Review Article | Published:

Concepts in the design and engineering of single-molecule electronic devices


Over the past two decades, various techniques for fabricating nano-gapped electrodes have emerged, promoting rapid development in the field of single-molecule electronics, on both the experimental and theoretical sides. To investigate intrinsic quantum phenomena and achieve desired functionalities, it is important to fully understand the charge transport characteristics of single-molecule devices. In this Review, we present the principles that have been developed for fabricating reliable molecular junctions and tuning their intrinsic properties from an engineering perspective. Through holistic consideration of the device structure, we divide single-molecule junctions into three intercorrelated components: the electrode, the contact (spacer–linker) interface and the molecular backbone or functional centre. We systematically discuss the selection of the electrode material and the design of the molecular components from the point of view of the materials, the interface and molecular engineering. The influence of the properties of these elements on the molecule–electrode interface coupling and on the relative energy gap between the Fermi level of the electrode and the orbital energy levels of the molecule, which directly influence the charge transport behaviour of single-molecule devices, is also a focus of our analysis. On the basis of these considerations, we examine various functionalities demonstrated in molecular junctions through molecular design and engineering.

Key points

  • Single-molecule electronics has become a burgeoning subfield of nanoscience and has begun to develop beyond the basic description of carrier transport, expanding in different research directions.

  • A single-molecule junction can be divided into three intercorrelated components: the electrode, the contact interface and the molecular backbone or functional centre.

  • Both the mechanical stability and electronic coupling of the molecule–electrode interface increase with the binding energy of the electrode–anchoring moiety interaction. A compromise between these factors can be achieved by inserting suitable spacers between the molecular kernel and anchoring groups.

  • To select suitable electrode materials, chemical inertness to air, good processability, suitable work function and good compatibility with molecules should be taken into consideration.

  • The structures of molecular bridges can be tuned by the molecular length, the geometry of the main chains, the responsivity of the functional centres and the types of side groups, offering opportunities to probe intrinsic physical properties and realize various functionalities.

  • Challenges in the field of single-molecule electronics include improving device-to-device uniformity, stability, integration capability and accuracy of theoretical models.


The physical limitations of the miniaturization of Si-based electronic devices1,2 motivate a growing interest in single-molecule electronics, a field being focused on by scientists with expertise spanning chemistry, materials science, physics, electronics and engineering. The field dates back to 1974, when Ratner and Aviram first proposed that a single molecule with an electron-donating group and an electron-withdrawing group at opposite ends could behave as a rectifier3. With developments in both experiments and theory, this topic has become a burgeoning subfield of nanoscience and has begun to develop beyond the basic description of carrier transport and to expand in different research directions, reflecting the interdisciplinarity of the field4,5,6,7,8,9.

Several approaches to building and studying molecular junctions have been developed4,10, including mechanically controllable break junctions (MCBJs)11,12,13, conductive atomic force microscopy14,15, electromigration16,17, scanning tunnelling microscopy (STM) break junctions18,19, on-wire lithography20, oxidative lithography21,22 or methods based on self-aligned templates23, thermally deposited metal films24, mercury drop electrodes25,26 or large-area molecular junctions27. These sophisticated techniques enable the probing of charge transport at the molecular level28,29,30,31. Because charge transport in single-molecule junctions is quantum mechanical in essence, molecular electronics also offers unique opportunities for the discovery of fundamental physical phenomena and for the direct observation of effects that are not accessible in bulk materials studied with traditional approaches. These effects include quantum interference (QI)32,33,34, the Coulomb blockade16 and the Kondo effect16,17. Moreover, devices with various remarkable functionalities — for example, single-molecule switches35,36,37,38, molecular thermoelectronic devices39,40, molecular diodes5,41, molecular spintronic devices42,43 and sensors with single-molecule sensitivity44,45,46,47 — have been realized within molecular junctions.

Over the past two decades, single-molecule electronic systems have matured into a platform that enables the study of fundamental properties of materials at the molecular or atomic level, in particular their charge and quantum transport characteristics, including the energy gap between the Fermi level of the electrode and the energy levels of the molecular orbitals, the electrode interface coupling and the intrinsic functions of molecules4,5,6,28,29,32,48,49,50,51,52,53. To realize precise control of these effects and to construct robust molecular junctions, it is helpful to start from a holistic analysis of the structure of single-molecule junctions, which consist of three intercorrelated components: the electrode, the contact interface and the molecular backbone or functional centre (Fig. 1). In this Review, we examine in detail these three components from an engineering perspective. This in-depth discussion is supplemented with a survey of important achievements in the application of single-molecule junctions to establish structure–function relationships. We conclude by outlining the crucial issues that will need to be solved to enable the successful development of next-generation, single-molecule optoelectronic devices for industrial applications.

Fig. 1: Structure of single-molecule junctions.

The schematic highlights the electrodes (yellow), contact interface (including the linker, dark grey, and the spacer, light grey) and functional molecular centre (blue). Various molecular junctions can be obtained by designing functional molecular bridges that respond to external stimuli, such as biological interactions, chemical stimuli, light, magnetic or electric fields and temperature.

Interface engineering

Interface coupling is one of the most critical factors influencing the properties of optoelectronic devices, such as solar cells and organic or polymer optoelectronic devices. In the study of single-molecule electronic devices, optimal interface engineering is also a focus of research (Box 1) and the most challenging issue that hampers the development of reliable molecular junctions. It was statistically proved that through-bond electrical contacts to octanedithiol monolayers are at least four orders of magnitude more conductive than physical contacts, emphasizing the key role of chemically bonded contacts in the measurement of intrinsic molecular properties14. The ideal interface between single molecules and the leads would be well defined, stable and highly conducting. Although notable efforts have been made towards this end, achieving the ideal molecule–electrode interface remains a formidable challenge.

Anchoring groups

Chemical synthesis offers many possibilities for optimizing the interface by tailoring the anchoring groups, which are the key to the mechanical stability of contacts and control the electronic coupling between molecules and electrodes. Molecular topologies have a direct effect on the transport mechanism and its efficiency. Indeed, the anchoring groups affect the charge injection barrier and the molecular orbitals, which are the pathways for electron tunnelling. The injection energy — the energy offset between the Fermi level of the electrode and the energy level of the molecular orbitals dominating the conductance (usually the highest occupied molecular orbital, HOMO, or the lowest unoccupied molecular orbital, LUMO) — is an important parameter to control.

Because studies of single-molecule charge transport are often based on nano-gapped gold electrodes, in this section, we focus our discussions on the interactions between anchoring groups and gold electrodes. According to the nature of the bonds between anchoring groups and Au atoms, anchoring groups can be divided into two kinds: covalent bonding groups and donor–acceptor bonding groups. Generally speaking, the interfacial electronic coupling achieved with covalent bonding is more efficient than that obtained with donor–acceptor bonding as a consequence of the higher bonding strength.

For covalent bonding, the thiol group (–SH) was the first and is currently the most widely employed anchoring group owing to its high binding energy and high probability of junction formation. However, multiple bonding scenarios are possible for Au–S covalent bonds and for the formation of Au–SH donor–acceptor bonds, resulting in a wide range of single-molecule conductance characteristics70,71,72,73,74,75. Another candidate for strong interface coupling is the covalent Au–C (sp) bond, which is established by either extrusion of a trimethyltin moiety or by post-deprotection of a trimethylsilyl moiety76,77,78,79. Compared with thiol anchoring groups, Au–C (sp) bonds lead to stronger hybridization of the molecular and metal states and to a more distinct energy shift of the peaks towards the Fermi energy, EF. This can be attributed to the hybridization of the molecular orbitals with the leads. As a result, molecular junctions with Au–C bonding exhibit improved mechanical stability and high electrical conductivity. Moreover, the conductance variations of Au–C bonds are substantially reduced owing to the more stable bonding configuration (top position).

Donor–acceptor bonding involves electron transfer from either π-donors or lone pair donors to Au atoms. Commonly used π-donors include fullerenes80,81 and other aromatic rings such as pyrene82,83. Most anchoring groups based on lone pair donors are general σ-donor ligands, similar to those found in coordination chemistry. Typical π-donor and lone pair donor anchoring groups are listed in Table 1. It has to be noted that donor–acceptor bonding results in a narrow conductance distribution in single-molecule junctions because of selective binding to undercoordinated adatoms on the surface of the gold electrode, which limits the Au-anchor geometry.

Table 1 Typical anchoring groups for donor–acceptor bonding

Au–N bonding has been widely used in single-molecule junctions. Among the three N-donor anchoring groups (Table 1), the stability is reported as pyridine > amine > nitrile, whereas the binding energy follows the sequence pyridine > nitrile > amine75. In addition to the lone pair donation from the N atoms, the delocalized π-character of pyridine and nitrile also contributes to the binding energy18,84,85. The low binding energy of amines can be attributed to the steric hindrance that is induced by the H atoms bonded to the N atom75,82,86. Because the Au–amine bond is not highly oriented, the formation of molecular junctions is unconstrained by the contact structure and is, in principle, straightforward71,74,87,88. The poor stability of the Au bond with nitrile is a result of its long and stiff structure, which prevents effective coupling with the molecular kernel. For nitrile, short biphenyl molecular junctions have been shown to be in two contact geometries with similar binding energies: one is a linear C–N–Au bond with a low-coordination-number Au atom; the other is attached to a ‘terrace-type’, high-coordination-number Au atom with an assumed C–N–Au angle of 160° (ref.89).

For more complex anchoring groups, the stability and conductivity both follow the sequence Au–NH2R < Au–SMeR < Au–PMe2R (refs70,72,90), which can be attributed to several factors. The σ-donation from lone pairs to metal atoms follows the sequence phosphines > amines > sulfides. Moreover, the π-backdonation from metal atoms to the ligands is more prominent in phosphines and sulfides than in amines. The enhanced availability of d states in sulfides and phosphine ligands affords a π-channel pathway for electron transport through SMe-bridged and PMe2-bridged molecular junctions. The additional π-channel can explain the conductance differences. The shape and size of lone pair orbitals also have an effect on the stability: larger and more diffused orbitals lead to higher tolerance of bonds to junction stretching. As a result, in a step-length histogram, the length steps of the SMe ligand are substantially longer than those of the NH2 ligand, although their bond strengths are roughly equal90.

Recently, molecular junctions using NCS and NCSe as anchoring groups have also been established, exploiting the excellent affinity of S and Se towards Au (refs76,79). These experiments indicated that replacing S with Se facilitates the orbital interactions between the Au electrode and the anchoring group and enhances the stability of the junction. Owing to its large molecule–metal interface and affinity to precious metals, fullerene has also been widely employed as an anchoring group. Indeed, fullerene moieties can induce a shift of the restrictive barriers for electron transfer from the molecule–metal contact interface to the molecular core, resulting in straightforward charge injection in the molecular kernel80,81.

Contact stability

To date, several strategies have been proposed to improve the contact stability and electronic coupling. One approach is to enhance the stability of electric contacts by interconnecting multipodal (bipodal or tripodal) anchoring groups at the end of the molecular kernel (Fig. 2a)91,92,93. Another strategy is to improve electron delocalization in the anchoring groups to increase the number of coupling conduction channels at the contact interface. The carbodithioate group (–CS2H)94,95 is a good candidate, as it has two S atoms at the end and a delocalized p-conjugated electronic structure, which can interact with Au leads through double-bonded S. Notably, the s and p orbitals of carbodithioate groups (CS2) can hybridize with the d orbitals of Au to generate an additional coupling pathway mediated by the p orbitals for electron transport. As a result, carbodithioate-bridged molecular junctions provide substantially improved conductivity in comparison with traditional thiol-linked molecular junctions, owing to the increased electronic coupling and reduced electron transport barrier. The dithiocarbamate group (–NCS2H)96 has also been employed to develop optimized electrical contacts for single-molecule junctions. As in the carbodithioate group, the s and p orbitals on the CS2 moiety of dithiocarbamate (NCS2) can hybridize with the d orbitals of Au atoms, whereas the non-bonding electron pair on the N atom can increase the delocalization and strength of Au–S antibonds, which are induced by the hybridization of thiolate frontier orbitals (S 3p orbitals) with the d and s orbitals of Au atoms. The electron-donating effect of the N lone pair can also reduce the injection gap between the Fermi level of the electrode and the HOMO. As a result, the delocalized electronic states of dithiocarbamate anchoring groups bonded to Au electrodes lead to a reduction in the contact resistance by two orders of magnitude as compared with thiolates on Au and to a stable molecular junction96.

Fig. 2: Strategies to control interface coupling.

a | Multipodal anchoring groups at the end of the molecular kernel can provide a sufficient number of stable electric contacts, improving the contact stability (chemical structures from refs91,92,93). b | Transition metal complexes with different numbers of methylene groups (zero or five) connecting a Co ion island with the anchoring groups (chemical structures from ref.16). c | Diarylethene derivatives designed by inserting methylene groups or electron-withdrawing groups to control interface coupling (chemical structures from refs35,60).


Overly strong interface coupling may trigger detrimental effects (Box 1), including the loss of intrinsic functionalities of single molecules and poor gating effects in three-terminal structural devices. By contrast, both the mechanical stability and electronic coupling increase with the binding energy between the electrode and the anchoring moiety, as mentioned above. Hence, a compromise between mechanical stability and electronic coupling is required to optimize the interface. This may be achieved by inserting methylene groups between the molecular kernel and anchoring groups as spacers. By effectively cutting off the π–electron delocalization, methylene groups can substantially decouple electronic interactions between the molecular functional centre and the electrodes while maintaining strong mechanical contacts. Nevertheless, few attempts have been made to control interfacial coupling by using this method.

The effect of spacers on quantum transport was investigated16 in three-terminal single-molecule transistors fabricated by electromigration. Specifically, two related molecules having a Co ion bonded to polypyridyl ligands in turn linked to insulating tethers (methylene groups) of different lengths were studied (Fig. 2b). The coupling strength between the ion and the electrodes could be effectively tuned by altering the number of methylene groups. Devices based on molecules with insulating tethers (weak interface coupling) showed a Coulomb blockade — a single-electron phenomenon occurring when the charging energy needed to move a single electron through a system exceeds the available energy, with potential applications in low-power and fast devices — owing to the presence of the Co ion island. By contrast, devices based on molecules without insulating tethers (intermediate interface coupling) presented a Kondo resonance, an increase in the conductance at low bias arising from the formation of a many-body singlet state caused by the scattering of conduction electrons in the metal electrodes on a local spin on the Co ion island. The interest in the Kondo effect lies in the fact that it is regarded as the simplest manifestation of the interaction of localized electrons with delocalized electrons, which is a question central to many problems in solid-state physics. Relatively weak coupling is also needed to conserve the QI effect, as was observed in a study of charge transport in benzene molecules bearing different numbers of methylenes at the meta positions of the anchoring groups97.

A series of single-molecule photoswitches based on diarylethene derivatives with different molecular structures (Fig. 2c) was proposed35,60, employing two strategies to effectively weaken the electronic coupling between the graphene electrodes and the diarylethene functional centre. One approach is to insert methylene groups between the diarylethene functional centre and the anchoring groups; the other consists in introducing electron-withdrawing groups in the diarylethene functional centre, for example, by substituting the hydrogenated cyclopentene in molecule I-1 by the fluorinated unit in molecules I-2 and I-3. The interface coupling strength Γ of graphene–molecule I-4 molecular junctions is much lower than those of the other three molecules (ΓI-4 < ΓI-3 < ΓI-2 < ΓI-1). Thus, only molecule I-4 achieves stable and reversible photoswitching, whereas the other three molecules exhibit unidirectional photoswitching (from open and non-conducting to closed and conducting diarylethene) as a consequence of the strong interface coupling that induces energy and electron transfer from the photoexcited molecule to the extended π–electron conjugated system in the graphene electrodes.

In addition to controlling the interface electronic coupling and mechanical stability of molecular junctions, anchoring groups also affect the energy levels of frontier molecular orbitals, which are determined by the electronegativity of the anchoring groups. Anchoring groups such as amine and thiol usually increase the energy of the frontier molecular orbitals owing to their electron-donating nature. Therefore, in SH-bound and NH2-bound molecular junctions, hole transport dominates transport, which happens mostly along the HOMO, the orbital closest in energy to the Fermi level of the electrode71,74. By contrast, charge transport in molecular wires bearing electron-withdrawing groups such as pyridine and nitrile is preferentially governed by the LUMO84,89,98. Further work will be needed to elucidate the intrinsic physical principles of interface coupling and the role of interface physics in determining the interfacial electronic structure and in tuning the charge transport characteristics.

Electrode materials

The electrode material is another key factor influencing the injection barrier and interface electronic coupling. To select suitable electrode materials, several factors must be taken into consideration: chemical inertness to air, good processability, suitable work function and good compatibility with organic or biological molecules. Currently, metal-based and carbon-based nanomaterials are widely employed as electrode materials.

Metal electrodes

Among metals, Au is commonly used in molecular junctions, because it meets most of the requirements above. Some other metals (such as Ag, Pt, Pd and Cu) have also been used as electrode materials for molecular junctions. Au, Ag, Pt, Pd and Cu are different from each other in terms of the work function, which in general results in different injection energies. Nevertheless, it has been reported that the injection barrier is independent of the work function and varies for conjugated and saturated systems99,100. The alignment of the molecular energy levels and the interface electronic coupling at the metal–organic contacts are also determined by subtle local interactions (rather than following simple rules), in which the density of states of the metal at the Fermi level has a key role.

Unlike Au, Ag and Cu, Pt and Pd are group 10 elements and thus have stronger d-orbital character and a larger local density of states near the Fermi level. By contrast, Au presents enhanced d states owing to the higher position of the d band edge (reflecting known relativistic effects). In general, the π-character of the bonds formed by Pt and Pd provides an alternative channel for electron transfer, resulting in superior conductance.

A study of isothiocyanate-terminated alkanes101 revealed that the conductance of Pd and Pt junctions was 2–3-fold higher than that of Au junctions, despite the fact that Au and Pd have almost identical work functions. The d band of metals has the right symmetry to couple with isothiocyanate π-orbitals near EF, and the relatively enhanced d character at EF of Pd and Pt increases the metal–molecule d–π interactions. The role of the d orbital was also demonstrated in oligoacene-based molecular junctions59. A strong hybridization between the Pt frontier orbitals and the dominant conducting molecular orbitals induces a smearing of the molecular features, yielding a large plateau of high transmission. By contrast, in Ag–oligoacene-based molecular junctions, the transmission is mostly controlled by the hybridization of the valence s-orbitals of Ag atoms with the molecular π-orbitals, and the junctions maintain the molecular level character owing to a small contribution from d orbitals around EF. Another study revealed that the value of 4,4ʹ-bipyridine conductance peaks is an order of magnitude lower when Ag electrodes are used rather than Au electrodes99. This difference can be attributed to reduced dπ* hybridization, as well as to a lower metal–molecule coupling caused by the weaker dyz-orbital character of the density of states of Ag at EF. Unlike Au and Ag, Cu forms a short atomic wire during the elongation of the junctions, leading to fewer adsorption sites available on the wire surface and to a relatively sharp peak in conductance histograms102,103,104.

Magnetic metals such as Ni (refs105,106,107) and Fe (ref.108) have also been used as electrodes in molecular junctions. Owing to spin-polarized orbital hybridization at the Fermi level of the electrode, interesting magnetic phenomena such as the gate-controlled Kondo effect109, which allows the precise control of the spin degree of freedom, providing information on the junction and holding promise for device applications, have been observed.

Carbon-based electrodes

Nevertheless, the applicability of metallic materials is limited by atomic mobility and incompatibility with single molecules in terms of size and work function. Carbon-based nanomaterials such as carbon nanotubes and graphene may be considered as alternative electrode materials for molecular electronics110. In particular, graphene is regarded as a viable candidate for the post-complementary metal oxide semiconductor (CMOS) electronics era, because high-quality monolayers of graphene can be grown at the wafer scale by using chemical vapour deposition. More importantly, graphene is atomically stiff and compatible with single molecules owing to its simple chemical composition and atomic bonding configuration, arising from its sp2-hybridized carbon atoms arranged in a honeycomb lattice. Patterning at the nanometre scale to create point contacts has been achieved in graphene by electron-beam lithography25 or electroburning111. Reliable room temperature molecular orbital gating has been demonstrated in graphene–molecule–graphene junctions111,112,113, which is impossible in metal–molecule–metal junctions owing to gate screening by the thick electrodes. These efforts have the advantage of bringing single-molecule electronics into a domain in which the junction dimensions are shrunk to two dimensions. Another merit of carbon-based electrodes is the contact flexibility, as the contact can be in either a covalent bonding or ππ stacking configuration. When molecules are covalently attached to graphene directly via anchoring groups, the electronic structure can be extended to the functional molecular kernel, making low-ohmic contacts possible25,112,114. Furthermore, an improved value of the contact resistance, of the order ~100 kΩ per 20 nm2, was obtained by exploiting a weak ππ stacking interaction111 that can be realized only with broad contact areas.

Increasing attention has been recently paid to other semiconductor materials that can be used as electrodes in single-molecule junctions. Among CMOS-compatible materials, Si (ref.115) and GaAs (refs116,117) are ideal candidates for the study of charge transport through single-molecule junctions. In comparison with metallic materials, the Fermi levels of these materials can be readily tuned, providing alternative approaches for the integration of novel functionalities into molecular junctions.

Molecular engineering

The structures of the molecular bridges at the core of molecular electronic devices are extremely diverse, offering the opportunity to probe the intrinsic relationships between the structure of a molecule and its physical properties (such as switching, thermal conductivity, rectification, spin transport and QI) and to install various functionalities through the precise design and engineering of the molecular structures. Parameters that can be tuned by flexible organic synthesis include the length of the molecules, the geometry of the main chains, the responsivity of functional centres and the type of side groups. In this section, the strategies developed for creating functional molecular devices are reviewed from the molecular engineering point of view, with the aim to distil some general principles for the rational design of single-molecule junctions.

Donor–acceptor asymmetry

Rectification is mainly induced by a structural asymmetry in molecular junctions or in the spatial profile of the electrostatic potential. For example, contact asymmetry is an efficient strategy for realizing the rectifying effect and was used to achieve rectification ratios in excess of 200 (ref.118). Another widely investigated approach is to use different electrode materials117,119,120,121,122 or design different anchoring groups123,124. From the molecular engineering point of view, rectification is still understood in the context of the Aviram–Ratner model, originally proposed in 1974 (ref.3), which is based on asymmetric donor–bridge–acceptor (DBA) molecules. The asymmetry here refers to the fact that electron transport from the acceptor to the donor molecule is favoured, because a transition from the excited D+BA to the ground D0BA0 is energetically favourable (Fig. 3a). Specifically, electron transport through a molecule involves three tunnelling steps, with the electron moving from the electrodes through the LUMO of the acceptor unit and the HOMO of the donor unit, which respond differently to the electric field between the electrodes upon application of a bias voltage. Under a forward bias, these two levels become closer in energy and align in the bias window (and vice versa). Notably, the bridge can be a σ-bond or a π-bond, or there can be no bond at all. The judicious design of the strongly electronegative and electropositive substituents, as well as the optimization of the interface coupling, is key to the improvement of the rectifying properties of molecular junctions. However, rectification has been achieved in only a few cases41,125,126,127,128 by using asymmetric molecular structures, owing to the challenging chemical synthesis (Fig. 3b). The performance of these systems is still far from that of bulk devices5.

Fig. 3: Single-molecule diodes.

a | Energy diagram of Aviram–Ratner rectification in a single-molecule device, showing that electrons can flow from the acceptor (A) to the donor (D) molecule more easily than from D to A because the barrier of a transition from the excited D+BA state to the ground D0BA0 state is lower. M represents the molecule in different states, and Γ represents the coupling between the different parts of the junction (chemical structures from refs41,126,127) b | Examples of asymmetric molecular structures that have been used to realize single-molecule diodes (chemical structures from ref.128). EF, Fermi energy; HOMO, highest occupied molecular orbital; LUMO, lowest unoccupied molecular orbital.

Molecular length

The molecular length is an important factor in the control of single-molecule conductance and has been extensively investigated in various molecular systems. First, it determines the distance that charges need to travel between the right and left electrode, thus affecting the single-molecule conductance. There are two distinct mechanisms of charge transport: coherent tunnelling independent of temperature and temperature-dependent incoherent hopping. Coherent tunnelling dominates in short molecules (usually <4 nm), whereas in an off-resonant situation, the molecular conductance decreases exponentially with the molecular length129,130 as G = G0 exp(–βL), where G is the molecular conductance, G0 is an effective constant conductance, L is the molecular length and β is the decay constant. Incoherent hopping is believed to be responsible for carrier transport through long molecular wires. In Marcus theory, which explains the rates of electron transfer131, the conductance obeys an Arrhenius relation, G exp(–EA/kBT), where EA is the hopping activation energy. Carrier hopping is characterized as a weak length-dependent process that influences the conductance, making it inversely proportional to the molecular length. The charge transport mechanism changes from tunnelling to hopping with increasing molecular length13. Here, we focus on single-molecule properties, instead of discussing molecular assemblies that are more complex to describe owing to intermolecular interactions. Because there have been only a few studies investigating the length-dependent hopping transport mechanism, we mainly discuss coherent tunnelling in different oligomeric backbones.

β-Quantitatively describes the ability of different oligomeric kernels to transport charge carriers and is mainly determined by the degree of conjugation between repeated units. β-Can also be affected by anchoring groups132,133, spacers134 and by the solvent environment135, most likely because of variations in the alignment of the Fermi level of the electrode within the HOMO–LUMO gap of the molecule and of charge transfer at the molecule–electrode interface. The mediation of long-range charge transport by the molecule degrades as the β-value increases. Indeed, the β-values of π-conjugated molecules are typically lower than those of aliphatic σ-bond molecules. π-Conjugated molecules can also function as highly conductive wires by virtue of the delocalization of the molecular orbitals and the small energy gap between the HOMO and LUMO. Typical β-values for different oligomeric materials are summarized in Table 2. Owing to the lack of delocalized charges, the β-value of alkanes is the highest (~0.94 Å–1)136. Despite the similar σ-bond structure in alkanes, silanes and germanes, the β-value decreases as the number of atoms increases. These conductivity trends arise from delocalization in the Si–Si and Ge–Ge σ-bonds — the same delocalization that makes Si and Ge excellent bulk semiconducting materials52.

Table 2 Conductance is dominated by coherent-tunnelling mechanisms

π-Conjugated molecular backbones tend to have lower β-values owing to effective charge delocalization. For alkenes137 and alkynes73, the spatial distribution of π-electron clouds is in the plane of the molecular backbone owing to the unique conformation of the backbone, and this results in more effective conjugation. Hence, alkenes and alkynes are better at mediating long-range charge transport than p-phenylenes138,139. In the quest to realize a larger degree of electron delocalization, several strategies have been proposed: using more electron-rich structures, such as thiophenes140,141,142 and metalloporphyrins143,144; locking the conformation of repeated units in the same plane to maximize the degree of conjugation146,147, as in cyclopentadifluorenes; and inserting alkynyl linkers between the repeated units to promote electronic conjugation along the oligomer, as in metalloporphyrins144,145,146.

Additionally, in conjugated oligomeric molecules, the HOMO–LUMO gap decreases as the molecular length increases, altering the injection energy. Length-dependent thermoelectricity has been observed in several oligomeric backbones138,140, but there is not such a clear trend for length-dependent conductance. This deficiency may be attributed to the fact that thermoelectricity depends on the characteristics of the molecular orbital that dominates conductance, as well as on the injection energy.

Switchable molecules

By virtue of their potential as building blocks for single-molecule electronics and ultrahigh-density storage devices, functional molecules with bistable or multistable states have been widely studied. Two kinds of conductance switching phenomenon have been observed in single-molecule electronics: stochastic and controllable switching. Stochastic switching results from changes in the molecular states induced by an external electric field or intrinsic vibration effects (often related to temperature)4,36. Here, we focus the discussion on molecular structures with an intrinsic and controllable switching function that promises to advance single-molecule switches towards practical applications. Switches based on three mechanisms have been reported: conformation-dependent switches, electrochemically induced switches and spintronics-triggered switches.

Conformational switches

For conformation-dependent switches, in principle, any molecular species that can isomerize in response to an external stimulus (usually light or the presence of ions) can serve as the core functional centre. The mechanical and conformational stability must be considered, as well as the fatigue resistance. Light stimulation is a commonly used approach to controlling molecular switches and can be integrated into solid-state electronic devices. Photochromic diarylethene derivatives are regarded as ideal candidates for light-driven molecular switches. Upon exposure to light, diarylethene derivatives can reversibly transform between two distinct states with open and closed conformations, a transformation accompanied by substantial changes in the molecular energy levels and electron delocalization but negligible changes in the molecular length. Moreover, diarylethene derivatives (Fig. 2c) have superior thermal stability and fatigue resistance148,149,150. However, the photophysical properties of individual diarylethenes are sensitive to the environment, and the electrode–molecule contact interface needs to be optimized to attain suitable interaction couplings60,61,62,151,152. Following almost 20 years of efforts, this challenge has finally been overcome, enabling the realization of fully reversible and stable molecular photoswitches based on single diarylethene molecules with excellent levels of accuracy, stability and reproducibility35. Conductance switching photothermally triggered in situ between two isomers of dimethyldihydropyrene molecules was also demonstrated (ON/OFF ratio, that is, the ratio between the conductances of the two states, is ~104)153. Despite its poor fatigue resistance, this molecular structure displayed good mechanical stability (with minimal length change between the two isomers) and good electronic properties.

Electrochemical switches

Redox-active molecules are particularly interesting as switches, because they can be reduced or oxidized by applying an electrochemical gate potential, which permanently changes the number of electrons on the molecule, the energy levels of molecular orbitals and the degree of conjugation, resulting in a switch in conductance. Electrochemical studies of single-molecule conductance focused primarily on organic redox moieties154,155,156,157,158,159 and organometallic compounds160,161,162,163,164. A special group of electrochemical switches, which includes catenanes and rotaxanes, exhibit stereoisomerization, that is, the 3D orientation of atoms in the molecule can change. These switches are mechanically interlocked molecules containing two molecules ‘embracing’ each other. In general, an outer ring can reversibly migrate between two stations (with different electron-donating abilities) of an inner molecule, producing two different conductance states. This switching process is regarded as intermolecular stereoisomerization, because in the first approximation, only one molecule exhibits changes in its position relative to the second molecule. Using this type of molecule, a molecular-scale, 160-kb electronic memory was realized with 1011 bits per square centimetre165.

Electrochemical approaches stabilize charged species, thus facilitating the investigation of the conducting properties of unstable states, such as radicals166,167 and anti-aromatic ions168. These two kinds of molecules exhibit ON/OFF ratios of ~200 for the radical ion and ~70 for the anti-aromatic ion, whereas oxidized/reduced structures exhibit ON/OFF ratios ≤10. Radical-based and anti-aromatic-based switches are similar in that the big change in the electronic structures occurs after oxidation, as seen in transmission spectroscopy data. This contributes greatly to their high ON/OFF ratios. Despite the absence of general principles guiding the design of electrochemically triggered switches with high ON/OFF ratios, these studies did provide new insight, motivating further work in this area.

Spintronic switches

Spintronics can also be used to achieve switching43,169,170,171. Different nuclear spin states should lead to different conductance states and could thus be used to encode information or induce switching. The most commonly used molecules in spin-based switches can be divided into two classes: spin-crossover compounds and valence-conversional molecules. Both molecule types have long magnetization relaxation times, and their electronic structures can change owing to charge rearrangement or atomic relaxation, leading to different states that are electrically readable. Bias-dependent switching was reported172 in molecular junctions with a spin-crossover coordination compound as the functional centre (Fig. 4a). Molecular junctions based on [FeII(tpy)2] complexes were fabricated using the mechanically controllable break junction technique. The FeII ion changes from a low-spin to a high-spin state at a threshold voltage owing to the distortion of the coordination sphere under a high electric field, resulting in bistability in the current–voltage curves.

Fig. 4: Typical spin-based switches.

a | Schematic representation of a spin-based switch with different Fe spin states. Under a small voltage, the FeII complex sandwiched between the two electrodes is in a low-spin state. When an electric field is applied, the coordination sphere of the FeII complex is distorted owing to the alignment of the push–pull system, and the system is in a high-spin state. b | Spin and charge states of a molecular junction in the presence of the electric field induced by the applied bias voltage. c | Schematic illustration of a spin-based transistor based on a single Tb3+ ion sandwiched between two phthalocyanine ligands in a Tb–Pc2 molecular magnet, in which the nuclear spin states of Tb3+ (coloured circles) can be manipulated with an electric field pulse (red). e, doubly degenerate; g, symmetric with respect to inversion centre; I, current; t, triply degenerate. Panel a is adapted with permission from ref.172, Wiley-VCH. Panel b is adapted from ref.173, Springer Nature Limited. Panel c is adapted with permission from ref.170, AAAS.

Valence-conversional molecules change their valence states as a function of the conductance state or of an applied magnetic field. Voltage-induced conductance switching was demonstrated173 in single-molecule, two-terminal break junctions based on a Mo-containing compound, yielding high-to-low current ratios exceeding 1,000 at a bias voltage of less than 1.0 V. This behaviour was attributed to the oxidation of and/or reduction in the Mo ion, mediated by a weakly coupled, localized molecular orbital with a spin-polarized ground state (Fig. 4b). Although the technologically relevant parameters still have to be determined in real device geometries, these efforts demonstrate the potential of these systems.

Reversible conductance switching was observed170 also for a Tb3+ ion sandwiched between two phthalocyanine (Pc) ligands (Fig. 4c). In this study, a three-terminal nuclear spin qubit transistor fabricated via electromigration and consisting of a Tb–Pc2 single-molecule magnet was used for electrical transport measurements. By sweeping the magnetic field at constant source–drain and gate biases, the electron spin changed between the |↑〉 and |↓〉 states, resulting in a conductance jump. Another reversible switch was realized171 that was based on Ho atoms supported on MgO, with an Fe atom next to the Ho to increase the magnetic field felt by Ho. These studies provide a universal route towards the electrical control of nuclear-spin-based devices by using the hyperfine Stark effect as a magnetic field transducer at the atomic level.

Switches based on quantum interference

Molecular electronic systems exhibit QI (Fig. 5)32,33,34,174,175,176,177,178,179,180,181,182,183,184,185. In molecular junctions, the propagation distance of electrons through the devices is comparable to the phase coherent length of the electron wave. Therefore, QI occurs in molecules with quasi-degenerate states (usually two), which are exactly the conducting channels. When partial electron waves propagating through the quasi-degenerate states interfere with each other destructively, the conductance is suppressed; when they interfere constructively, the conductance is enhanced. The phenomenon of constructive QI was observed177 in a double-backbone junction, which had a conductance larger than that of two single-backbone junctions measured in parallel. One signature of destructive QI in single-molecule electrical circuits is a sharp dip in theoretical transmission spectroscopy plots or in experimental differential conductance plots.

Fig. 5: Switches based on destructive quantum interference.

a | Two anthraquinone-based molecular structures used for realizing switches based on quantum interference (QI). b | Chemical structures of an oligomer with a meta-phenylene ethynylene skeleton (m-OPE) and of its derivatives obtained by intercalating a N atom in the middle benzene ring at different positions (M1, M2 and M3). c | Chemical structures of a parent compound para-OPE (p-OPE) and its daughter molecule (P) obtained with N substitution. Chemical structures in panels ac are from refs159,190. d | Corresponding energy (E)-dependent electron transmission coefficients, showing the destructive QI effect obtained when the N atom is in a meta position (M1). AQ, anthraquinone. Panel d is adapted from ref.191, CC-BY-4.0.

If a destructive QI transmission peak is close to the Fermi level of an electrode, the conductance can be extremely low. This behaviour is attractive because the destructive QI pathway — if it can be switched in a controllable manner — might serve as an ideal OFF state in devices with large ON/OFF ratios. Many theoretical proposals have been put forward for this kind of electrical device, suggesting the application of a gate voltage to regulate the anti-resonance position and/or switch the charge transport pathway between non-QI and destructive QI channels186,187,188,189. However, very few experiments have been performed to verify this prediction. QI switches have been constructed159,190 on the basis of the electrochemically triggered switching between cross-conjugated anthraquinone (destructive QI) and linearly conjugated hydroanthraquinone (no QI) (Fig. 5a). The ON/OFF ratio exceeded 10. The influence of heteroatom substitutions on QI in single-molecule devices was also investigated191. The conductance changes were induced by modifying a parent oligomer with a meta-phenylene ethynylene skeleton (m-OPE) by intercalating one N atom into the m-OPE backbone to obtain a daughter compound (Fig. 5b). When the N atom was inserted in a meta position relative to both acetylene linkers (M1), the daughter’s conductance was similar to that of the parent. When the N atom was in a para position relative to one acetylene linker and an ortho position relative to the other (M2), destructive QI was decreased, and the daughter’s conductance was substantially increased (Fig. 5d). When the N atom was in the para position relative to both acetylene linkers (M3), the conductance was between those of M1 and M2. By contrast, if the starting structure was connected in a para geometry (Fig. 5c), the conductance remained unchanged following N substitution (Fig. 5d). These observations are consistent with theoretically calculated transmission spectroscopy results.

Effect of substituents

Any small variation, electronic or geometric, of the molecular structure in the charge transport pathway can deeply influence the electrical conductance of single molecules. Moreover, changing the atoms or groups at the side-group position, which do not have continuous σ-bonds with the molecular junction, is an effective method to tune the electronic or geometric properties of the molecular backbone and the conductance behaviour. For instance, in the study of 1,4-diaminobenzene-based molecular wires, different substituents were incorporated at the 2-position, 3-position, 5-position and 6-position192, in which electron-donating groups (such as –OMe and –Me) and electron-withdrawing groups (such as –Br, –CF3, –F and –Cl) made positive and negative contributions to the molecular conductance, respectively. These opposite behaviours originate from the nature of HOMO-dominated charge transport of the amine anchors: substituents that donate electrons to the benzene unit elevate the HOMO energy towards the EF of Au, whereas substituents that withdraw electrons from the benzene unit stabilize the molecule and decrease the HOMO energy, moving it away from EF. These observations can be explained in terms of the energy offset between the conducting molecular orbital that is hybridized with metal electrodes and EF, in the same way that the energy difference between the ground state and the transition state determines chemical reaction rates.

Edge-on chemical modification

An interesting gating effect obtained through edge-on chemical modification in molecular wires (Fig. 6a) was demonstrated193 by using a pyridinoparacyclophane (PC) moiety with different substituent groups at the para–position of the pyridyl ring, ranging from strongly electron-withdrawing groups to strongly electron-donating groups. The conductance decreases when the substituent changes from a strong donor (N(CH3)2) to a strong acceptor (NO2; Fig. 6b,c). If the compound contains no nitro groups, the charge density on the N atom of the pyridine ring is directly affected by the electronegativity of the substituents. Electron-donating groups increase the negativity of the pyridine ring (and thus of the N atom), resulting in increased conductance by facilitating the hole current through the molecule. If the substituent is changed from an electron donor to an electron acceptor, the charge tunnelling barrier of compounds containing no nitro groups increases (Fig. 6b). For Cl, H, OCH3 and N(CH3)2 molecules, the HOMO is the dominant molecular orbital, whereas charge transport in nitro compounds occurs through the LUMO orbital, which is exclusively confined in the pyridine group. In this case, charges have to tunnel through the nitropyridine group, degrading the conductance. Regardless of the nature of the substituents, the molecules show similar conductance after protonation by trifluoroacetic acid (Fig. 6c)194. The effect of protonation is the same as that of the nitro groups: charges tunnel through the LUMO, which suppresses the conductance. In addition, protonation alters the symmetry of the molecular structure, and thus the interfacial potential decreases. In a similar way, the charge transport capabilities can be substantially tuned195,196 by incorporating a phosphonium group into metalla-aromatics or protonating azulene derivatives.

Fig. 6: Use of substituents to tune the conductance in single-molecule junctions.

a | Chemical structures of cyclophanes with different side groups, and the corresponding protonated forms (chemical structures from ref.193). b | Effect of substituent groups on the energy gaps between the dominant orbital (lowest unoccupied molecular orbital, LUMO, or highest occupied molecular orbital, HOMO) and the Fermi energy (EF). c | Difference between the conductances of the molecules with and without protonation in the cyclophane wires. d | Chemical structures of 4,4’-bipyridines with different side groups used to control their conductance (chemical structures from ref.197). e | Piezo-controlled conductance characteristics of II-3 and II-5 show larger conductance in II-5 owing to the interaction between the electrodes and the π-systems of the phenyl side groups. The 2D maps with piezo signals superimposed as grey lines show two distinctive conductance states for II-5 but not for II-3. G0, effective constant conductance. Panel b is reproduced with permission from refs193, ACS. Panel c is adapted with permission from ref.194, RSC. Panel e is adapted with permission from ref.197, Wiley-VCH.

Side-group chemistry

Side-group chemistry has also been used197 to control the conductance behaviour of molecular junctions based on 4,4ʹ-bipyridine. The introduction of bulky alkyl side groups in the phosphoryl-bridged compounds (Fig. 6d) effectively hinders the mechanically triggered conductance switching. The switching behaviour can be reinstated by substituting the bulky alkyl with a phenyl. In addition, bridging the two pyridine rings with Si-based groups can enhance the switching ratio. In relaxed junctions, the molecule is positioned parallel to the electrode axis, and carrier transport is mainly controlled by the LUMO, with a sharp resonance near EF. Upon junction compression, the molecule leans against the junction to form a geometric structure in which the pyridyl ring co-facially lies down on the electrode. In the bare bipyridine molecular junction, the compressed structure leads to strong interface coupling and high conductance. However, only a small difference in transmission between the relaxed and compressed junctions was observed in molecules II-2 and II-3: a bulky side group induces Au–N stretching, which reduces the electronic coupling with the electrode. As for molecules II-4 and II-5, although the binding geometric structure at the co-facial end is the same as in molecules II-2 and II-3, strong interactions between the electrodes and the π-systems of the phenyl side groups enhance the coupling, as well as the conductivity (Fig. 6e).

These results prove that it is possible to modulate in situ electronic structure (and thus the conductance) of single-molecule junctions by external stimuli, in this case, the rearrangement of the molecular electronic structures caused by either intermolecular interaction or chemical reactivity198. Because the substituent groups are affected in a limited way by interface coupling and their structural or electronic alterations result in minor changes in charge transport in the molecular backbone, the design of more controllable groups in the substituent position will provide more opportunities for the construction of stable molecular devices with specific physical properties. One key consideration to realize high-quality optoelectronic devices and switches is that the different states of the functional groups should have distinct electronic effects on the backbone. Because the substituent groups are not directly involved in charge transport, this strategy provides an ideal way to investigate the intrinsic effect of external stimuli (for example, the electric field between the electrodes) on the physical behaviour of the molecules without the interference from tunnelling currents. This might also lead to the direct observation of physical phenomena that are not accessible by conventional approaches. More importantly, these behaviours might enable a single-molecule realization of label-free, real-time electrical measurements of fast interaction dynamics with single-event sensitivity45,47,199,200,201,202.

Chemical reactions studied by single-molecule junctions

The use of single-molecule junctions to study step-by-step chemical reactions and interactions at the single-event level in a dynamic manner was recently demonstrated203,204,205,206,207,208. For instance, STM-based break junctions enabled the observation of the Diels–Alder reaction between a furan diene and dienophile initiated by an external electrical field204 (Fig. 7a); the researchers tried to electrostatically stabilize the resonance structure of the transition state using the downward electric field orientation at the negative bias. The photothermal reaction process of a photochromic dihydroazulene–vinylheptafulvene system was studied207 with MCBJs, revealing that the junction environment substantially influences the chemical process. Single-molecule junctions based on graphene51 were exploited to improve the stability of the device and duration of the measurement. A functional molecular bridge was covalently integrated with an electron-rich crown ether into graphene nanoelectrodes, enabling direct probing of the physical pseudorotaxane formation and deformation processes when a dicationic guest interacts with the crown ether with microsecond resolution (Fig. 7b)203. This technique can quantify the binding and unbinding rate constants and the activation energies for host–guest interactions (Fig. 7c).

Fig. 7: Single-molecule dynamic detection of intermolecular reactions or interactions.

a | Schematic representation of a Diels–Alder (D–A) reaction under the external electric field of a scanning tunnelling microscopy (STM)-based junction. The diene and dienophile were attached to the STM tip and to the flat gold surface through thiol groups. b | Schematic representation of the pseudorotaxane formation (right panel) and deformation (left panel) processes that occur when a dicationic guest interacts with the crown ether. c | Current–time curve of a pseudorotaxane-based device in a Me2SO solution containing 1 mM methyl viologen (MV)·2PF6 (293 K) with the corresponding idealized fit obtained from the segmental k-means method based on hidden Markov model analysis. The low and high conductance states were attributed to the deformation and formation states, respectively. The source–drain bias is 100 mV, and the gate bias is 0 mV. d | Schematic representation of a single-molecule junction based on a quadrupolar hydrogen-bonded system and current–time curves for a device in diphenyl ether at 323 K. e | Schematic diagram of each transformation process (left panels) with the low-lying energy (E) structures (middle panels) and corresponding transmission spectra at zero bias voltage (right panels). A, ammeter; EF, Fermi energy; T, temperature; V, voltage. Panel a is adapted from ref.204, Springer Nature Limited. Panels b and c are reproduced with permission from ref.203, AAAS. Panels d and e are adapted from ref.206, CC-BY-4.0.

In addition to the characterization of host–guest interactions, this technique was extended to address hydrogen-bond assembly dynamics with single-bond resolution206. A quadrupolar hydrogen-bonding system was covalently immobilized into graphene point contacts to establish a stable supramolecule-assembled single-molecule junction (Fig. 7d). The dynamics of individual hydrogen bonds in different solvents at different temperatures were studied in combination with density functional theory. In diphenyl ether, different current spikes and multiple levels of current signals were observed at 323 K (Fig. 7d), and the spikes and plateaux were classified into four microstates according to their amplitudes. Theoretical calculations for both the energy and transmission spectra at a zero bias voltage suggest that each current stage can be attributed to a different configuration. The transformation process was understood as follows (Fig. 7e): from the initial state (state 3), a 1,2,2ʹ,1ʹ lactam form, the hydrogen atom on N2ʹ is reversibly transferred to N3, forming a dissymmetric tautomer, the 1,2,3,1ʹ lactam form, with low conductivity (state 1); or through lactam–lactim tautomerism, the 1,2,2ʹ,1ʹ lactam form is converted into a 1,2,2ʹ,1ʹ lactim form that constitutes the intermediate conducting state of state 2. State 4 shows spike-like, high-frequency features. This probably results from the stabilizing effects of diphenyl ether molecules. Therefore, the observed multimodal distribution mainly results from stochastic rearrangements of the hydrogen-bond structure through either intermolecular proton transfer or lactam–lactim tautomerism. This work demonstrates an approach for probing weak bond interaction dynamics at the single-event level.

Beyond supramolecular chemistry, single-molecule electrical detection has potential for revealing temporal and reaction trajectories of individual intermediates in elementary reactions. To this end, a single diarylethene molecule with three methylene groups on each side was designed and synthesized, with the aim of decreasing the strong molecule–electrode coupling35. When covalently sandwiched between graphene electrodes (Fig. 8a), this molecule showed reversible linkage and breakage of a single σ-bond in the diarylethene centre driven by UV and visible light irradiation, thus leading to reversible and stable conductance photoswitching at room temperature (Fig. 8b). However, the attempt to capture the intermediates produced during the process of σ-bond linkage and breakage failed because the reaction is too quick to follow. To this end, most recently, a molecular wire with a 9-fluorenone centre was designed and covalently connected to nano-gapped graphene electrodes to establish functional single-molecule junctions (Fig. 8c)205. In situ electrical measurements at the molecular level demonstrated notable and reproducible current fluctuations with obvious solvent dependence in a nucleophilic addition reaction between hydroxylamine and a carbonyl group (Fig. 8d). In combination with theoretical simulations (Fig. 8e), it was demonstrated that this observation can be attributed to the reversible reaction between the ketone sidearm and an intermediate (Fig. 8d), which happens in a few microseconds. Beyond reaction chemistry, such a nanocircuit-based architecture offers a new strategy for the label-free exploration of rapid single-molecule (bio)physics or for single-molecule detection with high temporal resolution.

Fig. 8: Single-molecule dynamic detection of chemical reactions.

a | Schematic representation of a graphene–diarylethene–graphene single-molecule junction emphasizing the addition of three methylene groups to the molecule and showing the photoswitching mechanism. b | Reversible linkage and breakage of a single σ-bond driven by UV and visible (vis) light irradiation leads to reversible and stable conductance photoswitching at room temperature. The source–drain bias is 100 mV, and the gate bias is 0 mV. c | Schematic representation of fluorenone-bridged single-molecule junctions that emphasize a nucleophilic addition reaction between hydroxylamine and a carbonyl group. d | In situ single-molecule current–time measurements (top panel) in a mixed solution (EtOH:H2O = 1:4) containing NH2OH (10 μmol l–1) and NaOH (10 μmol l–1) at 298 K. The source–drain bias is 300 mV and the gate bias is 0 mV. The corresponding current histogram is presented in the bottom panel, showing a bimodal distribution. e | Transmission spectra of the reactant and an intermediate. The red and blue dashed lines highlight the transmission peaks of the perturbed highest occupied molecular orbital (p-HOMO) and perturbed lowest unoccupied molecular orbital (p-LUMO) for both states, whose interactions occur in a few microseconds. Panels a and b are reproduced with permission from ref.35, AAAS. Panels c, d, e are reproduced with permission from ref.205, AAAS.

Conclusions and perspectives

In this Review, adopting an engineering point of view encompassing three aspects — electrode material, interface and molecular bridge — we have systematically discussed current principles for the development of robust single-molecule electronic devices and for the integration of molecular functionalities into molecular electronic devices. The choice of electrode materials, the control of molecule–electrode interface coupling and the design of functional molecular kernels, working together as an intercorrelated holistic system, play a key role in device performance and stability. Molecule–electrode interface coupling, the strength of which is mainly determined by the nature of the contact (physical contact, ππ stacking or covalent binding), is intimately related to the choice of both electrode materials and anchoring groups. Through the flexible design of molecular bridges (anchoring end group, spacer and functional backbone) and a suitable choice of electrode materials, the molecule–electrode interface can be optimized to precisely control the relative energy gap between the molecular orbital energy levels and the Fermi level of the electrodes, thus contributing to the device stability. This stability is particularly important because it enables testing of different molecular engineering options and makes it possible to carry out reproducible electrical measurements, not only for probing the fundamental properties of materials at the molecular scale but also for imparting newly designed or even unexpected functionalities (such as switching, rectification, thermoelectricity, QI, sensing and stereoelectronic effects) to electrical nanocircuits. Although molecular electronics is a fairly mature field, tremendous challenges still exist in both scientific research and industrial manufacture.

One of the most critical challenges is the device-to-device uniformity. Once the size of a single electronic device is scaled down to the atomic or molecular level, even variations at the atomic level may influence its conductance performances. Currently, neither metal nor carbon-based electrodes guarantee atomic control of the electrode geometry, resulting in variant configurations at the molecule–electrode contact interface. For metal leads, the bonding sites for anchoring groups vary from device to device. In addition, the size of metal electrodes is not at the molecular scale. Hence, it is possible that only one molecule links two electrodes, while many others are adsorbed on the electrode surface. This configuration has a notable effect on the charge transport in the molecular bridge; thus, statistical conductivity data acquired from STM-based and MCBJ-based break junctions reveal fluctuations in the device performance. This is detrimental, especially for the functionalization of single-molecule electrical circuits. For carbon-based electrodes, conductance is affected by the edge configuration and inhomogeneous conductance of single-walled carbon nanotubes, even though the edges of the nanotubes and of graphene electrodes are at the atomic scale. The formation of nano-gapped electrodes with atomic-level precision and high yield and the precise control of the contact configuration and molecular conformation within the gaps on the substrate surface are the key issues in the evolution of molecular electronics from laboratory-based research to industrial applications.

Stability is an essential requirement for practical applications of molecular electronics. In single-molecule electronic circuits, molecular junctions, especially those based on metal electrodes, show poor stability. To achieve resonant transport, several volts typically need to be applied to junctions of only a few nanometres, leading to non-equilibrated dynamics and strong coupling between the molecular orbitals and the electric field gradient across the junction. Under such high bias voltages, atoms at both metal and carbon-based electrodes are mobile and tend to diffuse owing to heating effects. Additionally, lone pair species (such as Au–S bonds) are generally used to immobilize the molecules between two metal electrodes, but these coordination bonds are easily oxidized or ruptured. A precise choice of the measurement conditions and the formation of covalent bonds at the electrode–molecule contact interface might be an efficient way to improve device stability.

Another formidable challenge for single-molecule electronics is the integration capability, which is critical for applications. However, it seems that little attention has been paid to this aspect. For STM-based junctions and MCBJs, integration would be difficult owing to the incompatibility with current CMOS-based technologies. Carbon-based molecular junctions are advantageous in this respect owing to their three-terminal device architecture. To date, all reported measurements have been performed in a laboratory environment. However, practical devices are far more complicated and exposed to various operating and interference effects. To achieve efficient integration, two key factors should be considered. The first is that despite the intrinsically tiny size of their core parts, the long leads and large pads needed for outer connection hinder full exploitation of the potential of molecular devices. The second is that rather than replacing the CMOS technology, molecular devices are likely to be complementary parts within CMOS-based circuits. Hence, molecular devices should be CMOS-compatible to achieve practical applications209,210.

From a theoretical standpoint, the field needs further development. For instance, intrinsic misalignment exists between discrete molecular energy levels and continuous Fermi levels of the electrodes, making it difficult to understand how the voltage drops through the junction. Therefore, theoretical models that can fully explain experimental phenomena at a quantitative level are urgently needed. Moreover, theories should instruct experimental design — of both molecular materials and device architecture — to realize new functionalities. In an ideal scenario, when a specific molecular function is desired, it could be easily realized thanks to a good knowledge of the properties of molecules and of the synthetic routes that would realize the target structure.

The ultimate goal of microelectronics miniaturization is to manipulate the building blocks of matter with atomic-level precision. Only small molecules can offer such accurate control at subnanometre length scales and with the possibility of reproducibly fabricating exactly the same building blocks. Single-molecule electronics might be the only choice for moving beyond Si-based microelectronics. Consequently, there is strong motivation for the development of practical single-molecule optoelectronic devices. Apart from their small dimensions, such devices would also offer brand new functions beyond those achievable with traditional solid-state electrical devices, enabling new applications. Another research area that will profit from a deep understanding of the fundamental properties of materials at the single-molecule level is that of analytical chemistry, whose final goal is single-molecule detection. New modes of characterization might set up a mainstream methodology that enables single-molecule electrical detection for the investigation of single-molecule and single-event dynamics in an interdisciplinary setting. Considering the nature of this interdisciplinary field, only truly strong collaboration among materials scientists, engineers, physicists, electronic engineers, chemists and biologists will advance this powerful technology and foster its rapid development towards applications. Indeed, we trust that single-molecule electronics has a bright future for integrating the organic molecular world with hard electronics.


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The authors thank M. Schott and Y. Feng for giving feedback on the manuscript. The authors acknowledge primary financial support from the National Key R&D Program of China (2017YFA0204901; X.G.), the National Natural Science Foundation of China (21727806; X.G.), the Natural Science Foundation of Beijing (Z181100004418003; X.G.), Northwestern University (J.F.S. and M.A.R.), the Israel–US Binational Science Foundation (A.N.), the German Research Foundation (DFG TH 820/11–1; A.N.), the US National Science Foundation (grant no. CHE1665291; A.N.) and the University of Pennsylvania (A.N.).

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Correspondence to J. Fraser Stoddart or Xuefeng Guo.

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