Introduction

Metamaterials are artificial media that exhibit unusual electromagnetic properties such as anomalous refraction1,2,3,4,5, invisible cloak6,7 and strong chirality8,9. Light–matter interaction can be dramatically intensified with the use of electromagnetic responses around the resonance of specifically designed meta-atoms (MAs). Most of the wave properties, such as amplitude10, phase11 and polarization states12, and even the direction of light13 can be manipulated by the use of metamaterials or metasurfaces. Furthermore, variability in light–matter interaction is manifested through the external application of electrical10,14, mechanical15, optical16,17 and thermal18 stimuli when they are hybridized with natural active media. However, application of persistent stimuli is still required to sustain the transformed metamaterial properties unless there are memory functionalities. In this aspect, memory metamaterials are unique because long-lasting modification of the effective properties is possible even with the application of impulsive stimuli. This may lead to additional saving of energy resources that may otherwise have been used in sustaining the transformed properties. Previous memory metamaterials were implemented with natural memory media, such as phase-change materials19,20,21,22,23,24,25, that show memory behaviour with respect to electrically or optically induced thermal stimuli. The memory metamaterials have shown the possibility for unique performances, such as dynamic resonance tuning, multi-level data storage and bi-directionality14,19,20,21,22,23,24,25. However, they require a thermally isolated environment to obtain a longer retention of transformed properties or a strong optical pump for phase-change.

Here, we demonstrate electrically programmable nonvolatile memory metadevices operating at room temperature that are made possible by the hybridization of graphene, a ferroelectric and MAs/meta-molecules. The doping level of graphene embedded in the metadevices exhibits hysteretic behaviour with respect to external gate voltage26 that, in turn, leads to the hysteretic response in the effective properties of metadevices. Hence, their amplitude, phase and polarization states of light could be stored to multi-states with an appropriate MA structure. All stored states were stably maintained over 105 s even in the absence of additional electrical stimuli, from which a retention time over 10 years can be anticipated at room temperature. Beyond the single electrical input memory function, the operational principle has been proven to be scalable to a multi-input system; for example, two-input logic-gate operations such as AND, OR and XOR (complementary NOR, NAND and XNOR, respectively) were implemented. Furthermore, it is shown that the same logic-gate metadevice can be reconfigured to operate as a two-bit digital-to-analogue convertor by a slight change in the operating condition.

Results

Graphene–ferroelectric nonvolatile memory metadevice

A schematic representation of the graphene–ferroelectric nonvolatile memory metadevice (GF-NMM) is depicted in Fig. 1a. An array of hexagonal MAs, single-layer graphene, a ferroelectric polymer (poly(vinylidene fluoride-co-trifluoroethylene) or P(VDF-TrFE)) and a terahertz transparent electrode (TTE) composed of periodical subwavelength-scale metallic strips are placed sequentially on a polyimide substrate (fabrication details are described in the Methods, Supplementary Fig. 1 and Supplementary Note 1). An array of the hexagonal metallic pattern exhibiting polarization-independent inductance–capacitance (LC) resonance was chosen as the MA structure to intensify light–matter interaction. A large-size single-layer graphene synthesized by chemical vapour deposition27 on a Cu foil is transferred onto the array of MAs on polyimide using a ferroelectric polymer as a mechanically supporting film28. Since the dipoles in the ferroelectric polymer, P(VDF-TrFE), consist of weakly electronegative hydrogen atoms and strongly electronegative fluorine atoms, the application of an external gate voltage (VG) over the coercive voltage (VC) aligns the dipoles in the ferroelectric. These aligned dipoles, as a result, induce polarization (P) at the surface of the ferroelectric and exert an electrostatic force consistently on the charge carriers in the graphene layer (Fig. 1b). The TTE was carefully designed to apply a uniform electric field to the ferroelectric and transmit broadband terahertz waves vertically incident on the TTE without much loss as in previous works29. Pulsed external gate voltage (VG,pulse(V)) lasting for 1 s was applied between the TTE and the graphene/MAs in the measurement.

Figure 1: Graphene–ferroelectric amplitude and phase memory metadevice.
figure 1

(a) Schematic representation of the graphene–ferroelectric memory metadevice composed of a THz transparent electrode (TTE) with periodical metallic lines (4 μm linewidth and 2 μm spaces between the lines), ferroelectric polymer layer (2.1 μm, represented by green), single-layer graphene, hexagonal MAs and polyimide (1 μm, represented by light red) as substrate. Polarization of the incident THz is perpendicular to the TTE lines. (b) Schematic representation of the principle of nonvolatile doping in inherently p-doped graphene by ferroelectric polarization (P). Positive external voltage induces +PR at the surface of a ferroelectric, resulting in hole depletion in graphene while negative external voltage changes P to −PR, thereby resulting in the accumulation of holes in graphene. (c) Measured (open circles) and simulated (solid lines) THz transmission spectra for external pulsed gating voltage (VG,pulse) lasting for 1 s. The red, blue and yellow lines and circles represent the results of application of VG,pulse(+200 V), VG,pulse(−200 V) and VG,pulse(−120 V), respectively. (d) Hysteresis in the measured transmission amplitude (TA) and the calculated Fermi level of graphene for VG,pulse within a range of +200 and −200 V at a specific frequency of 0.5 THz. and are the positive and negative coercive voltages, respectively. Arrow refers to the VG,pulse sweep direction. Logic states denoted as 00, 01, 10 and 11 correspond to the multi-level transmission amplitudes for the retention time measurement. Error bars indicate the variation of each measured logic state. (e) Timing diagram of the transmission amplitude (TA) measured at 0.5 THz for various VG,pulse values of −80, −105, −115 and −130 V. Counting from the highest transmission amplitude, data states were designated as 00, 01, 10 and 11. Before each VG,pulse was applied, VG,pulse(+200 V) was applied to reset the ferroelectric polarization to +PR. (f) Transmission amplitude (TA) retention time measured at 0.5 THz for 1 × 105 s and a histogram for each state.

Terahertz time domain spectroscopy (THz-TDS) was carried out to characterize the fabricated GF-NMM as shown in Fig. 1c. On applying VG,pulse(+200 V) P, corresponding to positive remanent polarization (+PR), depletes the same polar charges out of graphene; THz transmission spectra through the GF-NMM showed a resonance dip at 1.1 THz. With the subsequent application of VG,pulse(−200 V), P changes to negative remanent polarization (−PR); the resonance frequency then shifted to 0.8 THz and the bandwidth was observed to slightly broaden.

Figure 1d shows the measured transmission amplitude (TA) through the GF-NMM and the quantitatively estimated Fermi level (EF) of graphene in the GF-NMM as a function of VG,pulse. Experimentally observed hysteretic variation of the spectral features is attributed to the change in graphene doping level resulting from the reversal of ferroelectric P (Supplementary Figs 2,3 and Supplementary Discussion). It is worthwhile to note that gradual transmission change is observed near positive and negative VC and multi-state memory operation can be achieved by utilizing this gradual change near VC. To validate multi-state memory operation, a timing diagram of TA was recorded at 0.5 THz for various VG,pulse values of −80, −105, −115 and −130 V and plotted in Fig. 1e. From the highest TA, data states were designated as 00, 01, 10 and 11. Before addressing each state, VG,pulse(+200 V) was applied to reset ferroelectric polarization to +PR.

Reliable nonvolatile memory operation requires not only data separation but also long retention time. Figure 1f depicts the retention time for each stored TA state; the GF-NMM has been observed to retain state information for all the states for over 105 s (the standard variation for TA, σstate is in the range between 5.62 × 10−3 and 7.58 × 10−3). The extrapolated TA for all states do not cross each other for over 8.5 × 108 s (10 years), which confirms that the demonstrated GF-NMM has indisputable nonvolatility. An additional measurement on THz-TDS system stability revealed that the slight variation in the TA was mostly a result of the fluctuations of the femtosecond laser output that was used for the THz-wave generation (the fluctuation of our femtosecond laser, σlaser, was 4.43 × 10−3; Supplementary Fig. 4 and Supplementary Table 1). As the MA structure used in the measurement is of a resonant type, the phase tunability and nonvolatility were also measured. In the case of phase response, VG,pulse-dependent hysteretic behaviour and multi-state stable retention properties were found to be similar to the transmission amplitude response (Supplementary Fig. 5).

Doping concentration in graphene is more resistant to change with time when graphene–ferroelectric hybrid devices operate in the accumulation mode compared with the depletion mode, especially at the beginning of the retention measurement30. Because the graphene used in our experiments is inherently p-doped and the intrinsic doping concentration (6.17 × 1012 cm−2) is larger than the extrinsic doping concentration modulated by the ferroelectric polarization (6.08 × 1012 cm−2), our device operates exclusively in the p-doped regime (Supplementary Fig. 6 and Supplementary Note 2). Moreover, all multi-states were addressed by applying a negative VG,pulse for further accumulation mode, so that the time-dependent drift in the EF of graphene in the GF-NMM is negligible, and, therefore, stable operation is possible. Ferroelectric polarization switching depends on the magnitude and duration of VG,pulse. For an electric field of 1 MV cm−1 corresponding to VG,pulse(+200 V), previous studies have reported a polarization switching time of 1 ms (refs 31, 32). Approximately 10 times faster switching would be expected by a VG,pulse with a one and a half times greater amplitude32.

The principle of amplitude and phase memory operation can also be applied to light polarization memory with a chiral metamaterial (chiral GF-NMM), in which the plane of linearly polarized incident light is rotated as the light travels through. Recently, it was shown that with the integration of active materials into metamaterials, polarization switching and modulation can be dynamically controlled33. However, optical activity such as circular dichroism and polarization rotation in most metamaterials can so far only be tuned by continuous external optical stimuli. With the incorporation of graphene and a ferroelectric into the chiral metamaterials, the polarization states of light passing through a chiral GF-NMM can be stored by VG,pulse(V). Strongly coupled chiral meta-molecules (MM) (ref. 34) were employed in the fabrication of the chiral GF-NMM as shown in Fig. 2a. The rest of the chiral GF-NMM is identical with the amplitude and phase GF-NMM described above (Supplementary Fig. 7 and Supplementary Note 3).

Figure 2: Graphene–ferroelectric chiral memory metadevice.
figure 2

(a) Schematic representation of the graphene–ferroelectric chiral memory metadevice composed of THz transparent electrode (TTE), ferroelectric polymer layer (2.1 μm, represented by green), single-layer graphene, CDZM with a spacer of 2 μm and a polyimide (1 μm, represented by light red) as the substrate. Polarization of the incident THz is perpendicular to the TTE lines. (b) Polarization rotation angle (θ) through chiral memory metadevice after the application of an external pulsed gating voltage (VG,pulse) lasting for 1 s, and the difference (Δθ) between θ+200V and θ−200V. (c) Polarization rotation angle (θ) in the VG,pulse within a range of +200 and −200 V at 1.1 THz. Arrows refer to the VG,pulse sweep direction. CDZM, conjugated double Z meta-molecules.

Figure 2b shows the azimuthal polarization rotation angle (θ) for two distinct VG,pulse values. Here, θ is extracted from the phase difference between the two circular polarizations (see Methods). On applying VG,pulse(+200 V), θ+200V shows a maximum value of 15° at 1.0 THz, while θ−200V exhibits a maximum value of 14° at 0.9 THz. It can be seen from Fig. 2b that Δθ (=θ+200V to θ−200V) attains the maximum value of 8° at 1.1 THz. To trace the hysteretic behaviour in the polarization states more clearly, θ measurement was carried out at 1.1 THz and is plotted in Fig. 2c. Because of ferroelectricity, θ changes gradually near positive and negative VC. Multi-level polarization states can also be stored for over 105 s without much degradation as shown in the operation of three different polarization states (Supplementary Fig. 8).

Graphene–ferroelectric reconfigurable logic-gate metadevice

The underlying concept for the operation of GF-NMM can be extended to a multi-input system such as a reconfigurable logic-gates metadevice (graphene–ferroelectric reconfigurable logic-gate metadevice (GF-RLM)). For example, a two-input system can be implemented by encapsulating graphene within two controllable ferroelectric layers as shown in Fig. 3a (Supplementary Fig. 9 and Supplementary Note 4). Independent pulsed gate control (VG,pulse) of each ferroelectric layer and the resulting combination of polarizations offered by the individual ferroelectric layers can lead to an increase in the degree of freedom in the manipulation of carrier concentration in graphene (NG) when compared with the GF-NMM having a single ferroelectric layer. Corresponding to the combination of two electrical inputs (the top electrode (T) and the bottom electrode (B)), NG as well as the THz transmission through the two-input system is expected to give unique logic outputs. Figure 3b shows the combination of polarization values in the ferroelectric layers that correspond to four kinds of logic inputs, (0, 0), (0, 1), (1, 0) and (1, 1). Input logic states 1 and 0 are prepared by applying VG,pulse(+200 V) and VG,pulse(−200 V) to the corresponding ferroelectric layers, respectively. If graphene in GF-RLM is inherently p-doped, logic input (1, 1) depletes majority carriers (holes) and logic input (0, 0) accumulates holes in the graphene. In the two intermediate states, (0, 1) and (1, 0), the hole concentration in graphene will be set to the values that are between those corresponding to input states (0, 0) and (1, 1). The variation in NG results in a change in the transmission spectrum as shown schematically in Fig. 3c, in which the resonance frequency is red-shifted as NG increases29. With the appropriate frequency choice for data reading (fREAD), the logic output can be decoded by comparing with TREF1 for the AND (complementary NOR) operation or TREF2 for the OR (complementary NAND) operation. Furthermore, XOR (complementary XNOR) operation can also be realized by simply rearranging the electric connections Supplementary Figs 10,11). All the logic-gate operations are measured using THz-TDS and shown in Fig. 3d (Supplementary Fig. 12 and Supplementary Table 2).

Figure 3: Graphene–ferroelectric reconfigurable logic-gate metadevice.
figure 3

(a) Schematic representation of the graphene–ferroelectric reconfigurable logic-gate metadevice composed of a top THz transparent electrode (top; TTE, T), a ferroelectric polymer layer (2.1 μm, represented by green), a single-layer graphene, hexagonal MAs, a ferroelectric polymer layer (2.1 μm, represented by green), a bottom THz transparent electrode (bottom; TTE, B) and a polyimide layer (1 μm, represented by light red) as the substrate. Polarization of the incident THz is perpendicular to the two TTE lines. (b) Schematic representation of the four kinds of polarization alignments for input logic states. Red arrow implies an application of positive pulsed gating voltage for logic state 1 and blue arrow refers to the application of negative pulsed gating voltage for logic state 0. (c) Schematic representation of the transmission spectra for input logic states. For each input logic state, the relationship fR(0,0)<fR(0,1)=fR(1,0)<fR(1,1) is satisfied in the graphene–ferroelectric reconfigurable logic-gate metadevice because of p-doped graphene. A frequency of fREAD was designated for data reading and two reference transmission amplitudes, TREF1 and TREF2 were defined to execute AND (complementary NOR) and OR (complementary NAND) gate operations. For AND gate operation, the reference transmission amplitude is set to TREF1. For OR gate operation, the reference is TREF2. (d) Experimental transmission amplitude (TA) measured at 0.5 THz for the four types of logic inputs in the AND/OR gates, the XOR gate and the two-bit DAC.

In addition to the logic operations, the device can also be configured as a digital-to-analogue converter if the remanant polarization in each of the ferroelectric layers assumes a different value. If the two ferroelectric layers supply two different PR values, four kinds of NG levels corresponding to (+PR1, +PR2), (+PR1, −PR2), (−PR1, +PR2) and (−PR1, −PR2) are possible, which implies that fR(0,1) is different from fR(1,0) as shown in Fig. 3c. The effective method to control polarization switching was demonstrated in a prior work35, in which ferroelectric switching was controlled by setting the current limitation (IC, compliance current). By setting different compliance current for bottom and top TTE, four distinct levels of transmission amplitude were measured as shown in Fig. 3d (Supplementary Fig. 12). The combination of two digital inputs resulting in four levels of optical analogue states validates the two-bit digital-to-analogue convertor operation. Although the transmission loss and optoelectric conversion should be considered in the compact integration of diverse functional metadevices, the platform and the principle of operation provided here might be extended to a certain class of multi-input systems in principle.

Discussion

In this work, electrically programmable nonvolatile memory and reconfigurable logic-gate metadevices were demonstrated with the hybridization of graphene, a ferroelectric and MAs/molecules. These functional metadevices are the first demonstration of superior nonvolatility and logic-gate operation at room temperature, which offer new pathways for emerging optoelectronic applications. Nonvolatile memory function liberates active metadevices from immovable power supply units, leading to saving of energy resources. Reconfigurability presents a user-oriented general-purpose metadevice that can be configured through electrical programming. More complex functionality can be made possible by the compact integration of diverse functional metadevices and/or by the design changes of the demonstrated metadevices. Ultimately, high-end metasystems to perform advanced functionalities may be developed by grafting the concept of GF-NMM and GF-RLM onto the diverse architectures of graphene-based nonvolatile memory, as recently demonstrated in the field of electronic devices36.

Methods

Fabrication processes for the GF-NMM and GF-RLM

All metallic parts of the hexagonal MAs/molecules and the TTE were made of 100-nm thick Au with a 10 nm thick Cr layer for enhanced adhesive strength. Single-layer graphene was synthesized by chemical vapour deposition on a Cu foil (G/Cu). Poly(vinylidene fluoride-trifluoroethylene), P(VDF-TrFE), manufactured by MSI Sensors Inc. was chosen as the ferroelectric polymer.

For the nonvolatile memory metadevice, a polyimide (PI, PI-2610, HD MicroSystems) was spin-coated and cured on a Si wafer. An array of hexagonal MAs was deposited by a photolithography, thermal evaporation and lift-off process (MA/PI/Si). On a SiO2/Si wafer, a ferroelectric polymer (FP) was spin-coated, annealed at 130 °C for 1 h, and cooled down to room temperature slowly. A TTE was patterned by a photolithography, thermal evaporation of Cr/Au and lift-off process (TTE/FP/SiO2/Si). By etching the SiO2 with an HF aqueous solution, the TTE/FP was transferred onto graphene (G) on Cu foil. By etching the Cu foil with the Cu etchant APS-100, the TTE/FP/G was transferred onto the MA/PI/Si and thermally treated for adhesion. Finally, Si was detached mechanically. For the polarization state memory metadevice, MA/PI on Si was replaced with MM/PI, which was fabricated by stacking conjugated double Z patterns with a polyimide spacer of 2 μm.

For the reconfigurable logic-gate metadevice, an MA layer was deposited on G/Cu. An FP was spin-coated on the MA/G/Cu. In addition, a TTE as the top electrode was deposited on the FP/MA/G/Cu. By etching the Cu foil with a Cu etchant of APS-100, a TTE/FP/MA/G hybrid film was prepared. On a Si wafer sacrificial substrate, PI was spin-coated and TTE as the bottom electrode was deposited on PI/Si (TTE/PI/Si). An FP was spin-coated onto the TTE/PI/Si (FP/TTE/PI/Si). Reconfigurable logic-gate metadevice was fabricated by transferring the TTE/FP/MA/G onto the FP/TTE/PI/Si. Finally, Si was detached mechanically.

All metadevices were mounted on a punched printed circuit board for THz-TDS measurements.

THz-TDS system

To generate the terahertz signal, we used a low-temperature grown GaAs THz emitter (Tera-SED, Gigaoptics) illuminated by a femtosecond Ti:sapphire laser pulse train of wavelength 800 nm and 80 MHz repetition rate, respectively. An electro-optic sampling method was used to detect the transmitted terahertz signals in the time domain by using a (110) oriented ZnTe crystal of 1 mm thickness. The THz-TDS system has a usable bandwidth of 0.3–2.5 THz and a signal to noise ratio (S/N) of over 10,000:1.

Measurement of the chiral GF-NMM

The chiral GF-NMM was characterized using conventional THz-TDS. The metadevice was positioned between two wire-grid THz polarizers, that are mounted on motorized rotational stages with parallel or crossed configurations, to measure the co-polarized (T||) and cross-polarized (T) transmission coefficients. The sample was carefully aligned to assure the TTE of the metadevice remains parallel to the front polarizer. From the measured transmission coefficients, the right and left circularly polarized transmission coefficients can be obtained as T+=T||+iT and T=T||iT. The azimuthal rotation angle can be calculated by the phase retardation between two circularly polarized waves as .

Additional information

How to cite this article: Kim, W. Y. et al. Graphene-ferroelectric metadevices for nonvolatile memory and reconfigurable logic-gate operations. Nat. Commun. 7:10429 doi: 10.1038/ncomms10429 (2016).