Covalent organic frameworks enable the topological connection of organic chromophores into π lattices, making them attractive for creating light-emitting polymers that are predesignable for both the primary- and high-order structures. However, owing to linkages, covalent organic frameworks are either unstable or poor luminescent, leaving the practical synthesis of stable light-emitting frameworks challenging. Here, we report the designed synthesis of sp2 carbon-conjugated frameworks that combine stability with light-emitting activity. The C=C linkages topologically connect pyrene knots and arylyenevinylene linkers into two-dimensional all sp2 carbon lattices that are designed to be π conjugated along both the x and y directions and develop layer structures, creating exceptionally stable frameworks. The resulting frameworks are capable of tuning band gap and emission by the linkers, are highly luminescent under various conditions and can be exfoliated to produce brilliant nanosheets. These results suggest a platform based on sp2 carbon frameworks for designing robust photofunctional materials.
Covalent organic frameworks (COFs) are a class of crystalline porous polymer with predesignable lattice structures of organic building blocks1,2,3,4,5,6,7,8. COFs can be predesigned by using topological diagram that enables the development of various lattices based on the combination of building units with different geometries9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,25. A diversity of chromophores has been explored for the synthesis of photofunctional and semiconducting COFs of different space groups26,27,28,29,30,31,32,33,34,35,36,37,38,39,40. However, owing to the shortage of a suitable linkage that combines stability with luminescence, stable COFs are less luminescent and luminescent COFs are chemically unstable. For example, boronate and boroxine linkages can form luminescent COFs but they are unstable under protic conditions or upon exposure to air26,27,28,29,30,31,32,33,34,35,36,37,38,39,30, while imine linkages are most widely used for the preparation of relatively stable frameworks that however, are less or not luminescent14,31,32. Developing a linkage to design COFs that combine luminescence activity and stability remains challenging.
In this work, we developed a C=C linkage for the construction of two-dimensional (2D) sp2 carbon-conjugated frameworks (sp2c-COFs) that are designed to be π conjugated along both the x and y directions and develop eclipsed layer structures. The C=C polycondensations of tetraphenylpyrene knots and phenyl, biphenyl, and terphenyl linkers enable the designed synthesis of sp2c-COFs with different π lattice sizes. The resulting sp2 carbon frameworks are exceptionally stable under various conditions upon immersion in acid and base solutions or exposure to air over a long period. We observed that the linkers adopt propeller conformation to constitute twisted arylenevinylene backbones so that the transmission of π delocalization along the x and y directions can be controlled by the linker units, enabling the tune of both band gap and emission colors. We elucidated the structure-photofunction correlation by disclosing the structural parameters that control photochemical events. We highlighted that the resulting frameworks are highly luminescent under various conditions and can be exfoliated to produce light-emitting sp2 carbon nanosheets.
Among various topologies, we explored a tetragonal topology for designing the sp2 carbon frameworks since it enables π conjugation along both the x and y directions to transmit the π cloud overlap over the 2D skeleton41. Among various linkages for the synthesis of COFs, recently we have developed a C=C linkage for synthesizing sp2 carbon-conjugated frameworks42. The C=C linkage is different from the boronate, boroxine, imine, hydrozone, imide, and phenazine bonds since it allows for the formation of fully conjugated systems from all sp2 carbon. In this study, we successfully explored the C=C linkage for the designed synthesis of sp2 carbon-conjugated COFs and disclosed their stability and photofunctionality.
We selected the C2+C2 topology diagram for the construction of 2D tetragonal sp2 carbon frameworks. The C=C polycondensation of 1,3,6,8-tetrakis(4-formylphenyl)pyrene (TFPPy) as knots with 2,2’-(1,4-phenylene)diacetonitrile (PDAN), 2,2’-(biphenyl-4,4’-diyl)diacetonitrile (BPDAN), and 2,2’-([1,1’:4’,1”-terphenyl]-4,4”-diyl)diacetonitrile (TPDAN) as linkers topologically connected pyrene units at regular intervals of 1.9, 2.4, and 2.8 nm into sp2 carbon lattices and develop eclipsed layer frameworks of sp2c-COF, sp2c-COF-2, and sp2c-COF-3, respectively (Fig. 1). To achieve high crystallinity, we optimized the reaction conditions, including solvents, reaction temperatures, and catalysts (ESI). High quality sp2c-COF and sp2c-COF-2 crystallites were prepared in 84% and 82% isolated yields by condensation in 1,4-dioxane in the presence of KOH catalyst at 90 °C and 110 °C, respectively. The polycondensation of TFPPy and TPDAN in o-dichlorobenzene (o-DCB) in the presence of a methanol (MeOH) solution of tetrabutylammonium hydroxide (TBAH) as catalyst for 3 days at 120 °C produced sp2c-COF-3 in 88% isolated yield. The chemical structures of sp2c-COFs were unambiguously characterized by various analytical methods (Supplementary Figures 1–21). Fourier transform infrared spectroscopy (FT IR) revealed the formation of sp2 carbon-conjugated COFs by showing a newly appeared C≡N vibration band at 2220 cm–1 and a greatly decreased vibration band at 2720 cm–1 that was assigned to the C–H stretching vibration of the aldehyde units (Suppelementary Fig. 1). Field-emission scanning electron microscope revealed that these sp2 carbon COFs were similar in morphology to assume belt shapes (Supplementary Figure 2). High resolution transmission electron microscope (HR-TEM) image revealed the tetragonal and layer structure (Supplementary Figure 3). The FFT and line profiles further indicate the lattice structures that clearly show a pore size of 2 nm and an interlayer separation of 3.5 Å.
Stability of COFs
To evaluate their chemical stability, we immersed sp2c-COF, sp2c-COF-2, and sp2c-COF-3 for 1 week in various solvents, including tetrahydrofuran (THF), N,N’-dimethylformamide (DMF), MeOH, water, concentrated HCl (12 M) and aqueous NaOH (14 M) solutions (ESI). Notably, these sp2 carbon COFs retained their original powder X-ray diffraction (PXRD) profiles (Fig. 2a–c). From the residual weight percentages, they exhibited nearly no weight loss (<0.1 wt%) in water and organic solvents (Fig. 2d–f). Even under strong acid (12 M HCl) and base (14 M NaOH) conditions, the residual weight percentages were as high as 90 wt%. FT IR spectroscopy revealed that the chemical structures were preserved (Supplementary Figure 4).
Surprisingly, we observed that the sp2 carbon frameworks are stable to keep crystallinity and porosity upon long-term exposure to air at room temperature. For example, both sp2c-COF and sp2c-COF-2 upon exposure to air for 1 year retained their structures by showing nearly the same intensities and peak positions in the PXRD patterns (Fig. 3a, b). The sp2c-COF and sp2c-COF-2 samples can keep their porosity; after 1-year exposure to air they exhibited the Brunauer–Emmett–Teller (BET) surface areas as high as 581 and 302 m2 g–1, respectively (Fig. 3c, d, red curves), which are close to those (sp2c-COF; 613 m2 g–1, sp2c-COF-2; 322 m2 g–1) of the as-synthesized samples (Fig. 3c, d, black curves). Pore size distribution profiles revealed that the pore size did not change (Supplementary Figure 5a–d). FT IR spectra revealed that the chemical structures were retained (Supplementary Figure 6a–d).
Along this line, we further investigated luminescent properties of sp2c-COF and sp2c-COF-2 upon 1-year exposure to air. Surprisingly, the sample retained its luminescent wavelength (Fig. 3e, f), absolute fluorescence quantum yield (sp2c-COF, 14% for as-synthesized versus 12% after 1-year exposure to air; sp2c-COF-2, 10% for as-synthesized versus 9% after 1-year exposure to air) and lifetime (Supplementary Figures 7 and 8). To the best of our knowledge, the sp2 carbon-conjugated COFs are the most stable and luminescent ones among all the COFs reported to date26,27,28,29,30,31,32,33,34,35,36,37,38,39,40. As a control, we investigated an imine-linked pyrene COF with a similar structure to that of sp2c-COF (Supplementary Figure 9). However, the imine-linked pyrene COF upon 1-year exposure to air cannot retain its crystallinity; in this case nearly no clear PXRD pattern was observable.
The PXRD patterns revealed that sp2c-COF, sp2c-COF-2, and sp2c-COF-3 were highly crystalline polymers (Fig. 4a–c, red curves). The sp2c-COF exhibited the PXRD peaks at 3.6°, 5.2°, 5.9°, 7.3°, 11.2°, 14.2°, and 24.7°, which were assigned to the (110), (200), (210), (220), (240), (520), and (001) facets, respectively (Fig. 4a, red curve). For sp2c-COF-2, the PXRD peaks at 3.1°, 5.9°, 6.8°, and 23.8° were assignable to the (110), (210), (120), and (001) facets, respectively (Fig. 4a, red curve). In the case of sp2c-COF-3, the PXRD peaks were observed at 2.7°, 5.5°, 8.2°, 10.9°, and 23.5°, which were attributed to the (110), (220), (240), (440), and (001) facets, respectively (Fig. 4c, red curve). The Pawley refined PXRD patterns of sp2c-COF, sp2c-COF-2, and sp2c-COF-3 (Fig. 4a–c, blue curves) can reproduce their experimentally observed curves with a negligible difference (Fig. 4a–c, black curves). sp2c-COF has a C2/m space group with the cell unit parameters of a = 33.9309 Å, b = 34.8219 Å, c = 3.7676 Å, α = 90°, β = 106.6756°, and γ = 90° (Supplementary Tables 1 and 2). On the other hand, sp2c-COF-2 adopts a P1 space group with the cell unit parameters of a = 29.1468 Å, b = 28.6019 Å, c = 3.7293 Å, α = 89.7834°, β = 90.2665°, and γ = 89.0697 (Supplementary Tables 3 and 4), while sp2c-COF-3 possesses a C2/m space group with the cell unit parameters of a = 48.8867 Å, b = 45.8095 Å, c = 3.6802 Å, α = 90°, β = 103.0632°, and γ = 90° (Supplementary Tables 5 and 6).
Among various possible stacking modes, the AA stacking mode is the most stable form in energy. The AA stacking mode yielded the PXRD patterns (Fig. 4a–c, green curves) that were in an agreement with the experimentally observed profiles. The AB stacking models cannot reproduce the experimentally observed PXRD patterns (Supplementary Figure 10, purple curves). Consequently, the 2D polymers adopt a tetragon skeleton with interweaved sp2 carbon-conjugated backbones and stack to form one type of tetragonal channels with the theoretical pore sizes of 1.9, 2.4, and 2.7 nm, respectively (Fig. 4d–f). The presence of the (001) facets suggests that the structural ordering is extended to the third dimension perpendicular to the 2D sheets. Based on the (001) facets, the interlayer distance of sp2c-COF, sp2c-COF-2, and sp2c-COF-3 was evaluated to be 3.58, 3.74, and 3.79 Å, respectively. The increased interlayer separation of sp2c-COF-2 and sp2c-COF-3 compared to that of sp2c-COF originates from the twisted biphenyl and terphenyl linkers in the frameworks.
The sp2c-COF, sp2c-COF-2, and sp2c-COF-3 samples exhibited reversible nitrogen sorption isotherm curves (Supplementary Figure 11). The BET surface areas were evaluated to be as high as 613, 322, and 737 m2 g–1 for sp2c-COF, sp2c-COF-2, and sp2c-COF-3, respectively. The sp2c-COF, sp2c-COF-2, and sp2c-COF-3 samples have pore volumes of 0.30, 0.14, and 0.32 cm3 g–1, respectively. The pore size distribution profiles calculated using nonlinear density functional theory (NLDFT) revealed that sp2c-COF, sp2c-COF-2, and sp2c-COF-3 have one type of pores. sp2c-COF is a microporous material with the pore size of 1.90 nm, while sp2c-COF-2 and sp2c-COF-3 are mesoporous polymers with the pore size of 2.38 and 2.69 nm, respectively.
Electronic absorption and π conjugation
The solid sample of sp2c-COF exhibited an electronic absorption band at 498 nm (Fig. 5a, black curve, Table 1). By contrast, the model compound exhibited an absorption band at 445 nm (Supplementary Figure 12, black curve). This 53-nm redshift in the electronic absorption band reflects extended π-conjugation over the 2D sp2 carbon framework. Since the imine-linked (C=N) pyrene COF has an absorption band at 477 nm42, the 21-nm redshift indicates that the C=C linkage is more efficient than the C=N bond in transmitting π conjugation over the 2D skeleton.
Notably, integration of the biphenyl and terphenyl units as linkers into the 2D sp2 carbon skeleton enables the tuning of electronic absorption bands. For example, sp2c-COF-2 exhibited an absorption band at 475 nm, which is 17-nm blueshifted from that of sp2c-COF (Fig. 5b, black curve, Table 1). More remarkably, sp2c-COF-3 displayed an absorption maximum at 462 nm that is 36-nm redshifted from that of sp2c-COF (Fig. 5c, black curve, Table 1). These blueshifts are clearly associated with the twisted structures of the linkers.
As shown in the crystal structure, sp2c-COF, sp2c-COF-2, and sp2c-COF-3 possess the phenyl, biphenyl and terphenyl units that connect the pyrene knots. Owing to the propeller alignment of the four phenyl units (the twisted angle is 37.81° for sp2c-COF, 30.45° for sp2c-COF-2 and 37.12° for sp2c-COF-3) at the focal pyrene core, the phenyl, biphenyl and terphenyl units adopt twisted confirmation relative to the pyrene plane. The phenyl linker has a twisted angle of 27.50° relative to the 2D plane, while the biphenyl unit has the twisted angles of 31.77° and 11.57° for each phenyl unit and the terphenyl linker adopts the twisted angles of 16.16°, 7.77°, and 17.24° relative to the 2D plane. The differences in the twisted angles cause different degrees of π cloud overlap along the sp2 carbon backbone. The propagation of twisted structures along the backbone decreases the degree of π cloud overlap between neighboring segments and weaken the extension of π conjugation over the 2D skeletons. Therefore, the linker units in the sp2 carbon frameworks are a key structural parameter that controls the π conjugation.
Frontier molecular orbital levels and band structure
From the onset of the electronic absorption band, the optical band gap of sp2c-COF was evaluated to be 2.05 eV (Table 2). As a result of decreased π conjugation, sp2c-COF-2 exhibited an increased band gap at 2.14 eV while sp2c-COF-3 yielded the largest band gap of 2.21 eV.
To investigate the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) levels of sp2 carbon-conjugated COFs, we further conducted cyclic voltammetry of powder samples coated on carbon glass electrode in the presence of tetrabutylammonia hexafulorophosphate electrolyte in acetonitrile at 25 °C (Table 2 and Supplementary Figure 13). sp2c-COF exhibited the oxidation and reduction potentials at 0.94 V and –0.96 V, respectively. Associated with the decreased π conjugation, sp2c-COF-2 and sp2c-COF-3 exhibited the oxidation potentials at 1.08 and 1.10 V, and the reduction potentials at −0.99 and −1.02 V, respectively. From the onset positions of oxidation and reduction potentials, the HOMO and LUMO levels were evaluated to be −5.74 and −5.88 eV for sp2c-COF, −5.90, and −3.84 eV for sp2c-COF-2 and −3.81 and −3.78 eV for sp2c-COF-3, respectively. Owing to the less π conjugation, sp2c-COF-2 and sp2c-COF-3 exhibited lowered HOMO and higher LUMO levels compared to those of sp2c-COF. Clearly, the linker units owing to their twisted conformation, enable the fine regulation of the HOMO and LUMO levels. As calculated from the HOMO and LUMO levels, the electrochemical band gaps of sp2c-COF, sp2c-COF-2, and sp2c-COF-3 were 1.90, 2.07, and 2.12 eV, respectively (Table 2). These results indicate that sp2c-COFs are semiconductors with predesigned lattices and tunable bad gap structures.
Light emitting in solutions
We dispersed sp2c-COF, sp2c-COF-2, and sp2c-COF-3 in different solvents and measured their fluorescence spectra (Supplementary Figures 14–16). sp2c-COF in THF emitted a strong red luminescence centered at 616 nm, whereas sp2c-COF-2 and sp2c-COF-3 emitted orange luminescence centered at 559 and 568 nm, respectively (Supplementary Figure 14g, 15 g and 16 g, Supplementary Table 8). The dispersed samples exhibited linker-dependent emission colors and are totally different from those of monomer and model compound (Fig. 5d). The absolute fluorescence quantum yields of sp2c-COF, sp2c-COF-2, and sp2c-COF-3 were evaluated to be 15%, 19%, and 12%, respectively (Fig. 5e, Supplementary Table 9). In water, sp2c-COF, sp2c-COF-2, and sp2c-COF-3 emitted at 606 nm, 592 nm, and 602 nm, respectively (Supplementary Figures 14a, 15a, 16a, Supplementary Table 8). Notably, their absolute fluorescence quantum yields were as high as 22%, 20%, and 18%, respectively (Fig. 5e, Supplementary Table 9). Moreover, in hexane, sp2c-COF, sp2c-COF-2, and sp2c-COF-3 emitted at 612 nm, 574 nm, and 571 nm (Supplementary Figures 14c, 15c and 16c, Supplementary Table 8) with absolute fluorescence quantum yields of 15%, 14%, and 7%, respectively (Fig. 5e, Supplementary Table 9). In other organic solvents, sp2c-COF, sp2c-COF-2, and sp2c-COF-3 retained fluorescence quantum yields of 15–20% (Fig. 5e, Supplementary Table 9). Fluorescence lifetime measurements revealed that these sp2c-COFs dispersed in different solvents have a fluorescence lifetime of 1.3–3.0 ns (Supplementary Table 9, Supplementary Figures 17–19). Therefore, sp2c-COFs are highly luminescent and are robust to emit luminescence in various solvents (Fig. 5e, Supplementary Table 9).
Light emitting in the solid state
The solid samples of sp2c-COF, sp2c-COF-2, and sp2c-COF-3 exhibited electronic absorption bands at 497, 475, and 462 nm, and emitted at 622, 606, and 609 nm, respectively (Fig. 5a–c, red curves, Table 1). The absolute fluorescence quantum yields of the sp2c-COF, sp2c-COF-2, and sp2c-COF-3 solids were 14%, 10%, and 6%, respectively (Fig. 5e, Table 1). Fluorescence microscopy confirmed that sp2c-COF is highly emissive across the entire belts (Supplementary Figure 20). The fluorescence lifetime of the solid samples was estimated to be 1.85, 2.93, and 3.43 ns for sp2c-COF, sp2c-COF-2, and sp2c-COF-3, respectively (Fig. 5f). By contrast, the imine-linked pyrene COF did not emit a luminescence in the solid state or when dispersed in organic solvents. Surprisingly, sp2c-COF and sp2c-COF-2 can keep the emission properties, including fluorescence wavelength, quantum yield and lifetime even upon 1-year exposure to air at room temperature (Fig. 3e, f, Supplementary Figures 7, 8). The combination of stability and light-emitting activity has been long pursued; the sp2 carbon frameworks offer a promising platform for designing luminescent and stable materials.
Light emitting in the exfoliated nanosheets
By virtue of the stable C=C linked 2D skeletons, the 2D sp2 carbon covalent organic nanosheets sp2c-CON, sp2c-CON-2, and sp2c-CON-3 were prepared by the sonication-assisted exfoliation of sp2c-COF, sp2c-COF-2, and sp2c-COF-3 in N-methyl-2-pyrrolidone (NMP), respectively (ESI). A clear Tyndall effect was observed as a laser light pass through the NMP solutions of the exfoliated sp2c-CONs (Fig. 6a).
sp2c-CON assumes an ultrathin and transparent sheet structure with crumpled shape as shown by the HR-TEM image (Fig. 6b), which is in contrast to that of sp2c-COF with bulk and opaque states. Upon filtration through anodic aluminum oxide (AAO) film, 2D sp2c-CON thin films with nearly single layer or limited few layers were prepared (Supplementary Figure 21). Notably, exfoliation induces great change in both absorption and emission. The thin film of sp2c-CON exhibited an absorption band at 437 nm (Fig. 6c, black curve) and emitted a luminescence at 565 nm (Fig. 6c, red curve), which are blueshifted from sp2c-COF. The thin films of sp2c-CON-2 and sp2c-CON-3 exhibited absorption bands at 418 and 438 nm (Fig. 6d, e, black curves), and emitted at 468 and 551 nm, respectively (Fig. 6d, e, red curves). The blueshift in the absorption and emission bands suggests that the photochemical events are controlled by the layered and exfoliated sheet status, which are strongly associated with their primary- (nanosheets) and high-order (layer framework) structures. Surprisingly, the sp2c-CON-2 and sp2c-CON-3 thin films exhibited fluorescence quantum yields of 21% and 16%, respectively (Fig. 6f, blue bars). These absolute quantum yields are 2.1- and 2.7-fold as high as those of sp2c-COF-2 and sp2c-COF-3, respectively. Moreover, the NMP solutions of exfoliated sp2c-CONs also exhibited high fluorescence quantum yields (Fig. 6f, red bars). Therefore, exfoliation produces brilliant sp2 carbon nanosheets.
The above robust light-emitting properties of sp2c-COFs and sp2c-CONs intrigued us to elucidate the key structural parameters that control the interactions with photons and their photochemical events. In sp2c-COFs, pyrene serves as knots to form 2D sp2 carbon layer that further stacks to form pyrene columns. Pyrene is a typical chromophore that tends to form excimer once aggregated. For example, boroxine-linked PPy-COF emit a blue luminescence at 484 nm, which is 63-nm redshifted from that (421 nm) of the monomeric pyrene27. Since the boroxine linkage does not offer π conjugation along the backbone and the framework does not contain other emissive moieties, the 63-nm redshift suggests that PPy-COF emits an emission from an excimer of pyrene units. The pyrene unit when excited to its singlet state can form an excimer with a ground-state pyrene unit of a neighboring layer to emit the fluorescence. Compared to the excimer emission of pyrene at 484 nm of PPy-COF, sp2c-COF emits at a far redshifted wavelength of 622 nm. This 134-nm redshift of emission cannot attribute to only the excimer formation but it is clearly associated with the sp2 carbon-conjugated backbone of sp2c-COF.
The backbone between two proximate pyrene knots in the same layer consists of the cyano-substituted phenylenevinylene segment, which adopts twisted conformation and is known as aggregation-induced emissive (AIE) chromophore43. Together with the excimer formation of the pyrene knots, the AIE feature of the linker backbone reveals a principle that in sp2c-COFs, the knot and linker are tightly correlated with the photochemical events, including excitation and emission.
For sp2c-COF, the adsorption band is 498 nm for the solid sample, which is blueshifted to 437 nm for the thin film of exfoliated nanosheets. The 61-nm blueshift suggests that in sp2c-COF the linkers adopt a more planar conformation so that they can extend the π cloud overlap in a more efficient way. On the other hand, in the exfoliated sp2c-CON nanosheets, the π–π stacking force that helps to planarize the sheet is released so that the backbones assume more twisted conformation to cause less π cloud overlap that leads to a blueshift of the absorption band. Indeed, density functional tight binding calculations confirmed that the phenyl twisted angle is 55.61° in the single layer and is 37.81° in the layer framework. Therefore, the photon absorption ruled by Franck-Cotton principle is regulated by the twisted status of the phenylenevinylene backbone. A 61-nm blueshift is observed for the emission band from 626 nm of sp2c-COF to 565 nm of the sp2c-CON thin film, changing the emission color from red to orange yellow. Notably, the fluorescence quantum yield retained nearly the same level (14% for sp2c-COF versus 12% for sp2c-CON). This observation suggests that the decreased AIE activity of the linkers in the exfoliated sp2c-CON film is balanced by the increased emission activity of the pyrene knots.
Similarly, sp2c-COF-2 shows a blueshift of the absorption band from 475 nm of the solid sample to 418 nm of the exfoliated sp2c-CON-2 thin film. This result reflects that the biphenyl linker greatly twists so that the transmission of the π conjugation along the x and y directions is suppressed in the exfoliated nanosheets. Therefore, the pyrene knots become to dominate the photon adsorption in the exfoliated nanosheets. Similarly, such a pyrene-knot dominance is also observable for the emission, which shows a blueshift from 606 (sp2c-COF-2) to 468 nm (sp2c-CON-2 thin film). Such an interruption of π conjugation enables the generation of a blue emission from the sp2c-CON-2 thin film. Interestingly, the fluorescence quantum yield is greatly enhanced from 10% for sp2c-COF-2 to 21% for the sp2c-CON-2 thin film. This improved activity originates from the enhanced emission from pyrene knots in the exfoliated state.
In the case of sp2c-COF-3, the terphenyl linkers also cause the blueshift of the adsorption and emission bands but the degree is the lowest among the series. The blueshift is 24 nm for the absorption band and is 58 nm for the emission band. Therefore, the terphenyl linkers could maintain certain degrees of π conjugation in the exfoliated sp2c-CON-3 films. Surprisingly, the fluorescence quantum yield is dramatically increased from the originally 6% of sp2c-COF-3 to 16% of the exfoliated sp2c-CON-3 film. These observations again indicate that in the exfoliated nanosheets the pyrene knots play a key role in determining the emission quantum yield, while the arylenevinylene linkers control the absorption and emission wavelengths.
As describe above, the sp2 carbon-conjugated skeletons offer a platform for designing stable and light-emitting frameworks. The C=C linkage enables the designed synthesis of sp2c-COFs and sp2c-CONs with different lattice sizes. The π conjugation is controlled by the linker units and their AIE feature is a key to achieve high luminescence quantum yields for the layered frameworks. This result is important for device application in which layer structure forms a basic configuration. The knot units play a key role in producing highly emissive covalent organic nanosheets. Interestingly, the exfoliated nanosheets enhance the fluorescence quantum yield by 2–3-fold compared to the bulk frameworks, leading to the generation of brilliant nanosheets. Clearly, the C=C linkage provides a suitable bridge that enables a strong electronic communication between knots and linkers through which they are cooperative in the photochemical events to achieve exceptional light-emitting activity in both layered frameworks and exfoliated nanosheets.
To ensure the significance of being a 2D structure in achieving the light-emitting function, we synthesized a one-dimensional 1,6-linear pyrene polymer as a control (Supplementary Figure 22a) by condensing (1,6-formylphenyl)pyrene with PDAN to yield a C=C linked sp2 carbon polymer that has the similar building units as that of sp2c-COF. Compared to sp2c-COF, the 1,6-linear pyrene polymer exhibited very weak luminescence in the solid state (Supplementary Figure 22b) and dispersed solutions. For example, the solid sample of 1,6-linear pyrene polymer exhibited the electronic absorption band at 434 nm and emitted at 574 nm (Supplementary Figure 22c); both of them are blueshifted from those of sp2c-COF. Moreover, its absolute fluorescence quantum yield is only 1% (Supplementary Figure 22d), which is even one order of magnitude lower than that of sp2c-COFs. The fluorescence lifetime is 1.2 ns (Supplementary Figure 22e). These results reflect that the 2D sp2 carbon lattice enables far extended π delocalization and greater emission activity and clearly demonstrate that 2D structure is essential for achieving light-emitting functions.
The highly emissive property of sp2c-COFs renders them able to detect specific guest molecules that can interact with the skeletons. In sp2c-COFs, the polymer backbones possess cyano (–CN) side groups that can serve as a ligand for triggering supramolecular interactions with specific metal species. To prove the concept, we selected Cu2+ as a target. Indeed, upon addition of Cu2+, the fluorescence intensity of sp2c-COF in THF was quenched (Supplementary Figure 23a). By contrast, addition of Zn2+ that cannot ligate with the –CN groups could not quench the emission, irrespective of its concentration (Supplementary Figure 23b). These results suggest that interaction with cyano groups is essential for triggering fluorescence sensing. Indeed, sp2c-COF is highly sensitive to the Cu2+ ion and achieves a detection limit of 88 ppb (ESI). From the Stern–Volmer plot, the fluorescence quenching rate constant kq (=kSV/τ) was calculated to be as high as 4.1 × 1014 M−1 s−1 (Supplementary Figure 23c). The extremely high kq-value revealed that the sp2 carbon-conjugated COF serves as a highly selective and effective sensor for detecting Cu2+ ions.
In summary, we have developed a C=C linkage for the designed synthesis of sp2 carbon-conjugated covalent organic frameworks. The C=C polycondensation enables the topology-directed connection of pyrene knots and arylenevinylene linkers into predesigned tetragonal sp2 carbon lattices that are π conjugated along both the x and y directions and develop layer frameworks that are stable under various conditions. The sp2 carbon frameworks consist of the pyrene knots linked with twisted arylenevinylene backbones so that the photochemical events are highly correlated with their primary- and high-order structures, constituting a class of unique photoactive semiconductors with enriched absorption and emission features. Comparative studies on the bulk frameworks and exfoliated nanosheets disclosed the structural parameters that control the photochemical events. The electronic communication and cooperation between the knots and linkers in the sp2 carbon lattices enable the simultaneous realization of highly emissive layered frameworks and exfoliated nanosheets. These characteristics are established in COFs and would exert great impact on the further advance of the field. We envisage that sp2 carbon frameworks could offer a promising platform for designing robust photoactive semiconductors that are useful in sensors, energy-harvesting antennae and photocatalysts.
A 1,4-dioxane (1.0 mL) solution of TFPPy (0.024 mmol, 15.0 mg) and PDAN (0.048 mmol, 7.58 mg) in the presence of KOH catalyst (4 M, 0.1 mL) in a Pyrex tube (10 mL) was degassed via three freeze–pump–thaw cycles. The tube was flame sealed and heated at 90 °C for 3 days. The precipitate was collected via centrifugation, washed three times with H2O, five times with THF and then subjected to Soxhlet extraction with THF for 1 day. The powder was collected and dried at 120 °C under vacuum overnight to yield sp2c-COF solid in an isolated yield of 84%.
A 1,4-dioxane (1.0 mL) solution of TFPPy (0.024 mmol, 15.0 mg) and BPDAN (0.048 mmol, 11.26 mg) in the presence of KOH catalyst (4 M, 0.1 mL) in a Pyrex tube (10 mL) was degassed via three freeze–pump–thaw cycles. The tube was sealed by flame and heated at 110 °C for 3 days. The precipitate was collected via centrifugation, washed three times with water, five times with THF and then subjected to Soxhlet extraction with THF for 1 day. The powder was collected and dried at 120 °C under vacuum overnight to yield sp2c-COF-2 in an isolated yield of 82%.
A 1,2-dichlorobenzene (ODCB, 500 μL) solution of TFPPy (0.016 mmol, 10.0 mg) and TPDAN (0.032 mmol, 9.97 mg) in the presence of TBAH catalyst (1 M in MeOH, 500 μL) in a Pyrex tube (10 mL) was degassed via three freeze–pump–thaw cycles. The tube was sealed by flame and heated at 120 °C for 3 days. The precipitate was collected via centrifugation, washed five times with THF and then subjected to Soxhlet extraction with THF for 1 day. The powder was collected and dried at 120 °C under vacuum overnight to yield sp2c-COF-3 in an isolated yield of 88%.
Stability test in solvents
The sp2c-COFs samples (15 mg) were kept in 2 mL of DMF, THF, water, MeOH, HCl (12 M) or NaOH (14 M), respectively for 1 week. The samples were washed with THF (for powders treated in organic solvents) or water (for powders treated in acid/base solutions), dried at 120 °C overnight under vacuum and subjected to PXRD, FT IR, and nitrogen sorption isotherm measurements.
Long-term stability test in air
The sp2c-COF and sp2c-COF-2 samples were kept in open glass tube and exposed to air for more than 1 year at room temperature. During the period, these samples were not avoided shining sunlight and room lamps. After 1 year, the samples were directly subjected to PXRD, BET, and luminescence measurements without any further treatment.
All data generated or analysed during this study are included in this published article (and its supplementary information).
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D.J. acknowledge the NUS start-up grant (R-143-000-A28-133).
The authors declare no competing interests.
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Jin, E., Li, J., Geng, K. et al. Designed synthesis of stable light-emitting two-dimensional sp2 carbon-conjugated covalent organic frameworks. Nat Commun 9, 4143 (2018). https://doi.org/10.1038/s41467-018-06719-8
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