An Expanded 2D Fused Aromatic Network with 90-Ring Hexagons.

Two-dimensional fused aromatic networks (2D FANs) have emerged as a highly versatile alternative to holey graphene. The synthesis of 2D FANs with increasingly larger lattice dimensions will enable new application perspectives. However, the synthesis of larger analogues is mostly limited by lack of appropriate monomers and methods. Herein, we describe the synthesis, characterisation and properties of an expanded 2D FAN with 90-ring hexagons, which exceed the largest 2D FAN lattices reported to date.

Introduction

Two‐dimensional fused aromatic networks (2D FANs) are a class of conjugated 2D polymers that have emerged as a highly versatile alternative to holey graphene. Similarly, 2D FANs combine an extended 2D π‐system with permanent nanometer‐sized pores, and have shown charge carrier mobility values reaching 1000 cm2 V−1 s−1. 2D FANs are synthesised from organic monomers that act as nodes and linkers and that can be designed at will. Hence by controlling the monomer structure and geometry, 2D FANs with different but predictable lattices and pore sizes can be obtained. In addition, heteroatoms, and substituents can be incorporated into the framework by modification of the monomers, which provides an additional way to modulate their electronic structure and their properties.

Among these, pyrazine‐fused 2D FANs[ , ] (Figure 1) are receiving increasing attention as they can be obtained by imine‐type cyclocondensation reactions between monomers equipped with sets of o‐quinone and o‐diamine groups. On one hand this type of condensation fuses together the π‐systems of both monomers through the formation of a pyrazine ring. On the other hand, the pyrazine linkage introduces simultaneously two electron‐withdrawing nitrogen atoms in the framework. This exchange of C atoms for N atoms in specific sites has given rise to materials with a lot of potential in electronics,[ , ] photovoltaics, gas separation and storage, membranes for proton conduction and water purification, organic catalysts, and metal‐free electrodes for the oxygen reduction reaction, oxygen evolution reaction, supercapacitors, and batteries.

Figure 1

Representative examples of 2D FANs with hexagons constituted of a) 12‐, b) 24‐,[ , ] c) 30‐, d) 42‐, and e) 54‐fused rings and the structures of c) [30]KL‐FAN and f) [90]KL‐FAN described in this work. The coloured dots in (c) and (f) indicate the assignments of the signals on Figures 2 c and 3 c.

Figure 2

Experimental and simulated structural characterisation of [30]KL‐FAN. a) FTIR; b) SS CP/MAS 1H NMR (* denotes side peaks); c) SS CP/MAS 13C NMR (the coloured dots on each signal correspond to the carbons marked in Figure 1 c); d) nitrogen adsorption and desorption isotherm profiles at 77 K; e) pore size distribution; f) experimental and simulated PXRD patterns; theoretical models showing the g) face‐on and h) side‐on projections; i) HRTEM images.

Figure 3

Experimental and simulated structural characterisation of [90]KL‐FAN. a) FTIR; b) SS CP/MAS 1H NMR (* denotes side peaks); c) SS CP/MAS 13C NMR (the coloured dots on each signal correspond to the carbons marked in Figure 1 f); d) nitrogen adsorption and desorption isotherm profiles at 77 K; e) pore size distribution; f) experimental and simulated PXRD patterns; theoretical models showing the g) face‐on and h) side‐on projections; i) HRTEM image.

Increasing the pore size of 2D FANs would allow the diffusion and encapsulation of organic, inorganic and biological macromolecules and would make available materials that combine both larger band gaps and porosities, broadening the application scope of 2D FANs into other fields, such as sensing and heterogeneous catalysis. However, synthesising 2D FANs with larger dimensions is a difficult task. Firstly, because of the limited number of monomers, the poor solubility of increasingly large monomers, and the harsh polymerisation conditions that are not always compatible with the functional groups of increasingly complex monomers. And secondly, in analogy to other framework materials, large pore 2D FANs are more prone to collapse upon activation. Nevertheless, an impressive wealth of honeycomb 2D FANs with hexagons constituted of 12‐, 18‐,[ , , ] 24‐,[ , , , , , , , ] 30‐, 36‐,[ , ] 42‐, and 54‐fused rings (highlighted in yellow in Figure 1) have been reported to date.

Herein we report the synthesis of a 2D FAN with 90‐ring hexagons (Figure 1 f, [90]KL‐FAN, where KL stands for Koke Lab), the largest yet reported. [90]KL‐FAN has been obtained by solvothermal cyclocondensation of a new set of large synthetic monomers that show an optimal solubility in the reaction media. The structural, optoelectronic and redox features of [90]KL‐FAN have been compared with those of a reference 2D FAN with 30‐ring sides (Figure 1, [30]KL‐FAN). The comparison reveals a lower band gap, a higher nitrogen uptake, and improved electrochemical properties for [90]KL‐FAN, while maintaining a similar degree of crystallinity and similar charge transporting properties, despite the larger dimensions.

Results and Discussion

[30]KL‐FAN was obtained by solvothermal condensation of hexaaminobenzene 1 and pyrene tetraone 2 (Figure 1 c) in N‐methyl‐2‐pyrrolidone (NMP) with a catalytic amount of H2SO4 at 250 °C. In this particular case, the reaction mixture must be kept at 0 °C before heating in order to ensure the reproducibility of the reaction. We attributed this behaviour to the high reactivity of hexaaminobenzene 1. [90]KL‐FAN was synthesised by condensation between dibenzotetraazahexacene tetraamine 3 and hexabenzohexaazatetracenylene hexaone 4 (Figure 1 f) in N‐methyl‐2‐pyrrolidone (NMP) with a catalytic amount of H2SO4 at 170 °C. In this case, the reaction proceeded without the need of precooling the mixture, which is consistent with the lower reactivity of tetraamine 3 in comparison to hexaamine 1. [30]KL‐FAN and [90]KL‐FAN were obtained as black powders after Soxhlet extraction. The structures of [30]KL‐FAN and [90]KL‐FAN were confirmed by a combination of different characterisation techniques.

The FT‐IR spectra of [30]KL‐FAN and [90]KL‐FAN (Figure 2 a and Figure 3 a) show the attenuation of the N−H (around 3100 cm−1) and C=O (around 1700 cm−1) bands of the corresponding monomers, which indicate that an efficient polymerisation has taken place.

Solid‐state cross‐polarisation/magic‐angle spinning (SS CP/MAS) NMR spectroscopy of [30]KL‐FAN and [90]KL‐FAN is consistent with the proposed structure. The SS CP/MAS 1H NMR spectra show two signals that correspond to the aromatic and tert‐butyl protons of the FANs in both cases because of the structural similarities (Figures 2 b and 3 b). The SS CP/MAS 13C NMR spectra also show a similar set of signals for both 2D FANs in agreement with their structural similarities, namely three signals in the 150–120 ppm region that correspond to the aromatic carbons and two signals around 30 ppm that correspond to the tert‐butyl carbons (Figures 2 c and 3 c). The absence of a sharp signal around 190 ppm indicates a low number of carbonyl groups in both FANs, which also indicates a good conversion.

X‐ray photoelectron spectroscopy (XPS; Figures S1 and S2) and energy‐dispersive X‐ray spectroscopy (EDX; Figure S3) confirm the presence of carbon, nitrogen and oxygen. The occurrence of carbon and nitrogen is consistent with the chemical composition of [30]KL‐FAN and [90]KL‐FAN. The presence of oxygen has been attributed to existence of unreacted ketone and amino groups and to the entrapment of water molecules, as illustrated by the deconvolution of the nitrogen and oxygen peaks (Figures S1 and S2). Elemental analysis showed that the carbon and nitrogen ratios were consistent with theoretical values, although the absolute percentages of carbon were lower than theoretical values (Tables S1 and S2). This discrepancy between the theoretical and observed values is also consistent with the presence of unreacted ketone and amino groups and of water, as indicated by XPS (Figures S1 and S2), thermal gravimetric analysis (Figure S4) and previous observations.[ , ]

In order to assess the porosity of [30]KL‐FAN and [90]KL‐FAN, N2 gas adsorption measurements at 77 K were performed. The isotherms confirm that [30]KL‐FAN and [90]KL‐FAN are porous materials (Figures 2 d and 3 d) that show, respectively, Brunauer–Emmet–Teller (BET) surface areas of 449 and 567 m2 g−1 and NLDFT pore sizes centred at 6 and 18 Å (Figures 2 e and 3 e).

The powder X‐ray diffraction (PXRD) of [30]KL‐FAN and [90]KL‐FAN reveals patterns of broad peaks that are similar to those observed in other 2D FANs.[ , , , , , , , , , ] The XRD peaks of 2D FANs are usually broad as the result of the limited reversibility of the pyrazine linkers and turbostratic disorder. In both cases, the diffractograms show two main diagnostic peaks that support the formation of the microporous honeycomb network. The first one, the low‐angle peak at 6.08° in the case of [30]KL‐FAN and at 1.77° in the case of [90]KL‐FAN, corresponds in both cases to the (100) reflection (Figures 2 f and 3 f). The second one, the peak around 25°, corresponds to the (001) reflection and to the d‐spacing of π‐stacked aromatic systems (≈3.4 Å).

To shine additional light on the structure of [30]KL‐FAN and [90]KL‐FAN, three general packing configurations (AA, AB and ABC) were computationally explored and their simulated PXRD patterns were compared with the experimental ones. In the case of [30]KL‐FAN, the simulated diffractogram for the slipped AA packing mode shows a better fit with the experimental one. Meanwhile, in the case of [90]KL‐FAN, the experimental diffractogram shows a better fit with the simulated diffractogram for the AB packing mode. This assignment is consistent with the NLDFT pore size distributions estimated from nitrogen adsorption measurements. In fact, the pore size of the [30]KL‐FAN model in an AA configuration (4 Å) is in excellent agreement with the experimental pore size (6 Å; Figure 2 e,g). Also, the pore size of the [90]KL‐FAN model in an AB configuration (17 Å) is in excellent agreement with the experimental pore size (18 Å; Figure 3 e,g).

High‐resolution transmission electron microscopy (HRTEM) images of [30]KL‐FAN and [90]KL‐FAN evidence their 2D layered structure by the presence of terraces and step‐edges of overlapping sheets (Figures 2 i and 3 i). In both cases, the micrographs show the projections of irregular pores, which were turbostratically disordered. In some particular areas of [30]KL‐FAN, seemingly crystalline regions can be observed (Figure 2 i) with some periodic features being attributed to the stacking arrangements of the individual layers. The unexpected mesopores within the structure (Figure 2 i) are likely to be caused by the presence of solvent molecules during the formation of the FAN lattice and terminated by unreacted carbonyl groups due to incomplete condensation, as we previously demonstrated for a conjugated microporous polymer.

The optical properties of [30]KL‐FAN and [90]KL‐FAN were studied by UV/Vis‐NIR spectroscopy (Figure 4 a,b). Thin films were obtained by drop‐casting dispersions of [30]KL‐FAN and [90]KL‐FAN in trifluoroacetic acid (TFA) directly onto a glass slide, which allowed estimating the optical band gap using Tauc's method (inset Figure 4 a,b). Band gaps of 2.05 and 1.95 eV were estimated, respectively, for [30]KL‐FAN and [90]KL‐FAN that illustrate their semiconducting nature.

Figure 4

UV/Vis‐NIR electronic absorption spectra of a) [30]KL‐FAN and b) [90]KL‐FAN. Inset corresponds to Tauc's plot. c) RRDE voltammograms (disk currents) recorded in O2‐saturated 0.1 M KOH at 1600 rpm. The disk potential was scanned at 10 mV s−1 and the ring potential was constant at 1.4 V versus RHE. Band structures of d) [30]KL‐FAN and e) [90]KL‐FAN. f) TMRC measurements (λ=355 nm, I 0=9.1×1015 photons cm−2).

The electrochemical properties of [30]KL‐FAN and [90]KL‐FAN were investigated by cyclic voltammetry in a rotating ring–disk electrode (RRDE; Figure 4 c and Table S3). For this purpose, freshly prepared dispersions of [30]KL‐FAN and [90]KL‐FAN in TFA were directly drop‐casted on a glassy carbon (GC) RRDE. The voltametric curves in an argon‐saturated aqueous 0.1 M KOH solution show no redox processes. However, in an oxygen‐saturated solution, the voltammograms reveal a reduction wave characteristic of the oxygen reduction reaction (ORR),[ , ] which is a key reaction in fuel cells. The voltammograms illustrate that the electrodes containing the 2D FANs show higher potentials at same current densities than the pristine GC electrode. This is consistent with a more efficient ORR as expected for the presence of catalytically active N atoms. When it comes to the 2D FANs, the electrodes containing [90]KL‐FAN show a significantly higher current density at same potential than [30]KL‐FAN, for example, at a potential of 0.1 V vs. RHE, their current densities are 2.02 mA cm−2 and 1.35 mA cm−2, respectively. The RRDE allows to monitor the formation of H2O2, and hence, to determine the average number of electrons (n) transferred per oxygen molecule with great accuracy. In the case of [90]KL‐FAN, n=3.00 (Figure S5). Meanwhile in the case of [30]KL‐FAN and GC, n=2.75 and 2.50, respectively. An electron number n larger than 2 indicates that in all cases the ORR may proceed simultaneously through the 2‐electron (from O2 to H2O2) and the 4‐electron mechanisms (from O2 to H2O) and, the higher the value of n is, the deeper oxygen gets reduced. This means [90]KL‐FAN is more efficient than [30]KL‐FAN for the ORR. The ORR performance of [90]KL‐FAN and [30]KL‐FAN is in line with that observed in current state‐of‐the‐art 2D FANs and other metal‐free state‐of‐the‐art 2D materials with the present additional advantage that no additive or carbonisation treatment was needed. Given the structural similarities and the similar nitrogen content, the higher electrocatalytic performance of [90]KL‐FAN over [30]KL‐FAN can be attributed to the larger pore size and surface area that facilitate in the case of [90]KL‐FAN the diffusion of oxygen within the framework.

The electronic band structures and the projected density of states of [30]KL‐FAN and [90]KL‐FAN were calculated by DFT to get an insight into their electronic structure and their charge transporting properties (Figures 4 d,e and S6). The calculations illustrate that both [30]KL‐FAN and [90]KL‐FAN are direct gap semiconductors and show the same trend as the optical band gaps. [30]KL‐FAN computed band gap is 1.82 eV at the Γ‐point (Figure 4 d). The frontier bands show weak dispersions of 37 meV and 15 meV for the highest occupied crystalline orbital (HOCO) and lowest unoccupied crystalline orbital (LUCO) respectively. In contrast, [90]KL‐FAN has a lower gap 1.51 eV, also at the Γ‐point, and shows degenerate HOCO and LUCO bands (Figure 4 e). For the larger FAN, the HOCO band shows further reduced dispersion, 15 meV, while the LUCO band is virtually flat with negligible energy dispersion (<1 meV).

The charge transport properties [30]KL‐FAN and [90]KL‐FAN were probed by flash‐photolysis time‐resolved microwave conductivity (FP‐TRMC). FP‐TRMC allows estimating the pseudo‐photoconductivity or intrinsic mobility (φΣμ, where φ: the charge carrier generation yield, Σμ: the sum of charge carrier mobilities). The samples of [30]KL‐FAN and [90]KL‐FAN showed similar φΣμ maximum values (φΣμ max) of 0.6×10−4 and 0.4×10−4 cm2 V−1 s−1, respectively (Figure 4 f). These φΣμ max values are of the same order of magnitude as those observed in molecular nanoribbons and nanographenes with the same fused‐ring structure[ , ] and in imine 2D covalent organic frameworks. The similar φΣμ max values of [30]KL‐FAN and [90]KL‐FAN are consistent with their structural similarities in terms of fused‐ring structure and interlayer distance.

Conclusion

We have described the successful solvothermal synthesis of a 2D FAN with a honeycomb lattice constituted of 90‐ring hexagons, which exceed the largest 2D FAN lattices reported to date. The synthesis of [90]KL‐FAN has been achieved by introducing a new set of monomers, which despite their large dimensions are sufficiently soluble in the reaction media. The structure of [90]KL‐FAN has been confirmed by a combination of FT‐IR, solid‐state NMR, porosimetry, PXRD, HRTEM and theoretical studies. [90]KL‐FAN‐containing electrodes showed enhanced electrocatalytic activity that was attributed to the larger pore size. UV/Vis‐NIR electronic absorption, theoretical studies and FP‐TRMC show that [90]KL‐FAN is a direct band gap semiconductor with an intrinsic charge carrier mobility comparable to those observed in state‐of‐the‐art nanographenes and imine 2D covalent organic frameworks. Overall, this work paves the way for the synthesis of 2D and 3D FANs with increasingly larger lattices. Such large‐pore semiconducting FANs may find applications in sensing, electrocatalysis, and energy conversion and storage.

Conflict of interest

The authors declare no conflict of interest.

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