journal article·2022-06-14

Soluble Two-Dimensional Donor–Acceptor Aza-Fused Aromatic Frameworks and their Electrochromism between the Visible and Near-Infrared Regions

Zilong Wang, Xing Xing, Igor F. Perepichka, Yue Sun, Bing Han, Yuting Wu, Yanan Zhu, Jiaoyi Ning, Mi Wang, Junpeng He, He Liu, Yaowu He, Clifton Kwang-Fu Shen, Hong Meng

Chemistry of Materials· Volume 34· Issue 11
Publisher page

Abstract

Two-dimensional (2D) covalent fused-ring aromatic frameworks (FAFs) can be regarded as holey graphene and hold considerable potential in many applications. However, the development of such materials has been seriously limited by their poor solubility. In this work, four soluble 2D fused-ring aromatic frameworks, FAF1–FAF4, soluble in common organic solvents, were successfully synthesized by creating large pore structures and attaching long side-chain substituents. They possess high molecular weights (Mw = 56,500–87,000 Da) and large hydrodynamic diameters (190–250 nm). Although FAFs are soluble in common organic solvents, they nevertheless show excellent ordering in the solid state with a layer spacing of ca. 0.36–0.37 nm, typical for π–π stacking. Due to the presence of electron-deficient pyrazine rings in the main skeleton and electron-rich alkoxyphenyl or alkylthienyl side-chain groups, these FAFs are electroactive in both n- and p-doping processes (Ered = −(0.80–0.93) V, Eox = 0.84–0.94 V vs Fc/Fc+). They possess low-lying lowest unoccupied molecular orbital (LUMO) energy levels of −(3.87–4.00) eV and narrow band gaps (EgCV = 1.64–1.87 eV), suggesting that they are good candidates as n-type semiconductors. Taking advantage of their good solubility, spray-coated films of FAF1 and FAF2 were prepared, and their cathodic electrochromic behavior in the ultraviolet–visible–near-infrared (UV–vis–NIR) region was investigated for the first time. The 2D framework with 4-(2-ethylhexyloxy)phenyl solubilizing groups, FAF1, demonstrated superior performance with short switching times between the neutral and n-doped states (few seconds), good contrast (ΔT up to 44%), high coloration efficiency (up to 171 cm2 C–1 at 515 nm), and good operational stability (>200 redox cycles). We envisage that such a type of 2D fused-ring framework possessing good solubility and strong π–π interactions between the layers should be a promising material for a wide range of electronic and optoelectronic applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China

Research & Development Institute of Northwestern Polytechnical University (Shenzhen), Northwestern Polytechnical University, Shenzhen 518057, China

Institute of Flexible Electronics, Northwestern Polytechnical University, 127 West Youyi Road, Xi’an 710072, China

Department of Materials Science & Engineering, Southern University of Science and Technology (SUSTech), Shenzhen 518055, China

Shenzhen Key Laboratory of Polymer Science and Technology, Guangdong Research Center for Interfacial Engineering of Functional Materials, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518060, China

Guangdong LEPUTAI New Materials Technology Co., Ltd., Dongguan 523808, China

Funding

National Natural Science Foundation of China · Postdoctoral Science Foundation of China · Guangdong Basic and Applied Basic Research Foundation · Shenzhen Science and Technology Research Grant · Special Funding for the Innovative R&D Team of Dongguan

References (88)

Show source-provided references
1. 10.1016/j.compositesb.2018.01.01310.1016/j.compositesb.2018.01.013 ↗
2. 10.1002/anie.20140278010.1002/anie.201402780 ↗
3. 10.1039/C8CS00773J10.1039/C8CS00773J ↗
4. 10.1016/j.jphotochemrev.2014.04.00210.1016/j.jphotochemrev.2014.04.002 ↗
5. 10.1021/acsami.8b0333810.1021/acsami.8b03338 ↗
6. 10.1021/acs.chemrev.7b0068910.1021/acs.chemrev.7b00689 ↗
7. 10.1021/acs.chemrev.8b0028810.1021/acs.chemrev.8b00288 ↗
8. 10.1002/adma.20150003310.1002/adma.201500033 ↗
9. 10.1039/C5CS00767D10.1039/C5CS00767D ↗
10. 10.1038/ncomms373610.1038/ncomms3736 ↗
11. 10.1038/ncomms748610.1038/ncomms7486 ↗
12. 10.1016/j.nanoen.2017.08.03810.1016/j.nanoen.2017.08.038 ↗
13. 10.1002/anie.20110349310.1002/anie.201103493 ↗
14. 10.1002/anie.20170027110.1002/anie.201700271 ↗
15. 10.1021/jacs.8b1148210.1021/jacs.8b11482 ↗
16. 10.1021/acs.chemrev.9b0055010.1021/acs.chemrev.9b00550 ↗
17. 10.1021/acs.accounts.5b0036910.1021/acs.accounts.5b00369 ↗
18. 10.1039/C2CS35072F10.1039/C2CS35072F ↗
19. 10.1002/adfm.20170555310.1002/adfm.201705553 ↗
20. 10.1021/jacs.8b1033410.1021/jacs.8b10334 ↗
21. 10.1002/advs.20180141010.1002/advs.201801410 ↗
22. 10.1039/C9CS00456D10.1039/C9CS00456D ↗
23. 10.1002/chem.20210113510.1002/chem.202101135 ↗
24. 10.1126/science.116542910.1126/science.1165429 ↗
25. 10.1038/s41563-020-0682-z10.1038/s41563-020-0682-z ↗
26. 10.1021/ja408355p10.1021/ja408355p ↗
27. 10.1002/adma.20180506210.1002/adma.201805062 ↗
28. 10.1039/C6MH00570E10.1039/C6MH00570E ↗
29. 10.1002/adma.20190310410.1002/adma.201903104 ↗
30. Meng, H. Organic Electronics for Electrochromic Materials and Devices; Wiley-VCH: Weinheim, 2021; p 528.10.1002/9783527830633 ↗
31. Chua M. H. · 2019 · 1
32. 10.1146/annurev-matsci-062910-10034410.1146/annurev-matsci-062910-100344 ↗
33. 10.1021/acs.accounts.6b0018310.1021/acs.accounts.6b00183 ↗
34. 10.1021/cr900129a10.1021/cr900129a ↗
35. 10.1039/C4CC00163J10.1039/C4CC00163J ↗
36. 10.1007/s11426-016-0305-910.1007/s11426-016-0305-9 ↗
37. 10.1002/aenm.20190043310.1002/aenm.201900433 ↗
38. 10.1021/jacs.9b0995610.1021/jacs.9b09956 ↗
39. 10.1038/s41467-020-19315-610.1038/s41467-020-19315-6 ↗
40. 10.1016/j.solmat.2020.11043810.1016/j.solmat.2020.110438 ↗
41. 10.1021/jacs.0c1239210.1021/jacs.0c12392 ↗
42. 10.1002/anie.20210087010.1002/anie.202100870 ↗
43. 10.1002/asia.20090059610.1002/asia.200900596 ↗
44. 10.1134/S0030400X1904014310.1134/S0030400X19040143 ↗
45. 10.1021/acs.chemmater.7b0131810.1021/acs.chemmater.7b01318 ↗
46. 10.1016/j.dyepig.2018.02.02110.1016/j.dyepig.2018.02.021 ↗
47. 10.1002/aenm.20170052210.1002/aenm.201700522 ↗
48. 10.1039/a606106k10.1039/a606106k ↗
49. 10.1021/jo980348110.1021/jo9803481 ↗
50. 10.1002/1521-3765(20021018)8:20<4656::AID-CHEM4656>3.0.CO;2-110.1002/1521-3765(20021018)8:20<4656::AID-CHEM4656>3.0.CO;2-1 ↗
51. 10.1002/anie.20035187610.1002/anie.200351876 ↗
52. 10.1021/ja309960m10.1021/ja309960m ↗
53. 10.1039/C9SC06143F10.1039/C9SC06143F ↗
54. 10.1002/pola.2732110.1002/pola.27321 ↗
55. 10.1126/sciadv.aav233610.1126/sciadv.aav2336 ↗
56. 10.1016/j.xcrp.2021.10046710.1016/j.xcrp.2021.100467 ↗
57. 10.1038/s41467-021-26173-310.1038/s41467-021-26173-3 ↗
58. 10.1002/asia.20170073210.1002/asia.201700732 ↗
59. 10.1002/tcr.20160009410.1002/tcr.201600094 ↗
60. 10.1039/C7CC09949E10.1039/C7CC09949E ↗
61. 10.1021/jacs.9b1152810.1021/jacs.9b11528 ↗
62. 10.1039/C4CC08146C10.1039/C4CC08146C ↗
63. 10.1002/adma.20170505210.1002/adma.201705052 ↗
64. 10.1021/jacs.0c0647410.1021/jacs.0c06474 ↗
65. 10.1007/s11426-020-9865-310.1007/s11426-020-9865-3 ↗
66. 10.1002/asia.20090037310.1002/asia.200900373 ↗
67. 10.1021/jo034549310.1021/jo0345493 ↗
68. 10.1039/b511075k10.1039/b511075k ↗
69. 10.1039/C6MH00051G10.1039/C6MH00051G ↗
70. 10.1002/adma.20160602510.1002/adma.201606025 ↗
71. 10.1039/C8TC04252G10.1039/C8TC04252G ↗
72. 10.1039/C6PY01847E10.1039/C6PY01847E ↗
73. 10.1039/C7TC05227H10.1039/C7TC05227H ↗
74. 10.1039/c2jm31035j10.1039/c2jm31035j ↗
75. 10.1039/C9TC02126D10.1039/C9TC02126D ↗
76. 10.1021/ar00118a00510.1021/ar00118a005 ↗
77. 10.1021/acs.macromol.8b0121310.1021/acs.macromol.8b01213 ↗
78. 10.1021/acscentsci.6b0007310.1021/acscentsci.6b00073 ↗
79. 10.1002/anie.20200692610.1002/anie.202006926 ↗
80. 10.1039/C9TC02861G10.1039/C9TC02861G ↗
81. 10.1021/cm102124510.1021/cm1021245 ↗
82. 10.1021/am301539410.1021/am3015394 ↗
83. 10.1039/C8PY01208C10.1039/C8PY01208C ↗
84. 10.1039/C4RA11827H10.1039/C4RA11827H ↗
85. 10.1021/ar400228410.1021/ar4002284 ↗
86. 10.1039/C9TC00416E10.1039/C9TC00416E ↗
87. 10.1016/j.tsf.2014.02.00210.1016/j.tsf.2014.02.002 ↗
88. Monk, P. M. S.; Mortimer, R. J.; Rosseinsky, D. R. Electrochromism and Electrochromic Devices; Cambridge University Press: Cambridge, 2007; p 510.10.1017/CBO9780511550959 ↗