journal article·2023-09-25

Dithiophenedione-Based Covalent Organic Frameworks for Supercapacitive Energy Storage

Shuang Li, Bidhan Kumbhakar, Bikash Mishra, Jérôme Roeser, Nicolas Chaoui, Johannes Schmidt, Arne Thomas, Pradip Pachfule

ACS Applied Energy Materials· Volume 6· Issue 18
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Abstract

Covalent organic frameworks (COFs) are organic materials with well-defined atomic arrangements, significant porosity, and tailorable chemical properties, which make them interesting for a variety of applications. In this study, we explore the synthesis of a crystalline COF based on dithiophenedione moieties in its backbone (TTT-DHTD), which has been further employed as an electrode material for supercapacitors. By comparison with a dimethoxybenzene-dithiophene-based COF (TTT-DMTD), it is shown that redox-active dithiophenedione moieties have a profound effect on the capacitance enhancement. Due to the synergistic impact of its high porosity, well-defined crystalline structure, and the presence of redox-active components, the TTT-DHTD COF exhibits both high energy storage density and long-term durability (273.3 F g –1 at 0.5 A g –1 and 163.7 F g –1 at 10 mV s –1 ).
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Research context

OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Supercapacitor Materials and Fabrication

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

Affiliations

College of Polymer Science & Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610065, China

Department of Chemical and Biological Sciences, S. N. Bose National Centre for Basic Sciences, Kolkata 700106, India

Department of Chemistry/Functional Materials, Technische Universität Berlin, Hardenbergstraße 40, 10623 Berlin, Germany

Funding

Bundesministerium f?r Bildung und Forschung · Science and Engineering Research Board · Deutsche Forschungsgemeinschaft

References (66)

Show source-provided references
1. 10.1021/acs.accounts.5b0036910.1021/acs.accounts.5b00369 ↗
2. 10.1038/s43586-022-00181-z10.1038/s43586-022-00181-z ↗
3. 10.1126/science.aal158510.1126/science.aal1585 ↗
4. 10.1038/nchem.69510.1038/nchem.695 ↗
5. 10.1021/jacs.8b1033410.1021/jacs.8b10334 ↗
6. 10.1021/acs.accounts.0c0038610.1021/acs.accounts.0c00386 ↗
7. 10.1038/s41467-019-10157-510.1038/s41467-019-10157-5 ↗
8. 10.1016/j.enchem.2020.10003510.1016/j.enchem.2020.100035 ↗
9. 10.1039/D0CS00009D10.1039/D0CS00009D ↗
10. 10.1021/acs.accounts.5b0001010.1021/acs.accounts.5b00010 ↗
11. 10.1021/acsnano.1c0319410.1021/acsnano.1c03194 ↗
12. 10.1021/jacs.7b0163110.1021/jacs.7b01631 ↗
13. 10.1039/C9CS00827F10.1039/C9CS00827F ↗
14. 10.1021/acsenergylett.7b0112310.1021/acsenergylett.7b01123 ↗
15. 10.1021/jacs.7b1125510.1021/jacs.7b11255 ↗
16. 10.1038/s41467-018-04910-510.1038/s41467-018-04910-5 ↗
17. 10.1039/D0CS00017E10.1039/D0CS00017E ↗
18. 10.1038/s41467-019-13739-510.1038/s41467-019-13739-5 ↗
19. 10.1002/anie.20230227610.1002/anie.202302276 ↗
20. 10.1021/acsenergylett.1c0076810.1021/acsenergylett.1c00768 ↗
21. 10.1021/ja409421d10.1021/ja409421d ↗
22. 10.1038/s41467-020-18427-310.1038/s41467-020-18427-3 ↗
23. 10.1002/chem.20140533010.1002/chem.201405330 ↗
24. 10.1021/jacs.9b0122610.1021/jacs.9b01226 ↗
25. 10.1039/D0CS01569E10.1039/D0CS01569E ↗
26. 10.1021/cr020730k10.1021/cr020730k ↗
27. 10.1093/nsr/nwx00910.1093/nsr/nwx009 ↗
28. 10.1038/nchem.251510.1038/nchem.2515 ↗
29. 10.1002/anie.20211628210.1002/anie.202116282 ↗
30. 10.1002/anie.20211238110.1002/anie.202112381 ↗
31. 10.1039/C7TA00863E10.1039/C7TA00863E ↗
32. 10.1021/acs.accounts.0c0046510.1021/acs.accounts.0c00465 ↗
33. 10.1002/adma.20180659910.1002/adma.201806599 ↗
34. 10.1021/acs.accounts.6b0034110.1021/acs.accounts.6b00341 ↗
35. 10.1002/adma.20220177910.1002/adma.202201779 ↗
36. 10.26599/NRE.2022.912000910.26599/NRE.2022.9120009 ↗
37. 10.3389/fmats.2016.0001810.3389/fmats.2016.00018 ↗
38. 10.1039/C9TA05252F10.1039/C9TA05252F ↗
39. 10.1016/S0378-7753(01)00735-210.1016/S0378-7753(01)00735-2 ↗
40. 10.1039/C7TA00527J10.1039/C7TA00527J ↗
41. 10.1021/acs.chemmater.5b0264810.1021/acs.chemmater.5b02648 ↗
42. 10.1002/adma.20170571010.1002/adma.201705710 ↗
43. 10.1002/celc.20190029810.1002/celc.201900298 ↗
44. 10.1021/acs.chemmater.6b0417810.1021/acs.chemmater.6b04178 ↗
45. 10.1002/asia.20190029610.1002/asia.201900296 ↗
46. 10.1021/acsami.8b2169610.1021/acsami.8b21696 ↗
47. 10.1021/acsami.5b0418510.1021/acsami.5b04185 ↗
48. 10.1039/C7CC01902E10.1039/C7CC01902E ↗
49. 10.1021/acsnano.7b0835410.1021/acsnano.7b08354 ↗
50. 10.1021/acscentsci.6b0022010.1021/acscentsci.6b00220 ↗
51. 10.1039/C9CC08107K10.1039/C9CC08107K ↗
52. 10.1021/am506095910.1021/am5060959 ↗
53. 10.1021/jacs.0c0701510.1021/jacs.0c07015 ↗
54. 10.1021/jacs.9b0473110.1021/jacs.9b04731 ↗
55. 10.1039/C8CC07289B10.1039/C8CC07289B ↗
56. 10.1002/anie.20180222010.1002/anie.201802220 ↗
57. 10.1021/jacs.8b1233910.1021/jacs.8b12339 ↗
58. 10.1039/C9SC06150A10.1039/C9SC06150A ↗
59. 10.1002/advs.20160038210.1002/advs.201600382 ↗
60. 10.1039/C9SC02601K10.1039/C9SC02601K ↗
61. 10.1016/j.joule.2017.08.01810.1016/j.joule.2017.08.018 ↗
62. 10.1038/nmat491910.1038/nmat4919 ↗
63. 10.1038/nature1290910.1038/nature12909 ↗
64. 10.1021/acsmacrolett.7b0084910.1021/acsmacrolett.7b00849 ↗
65. 10.1016/j.micromeso.2018.02.02610.1016/j.micromeso.2018.02.026 ↗
66. 10.1021/jacs.8b0646010.1021/jacs.8b06460 ↗