journal article·2020-02-12

Design Rules for Improving the Cycling Stability of High-Performance Donor–Acceptor-Type Electrochromic Polymers

Yuntao Han, Zhen Xing, Pinyi Ma, Su Li, Chong Wang, Zhenhua Jiang, Zheng Chen

Publisher page

Abstract

Although high-performance donor–acceptor (D–A)-type polymers have received much attention as an important class of electrochromic (EC) materials, the related studies have mostly focused on the influence of D and A units on the band gap, onset potential, and switching time, leaving the effect of D–A structures on cycling lifetime underexplored. Herein, we design and synthesize a series of poly(aryl amino sulfone)s (PAASs) as D–A polymers with triphenylamine-based donor units and the sulfone moiety as the acceptor unit. As a result, we present new rules to design and develop D–A structure polymers with high EC cycling stability: (1) the electron-donating and -withdrawing abilities of the donor and acceptor should be balanced during the electrochemical cycle process, and this balance can be measured by the ratio of Jred/Jox; (2) the D–A structure should benefit to generate lower Eonset. By these design rules, the best-performing polymer PAAS-TPPA-OMe exhibits an excellent long-term cycling stability (over 3,900 cycles), low onset potential (0.26 V), fast switching time (6.0/4.3 s for the EC process), high contrast (87% at 688 nm and 94% at 928 nm), and high coloration efficiency (500 cm2 C–1 at 688 nm and 1131 cm2 C–1 at 928 nm).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Conducting polymers and applications · Transition Metal Oxide Nanomaterials · Analytical Chemistry and Sensors

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

Affiliations

Key Laboratory of High-Performance Plastics (Jilin University), Ministry of Education, National & Local Joint Engineering Laboratory for Synthesis Technology of High-Performance Polymers, College of Chemistry, Jilin University, Xiuzheng Road 1788, Changchun 130012, China

Department of Analytical Chemistry, College of Chemistry, Jilin University, Xiuzheng Road 1788, Changchun 130012, China

Center of Applied Chemistry & School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 610054, China

Funding

People's Government of Jilin Province · Education Department of Jilin Province

References (51)

Show source-provided references
1. 10.3144/expresspolymlett.2014.6810.3144/expresspolymlett.2014.68 ↗
2. 10.1016/s0013-4686(99)00034-110.1016/s0013-4686(99)00034-1 ↗
3. 10.1002/1521-4095(20020605)14:11<845::aid-adma845>3.0.co;2-810.1002/1521-4095(20020605)14:11<845::aid-adma845>3.0.co;2-8 ↗
4. 10.18280/ijht.34s24110.18280/ijht.34s241 ↗
5. Byker, H. J. Electrochromic devices with bipyridinium salt solutions U.S. Patent 5,336,448 A 1994.
6. 10.1039/c6mh00165c10.1039/c6mh00165c ↗
7. 10.1146/annurev-matsci-062910-10034410.1146/annurev-matsci-062910-100344 ↗
8. 10.1039/c6tc01150k10.1039/c6tc01150k ↗
9. 10.1002/adfm.20180703310.1002/adfm.201807033 ↗
10. 10.1039/c9tc02861g10.1039/c9tc02861g ↗
11. 10.1016/s0927-796x(00)00029-210.1016/s0927-796x(00)00029-2 ↗
12. 10.1039/c6tc04002k10.1039/c6tc04002k ↗
13. 10.1039/c8cc00224j10.1039/c8cc00224j ↗
14. 10.1038/s41467-019-09054-810.1038/s41467-019-09054-8 ↗
15. 10.1021/cm202117d10.1021/cm202117d ↗
16. 10.1002/macp.20140017110.1002/macp.201400171 ↗
17. 10.1021/ma801227j10.1021/ma801227j ↗
18. 10.1002/macp.20120008710.1002/macp.201200087 ↗
19. 10.1016/s0927-0248(98)00183-410.1016/s0927-0248(98)00183-4 ↗
20. 10.1021/ja061274a10.1021/ja061274a ↗
21. 10.1002/adma.20090291710.1002/adma.200902917 ↗
22. 10.1021/ma300669710.1021/ma3006697 ↗
23. 10.1016/0379-6779(87)90907-610.1016/0379-6779(87)90907-6 ↗
24. 10.1002/masy.1998125010210.1002/masy.19981250102 ↗
25. 10.1016/s0379-6779(02)01250-x10.1016/s0379-6779(02)01250-x ↗
26. 10.1002/marc.20180057010.1002/marc.201800570 ↗
27. 10.1002/adom.20180056810.1002/adom.201800568 ↗
28. 10.1021/acs.jpcc.7b0629910.1021/acs.jpcc.7b06299 ↗
29. 10.1039/c7tc04064d10.1039/c7tc04064d ↗
30. 10.1021/ma060846910.1021/ma0608469 ↗
31. 10.1002/pola.2426910.1002/pola.24269 ↗
32. 10.1002/pola.2700110.1002/pola.27001 ↗
33. 10.1021/ma702146h10.1021/ma702146h ↗
34. 10.1021/ar100043u10.1021/ar100043u ↗
35. 10.1016/j.dyepig.2018.11.04510.1016/j.dyepig.2018.11.045 ↗
36. 10.1016/j.polymer.2011.02.03010.1016/j.polymer.2011.02.030 ↗
37. 10.1039/b612732k10.1039/b612732k ↗
38. 10.1023/a:101857040469310.1023/a:1018570404693 ↗
39. 10.1021/acs.macromol.9b0007910.1021/acs.macromol.9b00079 ↗
40. Frisch, M.; Trucks, G.; Schlegel, H.; Scuseria, G.; Robb, M.; Cheeseman, J.; Scalmani, G.; Barone, V.; Petersson, G.; Nakatsuji, H. Gaussian 16, Revision A. 03; Gaussian, Inc.: Wallingford CT, 2016. 2019.
41. 10.1002/jcc.2288510.1002/jcc.22885 ↗
42. 10.1021/jacs.5b0793210.1021/jacs.5b07932 ↗
43. 10.1021/cm901522210.1021/cm9015222 ↗
44. 10.1002/chem.20140462210.1002/chem.201404622 ↗
45. 10.1021/am405803z10.1021/am405803z ↗
46. 10.1016/j.electacta.2017.06.06110.1016/j.electacta.2017.06.061 ↗
47. 10.1021/ma202128e10.1021/ma202128e ↗
48. 10.1016/j.dyepig.2015.10.00110.1016/j.dyepig.2015.10.001 ↗
49. 10.1016/j.dyepig.2017.01.07810.1016/j.dyepig.2017.01.078 ↗
50. 10.1002/pola.2710310.1002/pola.27103 ↗
51. 10.1039/c3cc45838e10.1039/c3cc45838e ↗