Electrochromic Performance Fading and Restoration in Amorphous TiO2 Thin Films
Source abstract
Abstract
Abstract Electrochromic performance fading is inevitable upon extended cycling, and the limited lifetime greatly prevents large‐scale commercialization of electrochromism‐based devices. Here the origin of the performance degradation is uncovered and the performance restoration in TiO2 thin films is explored. It is shown that, depending on the applied potential windows, the inserted ions are immobilized in α‐traps resulting in a monotonous degradation of colored state, or immobilized in b‐ and modified α‐traps leading to mutual degradation of colored and bleached state of the films. It is found by releasing the resided ions in various traps, the initial performance can be restored accordingly. Moreover, reversible sites and all traps are demonstrated to be interconvertible through an ion trapping and detrapping process. These results provide a general scope in understanding the electrochromism in oxide thin films and offer the scheme for potential traps control or even elimination, aiming at superior electrochromic devices.
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Research context
OpenAlex topics: Transition Metal Oxide Nanomaterials · Advanced Memory and Neural Computing · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen 518055 China
Guangdong Provincial Key Laboratory of Functional Oxide Materials and Devices Southern University of Science and Technology Shenzhen 518055 China
Funding
Southern University of Science and Technology · National Natural Science Foundation of China
References (34)
Show source-provided references
1. 10.1016/j.ijsbe.2012.09.00110.1016/j.ijsbe.2012.09.001 ↗
2. 10.1038/nature1239810.1038/nature12398 ↗
3. 2014
4. 10.1002/adma.20200468610.1002/adma.202004686 ↗
5. 10.1021/acsami.6b0045710.1021/acsami.6b00457 ↗
6. 10.1002/adom.20210239910.1002/adom.202102399 ↗
7. 10.1021/jacs.5b0493310.1021/jacs.5b04933 ↗
8. 10.1038/383608a010.1038/383608a0 ↗
9. 10.1021/jacs.0c1062810.1021/jacs.0c10628 ↗
10. 10.1016/j.cej.2021.13282110.1016/j.cej.2021.132821 ↗
11. 10.1021/jp963939910.1021/jp9639399 ↗
12. Pankove J. I. · 1971
13. 10.1021/jp983040m10.1021/jp983040m ↗
14. 10.1016/j.joule.2018.12.01010.1016/j.joule.2018.12.010 ↗
15. 10.1038/nmat436810.1038/nmat4368 ↗
16. 10.1021/acs.chemmater.6b0150310.1021/acs.chemmater.6b01503 ↗
17. 10.1021/acsami.7b1381510.1021/acsami.7b13815 ↗
18. 10.1002/aenm.20190206610.1002/aenm.201902066 ↗
19. 10.1002/adma.20160110910.1002/adma.201601109 ↗
20. 10.1002/adma.20160192810.1002/adma.201601928 ↗
21. 10.1039/B709316K10.1039/B709316K ↗
22. 10.1021/jp045788c10.1021/jp045788c ↗
23. 10.1039/c4cp00630e10.1039/c4cp00630e ↗
24. 10.1002/aenm.20160229110.1002/aenm.201602291 ↗
25. 10.1016/S0013-4686(02)00102-010.1016/S0013-4686(02)00102-0 ↗
26. 10.1103/PhysRevB.77.23520310.1103/PhysRevB.77.235203 ↗
27. 10.1039/C7TA01132F10.1039/C7TA01132F ↗
28. 10.1016/j.mser.2019.10052410.1016/j.mser.2019.100524 ↗
29. 10.1021/acsami.0c1709710.1021/acsami.0c17097 ↗
30. 10.1021/ja028165q10.1021/ja028165q ↗
31. 10.1021/cr400624r10.1021/cr400624r ↗
32. 10.1021/jp202514j10.1021/jp202514j ↗
33. 10.1002/047174199X10.1002/047174199X ↗
34. 10.1016/j.elecom.2005.09.02110.1016/j.elecom.2005.09.021 ↗