电致变色
降级(电信)
材料科学
透射率
薄膜
离子障
无定形固体
纳米技术
光电子学
化学物理
离子
电致变色装置
俘获
化学
离子阱
电极
物理化学
有机化学
电子工程
结晶学
工程类
生物
生态学
作者
Rui‐Tao Wen,Claes G. Granqvist,Gunnar A. Niklasson
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2015-08-10
卷期号:14 (10): 996-1001
被引量:662
摘要
Although WO3 thin films are promising as electrodes for electrochromic devices, they suffer from degradation of optical modulation. Ion-trapping-induced degradation can now be successfully eliminated by constant-current-driven de-trapping. There is keen interest in the use of amorphous WO3 thin films as cathodic electrodes in transmittance-modulating electrochromic devices1,2,3,4. However, these films suffer from ion-trapping-induced degradation of optical modulation and reversibility on extended Li+-ion exchange. Here, we demonstrate that ion-trapping-induced degradation, which is commonly believed to be irreversible, can be successfully eliminated by constant-current-driven de-trapping; that is, WO3 films can be rejuvenated and regain their initial highly reversible electrochromic performance. Pronounced ion trapping occurs when x exceeds ∼0.65 in LixWO3 during ion insertion. We find two main kinds of Li+-ion-trapping site (intermediate and deep) in WO3, where the intermediate ones are most prevalent. Li+ ions can be completely removed from intermediate traps but are irreversibly bound in deep traps. Our results provide a general framework for developing and designing superior electrochromic materials and devices.
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