材料科学
非阻塞I/O
钙钛矿(结构)
异质结
紫外线
光电子学
氧化镍
辐照
卤化物
光伏系统
氧化物
化学工程
无机化学
催化作用
工程类
物理
生物
核物理学
化学
冶金
生物化学
生态学
作者
Xueliang Zhu,Cho Fai Jonathan Lau,Kangwei Mo,Siyang Cheng,Yalun Xu,Ruiming Li,Cheng Wang,Qixian Zheng,Yong Liu,Ti Wang,Qianqian Lin,Zhiping Wang
出处
期刊:Nano Energy
[Elsevier]
日期:2022-09-23
卷期号:103: 107849-107849
被引量:41
标识
DOI:10.1016/j.nanoen.2022.107849
摘要
Long-term stability remains a challenge for commercializing metal halide perovskites in photovoltaic (PV) applications. Ultraviolet-induced degradation (UV-ID) has been considered as one of the key stability issues for crystalline silicon PVs. However, limited studies have been performed on the long-term UV-ID of perovskite PVs, and none has been found related to operational stability under UV stressing. Here, we focus on UV-ID of inverted perovskite solar cells that comprise nickel oxide (NiO) as the hole transporting layer. Under continuous UV irradiation, we observe vacancies/voids generated in the vicinity of NiO/perovskite heterojunction. Time-resolved femtosecond transient absorption and double-ion injection current measurements indicate UV irradiation would induce interface shallow traps and severe ion migration. These UV-induced degradations can be greatly suppressed by modifying the heterojunction with a self-assembled monolayer [2-(9 H-Carbazol-9-yl)ethyl] phosphonic acid (2PACz). Unencapsulated NiO/2PACz devices, operated at maximum power point (MPP), retain over 90% of their initial efficiency after exposing to a total UV dose of 35 kWh/m2. The best-performing device reaches a stabilized efficiency of 22.2%, and retains 82% of its original efficiency after 2000 h of MPP tracking under one sun illumination (100 mW/cm2) at 45 ℃ in ambient air when encapsulated.
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