串联
钙钛矿(结构)
硅
材料科学
降级(电信)
光伏系统
PID控制器
光电子学
扩散
电子工程
电气工程
化学
物理
温度控制
工程类
复合材料
结晶学
热力学
作者
Lujia Xu,Jiang Liu,Wei Luo,Nimer Wehbe,Akmaral Seitkhan,Maxime Babics,Jingxuan Kang,Michele De Bastiani,Erkan Aydın,Thomas G. Allen,Mohammed Alamer,Wenbo Yan,Fuzong Xu,Atteq ur Rehman,Stefaan De Wolf
标识
DOI:10.1016/j.xcrp.2022.101026
摘要
Despite great progress in perovskite/silicon tandem solar cells’ device performance, their susceptibility to potential-induced degradation (PID) remains unexplored. In this study, we find that applying a voltage bias of −1,000 V to single-device perovskite/silicon tandem modules at 60°C for ∼1 day can cause a ∼50% loss in their power conversion efficiency, which raises concerns for tandem commercialization. We found no accumulation of Na+ in the perovskite or silicon photon absorbers. Consequently, no obvious shunt is observed in our silicon subcells. We also find that elements diffuse from the perovskite into the module encapsulant during PID testing. We argue that this diffusion is the main PID mechanism in our tandem modules. While applying a large positive voltage bias can partially recover this PID, introducing barriers or structures to prevent elemental diffusion out of the perovskite may be required to mitigate this degradation phenomenon.
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