降级(电信)
钙钛矿(结构)
基质(水族馆)
材料科学
钠
化学工程
化学
计算机科学
生物
工程类
冶金
电信
生态学
作者
Hasan Raza,Qisen Zhou,Zhaoyi Jiang,Aadil Mahboob,You Gao,Jianan Wang,Wenguang Liu,Yong Cai,Zhengtian Tan,Tianyin Miao,Salman Ali,Zonghao Liu,Wei Chen
出处
期刊:Solar RRL
[Wiley]
日期:2025-04-01
卷期号:9 (8)
被引量:3
标识
DOI:10.1002/solr.202400921
摘要
Perovskite solar cells (PSCs) are a promising photovoltaic (PV) technology due to their superior power conversion efficiency (PCE). However, potential‐induced degradation (PID) has been recognized as a critical issue in contemporary commercial solar systems, impeding reliability and commercialization. The migration of sodium (Na) ions from substrates is considered a key contributor to the PID of PV technologies under high‐voltage stress conditions. Strategies for mitigating or suppressing PID remain underexplored in PSCs. Here, for the first time, an approach using a Na‐free substrate is introduced to suppress the PID of PSCs under high humidity and elevated temperature, aligned with standard testing conditions (ICE 62804−1). It is demonstrated that Na‐free glass‐based devices maintained 91% of their initial PCE, while soda‐lime glass (SLG)‐based retained only 52%. After extended testing (1056 h), Na‐free glass‐based devices retained 96.61% of their initial PCE at 25°C and 60% relative humidity, outperforming SLG‐based devices, which failed entirely after 576 h. Na‐free glass‐based devices recovered 99.6% of their initial PCE after 96 h of post‐PID dark storage and retained 96.44% after 3072 h. These findings provide a pathway to accelerate the commercialization of PSCs.
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