钙钛矿(结构)
材料科学
热稳定性
降级(电信)
碘化物
耐久性
离子
图层(电子)
光伏系统
纳米技术
化学工程
光电子学
复合材料
化学
电气工程
计算机科学
无机化学
电信
工程类
有机化学
作者
Yifeng Shi,Yifan Zheng,X. Xiao,Yan Li,Dianfu Feng,Guodong Zhang,Yang Zhang,Tao Li,Yuchuan Shao
标识
DOI:10.1002/sstr.202400132
摘要
Ion migration presents a formidable obstacle to the stability and performance of perovskite solar cells (PSCs), hindering their progress toward commercial feasibility. Herein, the degradation mechanism of PSCs caused by iodide ion migration, which leads to abnormal changes in photoluminescence transients at the buried interface of perovskite films, is investigated. In light of this problem, a novel strategy is proposed to mitigate ion migration by introducing poly(2‐vinylnaphthalene) into poly[bis(4‐phenyl)(2,4,6‐trimethylphenyl)amine] as the hole transport layer with improved ion‐blocking capability. Consequently, this layer effectively reduces defect concentration, suppresses ion migration, and modulates energy level alignment, leading to an impressive efficiency exceeding 23% for doctor‐bladed FAPbI 3 PSCs. Moreover, the corresponding unencapsulated devices demonstrate remarkable durability, maintaining over 80% of their initial value after undergoing rigorous stress tests in accordance with the International Electrotechnical Commission 61215 standard for temperature, humidity, and illumination. These tests include 1000 h of thermal cycling and a long‐term operational test lasting 600 h under maximum power point tracking.
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