材料科学
能量转换效率
钝化
钙钛矿(结构)
晶界
结晶
化学工程
带隙
粒度
热稳定性
Crystal(编程语言)
光电子学
纳米技术
微观结构
复合材料
图层(电子)
程序设计语言
工程类
计算机科学
作者
Hu Li,Yingying Peng,Zhi‐Peng Wu,Guo Jun,Chao Gao,Yapeng He,Hui Huang,Jiangzhao Chen
标识
DOI:10.1002/adma.202511124
摘要
Abstract The grain boundaries (GBs) instability induced by photodecomposition of residual PbI 2 is long‐standing challenge for further simultaneous improvement of stability and power conversion efficiency (PCE) of perovskite solar cells (PSCs). Herein, a novel GB stabilization strategy through managing unstable residual PbI 2 within perovskite films is reported, which is realized by incorporating 2‐iodoimidazole (2‐IM) into perovskite precursor solution. The 2‐IM can in situ convert unstable residual PbI 2 at GBs into robust metallo‐organic complex 2‐IMPbI 2 exhibiting an orderly hexagonal layered crystal structure. 2‐IMPbI 2 is uncovered to have much better defect passivation effect and stability than PbI 2 . The formed 2‐IMPbI 2 facilitates perovskite crystallization, passivates GB defect, suppresses ion migration, mitigates phase segregation, and promotes carrier transport, contributing to simultaneously enhanced PCE and stability. Owing to the ingenious GB modulation strategy, the inverted 1.66 eV PSCs achieve a PCE of 24.12%, which is among the highest PCEs ever reported for 1.66 eV PSCs. This strategy demonstrates good universality by accomplishing efficient 1.53 eV PSCs with a PCE of 26.84%. Moreover, the inverted wide‐bandgap PSCs with 2‐IMPbI 2 maintain 94% and 90% of their initial efficiencies after 1000 h of continuous maximum power point operation and after 500 h of thermal stress at 85 °C, respectively.
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