吩恶嗪
材料科学
单层
钙钛矿(结构)
钙钛矿太阳能电池
纳米技术
光电子学
化学工程
能量转换效率
医学
药理学
工程类
吩噻嗪
作者
Anudari Dolgormaa,Yanjie Wu,Zigeng Xu,Helong Zhu,Yi Zhang,Shuang Lian,Wenping Wu,Binhe Li,Hongmei Zhan,Lixiang Wang,Chuanjiang Qin
标识
DOI:10.1002/adfm.202516065
摘要
Abstract While self‐assembled monolayers (SAMs) have demonstrated remarkable success in iodide‐based perovskite solar cells (PSCs), their application in bromide‐based PSCs is fundamentally constrained by poor crystallization behavior and interfacial energy level misalignment. To overcome these limitations, the SAMs of (3‐(3,7‐bis(diphenylphosphoryl)‐10H‐phenoxazin‐10‐yl)propyl) phosphonic acid (3,7‐POPA) are designed and synthesized to address these challenges in FAPbBr 3 ‐based PSCs. 3,7‐POPA not only facilitates oriented crystallization of perovskite and defect minimization but also optimizes energy level alignment at the hole‐selective interface, thereby significantly enhancing hole extraction efficiency. Consequently, optimized FAPbBr 3 ‐based PSCs achieve a power conversion efficiency (PCE) of 10.79% with a record open circuit voltage (Voc) of 1.51 V. Remarkably, after operating at maximum power point for 1000 h, the encapsulated device maintains 90% of its initial PCE. The novel SAM‐based hole transport strategy simultaneously resolves crystallization, defect, and energy‐level challenges in Br‐based PSCs, achieving record efficiency and stability for high‐performance PSCs.
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