材料科学
富勒烯
钙钛矿(结构)
堆积
能量转换效率
图层(电子)
化学工程
光电子学
纳米技术
化学
有机化学
工程类
作者
Xianglang Sun,Chunlei Zhang,Danpeng Gao,Xinyu Yu,Bo Li,Xin Wu,Shoufeng Zhang,Yaxin He,Zexin Yu,Liangchen Qian,Jianqiu Gong,Shuai Li,Nan Li,Zonglong Zhu,Zhong’an Li
标识
DOI:10.1002/anie.202412819
摘要
The electron transporting layer (ETL) used in high performance inverted perovskite solar cells (PSCs) is typically composed of C60, which requires time‐consuming and costly thermal evaporation deposition, posing a significant challenge for large‐scale production. To address this challenge, herein, we present a novel design of solution‐processible electron transporting material (ETM) by grafting a non‐fullerene acceptor fragment onto C60. The synthesized BTPC60 exhibits an exceptional solution processability and well‐organized molecular stacking pattern, enabling the formation of uniform and structurally ordered film with high electron mobility. When applied as ETL in inverted PSCs, BTPC60 not only exhibits excellent interfacial contact with the perovskite layer, resulting in enhanced electron extraction and transfer efficiency, but also effectively passivates the interfacial defects to suppress non‐radiative recombination. Resultant BTPC60‐based inverted PSCs deliver an impressive power conversion efficiency (PCE) of 25.3% and retain almost 90% of the initial values after aging at 85°C for 1500 hours in N2. More encouragingly, the solution‐processed BTPC60 ETL demonstrates remarkable film thickness tolerance, and enables a high PCE up to 24.8% with the ETL thickness of 200 nm. Our results highlight BTPC60 as a promising solution‐processed fullerene‐based ETM, opening an avenue for improving the scalability of efficient and stable inverted PSCs.
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