材料科学
串联
钙钛矿(结构)
锡
图层(电子)
铅(地质)
纳米技术
光电子学
化学工程
冶金
复合材料
地貌学
地质学
工程类
作者
Yuanjing Cai,Aidan Maxwell,Chongwen Li,Euidae Jung,Le Zeng,Boran Kumral,Peter Serles,Zhan’ao Tan,Runnan Yu,Sal Boccia,Hao Chen,Cheng Jiang,Dongcheng Chen,Yanjiang Liu,Zaiwei Wang,Luke Grater
出处
期刊:PubMed
日期:2024-09-23
卷期号:: e2411968-e2411968
标识
DOI:10.1002/adma.202411968
摘要
Despite high theoretical efficiencies and rapid improvements in performance, high-efficiency ≈1.2 eV mixed Sn-Pb perovskite solar cells (PSCs) generally rely on poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT: PSS) as the hole transport layer (HTL); a material that is considered to be a bottleneck for long-term stability due to its acidity and hygroscopic nature. Seeking to replace PEDOT: PSS with an alternative HTL with improved atmospheric and thermal stability, herein, a silole derivative (Silole-COOH) tuned with optimal electronic properties and efficient carrier transport by incorporating a carboxyl functional group is designed, which results in an optimal band alignment for hole extraction from Sn-Pb perovskites and robust air and thermal stability. Thin films composed of the Silole-COOH exhibit superior conductivity and carrier mobility compared to PEDOT: PSS, in addition to reduced nonradiative quasi-Fermi-level splitting losses at the HTL/perovskite interface and improved quality of Sn-Pb perovskite. Replacement of PEDOT: PSS with Silole-COOH leads to 23.2%-efficient single-junction Sn-Pb PSCs, 25.8%-efficient all-perovskite tandems, and long operating stability in ambient air.
科研通智能强力驱动
Strongly Powered by AbleSci AI