钙钛矿(结构)
钝化
配体(生物化学)
插层(化学)
材料科学
反应性(心理学)
能量转换效率
化学工程
铵
纳米技术
光电子学
无机化学
化学
有机化学
图层(电子)
医学
生物化学
受体
替代医学
病理
工程类
作者
So Min Park,Mingyang Wei,Jian Xu,Harindi R. Atapattu,Felix T. Eickemeyer,Kasra Darabi,Luke Grater,Yi Yang,Cheng Liu,Sam Teale,Bin Chen,Hao Chen,Tonghui Wang,Lewei Zeng,Aidan Maxwell,Zaiwei Wang,K.R.P.M. Rao,Zhuoyun Cai,Shaik M. Zakeeruddin,Jonathan T. Pham
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2023-07-13
卷期号:381 (6654): 209-215
被引量:322
标识
DOI:10.1126/science.adi4107
摘要
Perovskite solar cells (PSCs) consisting of interfacial two- and three-dimensional heterostructures that incorporate ammonium ligand intercalation have enabled rapid progress toward the goal of uniting performance with stability. However, as the field continues to seek ever-higher durability, additional tools that avoid progressive ligand intercalation are needed to minimize degradation at high temperatures. We used ammonium ligands that are nonreactive with the bulk of perovskites and investigated a library that varies ligand molecular structure systematically. We found that fluorinated aniliniums offer interfacial passivation and simultaneously minimize reactivity with perovskites. Using this approach, we report a certified quasi-steady-state power-conversion efficiency of 24.09% for inverted-structure PSCs. In an encapsulated device operating at 85°C and 50% relative humidity, we document a 1560-hour T85 at maximum power point under 1-sun illumination.
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