碘化物
钙钛矿(结构)
能量转换效率
卤化物
碘化锂
材料科学
图层(电子)
锂(药物)
电导率
制作
兴奋剂
钙钛矿太阳能电池
化学工程
无机化学
光电子学
光化学
电极
化学
纳米技术
物理化学
病理
内分泌学
工程类
替代医学
医学
电解质
作者
Tao Wang,Yao Zhang,Wei Wang,Liang Qiao,Bingguo Peng,Zhichao Shen,Qifeng Han,Han Chen,Zhiliang Yuan,Rongkun Zheng,Xudong Yang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-09-08
卷期号:377 (6611): 1227-1232
被引量:109
标识
DOI:10.1126/science.abq6235
摘要
Highly efficient halide perovskite solar cells generally rely on lithium-doped organic hole transporting layers that are thermally and chemically unstable, in part because of migration of iodide anions from the perovskite layer. We report a solution strategy to stabilize the hole transport in organic layers by ionic coupling positive polymer radicals and molecular anions through an ion-exchange process. The target layer exhibited a hole conductivity that was 80 times higher than that of the conventional lithium-doped layer. Moreover, after extreme iodide invasion caused by light-soaking at 85°C for 200 hours, the target layer maintained high hole conductivity and well-matched band alignment. This ion-exchange strategy enabled fabrication of perovskite solar cells with a certified power conversion efficiency of 23.9% that maintained 92% under standard illumination at 85°C after 1000 hours.
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