甲脒
铷
带隙
钙钛矿(结构)
卤化物
材料科学
光致发光
光电子学
化学
无机化学
结晶学
钾
冶金
作者
Likai Zheng,Mingyang Wei,Felix T. Eickemeyer,Jing Gao,Bin Huang,Ummugulsum Gunes,Pascal Schouwink,David Wenhua Bi,Virginia Carnevali,Mounir Mensi,Francesco Biasoni,Yuxuan Zhang,Lorenzo Agosta,Vladislav Sláma,Nikolaos Lempesis,Michael A. Hope,Shaik M. Zakeeruddin,Lyndon Emsley,Ursula Röthlisberger,Lukas Pfeifer
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-04-04
卷期号:388 (6742): 88-95
标识
DOI:10.1126/science.adt3417
摘要
A-site cation mixing can enhance the photovoltaic performance of a wide-bandgap (WBG) perovskite, but rubidium (Rb) cation mixing generally forms a nonperovskite phase. We report that lattice strain locks Rb ions into the α-phase of the lattice of a triple-halide WBG perovskite, preventing phase segregation into a nonperovskite Rb-cesium–rich phase. This process cooperates with chloride accommodation and promotes halide homogenization across the entire film volume. The resulting 1.67–electron volt WBG perovskite exhibits photoluminescence quantum yields exceeding 14% under 1-sun-equivalent irradiation, corresponding to a quasi–Fermi level splitting of ~1.34 electron volts. A WBG perovskite solar cell with an open-circuit voltage ( V OC ) of 1.30 volts was prepared, corresponding to 93.5% of the radiative V OC limit and representing the lowest photovoltage loss relative to the theoretical limit observed in WBG perovskites.
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