钙钛矿(结构)
串联
带隙
材料科学
光电子学
光伏系统
光伏
沉积(地质)
卤化物
纳米技术
化学
电气工程
无机化学
结晶学
复合材料
古生物学
工程类
生物
沉积物
作者
Yu‐Hsien Chiang,Kyle Frohna,Hayden Salway,Anna Abfalterer,Linfeng Pan,Bart Roose,Miguel Anaya,Samuel D. Stranks
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-05-24
卷期号:8 (6): 2728-2737
被引量:20
标识
DOI:10.1021/acsenergylett.3c00564
摘要
All-perovskite tandem solar cells beckon as lower cost alternatives to conventional single-junction cells. Solution processing has enabled rapid optimization of perovskite solar technologies, but new deposition routes will enable modularity and scalability, facilitating technology adoption. Here, we utilize 4-source vacuum deposition to deposit FA0.7Cs0.3Pb(IxBr1-x)3 perovskite, where the bandgap is changed through fine control over the halide content. We show how using MeO-2PACz as a hole-transporting material and passivating the perovskite with ethylenediammonium diiodide reduces nonradiative losses, resulting in efficiencies of 17.8% in solar cells based on vacuum-deposited perovskites with a bandgap of 1.76 eV. By similarly passivating a narrow-bandgap FA0.75Cs0.25Pb0.5Sn0.5I3 perovskite and combining it with a subcell of evaporated FA0.7Cs0.3Pb(I0.64Br0.36)3, we report a 2-terminal all-perovskite tandem solar cell with champion open circuit voltage and efficiency of 2.06 V and 24.1%, respectively. This dry deposition method enables high reproducibility, opening avenues for modular, scalable multijunction devices even in complex architectures.
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