材料科学
钙钛矿(结构)
锡
图层(电子)
混合层
铅(地质)
纳米技术
化学工程
冶金
气象学
地质学
地貌学
物理
工程类
作者
Mingyang Wei,Ke Xiao,Grant Walters,Renxing Lin,Yong‐Biao Zhao,Makhsud I. Saidaminov,Petar Todorović́,Andrew Johnston,Ziru Huang,Haijie Chen,Aidong Li,Jia Zhu,Zhenyu Yang,Ya‐Kun Wang,Andrew H. Proppe,Shana O. Kelley,Yi Hou,Oleksandr Voznyy,Hairen Tan,Edward H. Sargent
标识
DOI:10.1002/adma.201907058
摘要
Abstract The development of narrow‐bandgap ( E g ≈ 1.2 eV) mixed tin–lead (Sn–Pb) halide perovskites enables all‐perovskite tandem solar cells. Whereas pure‐lead halide perovskite solar cells (PSCs) have advanced simultaneously in efficiency and stability, achieving this crucial combination remains a challenge in Sn–Pb PSCs. Here, Sn–Pb perovskite grains are anchored with ultrathin layered perovskites to overcome the efficiency‐stability tradeoff. Defect passivation is achieved both on the perovskite film surface and at grain boundaries, an approach implemented by directly introducing phenethylammonium ligands in the antisolvent. This improves device operational stability and also avoids the excess formation of layered perovskites that would otherwise hinder charge transport. Sn–Pb PSCs with fill factors of 79% and a certified power conversion efficiency (PCE) of 18.95% are reported—among the highest for Sn–Pb PSCs. Using this approach, a 200‐fold enhancement in device operating lifetime is achieved relative to the nonpassivated Sn–Pb PSCs under full AM1.5G illumination, and a 200 h diurnal operating time without efficiency drop is achieved under filtered AM1.5G illumination.
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