甲脒
三碘化物
钙钛矿(结构)
钝化
卤化物
材料科学
涂层
相(物质)
能量转换效率
化学工程
化学
光电子学
无机化学
复合材料
有机化学
图层(电子)
物理化学
工程类
电解质
色素敏化染料
电极
作者
Jung‐Woo Yoo,Eunseo Noh,Jihun Jang,Kyoung Su Lee,Junseop Byeon,Man‐Young Choi,Jino Im,Sang Il Seok
出处
期刊:Joule
[Elsevier]
日期:2023-04-01
卷期号:7 (4): 797-809
被引量:9
标识
DOI:10.1016/j.joule.2023.03.003
摘要
The higher thermodynamic stability of formamidinium lead triiodide (FAPbI3) in the yellow non-perovskite (δ-phase) than the black perovskite (α-phase) at room temperature causes spontaneous α-phase to δ-phase transition. Stabilization of α-FAPbI3 by alloying the perovskite composition is limited by band gap broadening and halide segregation. Furthermore, commercial PSCs require coating methods suitable for large-area modules. Herein, we report α-phase stabilization of FAPbI3 without band gap broadening using R4N+ cations and Cl− anions. Subsequently, high-efficiency perovskite solar mini-modules (PSMs) were fabricated using a bar-coating process with simultaneous defect passivation and hole-transport promotion which exhibited a maximum power conversion efficiency (PCE) of 21.23% (certified 20.33%, 36.4-cm2 area). The PCE in the 1-cm2 area fabricated by bar-coating was 23.24% (certified 22.79%, the highest in those fabricated by scalable bar-coating method). Furthermore, the encapsulated PSM retained 93% of its initial PCE, even after 870 h under continuous one-sun illumination.
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