甲脒
钙钛矿(结构)
材料科学
卤化物
基质(水族馆)
硅
串联
蒸发
碘化物
图层(电子)
沉积(地质)
钙钛矿太阳能电池
薄膜
化学工程
能量转换效率
平面的
晶体硅
光电子学
外延
太阳能电池
光伏
降水
多孔性
热的
纳米技术
矿物学
衍射
多孔硅
作者
Mohamed A. A. Mahmoud,Tobias Schulz,Oliver Fischer,Michael Günthel,Christoph Messmer,Markus Knäbbeler‐Buß,Adrian Callies,Salar H. Sedani,Oussama Er‐raji,Adi Prasetio,Salma Al Khuwaitem,Stefaan De Wolf,Yashika Gupta,Jann B. Landgraf,Ilker Yildiz,Martin Bivour,Bhushan P. Kore,M Schubert,Martin Hermle,Stefan W. Glunz
出处
期刊:Joule
[Elsevier BV]
日期:2026-08-01
卷期号:: 102646-102646
标识
DOI:10.1016/j.joule.2026.102646
摘要
Thermal evaporation offers a scalable and solvent-free pathway for transitioning perovskite from laboratory prototypes to industrial production, yet it remains significantly underexplored. In this work, we present the first fully solvent-free top cell in a 2-terminal perovskite-silicon tandem solar cell. We systematically explore the structural and morphological evolution of sequentially evaporated perovskite films and the impact of silicon substrate topography on the perovskite film formation. Using in situ X-ray diffraction (XRD), we observed an enhanced conversion of lead halides to perovskite on micro-textured substrates compared with planar substrates. Correspondingly, morphological characterizations revealed a compact layer of lead halides on planar substrates compared with a porous one on textured substrates. Alongside this, an initial layer-by-layer deposition of lead halides is observed, followed by interlayer mixing after adding formamidinium iodide (FAI). These insights advance the understanding of sequential thermal evaporation and enable fully solvent-free perovskite-silicon tandem solar cells with a stabilized power conversion efficiency of 27.0 % .
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