材料科学
钙钛矿(结构)
光伏系统
化学工程
多孔性
沉积(地质)
纳米技术
形态学(生物学)
光伏
多孔介质
薄膜
科技与社会
钙钛矿太阳能电池
作者
Jiadi Pan,Yebin Li,翁长浩,Tianyi Yang,Xufeng Zang,Yajie Fu,Bin Cai,Haoliang Cheng
出处
期刊:Small
[Wiley]
日期:2026-05-08
卷期号:22 (34): e73723-e73723
摘要
ABSTRACT The two‐step sequential deposition method for perovskite solar cells (PSCs) is often limited by the dense PbI 2 film morphology, leading to incomplete conversion, residual PbI 2 , and high defect density. This review consolidates research showing that engineering a porous PbI 2 architecture is a universal and transformative solution. We categorize the key strategies: (1) Solvent Engineering: Using solvent extraction, vapor treatment, or anti‐solvent methods to create rapid nanoporosity; (2) Molecular Additives: Lewis bases or volatile amines that coordinate with Pb 2+ , disrupting crystallization and forming porous scaffolds; (3) Ionic Liquids and Salts: Multi‐functional agents templating porosity while passivating defects and boosting stability; (4) Sacrificial Agents and Frameworks: Pore‐forming compounds or MOFs/COFs that provide predefined porous structures; (5) Interfacial Engineering: Substrate modifications or low‐dimensional seeds guiding favorable PbI 2 porosity. A porous PbI 2 scaffold enhances organic salt diffusion, ensuring complete conversion to high‐quality perovskite films with larger grains, improved crystallinity, and lower trap densities. This consistently yields PSCs with efficiencies >25%–26% and outstanding stability, often retaining >90% performance after thousands of hours. Controlling PbI 2 morphology thus offers a scalable route to enhance perovskite photovoltaic performance and commercial viability.
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