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Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Toward Stable and Efficient Perovskite Solar Cells: Unlocking the Potential of Porous PbI2 Scaffolds via Two-Step
Jiadi Pan1, Yebin Li1, Changhao Weng1
1Zhejiang Engineering Research Center for Fabrication and Application of Advanced Photovoltaic Materials, School of Materials Science and Engineering, NingboTech University, Ningbo, P. R. China.
None:
The two-step sequential deposition method for perovskite solar cells (PSCs) is often limited by the dense PbI2 film morphology, leading to incomplete conversion, residual PbI2, and high defect density. This review consolidates research showing that engineering a porous PbI2 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 Pb2+, 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 PbI2 porosity. A porous PbI2 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 PbI2 morphology thus offers a scalable route to enhance perovskite photovoltaic performance and commercial viability.

