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Accessing Metal-Containing Species in Tin–Lead Perovskite Precursor Solutions via Molecular Strategies Guided by the Hard–Soft Acid–Base Principle

  • Shuaifeng Hu*
  • , Xinru Sun
  • , Wentao Liu
  • , Luca Gregori
  • , Pei Zhao
  • , Jorge Pascual*
  • , André Dallmann
  • , Akash Dasgupta
  • , Fengjiu Yang
  • , Guixiang Li
  • , Mahmoud Aldamasy
  • , Silver Hamill Turren-Cruz
  • , Marion A. Flatken
  • , Sheng Fu
  • , Yasuko Iwasaki
  • , Richard Murdey
  • , Armin Hoell
  • , Susan Schorr
  • , Steve Albrecht
  • , Shangfeng Yang
  • Antonio Abate, Atsushi Wakamiya, Filippo De Angelis, Meng Li*, Henry J. Snaith*
*此作品的通讯作者
  • University of Oxford
  • Henan University
  • Helmholtz Centre Berlin for Materials and Energy
  • University of Perugia
  • Institute for Molecular Science
  • University of the Basque Country
  • Humboldt University of Berlin
  • Southeast University, Nanjing
  • University of Valencia
  • Kyoto University
  • University of Science and Technology of China
  • University of Naples Federico II
  • Sungkyunkwan University

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

The properties of metal-centred species in metal halide perovskite precursor solutions substantially influence the formation and evolution of colloidal particles, which in turn dictate the crystallisation process and the film quality. In this work, we assess the “hard” and “soft” Lewis acid characteristics of Sn2+ and Pb2+ cations as a strategy to modulate the chemical environment of these metal-containing species in mixed-metal tin–lead perovskite precursor solutions. We observe enhanced simultaneous access to both metal centres upon adding compounds with functional groups suggested by the hard–soft acid–base principle. Theoretical calculations suggest that the hard base carboxyl group preferentially interacts with Sn2+-based species, while the softer base thiol group also targets Pb2+-based species. By effectively accessing and manipulating possible classes of inorganic species and their colloidal particle properties in the precursor solutions, we achieve 1.26 eV perovskite polycrystalline films exhibiting enhanced structural and optoelectronic quality, giving the best quasi-Fermi level splitting values of up to 0.95 eV. As a result, the solar cell devices demonstrate efficiency values of up to 23.3% with an extended operational lifetime, retaining 80% of their initial efficiency after over 280 and 180 h of maximum power point tracking under simulated AM1.5G illumination at 25 and 65 °C, respectively.

源语言英语
期刊论文编号e202514010
期刊Angewandte Chemie - International Edition
卷64
期41
DOI
出版状态已出版 - 6 10月 2025

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