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Fully Reduced Core-Shell Organotin-Polyoxometalate {Sn12Mo19}: A Synergistic Modulation Material for the Buried Interface of Inverted Perovskite Solar Cells.

Created on 29 Sep 2026

Authors

Yue Peng, Feifei Ren, Zhe Xin, Shiyi Liu, Weichao Chen, Dan Han, Xinlong Wang, Weilin Chen

Published in

Angewandte Chemie (International ed. in English). Pages e1019904. Sep 28, 2026. Epub Sep 28, 2026.

Abstract

The commercialization of inverted perovskite solar cells (PSCs) suffers from poor buried interface and interfacial charge loss at the hole transport layer. Therefore, designing and synthesizing materials that can precisely optimize the buried interface is crucial. Herein, we employ a molecular design strategy to synthesize an organotin-functionalized fully reduced polyoxometalate (POM), (NH4)2H15[SnIV 3(CH3)3(OH)3O]4[MoV 19O64]·20H2O ({Sn12Mo19}), which serves as a molecular-level synergistic interfacial layer between NiOx and a self-assembled monolayer (SAM) in PSCs. {Sn12Mo19} features a fully reduced Mo-oxo cluster core surrounded by four organotin shells, endowing the entire molecule with a Td-symmetric triply-nested architecture that enables ordered spatial organization of bifunctional moieties. Comprehensive experimental and theoretical results reveal that nanoscale, well-defined {Sn12Mo19} fills voids within the NiOx layer, where its Mo-oxo core suppresses detrimental Ni4+ and the organotin shell induces SAM homogenization via hydrogen bonding. Such synergistic effects substantially improve the quality of the buried interface by suppressing interfacial side reactions and SAM spatial mismatch. Consequently, the Voc of PSCs increases by 3.31%, and PCE rises from 23.81% to 26.11%, setting a new record for POM-modified PSCs and rendering {Sn12Mo19} universal across various SAMs. This work demonstrates that POM molecular engineering can precisely address interfacial challenges, offering new design concepts and technical routes for broader photovoltaic applications.

PMID:
42806466
Bibliographic data and abstract were imported from PubMed on 29 Sep 2026.

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