Phase Transition in Halide Double Perovskites for Solar-To-Chemical Energy Conversion

Chunhua Wang, Zhirun Xie, Pengshan Xie, Huiqiang Liang, Yang Ding, Yannan Wang, Michael K.H. Leung, Guosong Zeng, Johnny C. Ho, Sateesh Bandaru*, Ning Han*, Bao-Lian Su*, Yun Hau Ng*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

4 Citations (Scopus)
1 Downloads (CityUHK Scholars)

Abstract

Halide double perovskites have recently garnered significant interest in solar energy conversion applications owing to their non-toxic and high solar absorption properties. However, unanticipated structural distortion within these materials can compromise their performance, suppressing the structural distortion is essential and remains challenging. Here, it is reported that using phenylethylamine triggering the disorder-order phase transition can largely increase the ordering extent of octahedra in double perovskite Cs2AgBiBr6, which can suppress self-trapped exciton and defect and enable rapid charge separation, leading to exceptional photo-physics/chemistry properties with over sixfold photoactivity enhancement in the photocatalytic C−H bond activation compared to less ordered structures. This work provides an effective strategy to solve the challenging problem of the disorder phenomenon of halide double perovskites for boosting solar-to-chemical energy conversion. © 2025 The Author(s). Advanced Energy Materials published by Wiley-VCH GmbH.
Original languageEnglish
Article number2500921
JournalAdvanced Energy Materials
DOIs
Publication statusOnline published - 6 May 2025

Funding

This work was financially supported by the Hong Kong Research Grant Council (RGC) General Research Fund (GRF) (CityU 11305419, CityU 11306920, CityU 11308721, CityU 11316522), and SIRG 7020022.

Research Keywords

  • charge dynamics
  • halide double perovskite
  • phase transition
  • photocatalysis
  • photoelectric property

Publisher's Copyright Statement

  • This full text is made available under CC-BY-NC-ND 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/

RGC Funding Information

  • RGC-funded

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