Realizing improved CO2 photoreduction in Z-scheme Bi4O5Br2/AgBr heterostructure

  • Xiaoli Jin
  • , Jian Cao
  • , Huiqing Wang
  • , Chade Lv
  • , Haiquan Xie*
  • , Fengyun Su
  • , Xin Li
  • , Ruixue Sun
  • , Shukui Shi
  • , Mengfei Dang
  • , Liqun Ye
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Architecting Z-scheme heterojunction can restrain the recombination of photoinduced carriers to improve the photocatalytic performance. However, it still lacks high-efficiency catalysts for sustainable photoreduction of CO2. Herein, an Ag-bridged Z-scheme Bi4O5Br2/AgBr heterostructure is successfully developed, which enables room-temperature CO2 reduction driven by solar energy. In this catalyst, the Ag mediator acts as a bridge to shuttle electrons between Bi4O5Br2 and AgBr, separating the electron-hole pairs efficiently and maintaining the original strong reduction reaction. As a result, Z-scheme Bi4O5Br2/AgBr heterostructures show obviously promoted performance of photocatalytic CO2 reduction in contrast with pristine Bi4O5Br2, delivering a high CO2 conversion activity of 6.6 and 1.8 μmol g-1h−1 for CO and CH4 products, respectively. This study reports an effective reference of Z-scheme Bi4O5Br2/AgBr heterojunction for satisfactory photocatalytic solar energy conversion and synthesis of high value-added products from CO2.

Original languageEnglish
Article number153758
JournalApplied Surface Science
Volume598
DOIs
StatePublished - 1 Oct 2022
Externally publishedYes

Keywords

  • CO reduction
  • Carrier separation
  • Photocatalysis
  • Solar energy
  • Z-scheme heterojunction

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