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BiOI-SnO 2 Heterojunction Design to Boost Visible-Light-Driven Photocatalytic NO Purification

Author

Listed:
  • Han Chen

    (Key Laboratory for Technology in Rural Water Management of Zhejiang Province, Zhejiang University of Water Resources and Electric Power, Hangzhou 310018, China)

  • Yutao Hu

    (Key Laboratory of Microbial Technology for Industrial Pollution Control of Zhejiang Province, College of Environment, Zhejiang University of Technology, Hangzhou 310014, China)

  • Zanyun Ying

    (College of Science & Technology, Ningbo University, Ningbo 315212, China)

  • Yinfeng Xia

    (Key Laboratory for Technology in Rural Water Management of Zhejiang Province, Zhejiang University of Water Resources and Electric Power, Hangzhou 310018, China)

  • Jiexu Ye

    (Key Laboratory of Microbial Technology for Industrial Pollution Control of Zhejiang Province, College of Environment, Zhejiang University of Technology, Hangzhou 310014, China)

  • Jingkai Zhao

    (Key Laboratory of Microbial Technology for Industrial Pollution Control of Zhejiang Province, College of Environment, Zhejiang University of Technology, Hangzhou 310014, China)

  • Shihan Zhang

    (Key Laboratory of Microbial Technology for Industrial Pollution Control of Zhejiang Province, College of Environment, Zhejiang University of Technology, Hangzhou 310014, China)

Abstract

The efficient, stable, and selective photocatalytic conversion of nitric oxide (NO) into harmless products such as nitrate (NO 3 − ) is greatly desired but remains an enormous challenge. In this work, a series of BiOI/SnO 2 heterojunctions (denoted as X %B-S, where X % is the mass portion of BiOI compared with the mass of SnO 2 ) were synthesized for the efficient transformation of NO into harmless NO 3 − . The best performance was achieved by the 30%B-S catalyst, whose NO removal efficiency was 96.3% and 47.2% higher than that of 15%B-S and 75%B-S, respectively. Moreover, 30%B-S also exhibited good stability and recyclability. This enhanced performance was mainly caused by the heterojunction structure, which facilitated charge transport and electron-hole separation. Under visible light irradiation, the electrons gathered in SnO 2 transformed O 2 to ·O 2 − and ·OH, while the holes generated in BiOI oxidized H 2 O to produce ·OH. The abundantly generated ·OH, ·O 2 − , and 1 O 2 species effectively converted NO to NO − and NO 2 − , thus promoting the oxidation of NO to NO 3 − . Overall, the heterojunction formation between p-type BiOI and n-type SnO 2 significantly reduced the recombination of photo-induced electron-hole pairs and promoted the photocatalytic activity. This work reveals the critical role of heterojunctions during photocatalytic degradation and provides some insight into NO removal.

Suggested Citation

  • Han Chen & Yutao Hu & Zanyun Ying & Yinfeng Xia & Jiexu Ye & Jingkai Zhao & Shihan Zhang, 2023. "BiOI-SnO 2 Heterojunction Design to Boost Visible-Light-Driven Photocatalytic NO Purification," IJERPH, MDPI, vol. 20(5), pages 1-13, February.
  • Handle: RePEc:gam:jijerp:v:20:y:2023:i:5:p:4009-:d:1078350
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