Volume 57, Issue 1 pp. 122-138
Review

Oxygen Vacancy-Mediated Photocatalysis of BiOCl: Reactivity, Selectivity, and Perspectives

Dr. Hao Li

Dr. Hao Li

Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental Chemistry, College of Chemistry, Central China Normal University, Wuhan, 430079 P.R. China

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Dr. Jie Li

Dr. Jie Li

Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental Chemistry, College of Chemistry, Central China Normal University, Wuhan, 430079 P.R. China

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Prof. Zhihui Ai

Prof. Zhihui Ai

Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental Chemistry, College of Chemistry, Central China Normal University, Wuhan, 430079 P.R. China

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Prof. Falong Jia

Prof. Falong Jia

Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental Chemistry, College of Chemistry, Central China Normal University, Wuhan, 430079 P.R. China

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Prof. Lizhi Zhang

Corresponding Author

Prof. Lizhi Zhang

Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental Chemistry, College of Chemistry, Central China Normal University, Wuhan, 430079 P.R. China

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First published: 20 June 2017
Citations: 1,040

Graphical Abstract

Tiny concentrations of oxygen vacancies on the surface of real photocatalysts can influence the kinetics and energetics and the mechanisms of photocatalytic reactions decisively. Oxygen vacancies on BiOCl surfaces are described at the molecular level, and their structure correlated with reactivity and selectivity in photocatalytic reactions.

Abstract

Semiconductor photocatalysis is a trustworthy approach to harvest clean solar light for energy conversions, while state-of-the-art catalytic efficiencies are unsatisfactory because of the finite light response and/or recombination of robust charge carriers. Along with the development of modern material characterization techniques and electronic-structure computations, oxygen vacancies (OVs) on the surface of real photocatalysts, even in infinitesimal concentration, are found to play a more decisive role in determining the kinetics, energetics, and mechanisms of photocatalytic reactions. This Review endeavors to clarify the inherent functionality of OVs in photocatalysis at the surface molecular level using 2D BiOCl as the platform. Structure sensitivity of OVs on reactivity and selectivity of photocatalytic reactions is intensely discussed via confining OVs onto prototypical BiOCl surfaces of different structures. The critical understanding of OVs chemistry can help consolidate and advance the fundamental theories of photocatalysis, and also offer new perspectives and guidelines for the rational design of catalysts with satisfactory performance.

Conflict of interest

The authors declare no conflict of interest.

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