4.8 Article

Jointed Synchronous Photocatalytic Oxidation and Chromate Reduction Enabled by the Defect Distribution upon BiVO4: Mechanism Insight and Toxicity Assessment

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 15, 页码 17586-17598

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c01998

关键词

bismuth vanadate; defect distribution; jointed synchronous reaction; TC-HCl oxidation; Cr(VI) reduction

资金

  1. Program for the National Natural Science Foundation of China [51879101, 51579098, 51779090, 51709101, 51521006, 51809090, 51809293]
  2. National Program for Support of Top-Notch Young Professionals of China (2014)
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT-13R17]
  4. Hunan Provincial Science and Technology Plan Project [2018SK20410]
  5. Leading Talent of Technological Innovation of Hunan Province [2020RC4014]

向作者/读者索取更多资源

This study presents a facile defect-tailoring strategy for combined pollutants purification using BiVO4 photocatalysis, achieving a synchronous oxidation and reduction reaction in a coexistent environment. Results show that surface oxygen vacancies mediate these synchronous reactions, enhancing the reduction efficiency of Cr(VI) and maintaining the removal efficiency of TC-HCl.
Exploring active and ecological materials for the restoration of complex pollution system is highly desired. This study presents a facile defect-tailoring strategy for combined pollutants purification with BiVO4 photocatalysis in which the jointed synchronous reaction of oxidation and reduction is integrated instead of the sequential reaction in two individual systems. XPS and EPR reveal that BiVO4 with a suitable oxygen vacancies (OVs) concentration and distribution exhibits superior photocatalytic activity under the coexistence of TC-HCl and Cr(VI) with Cr(VI) reduction efficiency increased by 71 times compared with the individual Cr(VI) system along with TC-HCl removal efficiency comparable to a single TC-HCl system. The mechanism of synchronous redox reactions mediated by surface OVs is revealed by comprehensive characterization together with reaction kinetic analysis, and the electronic band structure adjustment induced by the OVs variation is confirmed. Active species identification tests and intermediate product analysis confirm that singlet oxygen (O-1(2)) accounts for the selective oxidation of TC-HCl, while electrons dominate the reduction of Cr(VI), under a coexistent environment. The influence of water quality parameters (e.g., pH, cations, anions, and organic substances) on the photocatalytic activity is investigated considering the complexity of the real aquatic environment. Importantly, toxicity assessment with Gram-negative strain E. coli as a model bacterium validates that the toxicity of the intermediates can be reduced to low or even ultralow levels. This work is dedicated to the mechanistic study of defect photocatalysis over BiVO4 and provides a jointed synchronous reaction system for combined pollutant purification.

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