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Fabrication of Multiple Heterojunctions with Tunable Visible-Light-Active Photocatalytic Reactivity in BiOBr–BiOI Full-Range Composites Based on Microstructure Modulation and Band Structures

ACS Applied Materials & Interfaces · 2014 · Vol. 7(1) · pp. 482–492
Hongwei HuangXu HanXiaowei LiShichao WangPaul K. ChuYihe Zhang

Abstract

The fabrication of multiple heterojunctions with tunable photocatalytic reactivity in full-range BiOBr-BiOI composites based on microstructure modulation and band structures is demonstrated. The multiple heterojunctions are constructed by precipitation at room temperature and characterized systematically. Photocatalytic experiments indicate that there are two types of heterostructures with distinct photocatalytic mechanisms, both of which can greatly enhance the visible-light photocatalytic performance for the decomposition of organic pollutants and generation of photocurrent. The large separation and inhibited recombination of electron-hole pairs rendered by the heterostructures are confirmed by electrochemical impedance spectra (EIS) and photoluminescence (PL). Reactive species trapping, nitroblue tetrazolium (NBT, detection agent of (•)O2(-)) transformation, and terephthalic acid photoluminescence (TA-PL) experiments verify the charge-transfer mechanism derived from the two types of heterostructures, as well as different enhancements of the photocatalytic activity. This article provides insights into heterostructure photocatalysis and describes a novel way to design and fabricate high-performance semiconductor composites.

Advanced Photocatalysis TechniquesPerovskite Materials and ApplicationsGas Sensing Nanomaterials and SensorsMaterials sciencePhotocatalysisHeterojunctionPhotoluminescencePhotocurrentMicrostructureOptoelectronicsSemiconductorDielectric spectroscopyComposite material

Funding

  • National Natural Science Foundation of China
  • Ministry of Education of the People's Republic of China
  • Ministry of Science and Technology of the People's Republic of China
Citations
719
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