4.7 Article

Construction of direct Z-scheme BPQDs-modified BiOBr thin film for enhanced photocatalytic performance under visible light irradiation

Journal

JOURNAL OF MATERIOMICS
Volume 7, Issue 5, Pages 1122-1130

Publisher

ELSEVIER
DOI: 10.1016/j.jmat.2021.01.009

Keywords

Photocatalytic thin films; Direct Z-scheme; Surface modification; BPQDs; BiOBr

Funding

  1. National Natural Science Foundation of China [52002301, U1806221, 51672198]
  2. Natural Science Foundation of Hubei Province [2020CFB308]
  3. Start-up Funding ofWuhan University of Technology [40120490]
  4. Innovation and Development Project of Zibo City [2017 C x 01 A022]
  5. Instruction & Development Project for National Funding Innovation Demonstration Zone of Shandong Province [2016-181-11, 2017-41-1, 2017-41-3, 2018ZCQZB01, 2019ZCQZB03]
  6. Central Guiding Local Science and Technology Development Special Funds [2060503]
  7. Key Research & Design Program of Shandong Province [2019GGX102011]

Ask authors/readers for more resources

In this study, a direct Z-scheme photocatalytic system was successfully constructed by integrating black phosphorus quantum dots (BPQDs) on the surface of BiOBr thin film, leading to enhanced degradation activity for methyl violet (MV) and tetracycline hydrochloride (TC). The improved efficiency of charge separation, enhanced visible light absorption, and enlarged specific surface area were the key factors contributing to the enhanced photocatalytic performance of BPQDs/BiOBr.
Surface modification on photocatalytic thin films is long considered as an effective strategy to improve the degradation performance, which in turn helps to alleviate the worldwide environmental pollution issue. In this study, a direct Z-scheme photocatalytic system is constructed successfully by integrating black phosphorus quantum dots (BPQDs) on the surface of BiOBr thin film prepared by hydrothermal method. The optimal BPQDs/BiOBr-1 thin film presents remarkable enhanced photocatalytic activity for degrading methyl violet (MV) and tetracycline hydrochloride (TC), which is 3 and 3.65 times higher than that of pure BiOBr counterpart. The active species involved in the reaction are h(+), center dot O-2(-), and center dot OH, which determined by radical trapping experiments. The formation of direct Z-scheme photocatalytic system makes electrons assembled in the conduction band (CB) of BPQDs and holes gathered in the valence band (VB) of BiOBr, which supports the generation of h(+) and center dot O-2(-) and in turn accelerates the photocatalytic reaction. Besides, the improved efficiency of charge separation, enhanced visible light absorption and enlarged specific surface area also contributed to the enhanced photocatalytic performance of BPQDs/BiOBr. This work provides a feasible strategy for optimizing photocatalytic thin films via detailed analyzing the role of BPQDs in the construction of direct Z-scheme photocatalysts. (C) 2021 The Chinese Ceramic Society. Production and hosting by Elsevier B.V.

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