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Author:

Kunfeng Zhang (Kunfeng Zhang.) | Hongxia Chen (Hongxia Chen.) | Wenbo Pei (Wenbo Pei.) | Hongxing Dai (Hongxing Dai.) | Junshan Li (Junshan Li.) | Yongfa Zhu (Yongfa Zhu.)

Abstract:

Herein,a series of three-dimensionally ordered macroporous(3DOM)Bi4O5Br2 photocatalysts with different macropore sizes were successfully fabricated via a polymethyl methacrylate(PMMA)template method.The photocatalytic activity for phenol degradation over 3DOM Bi4O5Br2 first increased and then decreased with the rise in macropore size.Specifically,3DOM Bi4O5Br2-255(macropore diameter ca.170 nm)exhibits the best photocatalytic activity in the static system,which is about 4.5,7.3,and 11.9 times higher than those of bulk Bi4O5Br2,Bi2WO6,and g-C3N4,respectively.Meanwhile,high phenol conversion(75%)is also obtained over 3DOM Bi4O5Br2-255 in the flow system under full spectrum irradiation.Furthermore,3DOM Bi4O5Br2-255 also shows strong mineralization capacity owing to the downward shift of valance band position(0.15 V)as compared with Bi4O5Br2.Total organic carbon(TOC)removal rate over 3DOM Bi4O5Br2-255(62%)is much higher than that of Bi4O5Br2(17%).The enhancement in photocatalytic performance of 3DOM Bi4O5Br2-255 is attributable to its better phenol adsorption,O2 activation,and charge separation and transfer abilities.This work combines the advantages of 3D structure and surface dangling bonds,providing new possibilities for designing highly efficient photocatalysts for pollutants removal.

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Author Community:

  • [ 1 ] [Kunfeng Zhang]Department of Chemistry,Tsinghua University,Beijing 100084,China;College of Environmental Engineering,Henan University of Technology,Zhengzhou 450001,China
  • [ 2 ] [Hongxia Chen]College of Environmental Engineering,Henan University of Technology,Zhengzhou 450001,China
  • [ 3 ] [Hongxing Dai]北京工业大学
  • [ 4 ] [Yongfa Zhu]清华大学
  • [ 5 ] [Wenbo Pei]北京工业大学
  • [ 6 ] [Junshan Li]成都大学

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Source :

纳米研究(英文版)

ISSN: 1998-0124

Year: 2023

Issue: 7

Volume: 16

Page: 8871-8881

9 . 9 0 0

JCR@2022

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count: -1

Chinese Cited Count:

30 Days PV: 5

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