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author:

Wang, Zhongming (Wang, Zhongming.) [1] | Wang, Xiaoxiao (Wang, Xiaoxiao.) [2] | Wang, Hong (Wang, Hong.) [3] | Chen, Xun (Chen, Xun.) [4] (Scholars:陈旬) | Dai, Wenxin (Dai, Wenxin.) [5] (Scholars:戴文新) | Fu, Xianzhi (Fu, Xianzhi.) [6] (Scholars:付贤智)

Indexed by:

EI Scopus SCIE

Abstract:

Visible-light-driven CO conversion has attracted many research efforts. Herein we study the reaction mechanism from the perspective of electron transfer behavior during CO adsorption (CO (ad)). The WO3 and CuWO4/WO3 films were in-situ synthesized, and then were investigated their behaviors for adsorbing CO and catalyzing CO conversion under visible light via gas sensing system and in-situ DRIFTS testing, respectively. It was found that the CO (ad) at W5+-W5+ site will form bridge adsorbed CO species over WO3, and donate electrons to W5+, resulting in its light-driven oxidation by O-2. The CO (ad) at W-0 site forms linear and gem-dicarbonyl adsorbed CO species over CuWO4/WO3, and accept electrons from W-0, then its reduction by H-2. The result shows the light-driven CO oxidation or reduction on WO3 and CuWO4/WO3 would be somewhat dependent on the electron transfer behavior induced by different modes of CO chemisorption and the Fermi level of sample itself.

Keyword:

CO chemisorption CO oxidation & reduction DFT calculations Electron transfer Photo-assisted gas response

Community:

  • [ 1 ] [Wang, Zhongming]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 2 ] [Wang, Xiaoxiao]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 3 ] [Wang, Hong]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 4 ] [Chen, Xun]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 5 ] [Dai, Wenxin]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 6 ] [Fu, Xianzhi]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 7 ] [Wang, Zhongming]Fujian Prov Univ, Fuzhou Univ, Key Lab Ecomat Adv Technol, Fuzhou 350002, Peoples R China
  • [ 8 ] [Wang, Xiaoxiao]Fujian Prov Univ, Fuzhou Univ, Key Lab Ecomat Adv Technol, Fuzhou 350002, Peoples R China
  • [ 9 ] [Wang, Hong]Fujian Prov Univ, Fuzhou Univ, Key Lab Ecomat Adv Technol, Fuzhou 350002, Peoples R China
  • [ 10 ] [Dai, Wenxin]Fujian Prov Univ, Fuzhou Univ, Key Lab Ecomat Adv Technol, Fuzhou 350002, Peoples R China

Reprint 's Address:

  • 戴文新 付贤智

    [Dai, Wenxin]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China;;[Fu, Xianzhi]Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China;;[Dai, Wenxin]Fujian Prov Univ, Fuzhou Univ, Key Lab Ecomat Adv Technol, Fuzhou 350002, Peoples R China

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Source :

APPLIED CATALYSIS B-ENVIRONMENTAL

ISSN: 0926-3373

Year: 2020

Volume: 265

1 9 . 5 0 3

JCR@2020

2 0 . 3 0 0

JCR@2023

ESI Discipline: CHEMISTRY;

ESI HC Threshold:160

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count: 28

SCOPUS Cited Count: 34

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 2

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