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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:

In this study, the reaction mechanisms of photodriven CO oxidation over both anatase and rutile TiO2 have been investigated from the hydrogen adsorption behavior. It can be beneficial when H-2 is introduced into CO oxidation system to increase the catalytic activity of rutile, while to decrease the catalytic activity of anatase. Further analysis revealed that H-2 molecule is dissociated on anatase surface, and then produce oxygen vacancies by dehydroxylation under UV irradiation. In contrast, the adsorbed H-2 (H-2 (ads)) with a non-dissociative mode does not activate the lattice oxygen (O-lat) over rutile. For anatase, CO oxidation reaction mainly undergoes the O-lat, activation process, while H-2 (ads) can inhibit the O-lat, activation, resulting in a suppressed CO oxidation. For rutile, the surface hydroxyls are the active species for CO oxidation, while H-2 (ads) can promote to form more surface hydroxyl species, resulting in a promoted CO oxidation.

Keyword:

Isotope labeling Light-driven CO oxidation Photo-assisted gas response Surface lattice oxygen TiO2

Community:

  • [ 1 ] [Wang, Zhongming]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 2 ] [Wang, Xiaoxiao]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 3 ] [Wang, Hong]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 4 ] [Chen, Xun]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 5 ] [Dai, Wenxin]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 6 ] [Fu, Xianzhi]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, 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, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China;;[Fu, Xianzhi]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China

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Source :

APPLIED CATALYSIS B-ENVIRONMENTAL

ISSN: 0926-3373

Year: 2020

Volume: 277

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: 27

SCOPUS Cited Count: 28

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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