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author:

Yue, Xuanyu (Yue, Xuanyu.) [1] | Zheng, Duojia (Zheng, Duojia.) [2] | Gao, Ming (Gao, Ming.) [3] | Wang, Ke (Wang, Ke.) [4] | Zhang, Zizhong (Zhang, Zizhong.) [5] (Scholars:张子重) | Dai, Wenxin (Dai, Wenxin.) [6] (Scholars:戴文新) | Fu, Xianzhi (Fu, Xianzhi.) [7] (Scholars:付贤智)

Indexed by:

EI Scopus SCIE

Abstract:

The direct decomposition of CO2 to produce CO and O-2 requires extremely high temperatures in catalysis. Here, we proposed the photoassisted oxygen vacancy active sites for CO2 dissociation to lower the reaction temperature. The designed low-crystalline Nb2O5 nanoribbons (LC-Nb2O5 NRs) showed a good CO production rate under mild conditions (<= 250 degrees C) with Xe lamp irradiation. Under light irradiation, the rate of CO yields of LC-Nb2O5 NRs increased to 68 mu mol g(-1) h(-1) at 250 degrees C, with no activity at all under light conditions. The high activity arose from unsaturated coordination with low crystallinity and CO2 reactants as an electron donor for forming an electron cycle with the Nb2O5 NRs, which played a key role in the generation of oxygen vacancies for the subsequent photoexcited electron transfer process at mild temperatures. The feasibility of this approach is further verified over Nb2O5/C nanofibers that make full use of photothermal and photoelectric effects to achieve long-term stable CO2 decomposition.

Keyword:

CO2 decomposition electron cycle low-crystallineNb(2)O(5) oxygen defects photothermal catalysis

Community:

  • [ 1 ] [Yue, Xuanyu]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 2 ] [Zheng, Duojia]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 3 ] [Wang, Ke]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
  • [ 4 ] [Zhang, Zizhong]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 ] [Yue, Xuanyu]Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
  • [ 8 ] [Zheng, Duojia]Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
  • [ 9 ] [Zhang, Zizhong]Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
  • [ 10 ] [Dai, Wenxin]Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
  • [ 11 ] [Fu, Xianzhi]Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
  • [ 12 ] [Gao, Ming]Sichuan Univ, Coll Architecture & Environm, State Key Lab Hydraul & Mt River Engn, Chengdu 610065, Peoples R China

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Source :

ACS CATALYSIS

ISSN: 2155-5435

Year: 2023

Issue: 24

Volume: 13

Page: 15841-15850

1 1 . 7

JCR@2023

1 1 . 7 0 0

JCR@2023

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count: 11

SCOPUS Cited Count: 3

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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