• Complex
  • Title
  • Keyword
  • Abstract
  • Scholars
  • Journal
  • ISSN
  • Conference
成果搜索

author:

Tian, Q. (Tian, Q..) [1] | Wei, W. (Wei, W..) [2] | Dai, J. (Dai, J..) [3] | Sun, Q. (Sun, Q..) [4] | Zhuang, J. (Zhuang, J..) [5] | Zheng, Y. (Zheng, Y..) [6] | Liu, P. (Liu, P..) [7] | Fan, M. (Fan, M..) [8] | Chen, L. (Chen, L..) [9]

Indexed by:

Scopus

Abstract:

Low light-absorption capacity and separation efficiency of photo-generated charges are two major limit factors to achieve high performance of photocatalysts. Herein, porous core-shell TixSn1-xO2 solid solutions with effective light-absorption capacity and charge separation are fabricated through one-pot mild solvothermal method without any surfactant and template. The self-development mechanism of the porous core-shell microspheres includes prior Ti-alkoxide hydrolysis and the spontaneous nucleation of TixSn1-xO2 combined with Ostwald ripening. Interestingly, although both TiO2 and SnO2 are wide band gap semiconductors, the prepared yellow TixSn1-xO2 solid solutions are of controllable band structure and broad-light response capacity. When Ti:Sn molar ratio is 7:3, the Ti0.7Sn0.3O2 sample shows the highest MO-photodegradation rate constant of 0.62 min−1 under UV irradiation, exceeding that of commercial TiO2 (0.04 min−1) by more than 15 times. Particularly, the sample also exhibits ultrahigh photocatalytic activity in MO-photodegradation (0.038 min−1) and As(III) removal (up to 100%) under visible-light (≥420 nm) irradiation. The mechanism study reveals that due to the proper redox potential of SnIV/SnII and the structural defects (e.g., oxygen vacancies) caused by lattice distortion, the photogenerated electrons would be trapped and the holes act as the main active species for the photooxidation reaction of MO and As(III) over TixSn1-xO2 photocatalysts. © 2018 Elsevier B.V.

Keyword:

Broad-light responsive; Ostwald ripening; Porous core-shell microspheres; TixSn1-xO2 solid solutions; Ultrahigh photooxidation performance

Community:

  • [ 1 ] [Tian, Q.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • [ 2 ] [Tian, Q.]State Key Laboratory of Photocatalysis on Energy and Environment, Research Institute of Photocatalysis, Fuzhou University, Fuzhou, 350002, China
  • [ 3 ] [Wei, W.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • [ 4 ] [Dai, J.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • [ 5 ] [Sun, Q.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • [ 6 ] [Zhuang, J.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • [ 7 ] [Zheng, Y.]State Key Laboratory of Photocatalysis on Energy and Environment, Research Institute of Photocatalysis, Fuzhou University, Fuzhou, 350002, China
  • [ 8 ] [Liu, P.]State Key Laboratory of Photocatalysis on Energy and Environment, Research Institute of Photocatalysis, Fuzhou University, Fuzhou, 350002, China
  • [ 9 ] [Fan, M.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • [ 10 ] [Chen, L.]College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou, 350002, China

Reprint 's Address:

  • [Zhuang, J.]College of Materials Engineering, Fujian Agriculture and Forestry UniversityChina

Show more details

Related Keywords:

Related Article:

Source :

Applied Catalysis B: Environmental

ISSN: 0926-3373

Year: 2019

Volume: 244

Page: 45-55

1 6 . 6 8 3

JCR@2019

2 0 . 3 0 0

JCR@2023

ESI HC Threshold:184

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

Affiliated Colleges:

Online/Total:79/10100226
Address:FZU Library(No.2 Xuyuan Road, Fuzhou, Fujian, PRC Post Code:350116) Contact Us:0591-22865326
Copyright:FZU Library Technical Support:Beijing Aegean Software Co., Ltd. 闽ICP备05005463号-1