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author:

Liang, S. (Liang, S..) [1] | Zhu, S. (Zhu, S..) [2] | Chen, Y. (Chen, Y..) [3] | Wu, W. (Wu, W..) [4] | Wang, X. (Wang, X..) [5] | Wu, L. (Wu, L..) [6]

Indexed by:

Scopus

Abstract:

Visible light-activated SnNb 2O 6 nanosheets (NSs) with high surface area and small crystallites have been prepared by a microwave-assisted template-free hydrothermal method without exfoliation for the first time. This approach could be used to prepare the functional materials efficiently and extended to synthesizing two-dimensional nanosheet materials directly as well. The crystalline phases, photoabsorption performances, and surface areas and porosity of the samples are characterized by XRD, UV-vis diffuse reflectance spectroscopy (UV-vis DRS), and N 2-adsorption. Results show that a hypsochromic shift of the photoabsorption edge is observed, which reflects an obvious quantum size effect. TEM images reveal SnNb 2O 6 nanosheets with a thickness of 1-4 nm versus several hundred nanometres in lateral size. Based on the experimental results, the formation mechanism of SnNb 2O 6 nanosheets is also studied and proposed, which reasonably follows a synergy interaction of reaction-crystallization and dissolution-recrystallization processes. Due to the unique morphology, larger surface area, smaller crystallites and stronger redox ability of the photogenerated hole-electron pair, these photocatalysts show much higher photocatalytic activities for the degradation of rhodamine B (RhB) compared with their counterparts prepared by the traditional solid-state reaction. The reaction rate is enhanced by over 4 times and the RhB molecule can be mineralized into CO 2 and H 2O over SnNb 2O 6 NSs. The decomposition mechanism of RhB over SnNb 2O 6 under visible light irradiation and the active species in the photocatalytic process have also been discussed. © 2012 The Royal Society of Chemistry.

Keyword:

Community:

  • [ 1 ] [Liang, S.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 2 ] [Zhu, S.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 3 ] [Chen, Y.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 4 ] [Wu, W.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 5 ] [Wang, X.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 6 ] [Wu, L.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 7 ] [Wu, L.]State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China

Reprint 's Address:

  • [Wu, L.]State Key Laboratory Breeding Base of Photocatalysis, Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China

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Source :

Journal of Materials Chemistry

ISSN: 0959-9428

Year: 2012

Issue: 6

Volume: 22

Page: 2670-2678

6 . 1 0 8

JCR@2012

6 . 6 2 6

JCR@2013

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 102

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 2

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