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author:

Xu, Chong (Xu, Chong.) [1] | Zhang, Jie (Zhang, Jie.) [2] (Scholars:张杰) | Qian, Xing (Qian, Xing.) [3] (Scholars:钱兴) | Wu, Weimin (Wu, Weimin.) [4] | Yang, Jiahui (Yang, Jiahui.) [5] | Hou, Linxi (Hou, Linxi.) [6] (Scholars:侯琳熙)

Indexed by:

EI Scopus SCIE

Abstract:

Due to the unique features including well-defined void space and high surface-to-volume ratio, non-noble metal catalysts with hollow structures have received intensive researches in dye-sensitized solar cells (DSSCs) and electrochemical water splitting. Herein, we prepare a series of cobalt-incorporated molybdenum sulfide hollow nanoboxes (denoted as Co-MoSx NBs) via a one-step fleet template conversion from cube-shaped Co-based zeolitic imidazolate framework-67 which precipitated without prolonged aged process. During above transformation, it is notable that the surface morphologies of nanobox can be effectively tailored by the proportion of MoS42-. The as-obtained Co-MoSx NBs with well-defined boxed structure and the appropriate doped ratio are developed as bifunctional catalysts for accelerating both reduction of I-3(-) in DSSCs and hydrogen evolution reaction (HER). As expected, a high power conversion efficiency (9.64%) is achieved by Co-MoSx-1/3 NBs based DSSC under AM 1.5G irradiation, which is much preceded to that of Pt (8.39%). Meanwhile, the practical utilization of Co-MoSx-1/3 NBs for HER yields a low onset overpotential (35 mV) and a small Tafel slope (61.4 mV decade(-1)) in alkaline medium. (C) 2018 Elsevier Ltd. All rights reserved.

Keyword:

Bifunctional electrocatalysts Cobalt molybdenum sulfide Dye-sensitized solar cells Hollow nanoboxes Hydrogen evolution reactions

Community:

  • [ 1 ] [Xu, Chong]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China
  • [ 2 ] [Zhang, Jie]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China
  • [ 3 ] [Qian, Xing]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China
  • [ 4 ] [Wu, Weimin]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China
  • [ 5 ] [Yang, Jiahui]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China
  • [ 6 ] [Hou, Linxi]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China

Reprint 's Address:

  • 钱兴 侯琳熙

    [Qian, Xing]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China;;[Hou, Linxi]Fuzhou Univ, Coll Chem Engn, Xueyuan Rd 2, Fuzhou 350116, Fujian, Peoples R China

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Source :

ELECTROCHIMICA ACTA

ISSN: 0013-4686

Year: 2018

Volume: 289

Page: 448-458

5 . 3 8 3

JCR@2018

5 . 5 0 0

JCR@2023

ESI Discipline: CHEMISTRY;

ESI HC Threshold:209

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count: 29

SCOPUS Cited Count: 32

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 4

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