Published March 2018 | Version v1
Journal article

The sesame ball-like CoS/MoS2 nanospheres as efficient counter electrode catalysts for dye-sensitized solar cells

  • 1. Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, Heilongjiang University, Harbin, 150080 (China)
  • 2. Key Laboratory for Photonic and Electric Bandgap Materials, Ministry of Education, Harbin Normal University, Harbin, 150025 (China)

Description

Highlights: • CoS nanoparticles grew on the MoS2 nanosheets to get the sesame structure. • CoS/MoS2 nanospheres exhibited a high power conversion efficiency of 7.48%. • Co atoms were the main catalytic active site for I3 reduction. In this work, the sesame ball-like CoS/MoS2 nanospheres were controllably synthesized via a facile hydrothermal and solvothermal consecutive reaction. MoS2 nanospheres were preferentially formed by assembly of nanosheets during the hydrothermal reaction. And then CoS nanoparticles were grown on the surface of MoS2 nanosheets during the solvothermal reaction method. Due to the space confinement effect, CoS grew as nanoparticles with size of 5 nm between MoS2 nanosheets, and the nanosheets assembled into nanospheres to get the sesame ball-like structure. Because this composite possessed two merits, that is, more active sites of CoS nanoparticles and high conductivity of MoS2 nanospheres, DSSCs based on this sesame ball-like CoS/MoS2 nanospheres got a higher power conversion efficiency of 7.48%, which was higher than that based on the solo CoS (7.10%) and solo MoS2 (4.84%). And it was similarly to the DSSCs based on Pt cathode (7.51%). Their excellent electrocatalytic activities for the I3/I redox reaction was confirmed by cyclic voltammetry, electrochemical impedance spectra and Tafel polarization measurements. Density functional theory was also used to calculate the adsorption of I3 on the surface of CoS/MoS2, and the adsorption energy and bond length results indicated Co atoms were the main catalytic active site for I3 reduction. The hybrid interactions took place between p orbital of I and 3d states of Co, which lead to I3 was activated and dissociated easily.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2017.12.345

Additional details

Identifiers

DOI
10.1016/j.jallcom.2017.12.345;
PII
S0925838817345577;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
739
Journal Page Range
p. 568-576
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2018 Elsevier B.V. All rights reserved.