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Improved performance in dye-sensitized solar cells via controlling crystalline structure of nickel selenide.

Authors :
Qingsong Jiang
Ruoting Chen
Haichao Chen
Jinlong Jiang
Xiao Yang
Yongfeng Ju
Rendong Ji
Yulin Zhang
Source :
Journal of Materials Science; May2018, Vol. 53 Issue 10, p7672-7682, 11p, 1 Color Photograph, 1 Black and White Photograph, 2 Charts, 5 Graphs
Publication Year :
2018

Abstract

Nickel selenide with the single-phase structure has been widely studied as counterelectrode nanomaterials for dye-sensitized solar cells (DSCs). However, the effect mechanism of the crystalline structure on the electrocatalytic activity is still needed to be explored and analyzed in nickel selenide with hybrid structure. Therefore, NiSe/NiSe<subscript>2</subscript> hybrid nanomaterials are synthesized via a simple solvothermal approach in this work. NiSe/NiSe<subscript>2</subscript> counterelectrodes are constructed by spraying NiSe/NiSe<subscript>2</subscript> hybrid nanomaterials onto fluorine-doped tin oxide glass. The hybrid nanostructure of NiSe/NiSe<subscript>2</subscript> counterelectrodes exhibits the more catalytic active sites, strong charge separation, and transfer ability for the reduction of triiodide owing to the well-controlled crystalline structure of nickel selenide. Therefore, the results from electrochemical measurements prove that the electrocatalytic activity of the optimized NiSe/NiSe<subscript>2</subscript> counterelectrode is higher than that of platinum electrode. As a result, the DSC with the optimized NiSe/NiSe<subscript>2</subscript> counterelectrode yields a remarkable photoelectrical conversion efficiency of 7.78%, which is larger than that of the DSC based on platinum electrode (7.09%). Our research work provides the insight into design and construct of nickel selenide counterelectrodes of DSCs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222461
Volume :
53
Issue :
10
Database :
Complementary Index
Journal :
Journal of Materials Science
Publication Type :
Academic Journal
Accession number :
128200118
Full Text :
https://doi.org/10.1007/s10853-018-2065-2