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Production of SnS2 Nanostructure as Improved Light-Assisted Electrochemical Water Splitting.
Song, Haizeng; Wu, Han; Gao, Yuan; Wang, Ka; Su, Xin; Yan, Shancheng; Shi, Yi.
  • Song H; Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, China.
  • Wu H; School of Electronic Science and Engineering, Nanjing University, Nanjing 210093, China.
  • Gao Y; Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, China.
  • Wang K; School of Electronic Science and Engineering, Nanjing University, Nanjing 210093, China.
  • Su X; School of Geography and Biological Information, Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
  • Yan S; School of Geography and Biological Information, Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
  • Shi Y; Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, China.
Nanomaterials (Basel) ; 9(9)2019 Sep 01.
Article en En | MEDLINE | ID: mdl-31480597
ABSTRACT
Tin disulfide (SnS2) has gained a lot of interest in the field of converting solar energy into chemical fuels in light-assisted electrochemical water splitting due to its visible-light band gap and high electronic mobility. However, further decreasing the recombination rate of electron-hole pairs and increasing the density of active states at the valence band edge of the photoelectrodes were a critical problem. Here, we were successful in fabricating the super-thin SnS2 nanostructure by a hydrothermal and solution etching method. The super-thin SnS2 nanostructure as a photo-electrocatalytic material exhibited low overpotential of 0.25 V at the current density of -10 mA·cm-2 and the potential remained basically unchanged after 1000 cycles in an H2SO4 electrolyte solution, which was better than that of the SnS2 nanosheet and SnS/SnS2 heterojunction nanosheet. These results show the potential application of super-thin SnS2 nanostructure in electrochemical/photo-electrocatalytic field.
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