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CuInS2Photocathodes with Atomic Gradation-Controlled (Ta,Mo) x(O,S) yPassivation Layers for Efficient Photoelectrochemical H2Production
  • Chae, Sang Youn ;
  • Kim, Yoolim ;
  • Park, Eun Duck ;
  • Im, Sang Hyuk ;
  • Joo, Oh Shim
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Publication Year
2021-12-15
Publisher
American Chemical Society
Citation
ACS Applied Materials and Interfaces, Vol.13, pp.58447-58457
Keyword
atomic gradationCuInS2passivation layerphotoelectrochemical celltantalum oxide
Mesh Keyword
Charge transportationE beam evaporationElectrocatalytic activityOnset potentialPassivation layerPhoto-electrodesPhotoelectrochemicalsTransient time
All Science Classification Codes (ASJC)
Materials Science (all)
Abstract
An atomic gradient passivation layer, (Ta,Mo)x(O,S)y, is designed to improve the charge transportation and photoelectrochemical activity of CuInS2-based photoelectrodes. We found that Mo spontaneously diffused to the a-TaOx layer during e-beam evaporation. This result indicates that the gradient profile of MoOx/TaOx is formed in the sublayer of (Ta,Mo)x(O,S)y. To understand the atomic-gradation effects of the (Ta,Mo)x(O,S)y passive layer, the composition and (photo)electrochemical properties have been characterized in detail. When this atomic gradient-passive layer is applied to CuInS2-based photocathodes, promising photocurrent and onset potential are seen without using Pt cocatalysts. This is one of the highest activities among reported CuInS2 photocathodes, which are not combined with noble metal cocatalysts. Excellent photoelectrochemical activity of the photoelectrode can be mainly achieved by (1) the electron transient time improved due to the conductive Mo-incorporated TaOx layer and (2) the boosted electrocatalytic activity by Mox(O,S)y formation.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32255
DOI
https://doi.org/10.1021/acsami.1c09560
Fulltext

Type
Article
Funding
This study was supported by the institutional program of the Korea Institute of Science and Technology (no. KIST-2E31241) and the C1 Gas Refinery Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (no. 2015M3D3A1A01064899). This research was also supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (no. 2020R1I1A1A01073326).
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PARK, EUN DUCK박은덕
Department of Chemical Engineering
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