Electrodeposited molybdenum sulfide as a cathode for proton exchange membrane water electrolyzer

Authors
Kim, Jung HwanKim, HyunkiKim, JunhyeongLee, Hye JinJang, Jong HyunAhn, Sang Hyun
Issue Date
2018-07-15
Publisher
ELSEVIER SCIENCE BV
Citation
JOURNAL OF POWER SOURCES, v.392, pp.69 - 78
Abstract
In this study, amorphous MoSx catalysts are fabricated on carbon paper using a simple one-step electrodeposition. Varying the deposition potential and time enables the simple control of the morphology and composition of MoSx catalysts, which affects their catalytic activity for hydrogen evolution reaction. The intrinsic activity based on their electrochemical surface area shows a significant relation with S atoms with higher binding energy. The lowest hydrogen evolving overpotential among the electrodeposited MoSx catalysts is - 159.8 mV at a current density of -10 mA cm(-2) with a Tafel slope of 42.3 mV dec(-1). The MoSx formed on carbon paper is directly implemented as a cathode in a proton exchange membrane water electrolyzer, and it displays acceptable cell performance. The following results demonstrate the potential for the use of amorphous MoSx catalysts as an alternative to noble metals in cathode of proton exchange membrane water electrolyzer.
Keywords
HYDROGEN EVOLUTION REACTION; MOS2 ULTRATHIN NANOSHEETS; ACTIVE EDGE SITES; EFFICIENT ELECTROCATALYST; CATALYTIC-ACTIVITY; SULFUR-ATOMS; DISULFIDE; NANOPARTICLES; PERFORMANCE; GRAPHENE; HYDROGEN EVOLUTION REACTION; MOS2 ULTRATHIN NANOSHEETS; ACTIVE EDGE SITES; EFFICIENT ELECTROCATALYST; CATALYTIC-ACTIVITY; SULFUR-ATOMS; DISULFIDE; NANOPARTICLES; PERFORMANCE; GRAPHENE; Proton exchange membrane water electrolyzer; Hydrogen evolution reaction; Electrodeposition; Amorphous molybdenum sulfide; High binding eergy sulfur
ISSN
0378-7753
URI
https://pubs.kist.re.kr/handle/201004/121149
DOI
10.1016/j.jpowsour.2018.04.087
Appears in Collections:
KIST Article > 2018
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