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Surface Wettability-Mediated Enhancement of Hydrogen Evolution Reaction Performance in Electron-Doped MoS<sub>2</sub> Monolayers

Authors
Lim, JungmoonKim, TaehunPark, HongjuEom, JaesikJung, MinByeon, JunsungLim, YounghoonPak, SangyeonCha, SeungNam
Issue Date
25-Mar-2024
Publisher
AMER CHEMICAL SOC
Keywords
MoS2 monolayer; hydrogen evolution reaction; halide doping; self-assembledmonolayer doping; energy level engineering; surfaceenergy
Citation
ACS APPLIED ENERGY MATERIALS, v.7, no.7, pp 2938 - 2945
Pages
8
Journal Title
ACS APPLIED ENERGY MATERIALS
Volume
7
Number
7
Start Page
2938
End Page
2945
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/33224
DOI
10.1021/acsaem.4c00189
ISSN
2574-0962
Abstract
Doping of monolayered MoS2 catalysts has drawn attention as the promising strategy that can improve the catalytic performance in hydrogen evolution reaction (HER) through enhancing charge transport properties in MoS2 catalysts. However, relatively little attention has been paid to identifying other parameters that affect the catalytic performance when the surface chemistry is altered. Here, we demonstrated that the doping strategies significantly affect not only the energy level of semiconducting catalysts but also the surface wettability of catalysts, which is crucial for the detachment of hydrogen gas bubbles in electrolyte solution. To evaluate the surface wettability-dependent hydrogen evolution performance in electron-donated MoS2 catalysts, we utilized halide atoms and self-assembled monolayer (SAM) molecules for dopants in the MoS2 monolayer, both of which are electron donors/acceptors that effectively improve/degrade catalytic performance compared with pristine MoS2. We found that halide doped Cl-MoS2 exhibited outstanding catalytic performance with 158 mV of overpotential at 10 mA/cm(2) compared to that of SAM-doped APTES-MoS2, which is attributed to the hydrophilic surface that led to rapid detachment of hydrogen gas bubbles, continuous reaction at the active sites of catalysts, and smooth ion diffusion in electrolyte.
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