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Patchwork-Structured Heterointerface of 1T-WS2/a-WO3 with Sustained Hydrogen Spillover as a Highly Efficient Hydrogen
Jinill Cho1, Minjun Kim2, Hyunho Seok2
1School of Mechanical Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
ACS Applied Materials & Interfaces
|May 13, 2022
Summary
This study enhances hydrogen evolution reaction (HER) electrocatalysis by creating a tungsten oxide (WO3) interface with tungsten disulfide (WS2). This novel WSO structure improves proton transfer, boosting HER performance for efficient water splitting.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Tungsten disulfide (WS2) is a promising electrocatalyst for the hydrogen evolution reaction (HER).
- Improving the intrinsic catalytic activity of WS2 is crucial for efficient water splitting.
- Facilitating proton transfer to active sites is key to enhancing HER performance.
Purpose of the Study:
- To introduce a nanodomain tungsten oxide (WO3) interface to 1T-WS2.
- To enhance HER performance by facilitating proton transfer to active sites.
- To develop a novel strategy for efficient water splitting.
Main Methods:
- Fabrication of a patchwork-structured heterointerface (WSO) of 1T-WS2/a-WO3 using H2S and O2 plasma treatments.
- Characterization of the WSO structure and its interface properties.
- Electrochemical evaluation of HER activity and density functional theory (DFT) calculations.
Main Results:
- The WSO interface, particularly WSO-1.2, demonstrated remarkable HER activity with an overpotential of 212 mV at 10 mA/cm².
- The hydrophilic WO3 interface facilitated the hydrogen spillover effect and acted as an efficient proton channel.
- DFT calculations confirmed higher proton binding energies on WO3 and reduced HER overpotential on 1T-WS2.
Conclusions:
- The developed 1T-WS2/a-WO3 heterointerface significantly enhances HER performance through improved proton transport.
- This strategy offers a novel approach for designing advanced electrocatalysts for water splitting.
- Efficient proton channeling is a viable pathway to boost catalytic activity in energy conversion reactions.
Keywords:
1T-WS2amorphous WO3hydrogen evolution reactionhydrogen spillover effectplasma-enhanced chemical vapor deposition
