JOURNAL ARTICLE

3D 1T‐MoS2/CoS2 Heterostructure via Interface Engineering for Ultrafast Hydrogen Evolution Reaction

Abstract

Abstract Metallic phase (1T) MoS 2 has been regarded as an appealing material for hydrogen evolution reaction. In this work, a novel interface‐induced strategy is reported to achieve stable and high‐percentage 1T MoS 2 through highly active 1T‐MoS 2 /CoS 2 hetero‐nanostructure. Herein, a large number of heterointerfaces can be obtained by interlinked 1T‐MoS 2 and CoS 2 nanosheets in situ grown from the molybdate cobalt oxide nanorod under moderate conditions. Owing to the strong interaction between MoS 2 and CoS 2 , high‐percentage of metallic‐phase (1T) MoS 2 of 76.6% can be achieved, leading to high electroconductivity and abundant active sites compared to 2H MoS 2 . Furthermore, the interlinked MoS 2 and CoS 2 nanosheets can effectively disperse the nanosheets so as to enlarge the exposed active surface area. The near zero free energy of hydrogen adsorption at the heterointerface can also be achieved, indicating the fast kinetics and excellent catalytic activity induced by heterojunction. Therefore, when applied in hydrogen evolution reaction (HER), 1T‐MoS 2 /CoS 2 heterostructure delivers low overpotential of 71 and 26 mV at the current density of 10 mA cm −2 with low Tafel slops of 60 and 43 mV dec −1 , respectively in alkaline and acidic conditions.

Keywords:
Tafel equation Heterojunction Materials science Overpotential Nanorod Catalysis Chemical engineering Hydrogen Nanostructure Metal Oxide Nanotechnology Molybdate Phase (matter) Optoelectronics Electrode Electrochemistry Chemistry Physical chemistry Metallurgy

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153
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49
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0.97
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Topics

Electrocatalysts for Energy Conversion
Physical Sciences →  Energy →  Renewable Energy, Sustainability and the Environment
Advanced battery technologies research
Physical Sciences →  Engineering →  Electrical and Electronic Engineering
Advanced Photocatalysis Techniques
Physical Sciences →  Energy →  Renewable Energy, Sustainability and the Environment

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