Shelling with MoS$_2$ Functional CuS@MoS2 Hybrids as Electrocatalysts for the Oxygen Reduction and Hydrogen Evolution Reactions

TL;DR

This paper presents MoS₂-based hybrid nanostructures with CuS cores that enhance electrocatalytic activity for both hydrogen evolution and oxygen reduction reactions, offering a noble-metal free alternative for clean energy applications.

Contribution

The study introduces a novel CuS@MoS₂ hybrid nanostructure with controlled morphology that improves catalytic performance for HER and ORR, expanding MoS₂'s application scope.

Findings

Enhanced HER activity with 225 mV overpotential at 10 mA/cm²

Improved ORR onset potential of 0.87 V vs RHE

Controlled morphology affects catalytic efficiency

Abstract

The development of noble-metal free electrocatalysts is of high importance for clean energy conversion applications. MoS$_2$ has been considered as a promising low cost catalyst for the hydrogen evolution reaction (HER), however its activity is limited by poor conductivity and low abundance of active sites. Moreover, its suitability as an effective catalyst for other reactions, in particluar the oxygen reduction reaction (ORR), was hardly explored to date. Herein, we show hybrid nanostructures of shelled CuS particles with MoS$_2$ layers, which produces several outcomes: The MoS$_2$ shell is strained and defective, and charge transfer from the core to MoS$_2$ occurs, enabling activation of the basal plane of MoS$_2$. Changing the feed ratio of the precursors led to control over morphology, such that the wrapping of the cores with the shell was continuously varied and characterized. We found an optimal hybrid structure, which provided high electrochemical active surface area and fast charge transfer kinetics, leading to improved activity not only towards HER (overpotential of 225 mV at 10 mA cm$^{-1}$), but also for the sluggish ORR (onset potential 0.87 V vs RHE).