2021
DOI: 10.1039/d0ma00688b
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Efficient electrochemical water splitting using copper molybdenum sulfide anchored Ni foam as a high-performance bifunctional catalyst

Abstract: A self-powered water electrolyzer system was constructed via integration of a solar cell with the fabricated CMS/Ni electrolyzer (acts as both anode (OER) and cathode (HER), which demonstrated potential application towards next-generation energy conversion and management systems.

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Cited by 14 publications
(14 citation statements)
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References 51 publications
(30 reference statements)
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“…Herein, we have developed P-doped and intercalated metallic (1T) copper molybdenum sulfide (P-1T-CMS) ultrathin nanosheet structures as a superior bifunctional electrocatalyst for low-potential overall water splitting. Previous reports showed that 2H-CMS bulk crystals have good EWS catalytical efficiency because of their crystallographic robustness with active edges and low hydrogen adsorption free energy, whereas bulk 2H-MoS 2 remains inert for EWS. , However, the nanostructures of 1T-CMS have not been investigated for EWS so far. We took the challenge for the first time in this report to fabricate stable P-doped and intercalated 1T-CMS nanostructures on carbon cloth (CC) and investigated their catalytic EWS efficacy.…”
Section: Introductionmentioning
confidence: 99%
“…Herein, we have developed P-doped and intercalated metallic (1T) copper molybdenum sulfide (P-1T-CMS) ultrathin nanosheet structures as a superior bifunctional electrocatalyst for low-potential overall water splitting. Previous reports showed that 2H-CMS bulk crystals have good EWS catalytical efficiency because of their crystallographic robustness with active edges and low hydrogen adsorption free energy, whereas bulk 2H-MoS 2 remains inert for EWS. , However, the nanostructures of 1T-CMS have not been investigated for EWS so far. We took the challenge for the first time in this report to fabricate stable P-doped and intercalated 1T-CMS nanostructures on carbon cloth (CC) and investigated their catalytic EWS efficacy.…”
Section: Introductionmentioning
confidence: 99%
“…The depletion of fossil energy resources coupled with the adverse effects of environmental pollution has enforced researchers to find a pollutant-free clean energy source. Electrocatalytic water splitting has emerged as a clean hydrogen-energy production method compared to steam-reforming natural gas and gasification of coal. The electrocatalytic water splitting consists of two reactions, hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). In an electrochemical cell, reduction occurs at the cathode where hydrogen evolution reactions occur (HER) and oxidation occurs at the anode where oxygen evolution reactions occur (OER). The equilibrium potentials for HERs and OERs are 0 and 1.23 V, respectively; however, we need some extra potential (overpotential) to split water due to sluggish reaction kinetics at the electrodes. It is highly essential to find a novel catalyst to accelerate the reaction rate at both the anode and cathode by promoting the charge transfer at the electrode–electrolyte interface.…”
Section: Introductionmentioning
confidence: 99%
“…For instance, copper molybdenum sulfide nanostructures anchored Ni foam has been demonstrated to act as bifunctional catalyst for overall water splitting. [ 28 ] Additionally, g‐C 3 N 4 nanosheets modified with Cu 2 MoS 4 have been utilized as efficient cocatalyst for photocatalytic water splitting under visible‐light illumination. [ 29 ] Another composite, namely, Ce‐MOF/Cu 2 MoS 4 , exhibited superior HER activity.…”
Section: Introductionmentioning
confidence: 99%