Issue 6, 2019

Asymmetric electrodes with a transition metal disulfide heterostructure and amorphous bimetallic hydroxide for effective alkaline water electrolysis

Abstract

Through hydro- and solvothermal methods and an electrodeposition-assisted in situ growth strategy, a transition metal disulfide (TMD)-assembled heterostructural cathode (Ni3S2/MoS2-CC) and derivative TMD superficial amorphous bimetallic hydroxide-coated anode (NiFe(OH)x@Ni3S2/MoS2-CC) were successfully prepared for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. The synthesized electrodes demonstrate first-rate performance with enhanced durability for electrolysis. Individually, Ni3S2/MoS2-CC affords an overpotential (η) of 173 mV (at 100 mA cm−2) in HER, while NiFe(OH)x@Ni3S2/MoS2-CC affords an η of 309 mV (at 100 mA cm−2) in OER. Tight interstratification between the nanosheet (NS) array and amorphous bimetallic hydroxides lead to enhanced affinity for OH/H+, improved conductivity, increased charge transfer, and enriched active sites. The two-electrode alkaline (1.0 M KOH) electrolyzer (NMC//NFNMC) requires a low overall voltage (ΔV) of 1.55 and 1.71 V to reach 10 and 100 mA cm−2, respectively. The rational combination of TMDs and TMDs/NiFe(OH)x delivers a useful methodology for designing and constructing low-cost, hierarchical, transition metal-based composite catalysts with high performance for water electrolysis.

Graphical abstract: Asymmetric electrodes with a transition metal disulfide heterostructure and amorphous bimetallic hydroxide for effective alkaline water electrolysis

Supplementary files

Article information

Article type
Paper
Submitted
31 Oct 2018
Accepted
02 Jan 2019
First published
03 Jan 2019

J. Mater. Chem. A, 2019,7, 2895-2900

Asymmetric electrodes with a transition metal disulfide heterostructure and amorphous bimetallic hydroxide for effective alkaline water electrolysis

X. H. Wang, Y. Ling, B. L. Li, X. L. Li, G. Chen, B. X. Tao, L. J. Li, N. B. Li and H. Q. Luo, J. Mater. Chem. A, 2019, 7, 2895 DOI: 10.1039/C8TA10458A

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