Issue 61, 2018, Issue in Progress

Morphology engineering of nickel molybdate hydrate nanoarray for electrocatalytic overall water splitting: from nanorod to nanosheet

Abstract

The morphology of nano-arrays plays an important role in their applications for catalysis, energy, environment. However, the morphology modulation of nano-arrays generally involves complex optimization of synthetic conditions including surfactants, pH, and solvent. In this work, we synthesize a NiMoO4·H2O nano-array by a simple hydrothermal method under mild conditions (pH = 6.47, aqueous solution, and without the aid of surfactants). The morphology modulation of the NiMoO4·H2O nano-array is realized by simply changing the hydrothermal temperature. When the hydrothermal temperature below 150 °C, a NiMoO4·H2O nanorod array is obtained. While the hydrothermal temperature is as high as 180 °C, the array on Ni foam is nanosheet instead of nanorod. The NiMoO4·H2O nanorod array synthesized at 150 °C shows a superior water splitting activity compared to the NiMoO4·H2O nanosheet array, affording a large current density of 10 mA cm−2 at an overpotential of <240 and 200 mV toward oxygen evolution reaction and hydrogen evolution reaction, respectively. Furthermore, the electrolyzer using NiMoO4·H2O nanorod array as both anode and cathode electrodes for catalyzing overall water splitting exhibits great performance, obtaining a current density of 10 mA cm−2 at 1.67 V, comparable to the integration of commercial noble-metal Pt/C and IrO2 electrodes.

Graphical abstract: Morphology engineering of nickel molybdate hydrate nanoarray for electrocatalytic overall water splitting: from nanorod to nanosheet

Supplementary files

Article information

Article type
Paper
Submitted
02 Sep 2018
Accepted
28 Sep 2018
First published
12 Oct 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 35131-35138

Morphology engineering of nickel molybdate hydrate nanoarray for electrocatalytic overall water splitting: from nanorod to nanosheet

J. Wang, L. Li, L. Meng, L. Wang, Y. Liu, W. Li, W. Sun and G. Li, RSC Adv., 2018, 8, 35131 DOI: 10.1039/C8RA07323F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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