Issue 20, 2021, Issue in Progress

A three-dimensional flower-like NiCo-layered double hydroxide grown on nickel foam with an MXene coating for enhanced oxygen evolution reaction electrocatalysis

Abstract

Electrolysis of water is currently one of the cleanest and most efficient ways to produce high-purity hydrogen. The oxygen evolution reaction (OER) at the anode of electrolysis is the key factor affecting the reaction efficiency, which involves the transfer of four electrons and can slow down the overall reaction process. In this work, using nickel foam coated with MXene (Ti3C2Tx) as the carrier, a three-dimensional flower-shaped layered double hydroxide (NiCo-LDH) is grown on Ti3C2Tx by a hydrothermal method to fabricate a NiCo-LDH/Ti3C2Tx/NF hybrid electrocatalyst for enhanced OER performance. The results reveal that the hybrid electrocatalyst has excellent OER activity in alkaline solution, in which a low overpotential of 223 mV and a small Tafel slope of 47.2 mV dec−1 can be achieved at a current density of 100 mA cm−2. The interface interaction and charge transfer between Ti3C2Tx and NiCo-LDH can accelerate the electron transfer rate during the redox process and improve the catalytic activity of the overall reaction. This NiCo-LDH/Ti3C2Tx/NF hybrid electrocatalyst may have important research significance and great application potential in catalytic electrolysis of water.

Graphical abstract: A three-dimensional flower-like NiCo-layered double hydroxide grown on nickel foam with an MXene coating for enhanced oxygen evolution reaction electrocatalysis

Supplementary files

Article information

Article type
Paper
Submitted
19 Feb 2021
Accepted
15 Mar 2021
First published
30 Mar 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 12392-12397

A three-dimensional flower-like NiCo-layered double hydroxide grown on nickel foam with an MXene coating for enhanced oxygen evolution reaction electrocatalysis

X. Li, Z. Zhang, Q. Xiang, R. Chen, D. Wu, G. Li and L. Wang, RSC Adv., 2021, 11, 12392 DOI: 10.1039/D1RA01368H

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