Issue 25, 2023

Novel high-entropy layered double hydroxide microspheres as an effective and durable electrocatalyst for oxygen evolution

Abstract

In this work, novel high-entropy layered double hydroxide (HELDH) microspheres consisting of nanosheets were synthesized via a simple hydrothermal method through utilizing the combination of low-cost active transition metal elements such as Ni, Fe, Mn, Zn, and Co, as well as non-active Mg and Al elements for electrocatalysis. The reported flower-like seven-element HELDH microspheres self-supported on a nickel foam substrate outperformed the hydroxide analogues with a similar structure in the electrocatalytic oxygen evolution reaction. Specifically, the optimal sample only requires a low overpotential of 183 mV to obtain a current density of 10 mA cm−2 with a small Tafel slope of 49.21 mV dec−1 (more active than RuO2 electrocatalysts) and has an outstanding cycling stability. Furthermore, in 1.0 mol L−1 KOH solution, the potential shows only a negligible increase (<5%) after a continuous test of 48 h even at a high current density of 250 mA cm−2, suggesting its robust durability and promising potential for practical industrial application as OER catalysts. Thus, the present work provided a new strategy to design and prepare high-performance HEM electrocatalysts. In addition, the theoretically calculated results based on density functional theory with the proposed models completely support our experimental results, which provide a new way to manipulate the catalytic performance of HEM electrocatalysts.

Graphical abstract: Novel high-entropy layered double hydroxide microspheres as an effective and durable electrocatalyst for oxygen evolution

Supplementary files

Article information

Article type
Paper
Submitted
09 Mar 2023
Accepted
22 May 2023
First published
23 May 2023

J. Mater. Chem. A, 2023,11, 13697-13707

Novel high-entropy layered double hydroxide microspheres as an effective and durable electrocatalyst for oxygen evolution

S. Li, L. Tong, Z. Peng, B. Zhang and X. Fu, J. Mater. Chem. A, 2023, 11, 13697 DOI: 10.1039/D3TA01454A

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