Inhibiting overoxidation of an α-MnO2 electrocatalyst by the lattice strain effect for efficient water oxidation†

EES catalysis Pub Date : 2025-06-23 DOI:10.1039/D5EY00106D
Fang-Yi Li, Shan Guan, Jianming Liu, Changhao Liu, Junfeng Zhang, Ju Gu, Zhaosheng Li, Zhigang Zou and Zhen-Tao Yu
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Abstract

The development of low-cost transition metal catalysts for use in alkaline water electrolysis (AWE) at high current densities is essential for achieving high-performance water splitting. Here, we reported a CrSb–MnO2 catalyst, which shows a low overpotential of 263 mV at 100 mA cm−2 and outstanding stability with only a small degradation of the catalyst after 100 h of operation at 1 A cm−2 (1 M KOH). In addition, the catalyst also achieved excellent performance in AWE (1.69 V@1 A cm−2). This enhanced performance is not only due to lattice-strain engineering, which effectively modulates the electronic configurations of the active sites, but also due to bimetallic synergy, which improves the dynamics of metal–metal charge transfer. In situ differential electrochemical mass spectrometry (DEMS) and Fourier-transform infrared (FTIR) analyses revealed that the CrSb–MnO2 catalyst preferred the adsorbate evolution mechanism (AEM) during the alkaline OER. This preference contributes to sustained stability under high current conditions in alkaline media. This work offers a novel approach for designing membrane electrodes that can operate efficiently and stably under large currents.

Abstract Image

通过晶格应变效应抑制α-MnO2电催化剂的过氧化,实现高效水氧化
开发用于高电流密度碱性电解(AWE)的低成本过渡金属催化剂是实现高效水分解的关键。在这里,我们报道了一种CrSb-MnO2催化剂,在100 mA cm - 2 (1 M KOH)下,其过电位低至263 mV,稳定性好,在1 a cm - 2 (1 M KOH)下运行100小时后,催化剂只发生了轻微的降解。此外,该催化剂在AWE中也取得了优异的性能(1.69 V@1 A cm−2)。这种增强的性能不仅是由于晶格应变工程,它有效地调节了活性位点的电子构型,而且由于双金属协同作用,它改善了金属-金属电荷转移的动力学。原位差示电化学质谱(dem)和傅里叶变换红外(FTIR)分析表明,CrSb-MnO2催化剂在碱性OER过程中倾向于吸附质演化机制(AEM)。这种偏好有助于在碱性介质的高电流条件下保持稳定性。这项工作为设计在大电流下高效稳定工作的膜电极提供了一种新的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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