Highly Corrugated Ni Films Electrodeposited onto Boron Doped Diamond Electrodes for Alkaline Water Electrolysis.

ACS electrochemistry Pub Date : 2025-10-20 eCollection Date: 2025-11-06 DOI:10.1021/acselectrochem.5c00319
Alexander W Black, Paul W May, David J Fermin
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Abstract

Ni-based electrocatalysts are among the most active materials for the hydrogen evolution reaction (HER) in alkaline media. In this work, we demonstrate the ability to use films of boron-doped diamond (BDD), a stable and corrosion-resistant electrode material, as a support for highly textured Ni films. Our approach is based on the electrodeposition of NiCu alloy thin-films, followed by electrochemical dealloying. The structure and composition of the electrocatalysts were characterized using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. In pH 13 KOH, a dealloyed Ni catalyst corresponding to an initial NiCu composition of 68% Ni, gave a HER overpotential at 10 mA cm-2 of 152 mV. With further analysis, we show that the rate of HER is 2nd order with respect to the number of Ni active sites, and that the kinetics are limited by the surface diffusion of adsorbed intermediates. Two Tafel slopes are additionally observed, suggesting a change in HER mechanism and intrinsic activity at dealloyed Ni catalysts.

高波纹镍膜电沉积在硼掺杂金刚石电极上用于碱性水电解。
镍基电催化剂是碱性介质中析氢反应最活跃的材料之一。在这项工作中,我们展示了使用硼掺杂金刚石(BDD)薄膜的能力,这是一种稳定且耐腐蚀的电极材料,作为高度纹理化的Ni薄膜的支撑。我们的方法是基于NiCu合金薄膜的电沉积,然后是电化学合金化。采用扫描电子显微镜、x射线衍射和x射线光电子能谱对电催化剂的结构和组成进行了表征。在pH为13 KOH的条件下,初始NiCu成分为68% Ni的合金镍催化剂在10 mA cm-2时产生了152 mV的HER过电位。通过进一步分析,我们发现,相对于Ni活性位点的数量,HER的速率是二阶的,并且动力学受到吸附中间体表面扩散的限制。另外还观察到两个Tafel斜率,表明合金镍催化剂的HER机制和固有活性发生了变化。
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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