Zihan Zhou, Liyang Xiao, Jun Zhao, Miao Zhou, Jingtong Zhang, Xiwen Du and Jing Yang
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引用次数: 0
Abstract
Pd-based catalytic electrodes for the hydrogen evolution reaction (HER) are promising as a replacement of Pt-based catalysts, but their strong hydrogen adsorption hinders hydrogen desorption and thus limits HER catalytic activity. Here, we report a function–structure integrated D-Ni3.5Pd/NF catalytic electrode with a very low Pd loading (0.19 mgPd cm−2) and a large number of edge dislocations, which was prepared by millisecond laser direct writing in liquid nitrogen. The plentiful dislocations induce a strain effect leading to reduced hydrogen adsorption energies of Pd sites and enhanced water dissociation ability of Ni sites. Thereby, the dense dislocations improve the alkaline HER intrinsic activity and electrochemical stability of D-Ni3.5Pd/NF under high current densities. The as-prepared electrodes can achieve fairly low overpotentials of 35 and 352 mV at 10 mA cm−2 and 1 A cm−2 in a 1 M KOH electrolyte, respectively, while the Tafel slope is only 62.3 mV dec−1. In addition, its overpotential only increases by 4.2% after 100 h of the chronoamperometric test at 500 mA cm−2, showing an outstanding electrochemical stability at high current densities.
用于析氢反应(HER)的Pd基催化电极有望取代Pt基催化剂,但其强烈的氢吸附阻碍了氢的解吸,从而限制了HER的催化活性。在这里,我们报道了一种功能-结构集成的D-Ni3.5Pd/NF催化电极,其具有非常低的Pd负载(0.19 mgPd cm−2)和大量的边缘位错,该电极是通过在液氮中的毫秒激光直接写入制备的。大量的位错引起应变效应,导致Pd位点的氢吸附能降低,Ni位点的水离解能力增强。因此,致密位错提高了D-Ni3.5Pd/NF在高电流密度下的碱性HER本征活性和电化学稳定性。在1M KOH电解质中,在10 mA cm−2和1 A cm−2下,所制备的电极可以分别获得35和352 mV的相当低的过电位,而Tafel斜率仅为62.3 mV dec−1。此外,在500 mA cm−2的计时电流测试100小时后,其过电位仅增加4.2%,在高电流密度下表现出出色的电化学稳定性。
期刊介绍:
Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome.
This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.