Youmei Kong, Wei Yang, Jingjing Bao, Licheng Sun, Yang Qiu, Yu Chen, Qiang Zhao, Min Du, Zhengyu Mo
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引用次数: 0
Abstract
Engineering a robust non-platinum electrode toward hydrogen evolution reaction (HER) is important for water electrolysis. Here we develop a nanotip-structured electrode through a solution phase etching procedure. Based on the experimental and finite element simulation, the results show that the nanotip-structured design of electrodes cannot only lower the adhesion force of bubbles, but also induce a local-concentrated electric field that can promote the formation of Marangoni effect, and K concentrated and local acid-like microenvironment, consequently facilitating the detachment of bubbles and the HER kinetics. The electrochemical measurements and density function theory (DFT) calculation indicate that the constructed electrode exhibits a low H* binding energy and an outstanding HER performance that outperforms the commercial Pt/C in pH-universal medium. Overall, this work provides a feasible strategy for electrode design with a pH-universal feasibility by precisely constructing electrode interfaces.
设计一种坚固耐用的非铂电极以实现氢进化反应(HER)对于电解水非常重要。在这里,我们通过溶液相蚀刻程序开发了一种纳米尖端结构电极。基于实验和有限元模拟的结果表明,纳米尖端结构的电极设计不仅能降低气泡的粘附力,还能诱导局部集中的电场,促进马兰戈尼效应的形成,以及 K 浓度和局部酸样微环境的形成,从而促进气泡的脱落和 HER 动力学的产生。电化学测量和密度函数理论(DFT)计算表明,所构建的电极具有较低的 H* 结合能和出色的 HER 性能,在 pH 值通用介质中优于商用 Pt/C。总之,这项研究通过精确构建电极界面,为具有 pH 通用性的电极设计提供了一种可行的策略。