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用于在宽pH介质中实现优于铂的析氢性能的顺序相转换诱导磷化物异质纳米棒阵列

Sequential Phase Conversion-Induced Phosphides Heteronanorod Arrays for Superior Hydrogen Evolution Performance to Pt in Wide pH Media.

作者信息

Yang Hongyuan, Guo Peifang, Wang Ruirui, Chen Ziliang, Xu Hongbin, Pan Hongge, Sun Dalin, Fang Fang, Wu Renbing

机构信息

Department of Materials Science, Fudan University, Shanghai, 200433, P. R. China.

Institute of Functional Nano and Soft Materials, Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, 215123, P. R. China.

出版信息

Adv Mater. 2022 May;34(20):e2107548. doi: 10.1002/adma.202107548. Epub 2022 Apr 11.

Abstract

Developing an efficient and non-precious pH-universal hydrogen evolution reaction electrocatalyst is highly desirable for hydrogen production by electrochemical water splitting but remains a significant challenge. Herein, a hierarchical structure composed of heterostructured Ni P-Ni P nanorod arrays rooted on Ni S film (Ni P-Ni P @Ni S ) via a simultaneous corrosion and sulfidation is built followed by a phosphidation treatment toward the metallic nickel foam. The combination of theoretical calculations with in/ex situ characterizations unveils that such a unique sequential phase conversion strategy ensures the strong interfacial coupling between Ni P and Ni P as well as the robust stabilization of 1D heteronanorod arrays by Ni S film, resulting in the promoted water adsorption/dissociation energy, the optimized hydrogen adsorption energy, and the enhanced electron/proton transfer ability accompanied with an excellent stability. Consequently, Ni P-Ni P @Ni S /NF requires only 32, 46, and 34 mV overpotentials to drive 10 mA cm in 1.0 m KOH, 0.5 m H SO , and 1.0 m phosphate-buffered saline electrolytes, respectively, exceeding almost all the previously reported non-noble metal-based electrocatalysts. This work may pave a new avenue for the rational design of non-precious electrocatalysts toward pH-universal hydrogen evolution catalysis.

摘要

开发一种高效且非贵金属的pH通用析氢反应电催化剂对于通过电化学水分解制氢非常有必要,但仍然是一项重大挑战。在此,通过同时腐蚀和硫化构建了一种分层结构,该结构由扎根于NiS薄膜(NiP-NiP@NiS)的异质结构NiP-NiP纳米棒阵列组成,随后对泡沫金属镍进行磷化处理。理论计算与原位/非原位表征相结合揭示,这种独特的顺序相转化策略确保了NiP和NiP之间的强界面耦合以及NiS薄膜对一维异质纳米棒阵列的稳健稳定作用,从而导致促进的水吸附/解离能、优化的氢吸附能以及增强的电子/质子转移能力,并具有出色的稳定性。因此,NiP-NiP@NiS/NF在1.0 m KOH、0.5 m H2SO4和1.0 m磷酸盐缓冲盐电解质中驱动10 mA cm-2分别仅需要32、46和34 mV的过电位,超过了几乎所有先前报道的非贵金属基电催化剂。这项工作可能为合理设计用于pH通用析氢催化的非贵金属电催化剂开辟一条新途径。

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