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用于水电解析氢反应的磷化镍的合成、物理性质及电催化性能

Synthesis, Physical Properties and Electrocatalytic Performance of Nickel Phosphides for Hydrogen Evolution Reaction of Water Electrolysis.

作者信息

Liu Gaoyang, Hou Faguo, Peng Shanlong, Wang Xindong, Fang Baizeng

机构信息

Department of Energy Storage Science and Technology, University of Science and Technology Beijing, 30 College Road, Beijing 100083, China.

Department of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, 30 College Road, Beijing 100083, China.

出版信息

Nanomaterials (Basel). 2022 Aug 25;12(17):2935. doi: 10.3390/nano12172935.

Abstract

Nickel phosphides have been investigated as an alternative to noble metals and have emerged as potential catalysts that can efficiently catalyze the hydrogen evolution reaction (HER). However, the impacts of facet morphology and crystal structure of the nickel phosphides on their catalytic reactivity have not been systematically investigated. Herein, nickel phosphides with different crystalline states were prepared through a facile calcination treatment. It was found that the calcination treatment had important effects on the phase compositions, morphologies, and crystallinity of nickel phosphides, which are closely related to their HER activity. Generally, the crystallized Ni-P catalysts exhibited faster kinetics than the amorphous Ni-P. In particular, the Ni-P 300 showed remarkable HER performance with η10 of ca. 65 mV, along with a very low Tafel slope of ca. 44 mV dec due to the increased catalytically active sites. Furthermore, the Ni-P 300 exhibited negligible decay during the 140 h galvanostatic electrolysis, showing better catalytic stability than the commercial Pt/C catalyst. Compared with the amorphous Ni-P, the boosted HER activity of the Ni-P 300 could benefit from the mixed nanocrystalline NiP and NiP, which could contribute to the H adsorption/desorption abilities and helped provide more activity sites, promoting the HER performance.

摘要

磷化镍已被作为贵金属的替代品进行研究,并已成为能够有效催化析氢反应(HER)的潜在催化剂。然而,磷化镍的晶面形态和晶体结构对其催化活性的影响尚未得到系统研究。在此,通过简便的煅烧处理制备了具有不同晶态的磷化镍。发现煅烧处理对磷化镍的相组成、形貌和结晶度有重要影响,而这些与它们的析氢活性密切相关。一般来说,结晶态的Ni-P催化剂比非晶态的Ni-P表现出更快的动力学。特别是,Ni-P 300表现出显著的析氢性能,η10约为65 mV,同时由于催化活性位点的增加,塔菲尔斜率非常低,约为44 mV dec。此外,Ni-P 300在140 h恒电流电解过程中表现出可忽略不计的衰减,显示出比商业Pt/C催化剂更好的催化稳定性。与非晶态Ni-P相比,Ni-P 300增强的析氢活性得益于混合的纳米晶NiP和NiP,这有助于提高H吸附/脱附能力,并有助于提供更多活性位点,从而促进析氢性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6c4/9458097/53379887a55d/nanomaterials-12-02935-g001.jpg

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