拉曼光谱
原位
催化作用
碱金属
氢
光谱学
活动站点
材料科学
离子
化学
制氢
化学工程
纳米技术
物理
光学
有机化学
量子力学
工程类
作者
Mingpeng Chen,Di Liu,Yuyun Chen,Dong Liu,Xinyu Du,Jinxian Feng,Pengfei Zhou,Baoye Zi,Qingju Liu,Kin Ho Lo,Shi Chen,Shuangpeng Wang,Weng Fai Ip,Hui Pan
标识
DOI:10.1016/j.apmt.2021.101343
摘要
Low-cost and efficient electrocatalysts have been extensively studied for hydrogen evolution reaction (HER) in large-scale hydrogen production. However, the actual active sites on their surfaces in working condition have not been understood clearly. Herein, we carry out a systematic study to figure out the active sites on the Ni/NixP hybrids grown on carbon cloth (Ni/NixP/CC) for HER in both acidic and alkaline conditions, by a series of combined in-situ and ex-situ characterizations. Interestingly, we find that their current densities gradually increase (maximum: 106.1%) at a voltage of −0.16 V (vs. RHE) in acid, but show slight reduction in alkali at a voltage of −0.2 V (vs. RHE). Ex-situ studies show that Ni/NixP/CC electrodes undergo significant morphology remodeling and surface reconstruction after working in both acid and alkali. However, in-situ Raman spectroscopy shows that the surface reconstruction does not happen during the HER process. Most importantly, in-situ Raman spectroscopy reveals that the negatively charged P ions act as active sites that attract the positively charged protons for HER. Our findings demonstrate that tracking the dynamic structure evolution may be significant to gain insightful understanding on the reaction mechanism, which shall provide meaningful guidance to the design of catalysts for practical applications.
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