Engineering single atomic ruthenium on defective nickel vanadium layered double hydroxide for highly efficient hydrogen evolution

被引:0
|
作者
Xiaoyu Chen
Jiawei Wan
Meng Zheng
Jin Wang
Qinghua Zhang
Lin Gu
Lirong Zheng
Xianzhu Fu
Ranbo Yu
机构
[1] Shenzhen University,College of Materials Science and Engineering
[2] Shenzhen University,College of Physics and Optoelectronic Engineering
[3] University of Science and Technology Beijing Institution,Department of Physical Chemistry, School of Metallurgical and Ecological Engineering
[4] Chinese Academy of Sciences,State Key Laboratory of Biochemical Engineering, Institute of Process Engineering
[5] Chinese Academy of Sciences,Beijing National Laboratory for Condensed Matter Physics, Institute of Physics
[6] Tsinghua University,Beijing National Center for Electron Microscopy and Laboratory of Advanced Materials, Department of Materials Science and Engineering
[7] Chinese Academy of Sciences,Beijing Synchrotron Radiation Facility, Institute of High Energy Physics
[8] Zhengzhou University,Key Laboratory of Advanced Material Processing & Mold, Ministry of Education
来源
Nano Research | 2023年 / 16卷
关键词
hydrogen evolution reaction; layered double hydroxide; ruthenium atomic site; ultrathin nanoribbons;
D O I
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中图分类号
学科分类号
摘要
Fabricating single-atom catalysts (SACs) with high catalytic activity as well as great stability is a big challenge. Herein, we propose a precise synthesis strategy to stabilize single atomic ruthenium through regulating vanadium defects of nickel vanadium layered double hydroxides (NiV-LDH) ultrathin nanoribbons support. Correspondingly, the isolated atomically Ru doped NiV-LDH ultrathin nanoribbons (NiVRu-R) were successfully fabricated with a super-high Ru load of 12.8 wt.%. X-ray absorption spectrum (XAS) characterization further confirmed atomic dispersion of Ru. As catalysts for electrocatalytic hydrogen evolution reaction (HER) in alkaline media, the NiVRu-R demonstrated superior catalytic properties to the commercial Pt/C. Moreover, it maintained exceptional stability even after 5,000 cyclic voltammetry cycles. In-situ XAS and density functional theory (DFT) calculations prove that the Ru atomic sites are stabilized on supports through forming the Ru-O-V structure, which also help promote the catalytic properties through reducing the energy barrier on atomic Ru catalytic sites. [graphic not available: see fulltext]
引用
收藏
页码:4612 / 4619
页数:7
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