Nanocrystalline and coarse grained polycrystalline nickel catalysts for the hydrogen evolution reaction

被引:26
|
作者
Grubac, Z. [1 ]
Metikos-Hukovic, M. [2 ]
Babic, R. [2 ]
机构
[1] Univ Split, Dept Gen & Inorgan Chem, Fac Chem & Technol, Split 21000, Croatia
[2] Univ Zagreb, Dept Electrochem, Fac Chem Engn & Technol, Zagreb 10000, Croatia
关键词
Hydrogen evolution; Electrocatalysts; Microstructure; Spillover; Nanocrystalline nickel; EIS; ELECTROCHEMICAL IMPEDANCE; ELECTROCATALYTIC ACTIVITY; NI; KINETICS; SIZE; MECHANISM; DIFFUSION; ELECTRODE; COATINGS; ALLOY;
D O I
10.1016/j.ijhydene.2013.01.113
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The objective of this work was to rationalize effects on electrocatalytic reactivity of the coarse grained polycrystalline Ni-cathodes: bulk (Ni), foam (3D-Ni), and electrodeposited (ed-Ni) in comparison with effects on reactivity of nanocrystalline nickel catalyst (nc-Ni) for the hydrogen evolution reaction (HER) in 1.0 M NaOH solution. Nickel crystal nanoparticles of the average grain size d = 17 nm in the nc-Ni catalyst initiate spillover of adsorbed hydrogen species while the intercrystalline volume fraction (equal to 39%) acts as the acceptor of these species. The influence of the spillover effect of adsorbed hydrogen to overall rate of HER was investigated in situ using electrochemical impedance spectroscopy (EIS). According to both voltammetry and EIS results the intrinsic reactivity of the polycrystalline Ni-cathodes investigated for the hydrogen evolution reaction increases as follows: ed-Ni < 3D-Ni < bulk Ni. The highest catalytic reactivity of nc-Ni cathode results from its favourable microstructural properties. Copyright (c) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4437 / 4444
页数:8
相关论文
共 50 条
  • [1] XPS study on the passivity of coarse-grained polycrystalline and electrodeposited nanocrystalline nickel-iron (NiFe) alloys
    Monaco, Leo
    Sodhib, Rana N. S.
    Palumbo, Gino
    Erb, Uwe
    CORROSION SCIENCE, 2020, 176
  • [2] Nickel cobalt hydroxide nanoflakes as catalysts for the hydrogen evolution reaction
    Baranton, Steve
    Coutanceau, Christophe
    APPLIED CATALYSIS B-ENVIRONMENTAL, 2013, 136 : 1 - 8
  • [3] COMPARISON OF STRUCTURE AND PROPERTIES OF ALLOYS IN AMORPHOUS, NANOCRYSTALLINE AND COARSE-GRAINED POLYCRYSTALLINE STATES
    LIU, XD
    WANG, JT
    ZHU, J
    JOURNAL OF MATERIALS SCIENCE, 1994, 29 (04) : 929 - 933
  • [4] Unveiling hydrogen evolution dependence on KOH concentration for polycrystalline and nanostructured nickel-based catalysts
    Alaa Y. Faid
    Faranak Foroughi
    Svein Sunde
    Bruno Pollet
    Journal of Applied Electrochemistry, 2022, 52 : 1819 - 1826
  • [5] Unveiling hydrogen evolution dependence on KOH concentration for polycrystalline and nanostructured nickel-based catalysts
    Faid, Alaa Y.
    Foroughi, Faranak
    Sunde, Svein
    Pollet, Bruno
    JOURNAL OF APPLIED ELECTROCHEMISTRY, 2022, 52 (12) : 1819 - 1826
  • [6] Isothermal oxidation kinetics of nanocrystalline and coarse grained nickel: Experimental results and theoretical approach
    Rashidi, A. M.
    SURFACE & COATINGS TECHNOLOGY, 2011, 205 (17-18): : 4117 - 4123
  • [7] Nickel-based electrodes as catalysts for hydrogen evolution reaction in alkaline media
    Zhu, Yanbing
    Liu, Tao
    Li, Liming
    Song, Shili
    Ding, Rui
    IONICS, 2018, 24 (04) : 1121 - 1127
  • [8] Nickel-based electrodes as catalysts for hydrogen evolution reaction in alkaline media
    Yanbing Zhu
    Tao Liu
    Liming Li
    Shili Song
    Rui Ding
    Ionics, 2018, 24 : 1121 - 1127
  • [9] Reaction modelling of hydrogen evolution on nickel phosphide catalysts: density functional investigation
    Sadan, Syam
    Svenum, Ingeborg-Helene
    Hanslin, Sander o.
    Akola, Jaakko
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2024, 26 (40) : 25957 - 25968
  • [10] Asymmetrically coordinated nickel-based catalysts for enhanced hydrogen evolution reaction
    Li, Shiyi
    Wang, Keyu
    Liang, Chen
    Lei, Linfeng
    Wang, Yixing
    Zhuang, Linzhou
    Xu, Zhi
    AICHE JOURNAL, 2025, 71 (05)