A Universal Descriptor for the Screening of Electrode Materials for Multiple-Electron Processes: Beyond the Thermodynamic Overpotential

被引:115
作者
Exner, Kai S. [1 ]
机构
[1] Univ Duisburg Essen, Fac Chem, Theoret Chem, D-45141 Essen, Germany
来源
ACS CATALYSIS | 2020年 / 10卷 / 21期
关键词
D O I
10.1021/acscatal.0c03865
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
On the way toward a sustainable energy economy, electrode materials that do not contain scarce noble metals need to be developed. Operating at low computational costs, material screening is a powerful tool to assess the performance of potential electrode compositions by categorizing materials into active and inactive. Most commonly, linear scaling relationships are analyzed by the construction of a volcano plot, in which the thermodynamic overpotential, eta(TD), serves as activity descriptor. Even if this descriptor identifies the majority of active electrode materials, it has been reported that eta(TD) lacks thorough sorting of catalysts according to their activity. This failure is mainly related to the fact that eta(TD) is defined by a single free-energy change (thermodynamics), whereas the applied overpotential and kinetics are not factored in the analysis. Based on the discussion of free-energy diagrams and the rate-determining reaction step, this Viewpoint introduces an alternate activity descriptor, G(max)(eta), for multiple-electron processes, thereby including the applied overpotential and kinetic effects in the evaluation. On the example of the oxygen evolution reaction, the application of G(max)(eta) for the screening and optimization of electrode materials is discussed, providing a different perspective compared with the conventional scheme of eta(TD).
引用
收藏
页码:12607 / 12617
页数:11
相关论文
共 91 条
  • [81] A Density Functional plus U Assessment of Oxygen Evolution Reaction Mechanisms on β-NiOOH
    Tkalych, Alexander J.
    Zhuang, Houlong L.
    Carter, Emily A.
    [J]. ACS CATALYSIS, 2017, 7 (08): : 5329 - 5339
  • [82] From 3D to 2D Co and Ni Oxyhydroxide Catalysts: Elucidation of the Active Site and Influence of Doping on the Oxygen Evolution Activity
    Tripkovic, Vladimir
    Hansen, Heine Anton
    Vegge, Tejs
    [J]. ACS CATALYSIS, 2017, 7 (12): : 8558 - 8571
  • [83] Reactivity Theory of Transition-Metal Surfaces: A Bronsted-Evans-Polanyi Linear Activation Energy-Free-Energy Analysis
    van Santen, Rutger A.
    Neurock, Matthew
    Shetty, Sharan G.
    [J]. CHEMICAL REVIEWS, 2010, 110 (04) : 2005 - 2048
  • [84] VANSANTEN RA, 2006, MOL HETEROGENEOUS CA, P19
  • [85] Universality in Oxygen Reduction Electrocatalysis on Metal Surfaces
    Viswanathan, Venkatasubramanian
    Hansen, Heine Anton
    Rossmeisl, Jan
    Norskov, Jens K.
    [J]. ACS CATALYSIS, 2012, 2 (08): : 1654 - 1660
  • [86] Catalysis-Hub.org an open electronic structure database for surface reactions
    Winther, Kirsten T.
    Hoffmann, Max J.
    Boes, Jacob R.
    Mamun, Osman
    Bajdich, Michal
    Bligaard, Thomas
    [J]. SCIENTIFIC DATA, 2019, 6 (1)
  • [87] Identification of Hydroperoxy Species as Reaction Intermediates in the Electrochemical Evolution of Oxygen on Gold
    Yeo, Boon Siang
    Klaus, Shannon L.
    Ross, Philip N.
    Mathies, Richard A.
    Bell, Alexis T.
    [J]. CHEMPHYSCHEM, 2010, 11 (09) : 1854 - 1857
  • [88] Role of Lattice Oxygen Participation in Understanding Trends in the Oxygen Evolution Reaction on Perovskites
    Yoo, Jong Suk
    Rong, Xi
    Liu, Yusu
    Kolpak, Alexie M.
    [J]. ACS CATALYSIS, 2018, 8 (05): : 4628 - 4636
  • [89] Is a major breakthrough in the oxygen electrocatalysis possible?
    Zeradjanin, Aleksandar R.
    [J]. CURRENT OPINION IN ELECTROCHEMISTRY, 2018, 9 : 214 - 223
  • [90] Unconventional Oxygen Reduction Reaction Mechanism and Scaling Relation on Single-Atom Catalysts
    Zhong, Lixiang
    Li, Shuzhou
    [J]. ACS CATALYSIS, 2020, 10 (07): : 4313 - 4318