Venugopal Anirudh, Egberts Laurentius H T, Meeprasert Jittima, Pidko Evgeny A, Dam Bernard, Burdyny Thomas, Sinha Vivek, Smith Wilson A
Materials for Energy Conversion and Storage (MECS), Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, Delft 2629HZ, The Netherlands.
Inorganic Systems Engineering (ISE), Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, Delft 2629HZ, The Netherlands.
ACS Energy Lett. 2022 May 13;7(5):1586-1593. doi: 10.1021/acsenergylett.2c00199. Epub 2022 Apr 4.
Finding alternative ways to tailor the electronic properties of a catalyst to actively and selectively drive reactions of interest has been a growing research topic in the field of electrochemistry. In this Letter, we investigate the tuning of the surface electronic properties of electrocatalysts via polymer modification. We show that when a nickel oxide water oxidation catalyst is coated with polytetrafluoroethylene, stable Ni-CF bonds are introduced at the nickel oxide/polymer interface, resulting in shifting of the reaction selectivity away from the oxygen evolution reaction and toward hydrogen peroxide formation. It is shown that the electron-withdrawing character of the surface fluorocarbon molecule leaves a slight positive charge on the water oxidation intermediates at the adjacent active nickel sites, making their bonds weaker. The concept of modifying the surface electronic properties of an electrocatalyst via stable polymer modification offers an additional route to tune multipathway reactions in polymer/electrocatalyst environments, like with ionomer-modified catalysts or with membrane electrode assemblies.
寻找替代方法来调整催化剂的电子性质,以积极且选择性地驱动感兴趣的反应,一直是电化学领域中一个不断发展的研究课题。在本信函中,我们研究了通过聚合物改性来调节电催化剂的表面电子性质。我们表明,当用聚四氟乙烯包覆氧化镍水氧化催化剂时,在氧化镍/聚合物界面处引入了稳定的Ni-CF键,导致反应选择性从析氧反应转向过氧化氢生成。结果表明,表面碳氟化合物分子的吸电子特性在相邻活性镍位点的水氧化中间体上留下轻微正电荷,使其键变弱。通过稳定的聚合物改性来改变电催化剂表面电子性质的概念,为调节聚合物/电催化剂环境中的多途径反应提供了一条额外途径,如离子聚合物改性催化剂或膜电极组件的情况。