Fabbri Emiliana, Schmidt Thomas J
Electrochemistry Laboratory, Paul Scherrer Institute, Forschungsstrasse 111, CH-5232 Villigen PSI, Switzerland.
Institute for Molecular Physical Sciences, ETH Zurich, CH-8093 Zurich, Switzerland.
Chimia (Aarau). 2024 May 29;78(5):320-325. doi: 10.2533/chimia.2024.320.
The development of a sustainable and environmentally friendly energy economy encompasses efficient hydrogen production from renewable energy via electrolysis. In this context, great efforts have recently been dedicated to the development of more efficient and cost-effective electrocatalysts. Understanding the mechanism of the oxygen evolution reaction (OER) on transition metal oxide catalysts is of great interest, but the reaction and system complexity render the characterization of active sites and the understanding of reaction mechanisms challenging. Time resolved Quick X-ray Absorption Spectroscopy (XAS) can provide dynamic snapshots of the electronic and local structure of nanocatalysts, revealing the 'real active phase' of the catalyst, which can substantially differ from the as-prepared catalyst powder or the catalyst in form of an electrode under non-operating conditions. In this contribution, several examples will be presented showing how operando XAS can reveal catalyst-support interactions, changes in the reaction mechanism, and dynamic reversible/irreversible changes in the electronic and local structure of OER catalysts.
可持续且环境友好型能源经济的发展包括通过电解从可再生能源中高效制氢。在此背景下,近来人们付出了巨大努力来研发更高效且更具成本效益的电催化剂。了解过渡金属氧化物催化剂上析氧反应(OER)的机理备受关注,但反应和体系的复杂性使得活性位点的表征以及反应机理的理解颇具挑战性。时间分辨快速X射线吸收光谱(XAS)能够提供纳米催化剂电子结构和局部结构的动态快照,揭示催化剂的“真实活性相”,这可能与制备好的催化剂粉末或非工作条件下电极形式的催化剂有很大不同。在本论文中,将给出几个实例,展示原位XAS如何揭示催化剂-载体相互作用、反应机理的变化以及OER催化剂电子结构和局部结构的动态可逆/不可逆变化。