Griesser Christoph, Diaz-Coello Sergio, Olgiati Matteo, do Valle Wanderson Ferraz, Moser Toni, Auer Andrea, Pastor Elena, Valtiner Markus, Liebhäuser Julia Kunze
Department of Physical Chemistry, University of Innsbruck, Innrain 52 c, Innsbruck, 6020, Austria.
Institute of Applied Physics, Vienna University of Technology, Vienna, 1040, Austria.
Angew Chem Int Ed Engl. 2025 Jun 24;64(26):e202500965. doi: 10.1002/anie.202500965. Epub 2025 Mar 31.
Tungsten carbide (WC) is a renowned compound catalyst material for electrochemical water splitting, and its high electrocatalytic activity toward the hydrogen evolution reaction (HER) has been repeatedly reported. However, its susceptibility to oxidation raises the fundamental question of the underlying reason for its high activity, especially since passivation and thus potential deactivation can occur not only in air but also during reaction. Hence, the investigation of the surface chemistry under true operating conditions is crucial for a fundamental understanding of the electrocatalytic process. In this work, we use electrochemical X-ray photoelectron spectroscopy (EC-XPS) to revisit the surface chemistry of WC powder electrodes in alkaline electrolyte in situ and under full potential control. Our results show that although the surface is initially covered with oxide, this passive film dissolves in the electrolyte under electrochemical reaction conditions. This clarifies the active surface termination during the HER and highlights the potential of laboratory-based EC-XPS to study applied energy conversion materials.
碳化钨(WC)是一种著名的用于电化学水分解的复合催化剂材料,其对析氢反应(HER)的高电催化活性已被多次报道。然而,它易被氧化这一特性引发了关于其高活性根本原因的基本问题,特别是因为不仅在空气中,而且在反应过程中都可能发生钝化并因此导致潜在的失活。因此,在真实操作条件下研究表面化学对于从根本上理解电催化过程至关重要。在这项工作中,我们使用电化学X射线光电子能谱(EC-XPS)在碱性电解质中原位且在全电位控制下重新研究WC粉末电极的表面化学。我们的结果表明,尽管表面最初覆盖有氧化物,但这种钝化膜在电化学反应条件下会溶解在电解质中。这阐明了HER过程中的活性表面终止情况,并突出了基于实验室的EC-XPS在研究应用能量转换材料方面的潜力。