Ngoipala Apinya, Schott Christian, Briega-Martos Valentin, Qamar Minaam, Mrovec Matous, Javan Nikkhah Sousa, Schmidt Thorsten O, Deville Lewin, Capogrosso Andrea, Moumaneix Lilian, Kallio Tanja, Viola Arnaud, Maillard Frédéric, Drautz Ralf, Bandarenka Aliaksandr S, Cherevko Serhiy, Vandichel Matthias, Gubanova Elena L
School of Chemical Sciences and Chemical Engineering, Bernal Institute, University of Limerick, Limerick, V94 T9PX, Ireland.
Physics of Energy Conversion and Storage, Department of Physics, Technical University of Munich, James-Franck-Straße 1, 85748, Garching, Germany.
Adv Mater. 2025 Jan;37(4):e2410951. doi: 10.1002/adma.202410951. Epub 2024 Dec 4.
Designing electrocatalysts with optimal activity and selectivity relies on a thorough understanding of the surface structure under reaction conditions. In this study, experimental and computational approaches are combined to elucidate reconstruction processes on low-index Pd surfaces during H-insertion following proton electroreduction. While electrochemical scanning tunneling microscopy clearly reveals pronounced surface roughening and morphological changes on Pd(111), Pd(110), and Pd(100) surfaces during cyclic voltammetry, a complementary analysis using inductively coupled plasma mass spectrometry excludes Pd dissolution as the primary cause of the observed restructuring. Large-scale molecular dynamics simulations further show that these surface alterations are related to the creation and propagation of structural defects as well as phase transformations that take place during hydride formation.
设计具有最佳活性和选择性的电催化剂依赖于对反应条件下表面结构的透彻理解。在本研究中,结合实验和计算方法来阐明质子电还原后H插入过程中低指数Pd表面的重构过程。虽然电化学扫描隧道显微镜清楚地揭示了在循环伏安法期间Pd(111)、Pd(110)和Pd(100)表面明显的表面粗糙化和形态变化,但使用电感耦合等离子体质谱的补充分析排除了Pd溶解是观察到的重构的主要原因。大规模分子动力学模拟进一步表明,这些表面变化与结构缺陷的产生和传播以及氢化物形成过程中发生的相变有关。