Zeolite supported Pt electrocatalysts, made by ion exchange method using Pt/Y type zeolite, have been investigated to determine Pt electrochemical activity of HCOOH and CH3OH oxidation using the cyclic voltammetry (CV) and the extended X-ray adsorption fine structure (EXAFS) techniques. The study reveals that the introduction of excess H+ ions during electrocatalyst pre-treatment could enhance electrochemical reaction on Pt surface due to higher Pt dispersion, regardless of zeolite being a direct current electronic conducting insulator. Two possible conduction pathways might contribute to the electrocatalytic reaction on Pt surface with Pt particle size and loading: (1) hydrogen atoms/H+ ions spillover through zeolite framework and at the electrode and solution interface; (2) surface mobility of adsorbed species on electrode surface. The water may act as a carrier in assisting the migration of the H+ ions throughout zeolite channels to facilitate the charger and electron transfer in such an electrical system.
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机译:已经研究了使用Pt / Y型沸石通过离子交换方法制备的沸石负载Pt电催化剂,以循环伏安法(CV)和扩展X射线吸附精细结构(EXAFS)技术测定HCOOH和CH3OH氧化的Pt电化学活性。 。研究表明,由于沸石具有较高的Pt分散度,因此在电催化剂预处理过程中引入过量的H +离子可增强Pt表面的电化学反应,而与沸石是直流电子绝缘体无关。有两种可能的传导途径可能有助于Pt表面上具有Pt粒径和负载的电催化反应:(1)氢原子/ H +离子通过沸石骨架以及在电极和溶液界面溢出。 (2)电极表面上被吸附物质的表面迁移率。水可以充当载体,以帮助H +离子在整个沸石通道中迁移,从而促进此类电子系统中的电荷和电子转移。
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