{"title":"In-situ Raman Observation on Gas Diffusion Electrode/Polyelectrolyte Interface","authors":"Guangzhe Wang, Gongwei Wang, Lin Zhuang, Li Xiao","doi":"10.1016/j.electacta.2024.145348","DOIUrl":null,"url":null,"abstract":"Polyelectrolytes (PEs) serve as the critical medium for electrochemical reactions in membrane-based electrochemical devices, such as fuel cells and membrane electrolyzers. To optimize membrane-based electrochemical device performance and elucidate reaction mechanisms, there is a pressing need for detailed microscopic molecular information at gas diffusion electrode/PE interfaces. In this work, we designed a novel membrane-based-electrochemical-device-like gas diffusion electrode/polyelectrolyte electrochemical <em>in-situ</em> Raman cell. The cell's configuration and gas transfer characteristics closely mimic those of MBEDs under working conditions. We created a Pt/Nafion(<em>s</em>) interface by hot-pressing satellite Au@SiO<sub>2</sub>-Pt loaded carbon cloth with a Nafion membrane, and used this interface for electrochemical <em>in-situ</em> surface enhanced Raman spectroscopy (SERS) observation, including oxygen adsorption/desorption processes, structure of interfacial water and functional groups of Nafion under Ar. The cell enables negatively polarize the potential down to -1.6 V vs. RHE without stripping of the solid/solid interface, despite vigorous H<sub>2</sub> generation. The stability of the interface under extreme conditions demonstrates rapid gas transfer at the interface. This observation underscores the potential of our <em>in-situ</em> Raman cell for studying various gas-involved reactions under conditions that closely resemble those in operational MBEDs.","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":null,"pages":null},"PeriodicalIF":5.5000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.electacta.2024.145348","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Polyelectrolytes (PEs) serve as the critical medium for electrochemical reactions in membrane-based electrochemical devices, such as fuel cells and membrane electrolyzers. To optimize membrane-based electrochemical device performance and elucidate reaction mechanisms, there is a pressing need for detailed microscopic molecular information at gas diffusion electrode/PE interfaces. In this work, we designed a novel membrane-based-electrochemical-device-like gas diffusion electrode/polyelectrolyte electrochemical in-situ Raman cell. The cell's configuration and gas transfer characteristics closely mimic those of MBEDs under working conditions. We created a Pt/Nafion(s) interface by hot-pressing satellite Au@SiO2-Pt loaded carbon cloth with a Nafion membrane, and used this interface for electrochemical in-situ surface enhanced Raman spectroscopy (SERS) observation, including oxygen adsorption/desorption processes, structure of interfacial water and functional groups of Nafion under Ar. The cell enables negatively polarize the potential down to -1.6 V vs. RHE without stripping of the solid/solid interface, despite vigorous H2 generation. The stability of the interface under extreme conditions demonstrates rapid gas transfer at the interface. This observation underscores the potential of our in-situ Raman cell for studying various gas-involved reactions under conditions that closely resemble those in operational MBEDs.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.