Jing Xu, D. Scherson
{"title":"多晶铂在酸性水溶液中氧化的定量原位差分反射光谱分析","authors":"Jing Xu, D. Scherson","doi":"10.1149/2.0061509EEL","DOIUrl":null,"url":null,"abstract":"A method is herein described that allows the coverage of the two forms of oxide believed to form on polycrystalline Pt, Pt(poly), surfaces in aqueous solutions to be determined based on the analysis of in situ differential reflectance spectroscopy, R/R, and voltammetric data recorded simultaneously. The model employed assumes R/R can be expressed as the sum of contributions due to each type of surface site, i, represented by the product of their potential dependent coverage, θi(E), and a linear function of E obtained empirically. Values of θi(E) for the unoxidized and oxidized sites are calculated by solving a system of three non-linear equations that relate θi(E) to the charge associated with the formation of the oxide layer based on coulometric analyses and accepted values for the number of electrons transferred for each of the oxides. Data collected for Pt(poly) electrodes in aqueous 0.1 M HClO4 was found to be consistent with the coexistence of the two forms of Pt oxide and unoxidized sites on the surface over a potential range extending from ca. 1.0 to 1.25 V. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0061509eel] All rights reserved.","PeriodicalId":11470,"journal":{"name":"ECS Electrochemistry Letters","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1149/2.0061509EEL","citationCount":"1","resultStr":"{\"title\":\"Quantitative In Situ Differential Reflectance Spectroscopy Analysis of Polycrystalline Platinum Oxidation in an Aqueous Acidic Electrolyte\",\"authors\":\"Jing Xu, D. Scherson\",\"doi\":\"10.1149/2.0061509EEL\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A method is herein described that allows the coverage of the two forms of oxide believed to form on polycrystalline Pt, Pt(poly), surfaces in aqueous solutions to be determined based on the analysis of in situ differential reflectance spectroscopy, R/R, and voltammetric data recorded simultaneously. The model employed assumes R/R can be expressed as the sum of contributions due to each type of surface site, i, represented by the product of their potential dependent coverage, θi(E), and a linear function of E obtained empirically. Values of θi(E) for the unoxidized and oxidized sites are calculated by solving a system of three non-linear equations that relate θi(E) to the charge associated with the formation of the oxide layer based on coulometric analyses and accepted values for the number of electrons transferred for each of the oxides. Data collected for Pt(poly) electrodes in aqueous 0.1 M HClO4 was found to be consistent with the coexistence of the two forms of Pt oxide and unoxidized sites on the surface over a potential range extending from ca. 1.0 to 1.25 V. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0061509eel] All rights reserved.\",\"PeriodicalId\":11470,\"journal\":{\"name\":\"ECS Electrochemistry Letters\",\"volume\":\"4 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1149/2.0061509EEL\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ECS Electrochemistry Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1149/2.0061509EEL\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Electrochemistry Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/2.0061509EEL","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Quantitative In Situ Differential Reflectance Spectroscopy Analysis of Polycrystalline Platinum Oxidation in an Aqueous Acidic Electrolyte
A method is herein described that allows the coverage of the two forms of oxide believed to form on polycrystalline Pt, Pt(poly), surfaces in aqueous solutions to be determined based on the analysis of in situ differential reflectance spectroscopy, R/R, and voltammetric data recorded simultaneously. The model employed assumes R/R can be expressed as the sum of contributions due to each type of surface site, i, represented by the product of their potential dependent coverage, θi(E), and a linear function of E obtained empirically. Values of θi(E) for the unoxidized and oxidized sites are calculated by solving a system of three non-linear equations that relate θi(E) to the charge associated with the formation of the oxide layer based on coulometric analyses and accepted values for the number of electrons transferred for each of the oxides. Data collected for Pt(poly) electrodes in aqueous 0.1 M HClO4 was found to be consistent with the coexistence of the two forms of Pt oxide and unoxidized sites on the surface over a potential range extending from ca. 1.0 to 1.25 V. © The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0061509eel] All rights reserved.