{"title":"Electrocatalytic Activity of Pt Oxide Electrode for CO2 Reduction","authors":"K. Ohkubo, Hiroki Takahashi, M. Taguchi","doi":"10.2473/JOURNALOFMMIJ.135.8","DOIUrl":null,"url":null,"abstract":"CO 2 electrochemical reduction. Cyclic voltammetry of the Pt oxide electrode in a CO 2 -saturated H 2 SO 4 solution showed a definite anodic peak at 0.6-0.8 V vs. SHE, which was not observed in an Ar-deaerated electrolyte. Thus, it was determined that the anodic peak could be related to the re-oxidation of the reduction product of CO 2 during cathodic polarization. The activity of the Pt oxide electrode for CO 2 reduction was much higher than that of the Pt electrode. It was concluded that the residual oxygen, which was hardly detected in the Pt electrode, improved the activity for CO 2 electrochemical reduction on the Pt oxide electrode. Gas chromatography-mass spectrometry of the electrolytic solution after CO 2 reduction revealed that the reduction product was mainly CH 3 OH. These results should be very useful for developing a new electrochemical reduction system for converting CO 2 into CH 3 OH.","PeriodicalId":16502,"journal":{"name":"Journal of Mmij","volume":"47 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Mmij","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2473/JOURNALOFMMIJ.135.8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
CO 2 electrochemical reduction. Cyclic voltammetry of the Pt oxide electrode in a CO 2 -saturated H 2 SO 4 solution showed a definite anodic peak at 0.6-0.8 V vs. SHE, which was not observed in an Ar-deaerated electrolyte. Thus, it was determined that the anodic peak could be related to the re-oxidation of the reduction product of CO 2 during cathodic polarization. The activity of the Pt oxide electrode for CO 2 reduction was much higher than that of the Pt electrode. It was concluded that the residual oxygen, which was hardly detected in the Pt electrode, improved the activity for CO 2 electrochemical reduction on the Pt oxide electrode. Gas chromatography-mass spectrometry of the electrolytic solution after CO 2 reduction revealed that the reduction product was mainly CH 3 OH. These results should be very useful for developing a new electrochemical reduction system for converting CO 2 into CH 3 OH.