Qasim Z. Adesope, Mohammad Z. Altafi, Stella Z. Amagbor, Kabirat Z. Balogun, Manan Guragain, Alankar Kafle, V. Mesilov, Francis D’Souza, Tom Cundari, Jeffry Kelber
{"title":"Electrocatalytic Reduction of Nitrate to Ammonia at Oxidized Vanadium Surfaces with V(3+) and V(4+) Oxidation States","authors":"Qasim Z. Adesope, Mohammad Z. Altafi, Stella Z. Amagbor, Kabirat Z. Balogun, Manan Guragain, Alankar Kafle, V. Mesilov, Francis D’Souza, Tom Cundari, Jeffry Kelber","doi":"10.1149/1945-7111/ad60f8","DOIUrl":null,"url":null,"abstract":"\n The electrochemical reduction of nitrate to ammonia is of interest as an energy/environmentally friendly source of ammonia for agriculture and energy applications and as a route toward groundwater purification. We report in situ photoemission data, electrochemical results, and density functional theory calculations that demonstrate vanadium oxide – prepared by ambient exposure of V metal, with a distribution of surface V3+ and V4+ oxidation states – specifically adsorbs and reduces nitrate to ammonia at pH 3.2 at cathodic potentials. Negligible cathodic activity in the absence of NO3- indicates high selectivity with respect to non-nitrate reduction processes. In situ photoemission data indicate that nitrate adsorption and reduction to adsorbed NO2 is a key step in the reduction process. NO3RR activity is also observed at pH 7, albeit at a much slower rate. The results indicate that intermediate (non-d0) oxidation states are important for both molecular nitrogen and nitrate reduction to ammonia.","PeriodicalId":509718,"journal":{"name":"Journal of The Electrochemical Society","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Electrochemical Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/1945-7111/ad60f8","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
The electrochemical reduction of nitrate to ammonia is of interest as an energy/environmentally friendly source of ammonia for agriculture and energy applications and as a route toward groundwater purification. We report in situ photoemission data, electrochemical results, and density functional theory calculations that demonstrate vanadium oxide – prepared by ambient exposure of V metal, with a distribution of surface V3+ and V4+ oxidation states – specifically adsorbs and reduces nitrate to ammonia at pH 3.2 at cathodic potentials. Negligible cathodic activity in the absence of NO3- indicates high selectivity with respect to non-nitrate reduction processes. In situ photoemission data indicate that nitrate adsorption and reduction to adsorbed NO2 is a key step in the reduction process. NO3RR activity is also observed at pH 7, albeit at a much slower rate. The results indicate that intermediate (non-d0) oxidation states are important for both molecular nitrogen and nitrate reduction to ammonia.