Electrocatalytic Reduction of Nitrate to Ammonia at Oxidized Vanadium Surfaces with V(3+) and V(4+) Oxidation States

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.
在具有 V(3+)和 V(4+)氧化态的氧化钒表面电催化硝酸盐还原为氨气
硝酸盐通过电化学还原成氨,作为一种能源/环境友好型氨源用于农业和能源应用,并作为净化地下水的一种途径,引起了人们的兴趣。我们报告了原位光发射数据、电化学结果和密度泛函理论计算,这些数据证明了氧化钒--通过 V 金属的环境暴露制备而成,其表面 V3+ 和 V4+ 氧化态分布--在 pH 值为 3.2 的阴极电位下能特异性地吸附硝酸盐并将其还原成氨。在没有 NO3- 的情况下,其阴极活性可忽略不计,这表明其对非硝酸盐还原过程具有很高的选择性。原位光辐射数据表明,硝酸盐吸附并还原为吸附的二氧化氮是还原过程的关键步骤。在 pH 值为 7 时也能观察到 NO3RR 活性,尽管速度要慢得多。结果表明,中间(非 d0)氧化态对分子氮和硝酸盐还原成氨都很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信