{"title":"在 Co3O4 上进行原位面转化工程,实现硝酸盐到氨的高效电还原","authors":"Suwei Lu, Guanting Lin, Hongping Yan, Yuhang Li, Tingting Qi, Yuanjin Li, Shijing Liang, Lilong Jiang","doi":"10.1021/acscatal.4c05292","DOIUrl":null,"url":null,"abstract":"Various exposed facets can cause a huge difference in the catalytic activity. Here we prepared Co<sub>3</sub>O<sub>4</sub> hexagonal nanosheets with exposed {112}, {112}&{111}, and {111} facets for the electrochemical nitrate reduction reactions (NO<sub>3</sub>RR). The reaction pathways of the NO<sub>3</sub>RR on Co<sub>3</sub>O<sub>4</sub> {111} and {112} facets are clarified through in situ electrochemical characterizations and theoretical analysis. As the dominating facet of Co<sub>3</sub>O<sub>4</sub> transforms from {112} to {111}, the rate-determining step changes from *NO<sub>2</sub> → *NO<sub>2</sub>H to *NO<sub>3</sub>H → *NO<sub>2</sub>, with the energy barrier decreasing to 0.48 eV. And the {111} facet promotes the hydrogenation of NO<sub><i>x</i></sub> and NH<sub><i>x</i></sub> intermediates. Notably, the Co<sub>3</sub>O<sub>4</sub>-{111} catalyst shows exceptional NO<sub>3</sub>RR performance, achieving an NH<sub>3</sub> yield of 5.73 mg mg<sub>cat.</sub><sup>–1</sup> h<sup>–1</sup>, surpassing the majority of the reported activities.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In Situ Facet Transformation Engineering over Co3O4 for Highly Efficient Electroreduction of Nitrate to Ammonia\",\"authors\":\"Suwei Lu, Guanting Lin, Hongping Yan, Yuhang Li, Tingting Qi, Yuanjin Li, Shijing Liang, Lilong Jiang\",\"doi\":\"10.1021/acscatal.4c05292\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Various exposed facets can cause a huge difference in the catalytic activity. Here we prepared Co<sub>3</sub>O<sub>4</sub> hexagonal nanosheets with exposed {112}, {112}&{111}, and {111} facets for the electrochemical nitrate reduction reactions (NO<sub>3</sub>RR). The reaction pathways of the NO<sub>3</sub>RR on Co<sub>3</sub>O<sub>4</sub> {111} and {112} facets are clarified through in situ electrochemical characterizations and theoretical analysis. As the dominating facet of Co<sub>3</sub>O<sub>4</sub> transforms from {112} to {111}, the rate-determining step changes from *NO<sub>2</sub> → *NO<sub>2</sub>H to *NO<sub>3</sub>H → *NO<sub>2</sub>, with the energy barrier decreasing to 0.48 eV. And the {111} facet promotes the hydrogenation of NO<sub><i>x</i></sub> and NH<sub><i>x</i></sub> intermediates. Notably, the Co<sub>3</sub>O<sub>4</sub>-{111} catalyst shows exceptional NO<sub>3</sub>RR performance, achieving an NH<sub>3</sub> yield of 5.73 mg mg<sub>cat.</sub><sup>–1</sup> h<sup>–1</sup>, surpassing the majority of the reported activities.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.4c05292\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c05292","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
In Situ Facet Transformation Engineering over Co3O4 for Highly Efficient Electroreduction of Nitrate to Ammonia
Various exposed facets can cause a huge difference in the catalytic activity. Here we prepared Co3O4 hexagonal nanosheets with exposed {112}, {112}&{111}, and {111} facets for the electrochemical nitrate reduction reactions (NO3RR). The reaction pathways of the NO3RR on Co3O4 {111} and {112} facets are clarified through in situ electrochemical characterizations and theoretical analysis. As the dominating facet of Co3O4 transforms from {112} to {111}, the rate-determining step changes from *NO2 → *NO2H to *NO3H → *NO2, with the energy barrier decreasing to 0.48 eV. And the {111} facet promotes the hydrogenation of NOx and NHx intermediates. Notably, the Co3O4-{111} catalyst shows exceptional NO3RR performance, achieving an NH3 yield of 5.73 mg mgcat.–1 h–1, surpassing the majority of the reported activities.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.