Daopeng Li, Shengbo Zhang, Zhixian Mao, Min Liu, Kui Hu, Dongnan Zhao, Zhengguo Qv, Li Zhou and Tongfei Shi
{"title":"Highly selective electrocatalytic reduction of nitrate to ammonia over a copper–cobalt bimetallic catalyst†","authors":"Daopeng Li, Shengbo Zhang, Zhixian Mao, Min Liu, Kui Hu, Dongnan Zhao, Zhengguo Qv, Li Zhou and Tongfei Shi","doi":"10.1039/D5RA00860C","DOIUrl":null,"url":null,"abstract":"<p >The electrocatalytic nitrate reduction reaction (NitRR) is a promising alternative to the traditional Haber–Bosch process. However, the competitive hydrogen evolution reaction results in poor NH<small><sub>3</sub></small> selectivity (<em>S</em><small><sub>NH3</sub></small>). Here, a Cu–Co bimetallic catalyst supported on biomass-derived porous carbon (Cu–Co/BPC) is designed and synthesized. Interestingly, the catalyst presents a high NH<small><sub>3</sub></small> yield rate of 9114.1 ± 244.8 μg h<small><sup>−1</sup></small> cm<small><sup>−2</sup></small> at −1.4 V (<em>vs.</em> RHE) and a high faradaic efficiency (FE) of 84.5 ± 1.6% at −1.0 V (<em>vs.</em> RHE). Notably, the <em>S</em><small><sub>NH<small><sub>3</sub></small></sub></small> of Cu–Co/BPC catalyst is kept above 94.2% under a broad range from −1.0 to −1.4 V (<em>vs.</em> RHE), indicating the high NitRR-to-NH<small><sub>3</sub></small> selectivity of Cu–Co/BPC. The combination of <em>in situ</em> characterization and experimental results indicates that the electron transfer occurs between Cu and Co, and many active sites are generated for adsorption and activation of N<img>O double bonds, and hydrogenation reactions occur with adjacent H protons to improve the selectivity of NH<small><sub>3</sub></small>.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 12","pages":" 9461-9466"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d5ra00860c?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra00860c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The electrocatalytic nitrate reduction reaction (NitRR) is a promising alternative to the traditional Haber–Bosch process. However, the competitive hydrogen evolution reaction results in poor NH3 selectivity (SNH3). Here, a Cu–Co bimetallic catalyst supported on biomass-derived porous carbon (Cu–Co/BPC) is designed and synthesized. Interestingly, the catalyst presents a high NH3 yield rate of 9114.1 ± 244.8 μg h−1 cm−2 at −1.4 V (vs. RHE) and a high faradaic efficiency (FE) of 84.5 ± 1.6% at −1.0 V (vs. RHE). Notably, the SNH3 of Cu–Co/BPC catalyst is kept above 94.2% under a broad range from −1.0 to −1.4 V (vs. RHE), indicating the high NitRR-to-NH3 selectivity of Cu–Co/BPC. The combination of in situ characterization and experimental results indicates that the electron transfer occurs between Cu and Co, and many active sites are generated for adsorption and activation of NO double bonds, and hydrogenation reactions occur with adjacent H protons to improve the selectivity of NH3.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.