{"title":"Copper-nickel-MOF/nickel foam catalysts grown in situ for efficient electrochemical nitrate reduction to ammonia.","authors":"Chenxia Yang, Ying Tang, Qian Yang, Bo Wang, Xianghao Liu, Yuxiang Li, Weixia Yang, Kunxuan Zhao, Gang Wang, Zongyuan Wang, Feng Yu","doi":"10.1016/j.jhazmat.2024.136036","DOIUrl":null,"url":null,"abstract":"<p><p>Reducing nitrate (NO<sub>3</sub><sup>-</sup>) in an aqueous solution to ammonia under ambient conditions can provide a green and sustainable NH<sub>3</sub>-synthesis technology and mitigate global energy and pollution issues. In this work, a CuNi<sub>0.75</sub>-1,3,5-benzenetricarboxylic acid/nickel foam (CuNi<sub>0.75</sub>-MOF/NF) catalyst grown in situ was prepared via a one-pot method as an efficient cathode material for electrocatalytic nitrate reduction reaction (NO<sub>3</sub>RR). The CuNi<sub>0.75</sub>-MOF/NF catalyst exhibited excellent electrocatalytic NO<sub>3</sub>RR performance at -1.0 V versus a reversible hydrogen electrode, achieving an outstanding faradaic efficiency of 95.88 % and an NH<sub>3</sub> yield of 51.78 mg h<sup>-1</sup> cm<sup>-2</sup>. The <sup>15</sup>N isotope labeling experiments confirmed that the sole source of N in the electrocatalytic NO<sub>3</sub>RR was the NO<sub>3</sub><sup>-</sup> in the electrolyte. The reaction pathway for the electrocatalytic NO<sub>3</sub>RR was derived by in situ Fourier transform infrared spectroscopy and in situ differential electrochemical mass spectrometry. Density functional theory calculations revealed that the Ni element in the CuNi<sub>0.75</sub>-MOF/NF catalyst had excellent O-H activation ability and strong *H adsorption capacity. These *H species were transferred from the Ni sites to the *NO adsorption intermediates located on the Cu sites, providing a continuous supply of *H to Cu, thereby promoting the formation of *NOH intermediates and enhancing the hydrogenation process of the electrocatalytic NO<sub>3</sub>RR.</p>","PeriodicalId":94082,"journal":{"name":"Journal of hazardous materials","volume":"480 ","pages":"136036"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of hazardous materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.jhazmat.2024.136036","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/3 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Reducing nitrate (NO3-) in an aqueous solution to ammonia under ambient conditions can provide a green and sustainable NH3-synthesis technology and mitigate global energy and pollution issues. In this work, a CuNi0.75-1,3,5-benzenetricarboxylic acid/nickel foam (CuNi0.75-MOF/NF) catalyst grown in situ was prepared via a one-pot method as an efficient cathode material for electrocatalytic nitrate reduction reaction (NO3RR). The CuNi0.75-MOF/NF catalyst exhibited excellent electrocatalytic NO3RR performance at -1.0 V versus a reversible hydrogen electrode, achieving an outstanding faradaic efficiency of 95.88 % and an NH3 yield of 51.78 mg h-1 cm-2. The 15N isotope labeling experiments confirmed that the sole source of N in the electrocatalytic NO3RR was the NO3- in the electrolyte. The reaction pathway for the electrocatalytic NO3RR was derived by in situ Fourier transform infrared spectroscopy and in situ differential electrochemical mass spectrometry. Density functional theory calculations revealed that the Ni element in the CuNi0.75-MOF/NF catalyst had excellent O-H activation ability and strong *H adsorption capacity. These *H species were transferred from the Ni sites to the *NO adsorption intermediates located on the Cu sites, providing a continuous supply of *H to Cu, thereby promoting the formation of *NOH intermediates and enhancing the hydrogenation process of the electrocatalytic NO3RR.