Delei Yu, Ying Chen, Yao Chen, Xiangchun Liu, Xianwen Wei, Ping Cui
{"title":"Single-Ni-atoms on nitrogenated humic acid based porous carbon for CO2 electroreduction","authors":"Delei Yu, Ying Chen, Yao Chen, Xiangchun Liu, Xianwen Wei, Ping Cui","doi":"10.1007/s11705-024-2411-7","DOIUrl":null,"url":null,"abstract":"<div><p>We proposed a facile synthesis of single-Ni-atom catalysts on low-cost porous carbon using a calcination method at the temperatures of 850–1000 °C, which were used for CO<sub>2</sub> electrochemical reduction to CO. The porous carbon was prepared by carbonizing cheap and abundant humic acid. The structural characterizations of the as-synthesized catalysts and their electrocatalytic performances were analyzed. The results showed that the single-Ni-atom catalyst activated at 950 °C showed an optimum catalytic performance, and it reached a CO Faradaic efficiency of 91.9% with a CO partial current density of 6.9 mA·cm<sup>−2</sup> at −0.9 V <i>vs.</i> reversible hydrogen electrode (RHE). Additionally, the CO Faradaic efficiency and current density of the optimum catalyst changed slightly after 8 h of continuous operation, suggesting that it possessed an excellent stability. The structure-activity relations indicate that the variation in the CO<sub>2</sub> electrochemical reduction performance for the as-synthesized catalysts is ascribed to the combined effects of the increase in the content of pyrrolic N, the evaporation of Ni and N, the decrease in pore volume, and the change in graphitization degree.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":571,"journal":{"name":"Frontiers of Chemical Science and Engineering","volume":"18 5","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers of Chemical Science and Engineering","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s11705-024-2411-7","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
We proposed a facile synthesis of single-Ni-atom catalysts on low-cost porous carbon using a calcination method at the temperatures of 850–1000 °C, which were used for CO2 electrochemical reduction to CO. The porous carbon was prepared by carbonizing cheap and abundant humic acid. The structural characterizations of the as-synthesized catalysts and their electrocatalytic performances were analyzed. The results showed that the single-Ni-atom catalyst activated at 950 °C showed an optimum catalytic performance, and it reached a CO Faradaic efficiency of 91.9% with a CO partial current density of 6.9 mA·cm−2 at −0.9 V vs. reversible hydrogen electrode (RHE). Additionally, the CO Faradaic efficiency and current density of the optimum catalyst changed slightly after 8 h of continuous operation, suggesting that it possessed an excellent stability. The structure-activity relations indicate that the variation in the CO2 electrochemical reduction performance for the as-synthesized catalysts is ascribed to the combined effects of the increase in the content of pyrrolic N, the evaporation of Ni and N, the decrease in pore volume, and the change in graphitization degree.
我们提出了一种在 850-1000 °C 温度下利用煅烧法在低成本多孔碳上简便合成单-镍原子催化剂的方法,该催化剂用于将 CO2 电化学还原为 CO。多孔碳是通过碳化廉价而丰富的腐植酸制备的。分析了合成催化剂的结构特征及其电催化性能。结果表明,在 950 ℃ 下活化的单镍原子催化剂具有最佳催化性能,在 -0.9 V 相对于可逆氢电极(RHE)电压为 6.9 mA-cm-2 时,一氧化碳法拉第效率达到 91.9%,一氧化碳部分电流密度为 6.9 mA-cm-2。此外,最佳催化剂的一氧化碳法拉第效率和电流密度在连续运行 8 小时后略有变化,表明其具有极佳的稳定性。结构-活性关系表明,所合成催化剂的 CO2 电化学还原性能的变化是由吡咯烷酮 N 含量的增加、Ni 和 N 的蒸发、孔体积的减少以及石墨化程度的变化等综合因素造成的。
期刊介绍:
Frontiers of Chemical Science and Engineering presents the latest developments in chemical science and engineering, emphasizing emerging and multidisciplinary fields and international trends in research and development. The journal promotes communication and exchange between scientists all over the world. The contents include original reviews, research papers and short communications. Coverage includes catalysis and reaction engineering, clean energy, functional material, nanotechnology and nanoscience, biomaterials and biotechnology, particle technology and multiphase processing, separation science and technology, sustainable technologies and green processing.