{"title":"Carburization induced phase transition of Ni3In to Ni3InC0.5 intermetallic carbide for acetylene semihydrogenation","authors":"Xiaohu Ge, Nina Fei, Yueqiang Cao, Hao Jiang, Jing Zhang, Gang Qian, Xinggui Zhou, Xuezhi Duan","doi":"10.1002/aic.18842","DOIUrl":null,"url":null,"abstract":"In this work, we develop a carburization strategy to transform hexagonal Ni<sub>3</sub>In into face-centered cubic Ni<sub>3</sub>InC<sub>0.5</sub> intermetallic carbide, leveraging partially isolated Ni sites for improved acetylene semihydrogenation. The catalyst synthesized via carburization of Ni<sub>3</sub>In intermetallic compound derived from Ni/In/Mg/Al layered double hydroxides in a C<sub>2</sub>H<sub>2</sub>/H<sub>2</sub> atmosphere is evidenced to show Ni<sub>3</sub>InC<sub>0.5</sub> intermetallic carbide phase through detailed characterizations, including high-resolution transmission electron microscopy and X-ray absorption spectroscopy. Catalytic tests reveal that the Ni<sub>3</sub>InC<sub>0.5</sub> catalyst achieves 92.0% ethylene selectivity at full acetylene conversion, outperforming the Ni and Ni<sub>3</sub>In catalysts. Both experimental and theoretical evidence demonstrate that interstitial carbon atoms in Ni<sub>3</sub>InC<sub>0.5</sub> synergize with neighboring In atoms to modify the electronic structure of surface Ni sites via significant hybridization between Ni 3<i>d</i>, In 5<i>p</i>, and C 2<i>p</i> orbitals. These unique features enable higher kinetic favorability of ethylene desorption over its further hydrogenation on the Ni<sub>3</sub>InC<sub>0.5</sub> catalyst and thus contribute to the enhanced semihydrogenation.","PeriodicalId":120,"journal":{"name":"AIChE Journal","volume":"38 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIChE Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/aic.18842","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
In this work, we develop a carburization strategy to transform hexagonal Ni3In into face-centered cubic Ni3InC0.5 intermetallic carbide, leveraging partially isolated Ni sites for improved acetylene semihydrogenation. The catalyst synthesized via carburization of Ni3In intermetallic compound derived from Ni/In/Mg/Al layered double hydroxides in a C2H2/H2 atmosphere is evidenced to show Ni3InC0.5 intermetallic carbide phase through detailed characterizations, including high-resolution transmission electron microscopy and X-ray absorption spectroscopy. Catalytic tests reveal that the Ni3InC0.5 catalyst achieves 92.0% ethylene selectivity at full acetylene conversion, outperforming the Ni and Ni3In catalysts. Both experimental and theoretical evidence demonstrate that interstitial carbon atoms in Ni3InC0.5 synergize with neighboring In atoms to modify the electronic structure of surface Ni sites via significant hybridization between Ni 3d, In 5p, and C 2p orbitals. These unique features enable higher kinetic favorability of ethylene desorption over its further hydrogenation on the Ni3InC0.5 catalyst and thus contribute to the enhanced semihydrogenation.
期刊介绍:
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