Zhe Feng, Xin Liu*, Huimin Guo* and Changgong Meng*,
{"title":"MFI沸石丙烷脱氢条件下[Ga]+和[GaH2]+演化的理论研究","authors":"Zhe Feng, Xin Liu*, Huimin Guo* and Changgong Meng*, ","doi":"10.1021/acs.jpcc.4c0881310.1021/acs.jpcc.4c08813","DOIUrl":null,"url":null,"abstract":"<p >Ga/ZSM-5 is among the most promising catalysts for propane dehydrogenation (PDH) to selectively produce propylene, which is one of the most important feedstocks in chemical industry. PDH over Ga/ZSM-5 operates at harsh conditions (<i>T</i> > 800 K), limiting the in-depth and in situ characterization of the catalysts. The Ga speciation and the structures of active sites on Ga/H-ZSM-5 in dehydrogenation have remained in active discussion as they have not been solved clearly. Furthermore, Ga species stabilized by mono-Al sites would be the most abundant Ga species; the PDH pathways over them would be different from those of Ga-oxo or reduced Ga species trapped by dual-Al sites in Ga/ZSM-5, and were reported to exhibit unexpectedly high performance. To bridge these gaps, the potential catalytic roles and evolution of [Ga]<sup>+</sup>, [GaH<sub>2</sub>]<sup>+</sup>, and [Ga]<sup>3+</sup> in the channel and on the surface of ZSM-5 in PDH were investigated with first-principles-based calculations. We showed that dynamically generated undercoordinated [GaH<sub>2</sub>]<sup>+</sup> (Sin-[GaH<sub>2</sub><sup>]+</sup>) would exhibit superior catalytic performance as compared with other mononuclear reduced Ga species stabilized by mono-Al sites at the operation conditions. Though [Ga]<sup>+</sup> is thermodynamically more plausible, [GaH<sub>2</sub>]<sup>+</sup> is also kinetically favored on PDH pathways. A catalytic cycle of PDH was proposed connecting the concerted pathway over [Ga]<sup>+</sup> and the alkyl pathway over [GaH<sub>2</sub>]<sup>+</sup>, showing the strong coupling between the evolution of Ga species and the conversion of propane. We also proposed that, competing with PDH and the interconversion, [Ga]<sup>+</sup> and [GaH<sub>2</sub>]<sup>+</sup> may also evolve and transport to form [Ga]<sup>3+</sup> in channels or on the surface of zeolites, and this transportation also changes the Ga/Al ratio, forming Ga species that are more active than [GaH<sub>2</sub>]<sup>+</sup> and [Ga]<sup>+</sup> in situ and may account for the observed PDH performance of Ga/ZSM-5. The findings may help to rationalize the understanding of PDH performance of Ga/ZSM-5 and benefit the design of novel catalysts with superior PDH performance.</p>","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"129 17","pages":"8106–8120 8106–8120"},"PeriodicalIF":3.2000,"publicationDate":"2025-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evolution of [Ga]+ and [GaH2]+ at Propane Dehydrogenation Conditions in MFI Zeolite: A Theoretical Investigation\",\"authors\":\"Zhe Feng, Xin Liu*, Huimin Guo* and Changgong Meng*, \",\"doi\":\"10.1021/acs.jpcc.4c0881310.1021/acs.jpcc.4c08813\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Ga/ZSM-5 is among the most promising catalysts for propane dehydrogenation (PDH) to selectively produce propylene, which is one of the most important feedstocks in chemical industry. PDH over Ga/ZSM-5 operates at harsh conditions (<i>T</i> > 800 K), limiting the in-depth and in situ characterization of the catalysts. The Ga speciation and the structures of active sites on Ga/H-ZSM-5 in dehydrogenation have remained in active discussion as they have not been solved clearly. Furthermore, Ga species stabilized by mono-Al sites would be the most abundant Ga species; the PDH pathways over them would be different from those of Ga-oxo or reduced Ga species trapped by dual-Al sites in Ga/ZSM-5, and were reported to exhibit unexpectedly high performance. To bridge these gaps, the potential catalytic roles and evolution of [Ga]<sup>+</sup>, [GaH<sub>2</sub>]<sup>+</sup>, and [Ga]<sup>3+</sup> in the channel and on the surface of ZSM-5 in PDH were investigated with first-principles-based calculations. We showed that dynamically generated undercoordinated [GaH<sub>2</sub>]<sup>+</sup> (Sin-[GaH<sub>2</sub><sup>]+</sup>) would exhibit superior catalytic performance as compared with other mononuclear reduced Ga species stabilized by mono-Al sites at the operation conditions. Though [Ga]<sup>+</sup> is thermodynamically more plausible, [GaH<sub>2</sub>]<sup>+</sup> is also kinetically favored on PDH pathways. A catalytic cycle of PDH was proposed connecting the concerted pathway over [Ga]<sup>+</sup> and the alkyl pathway over [GaH<sub>2</sub>]<sup>+</sup>, showing the strong coupling between the evolution of Ga species and the conversion of propane. We also proposed that, competing with PDH and the interconversion, [Ga]<sup>+</sup> and [GaH<sub>2</sub>]<sup>+</sup> may also evolve and transport to form [Ga]<sup>3+</sup> in channels or on the surface of zeolites, and this transportation also changes the Ga/Al ratio, forming Ga species that are more active than [GaH<sub>2</sub>]<sup>+</sup> and [Ga]<sup>+</sup> in situ and may account for the observed PDH performance of Ga/ZSM-5. The findings may help to rationalize the understanding of PDH performance of Ga/ZSM-5 and benefit the design of novel catalysts with superior PDH performance.</p>\",\"PeriodicalId\":61,\"journal\":{\"name\":\"The Journal of Physical Chemistry C\",\"volume\":\"129 17\",\"pages\":\"8106–8120 8106–8120\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-04-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry C\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jpcc.4c08813\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpcc.4c08813","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Evolution of [Ga]+ and [GaH2]+ at Propane Dehydrogenation Conditions in MFI Zeolite: A Theoretical Investigation
Ga/ZSM-5 is among the most promising catalysts for propane dehydrogenation (PDH) to selectively produce propylene, which is one of the most important feedstocks in chemical industry. PDH over Ga/ZSM-5 operates at harsh conditions (T > 800 K), limiting the in-depth and in situ characterization of the catalysts. The Ga speciation and the structures of active sites on Ga/H-ZSM-5 in dehydrogenation have remained in active discussion as they have not been solved clearly. Furthermore, Ga species stabilized by mono-Al sites would be the most abundant Ga species; the PDH pathways over them would be different from those of Ga-oxo or reduced Ga species trapped by dual-Al sites in Ga/ZSM-5, and were reported to exhibit unexpectedly high performance. To bridge these gaps, the potential catalytic roles and evolution of [Ga]+, [GaH2]+, and [Ga]3+ in the channel and on the surface of ZSM-5 in PDH were investigated with first-principles-based calculations. We showed that dynamically generated undercoordinated [GaH2]+ (Sin-[GaH2]+) would exhibit superior catalytic performance as compared with other mononuclear reduced Ga species stabilized by mono-Al sites at the operation conditions. Though [Ga]+ is thermodynamically more plausible, [GaH2]+ is also kinetically favored on PDH pathways. A catalytic cycle of PDH was proposed connecting the concerted pathway over [Ga]+ and the alkyl pathway over [GaH2]+, showing the strong coupling between the evolution of Ga species and the conversion of propane. We also proposed that, competing with PDH and the interconversion, [Ga]+ and [GaH2]+ may also evolve and transport to form [Ga]3+ in channels or on the surface of zeolites, and this transportation also changes the Ga/Al ratio, forming Ga species that are more active than [GaH2]+ and [Ga]+ in situ and may account for the observed PDH performance of Ga/ZSM-5. The findings may help to rationalize the understanding of PDH performance of Ga/ZSM-5 and benefit the design of novel catalysts with superior PDH performance.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.