MFI沸石丙烷脱氢条件下[Ga]+和[GaH2]+演化的理论研究

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
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,&nbsp;Xin Liu*,&nbsp;Huimin Guo* and Changgong Meng*,&nbsp;","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> &gt; 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,&nbsp;Xin Liu*,&nbsp;Huimin Guo* and Changgong Meng*,&nbsp;\",\"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> &gt; 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}
引用次数: 0

摘要

Ga/ZSM-5是丙烷脱氢(PDH)选择性生产丙烯的催化剂之一,丙烯是化工领域最重要的原料之一。Ga/ZSM-5上的PDH在恶劣条件下工作(T >;800 K),限制了催化剂的深入和原位表征。Ga/H-ZSM-5脱氢过程中Ga的形态和活性位点的结构一直没有得到明确的解答。此外,单al位点稳定的Ga物种是最丰富的Ga物种;它们上的PDH通路与Ga/ZSM-5中双al位点捕获的Ga-oxo或还原Ga物种的PDH通路不同,并且据报道表现出意想不到的高性能。为了弥补这些空白,利用第一性原理计算研究了[Ga]+, [GaH2]+和[Ga]3+在PDH中ZSM-5通道和表面的潜在催化作用和演变。结果表明,在操作条件下,动态生成的欠配位[GaH2]+ (Sin-[GaH2]+)与其他由单al位稳定的单核还原Ga相比,具有优越的催化性能。虽然[Ga]+在热力学上更合理,但[GaH2]+在动力学上也有利于PDH途径。提出了一个PDH的催化循环,连接了[Ga]+的协同途径和[GaH2]+的烷基途径,表明了Ga物种的进化与丙烷转化之间的强耦合。我们还提出,与PDH和相互转化竞争,[Ga]+和[GaH2]+也可能在通道或沸石表面演化和运输形成[Ga]3+,并且这种运输也改变了Ga/Al比,形成比[GaH2]+和[Ga]+更活跃的Ga物种,这可能是Ga/ZSM-5观察到的PDH性能的原因。研究结果有助于进一步理解Ga/ZSM-5的PDH性能,并有助于设计具有优异PDH性能的新型催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evolution of [Ga]+ and [GaH2]+ at Propane Dehydrogenation Conditions in MFI Zeolite: A Theoretical Investigation

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信