Evolution of [Ga]<sup>+</sup> and [GaH<sub>2</sub>]<sup>+</sup> 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.

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2025-04-21
DOI
https://doi.org/10.1021/acs.jpcc.4c08813
Citations
3
Primary Topic
Zeolite Catalysis and Synthesis
Type
article
Field-Weighted Citation Impact
1.61
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article

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

Changgong Meng, Huimin Guo, Xin Liu, Feng Zhe
3 citations
The Journal of Physical Chemistry C
Zeolite Catalysis and Synthesis
1.61
article

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

Changgong Meng, Huimin Guo, Xin Liu, Feng Zhe
article en
3 citations

Abstract

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.

The Journal of Physical Chemistry CVol. 129(17)
Dalian University of Technology (CN), Smart Material (Germany) (DE), State Key Laboratory of Fine Chemicals
Openalex Percentile: Top 17%
Zeolite Catalysis and Synthesis
1.61
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