Boosting Propane Dehydrogenation to Propylene via Electron Hole‐Hydrogen Coupling on Cobalt Metal Surface

Abstract Nonoxidative dehydrogenation of propane is useful for the high selectivity to propylene but is suffering from the heavy coke deposition on the catalyst surface. Herein, we present a proof‐of‐concept application of a hole‐hydrogen (H) couple on a metallic cobalt surface to decrease the deactivation rate. The coupled H atoms on the Cobalt (Co) surface, partially resulting from propane dehydrogenation, enabled the desorption of propylene to avoid deep hydrogenolysis and coke deposition and realize selective and durable propylene production, while conventional Co metal‐based catalysts do not generate propylene. The optimized hole‐H coupled Co catalyst provided a low deactivation rate (0.0036 h −1 ) and a high turnover frequency (55.6 h −1 ) for propylene production with a high propane flux (48 vol.% C 3 H 8 in gas feeds) at 550 °C.

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Publication Details

Journal
Angewandte Chemie
Published
2024-10-24
DOI
https://doi.org/10.1002/ange.202419816
Citations
1
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
0.34
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article

Boosting Propane Dehydrogenation to Propylene via Electron Hole‐Hydrogen Coupling on Cobalt Metal Surface

Yu-Shuai Xu, Qiang Su, Jie‐Sheng Chen, Bing‐Liang Leng et al.
1 citations
Angewandte Chemie
Advanced Chemical Physics Studies
0.34
article

Boosting Propane Dehydrogenation to Propylene via Electron Hole‐Hydrogen Coupling on Cobalt Metal Surface

Yu-Shuai Xu, Qiang Su, Jie‐Sheng Chen, Bing‐Liang Leng, Xiu Lin, Xin‐Hao Li, Qiyuan Li, Dong Xu, Siyuan Xia, Liu-Yin Fan
article en
1 citations

Abstract

Abstract Nonoxidative dehydrogenation of propane is useful for the high selectivity to propylene but is suffering from the heavy coke deposition on the catalyst surface. Herein, we present a proof‐of‐concept application of a hole‐hydrogen (H) couple on a metallic cobalt surface to decrease the deactivation rate. The coupled H atoms on the Cobalt (Co) surface, partially resulting from propane dehydrogenation, enabled the desorption of propylene to avoid deep hydrogenolysis and coke deposition and realize selective and durable propylene production, while conventional Co metal‐based catalysts do not generate propylene. The optimized hole‐H coupled Co catalyst provided a low deactivation rate (0.0036 h −1 ) and a high turnover frequency (55.6 h −1 ) for propylene production with a high propane flux (48 vol.% C 3 H 8 in gas feeds) at 550 °C.

Angewandte ChemieVol. 137(7)
Shanghai Jiao Tong University (CN)
Openalex Percentile: Top 39%
Advanced Chemical Physics Studies
0.34
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