Photocatalytic non-oxidative dehydrogenation of ethane to ethene with near unit selectivity

The non-oxidative dehydrogenation of light alkanes to alkenes is thermodynamically limited by the trade-off between the cleavage of C-H and C-C bonds. Unlocking the thermodynamic bottleneck with photocatalysis is prone to eliminate undesirable side reactions such as deep dehydrogenation, cracking, isomerization, and polymerization. Herein, we show the photocatalytic non-oxidative dehydrogenation of ethane to ethene and hydrogen at ambient conditions, which is enabled by grafting of Ni single atoms to modulate the surface electronic structure of Pd nanoparticles photo-deposited on the surface of anatase TiO<sub>2</sub> nanoparticles, modifying the ethane dehydrogenation pathway. A high rate of 8.2 ± 0.2 mmol·g<sup>-1</sup>·h<sup>-1</sup> for the stoichiometric conversion of ethane to ethene and hydrogen is achieved with a 100% ethene selectivity in a flow reactor under solar light irradiation. The apparent quantum efficiency reaches ~22.3% at 350 nm by using the optimal T-Ni<sub>0.6</sub>Pd<sub>0.24</sub> photocatalyst. Solar-driven non-oxidative alkane dehydrogenation offers a route to light alkenes with high performance, and selectivity.

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Publication Details

Journal
Nature Communications
Published
2025-10-23
DOI
https://doi.org/10.1038/s41467-025-64389-9
Citations
4
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
1.56

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article

Photocatalytic non-oxidative dehydrogenation of ethane to ethene with near unit selectivity

Yanyan Jia, Jiwu Zhao, Jinlin Long, Sheng Dai et al.
4 citations
Nature Communications
Catalysis and Oxidation Reactions
1.56
article

Photocatalytic non-oxidative dehydrogenation of ethane to ethene with near unit selectivity

Yanyan Jia, Jiwu Zhao, Jinlin Long, Sheng Dai, Pengzhao Wang, Na Wen, Hangbin Zheng, Wenxin Dai, Xiaoyu Sui, Zizhong Zhang, Zhengxin Ding, Rusheng Yuan, Chao Xu, Pu Zhang, Ying Wang, Xianzhi Fu, Haihua Zeng
article en
4 citations

Abstract

The non-oxidative dehydrogenation of light alkanes to alkenes is thermodynamically limited by the trade-off between the cleavage of C-H and C-C bonds. Unlocking the thermodynamic bottleneck with photocatalysis is prone to eliminate undesirable side reactions such as deep dehydrogenation, cracking, isomerization, and polymerization. Herein, we show the photocatalytic non-oxidative dehydrogenation of ethane to ethene and hydrogen at ambient conditions, which is enabled by grafting of Ni single atoms to modulate the surface electronic structure of Pd nanoparticles photo-deposited on the surface of anatase TiO<sub>2</sub> nanoparticles, modifying the ethane dehydrogenation pathway. A high rate of 8.2 ± 0.2 mmol·g<sup>-1</sup>·h<sup>-1</sup> for the stoichiometric conversion of ethane to ethene and hydrogen is achieved with a 100% ethene selectivity in a flow reactor under solar light irradiation. The apparent quantum efficiency reaches ~22.3% at 350 nm by using the optimal T-Ni<sub>0.6</sub>Pd<sub>0.24</sub> photocatalyst. Solar-driven non-oxidative alkane dehydrogenation offers a route to light alkenes with high performance, and selectivity.

Nature CommunicationsVol. 16(1)
East China University of Science and Technology (CN), Fuzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 16%
Catalysis and Oxidation Reactions
1.56
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