Thermal Management Approach to Stabilization of Disordered Active Sites for Sabatier Reaction

The transition metal nanocatalysts containing disordered active sites can potentially achieve efficient Sabatier reactions with high selectivity. However, it remains a challenge to maintain the stability of these active sites in such an exothermic reaction. Here, a thermal management approach is reported to address this challenge. Specifically, an efficient and stable catalytic system is developed by integrating urchin-like Ru nanoparticles with disordered active sites (d-RuNUs) and multi-walled carbon nanotubes (MWCNTs) as heat transfer framework, which achieves a CH<sub>4</sub> yield of 3.3 mol g<sup>-1</sup> h<sup>-1</sup> with nearly 100% selectivity in 12 h. The characterizations reveal that the thermal-induced crystallization seriously weakens the adsorption of CO<sub>2</sub>, leading to significant degradation of catalytic performance. The heat transfer simulation confirms that the MWCNTs with high thermal conductivity play a key role in rapidly redistributing the reaction heat, thereby preventing the crystallization of disordered structures. This work elucidates the deactivation mechanism of disordered active sites in exothermic reactions and opens the avenue for local thermal management of non-thermal equilibrium reactions.

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Publication Details

Journal
Advanced Science
Published
2024-12-04
DOI
https://doi.org/10.1002/advs.202409048
Citations
2
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.36

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article

Thermal Management Approach to Stabilization of Disordered Active Sites for Sabatier Reaction

Chuansheng Hu, Yingpu Bi, Ran Long, Di Wu et al.
2 citations
Advanced Science
Carbon dioxide utilization in catalysis
0.36
article

Thermal Management Approach to Stabilization of Disordered Active Sites for Sabatier Reaction

Chuansheng Hu, Yingpu Bi, Ran Long, Di Wu, Canyu Hu, Hongwei Shou, Delong Duan, Yujie Xiong, Min Zhou
article en
2 citations

Abstract

The transition metal nanocatalysts containing disordered active sites can potentially achieve efficient Sabatier reactions with high selectivity. However, it remains a challenge to maintain the stability of these active sites in such an exothermic reaction. Here, a thermal management approach is reported to address this challenge. Specifically, an efficient and stable catalytic system is developed by integrating urchin-like Ru nanoparticles with disordered active sites (d-RuNUs) and multi-walled carbon nanotubes (MWCNTs) as heat transfer framework, which achieves a CH<sub>4</sub> yield of 3.3 mol g<sup>-1</sup> h<sup>-1</sup> with nearly 100% selectivity in 12 h. The characterizations reveal that the thermal-induced crystallization seriously weakens the adsorption of CO<sub>2</sub>, leading to significant degradation of catalytic performance. The heat transfer simulation confirms that the MWCNTs with high thermal conductivity play a key role in rapidly redistributing the reaction heat, thereby preventing the crystallization of disordered structures. This work elucidates the deactivation mechanism of disordered active sites in exothermic reactions and opens the avenue for local thermal management of non-thermal equilibrium reactions.

Advanced ScienceVol. 12(4)
University of Science and Technology of China (CN), Chinese Academy of Sciences (CN), Suzhou University of Science and Technology (CN), Lanzhou Institute of Chemical Physics (CN), National Synchrotron Radiation Laboratory (CN)
Salt Science Research Foundation, National Key Laboratory of Human Factors Engineering, National Natural Science Foundation of China, Chinese Academy of Sciences, University of Science and Technology of China, National Synchrotron Radiation Laboratory, West Light Foundation of the Chinese Academy of Sciences, Natural Science Foundation of Anhui Province, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Clean water and sanitation
Openalex Percentile: Top 50%
Carbon dioxide utilization in catalysis
0.36
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