image: The tandem reaction achieved by the synergistic effect of Zn-O-Zr sites and oxygen vacancies, the ethane C–H bond was selectively clipped over the Zn-O-Zr sites and the CO2 C=O bonds was activated over the oxygen vacancies.
Credit: Chinese Journal of Catalysis
Ethylene, as one of the most important light olefins, serves as a fundamental feedstock for producing various high-value-added chemical products. Industrial ethylene production primarily relies on steam cracking of ethane and naphtha feedstock, which suffers from several drawbacks including excessive energy consumption, significant carbon emissions, and severe coke deposition.
The CO₂-assisted oxidative dehydrogenation of ethane (CO₂-ODHE) represents an eco-friendly process that enables resource utilization of ethane with the greenhouse gas CO₂. This technology demonstrates significant potential for advancing carbon neutrality initiatives and establishing sustainable chemical production systems. The current catalyst systems exhibit inherent limitations originating from the activity-selectivity trade-off and insufficient stability. The design of catalysts capable of simultaneously achieving selective C–H bond scission of ethane and efficient CO₂ activation represents a key challenge in CO₂-ODHE.
The ZnxZrO bifunctional catalyst developed in this study exhibits synergistic effects in the simultaneous activation of C–H and C=O bonds. Comprehensive characterization techniques were employed to probe the surface chemical states of ZnxZrO catalysts during CO₂-ODHE, identifying distinct functions of active sites. The Zn-O-Zr sites selectively cleave C–H bonds of ethane, while oxygen vacancies effectively activate CO₂ C=O bonds, enabling synergistic conversion of ethane and CO₂. In situ FTIR further elucidated the tandem reaction mechanism involving ethane dehydrogenation and reverse water-gas shift (RWGS).
This study provides fundamental insights into developing cost-effective, highly active, and stable catalysts for CO₂-ODHE, while establishing a novel catalyst design strategy for targeting alkane C–H bond scission in olefin production and CO₂ utilization. The results were published in Chinese Journal of Catalysis (DOI: 10.1016/S1872-2067(24)60235-4)
About the Journal
Chinese Journal of Catalysis is co-sponsored by Dalian Institute of Chemical Physics, Chinese Academy of Sciences and Chinese Chemical Society, and it is currently published by Elsevier group. This monthly journal publishes in English timely contributions of original and rigorously reviewed manuscripts covering all areas of catalysis. The journal publishes Reviews, Accounts, Communications, Articles, Highlights, Perspectives, and Viewpoints of highly scientific values that help understanding and defining of new concepts in both fundamental issues and practical applications of catalysis. Chinese Journal of Catalysis ranks among the top one journals in Applied Chemistry with a current SCI impact factor of 15.7. The Editors-in-Chief are Profs. Can Li and Tao Zhang.
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Journal
Chinese Journal of Catalysis
Article Title
Synergistic sites over the ZnxZrO catalyst for targeted cleavage of the C–H bonds of ethane in tandem with CO2 activation
Article Publication Date
20-Mar-2025