CO2-mediated oxidative dehydrogenation of light alkanes to olefins: Advances and perspectives in catalyst design and process improvement

• Upgrading CO 2 and light alkanes (C 2 -C 4 ), isobutane, ethylbenzene into olefins. • CO 2 -mediated oxidative dehydrogenation (CO 2 -ODH) are environmentally benign routes. • Insights on CO 2 activation and activation mechanisms in CO 2 -ODH were provided. • Advances and perspectives on catalyst design strategies were discussed. • Integrated CO 2 capture-utilization via CO 2 -ODH is possible with dual-function materials. Simultaneous valorization of anthropogenic CO 2 and underutilized light alkanes (C 2 -C 4 ) in shale gas and other feedstock into valuable platform chemicals (olefins) is a highly promising green alternative. The route involves CO 2 -assisted oxidative dehydrogenation of the feedstock (CO 2 -ODH) with zero direct H 2 input, and can bring about a paradigm shift in the chemical industry towards becoming more environmentally benign. Herein, we reviewed and discussed recent advances in these processes under common themes related to activation mechanism, catalyst development, and process improvement. Notably, we elucidated various catalyst design and tuning strategies that can potentially guide in future design of novel CO 2 -ODH catalysts with high activity, high olefin selectivity, and long-term stability. The design strategies were illustrated in the light of crucial catalytic features and various nanoscale phenomena such as oxygen mobility, charge transfer, defect creation, interfacial synergy, and balanced acidity that strongly influence and regulate overall catalytic performance. In addition, the review captured a discussion on prospects of dual-function materials for integrated CO 2 capture-utilization via CO 2 -ODH. Moreover, challenges and perspectives have been provided to stimulate further progress in the CO 2 -ODH processes towards becoming commercially and industrially viable alternatives.