Affiliation:
1. School of Environmental Science and Engineering Shaanxi University of Science and Technology Xian 710021 P. R. China
2. Department of Biology College of Science Princess Nourah bint Abdulrahman University Riyadh 11671 Saudi Arabia
3. Department of Biology College of Science Imam Mohammad Ibn Saud Islamic University Riyadh 11623 Saudi Arabia
4. Institute for Technical Chemistry Leibniz University Hannover 30167 Hannover Germany
5. Laboratory of Photoactive Nanocomposite Materials Saint Petersburg State University Saint-Petersburg 198504 Russia
Abstract
AbstractOver the past decades, CO2 greenhouse emission has been considerably increased, causing global warming and climate change. Indeed, converting CO2 into valuable chemicals and fuels is a desired option to resolve issues caused by its continuous emission into the atmosphere. Nevertheless, CO2 conversion has been hampered by the ultrahigh dissociation energy of C=O bonds, which makes it thermodynamically and kinetically challenging. From this prospect, photocatalytic approaches appear promising for CO2 reduction in terms of their efficiency compared to other traditional technologies. Thus, many efforts have been made in the designing of photocatalysts with asymmetric sites and oxygen vacancies, which can break the charge distribution balance of CO2 molecule, reduce hydrogenation energy barrier and accelerate CO2 conversion into chemicals and fuels. Here, we review the recent advances in CO2 hydrogenation to C1 and C2 products utilizing photocatalysis processes. We also pin down the key factors or parameters influencing the generation of C2 products during CO2 hydrogenation. In addition, the current status of CO2 reduction is summarized, projecting the future direction for CO2 conversion by photocatalysis processes.
Funder
National Natural Science Foundation of China
Cited by
2 articles.
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