Citation: Yang Yan, Zhang Yun, Hu Jin-Song, Wan Li-Jun. Progress in the Mechanisms and Materials for CO₂ Electroreduction toward C₂₊ Products[J]. Acta Physico-Chimica Sinica, ;2020, 36(1): 190608. doi: 10.3866/PKU.WHXB201906085 shu

Progress in the Mechanisms and Materials for CO₂ Electroreduction toward C₂₊ Products

Yang Yan ^1,2 ,
Zhang Yun ¹ ,
Hu Jin-Song ^1,2,, ,
Wan Li-Jun ¹

1.
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China
2.
University of Chinese Academy of Sciences, Beijing 100049, P. R. China

Author Bio:

Jin-Song Hu is currently a professor at the Institute of Chemistry, Chinese Academy of Sciences (ICCAS). After receiving Ph.D. degree in Physical Chemistry at ICCAS in 2005, he joined in ICCAS as an assistant professor and was then promoted as an associated professor in 2007. He worked in professor Charles M. Lieber's group at Harvard University in 2008-2011, then moved back to ICCAS as a Full Professor. His research currently focuses on developing new functional nanomaterials for efficient electrochemical energy conversion and solar energy conversion
Corresponding author: Hu Jin-Song, hujs@iccas.ac.cn
Received Date: 27 June 2019
Revised Date: 4 August 2019
Accepted Date: 22 August 2019
Available Online: 2 January 2019
Fund Project: The project was supported by the National Key Research and Development Program of China (2016YFB0101202) and the National Natural Science Foundation of China (21773263, 91645123)the National Natural Science Foundation of China 21773263the National Key Research and Development Program of China 2016YFB0101202the National Natural Science Foundation of China 91645123

Over the past decades, advances in science and technology have greatly benefitted the society. However, the exploitation of fossil fuels and excessive emissions of polluting gases have disturbed the balance of the normal carbon cycle, causing serious environmental issues and energy crises. Global warming caused by heavy CO₂ emissions is driving new attempts to mitigate the increase in the concentration of atmospheric CO₂. Significant efforts have been devoted for CO₂ conversion. To date, the electroreduction of CO₂, which is highly efficient and offers a promising strategy for both storing energy and managing the global carbon balance, has attracted great attention. In addition, the electrosynthesis of value-added C₂₊ products from CO₂ addresses the need for the long-term storage of renewable energy. Therefore, developing catalysts that function under ambient conditions to produce C₂ selectively over C₁ products will increase the utility of renewable feedstocks in industrial chemistry applications. Recently, great progress has been made in the development of materials for electrocatalytic CO₂ reduction (ECR) toward C₂₊ products; however, some issues (e.g., low selectivity, low current efficiency, and poor durability) remain to be addressed. In addition, the elementary reaction mechanism of each C₂₊ product remains unclear, contributing to the blindness of catalyst design. In this regard, the development of proposed mechanisms of ECR toward C₂₊ products is summarized herein. The key to generating C₂₊ products is improving the chances of C―C coupling. Test conditions significantly influence the reaction path of the catalyst. Thus, three different paths that that are most likely to occur during ECR to C₂₊ products are proposed, including the CO, CO-COH, and CO-CO paths. In addition, typical material regulatory strategies and technical designs for ECR toward C₂₊ products (e.g. crystal facet modulation, defect engineering, size effect, confinement effects, electrolyzer design, and electrolyte pH) are introduced, focusing on their effects on the selectivity, current efficiency, and durability. The four strategies for catalyst design (crystal facet modulation, defect engineering, size effect, and confinement effect) primarily affect the selectivity of the ECR via adjustment of the adsorption of reaction intermediates. The last two strategies for technique design (electrolyzer design and electrolyte pH) contributing greatly toward improving the current efficiency than selectivity. Finally, the challenges and perspectives for ECR toward C₂₊ products and their future prospects are discussed herein. Therefore, breakthroughs in the promising field of ECR toward the generation of C₂₊ products are possible when these catalyst design strategies and mechanisms are applied and novel designs are developed.
- CO₂ electroreduction,
- High value-added product,
- Selectivity,
- Faradaic efficiency,
- Durability
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Progress in the Mechanisms and Materials for CO2 Electroreduction toward C2+ Products

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Progress in the Mechanisms and Materials for CO₂ Electroreduction toward C₂₊ Products