期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 8, 页码 3905-3932出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta09659a
关键词
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资金
- National Natural Science Foundation of China [51779090, 51879101, 51579098, 51709101, 51521006, 51809090, 51909084]
- National Program for Support of Top-Notch Young Professionals of China (2014)
- Program for Changjiang Scholars and Innovative Research Team in University [IRT13R17]
- Hunan Provincial Science and Technology Plan Project [2018SK20410, 2017SK2243, 2016RS3026]
- Fundamental Research Funds for the Central Universities [531119200086, 531118010114, 531107050978, 541109060031]
The review discusses the feasibility of utilizing Graphynes (GYs) as supports for Single Atom Catalysts (SACs), and outlines various synthetic methods and applications for GY-supported SACs in electrochemical energy conversion. It also highlights the challenges and future research directions of GY-supported SACs for further development.
Single atom catalysts (SACs) with maximum atom utilization, well-distributed active sites, and various metal-support interactions have been proven to be new frontiers in electrocatalysis. A suitable support is usually desirable for SACs to prevent the aggregation of metal atoms and improve their dispersity, thereby enhancing their performance for electrochemical energy conversion. Graphynes (GYs), the rising stars of two-dimensional carbon allotropes with monolayer thickness, are composed of sp- and sp(2)-hybridized carbon atoms. The presence of sp-hybridized carbon atoms in GY networks endows them with unique structures and properties, such as well-distributed pores, high carrier mobility, excellent stability, a large specific surface area, and superior electrical conductivity. These unique structures and properties make GYs ideal supports for SACs. In this review, the feasibility of applying GYs as supports for SACs is analyzed with respect to the structure and properties. Then, various synthetic methods for GY-supported SACs are summarized. Moreover, the applications of GY-supported SACs for electrochemical energy conversion are summarized. Finally, the challenges and future research directions of GY-supported SACs for further development are highlighted. We believe that such a comprehensive summary not only provides a profound understanding of GY-supported SACs for electrochemical energy conversion, but also opens up promising channels for SAC design.
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