Molten Salt Electrolytic CO2-Derived Carbon-Based Nanomaterials for Energy Storage and Electrocatalysis: A Review

被引:2
作者
Yu, Ao [1 ]
Liu, Shengwen [1 ]
Zhang, Wei [1 ,2 ]
Yang, Yang [3 ,4 ]
机构
[1] Univ Cent Florida, NanoSci Technol Ctr, Orlando, FL 32826 USA
[2] Univ Cent Florida, Dept Mat Sci & Engn, Orlando, FL 32826 USA
[3] Univ Cent Florida, Nano Sci Technol Ctr, Renewable Energy & Chem Transformat Cluster, Dept Mat Sci & Engn,Dept Chem, Orlando, FL 32826 USA
[4] Univ Cent Florida, Stephen W Hawking Ctr Micrograv Res & Educ, Orlando, FL 32826 USA
基金
美国国家科学基金会;
关键词
molten salt electrolysis; CO2; nanomaterials; capacitors; batteries; electrocatalysts; OXYGEN REDUCTION; ELECTROCHEMICAL CONVERSION; CO2; CAPTURE; MSCC-ET; TEMPERATURE; ION; DIOXIDE; H2O2; PERFORMANCE; CATALYSTS;
D O I
10.1021/acsanm.4c00010
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The electroreduction of CO2 in molten salt presents a promising strategy for achieving decarbonization while simultaneously producing highly valuable CO2-derived carbon-based nanomaterials. Although electrolytic nanocarbons have been explored for an extended period, their applications in energy storage and as electrocatalysts still require an in-depth study. This paper initially introduces the advantages and basic mechanisms of CO2 reduction in molten salt and then discusses the progress of CO2-derived carbon-based nanomaterials. More importantly, the paper summarizes the applications in capacitors, batteries, and electrocatalysts based on research progress and material characteristics. It is highlighted that CO2-derived carbon-based nanomaterials were initially used in capacitors and batteries and have recently begun to be utilized as electrocatalysts for two-electron oxygen reduction reaction, oxygen evolution reaction, and hydrogen evolution reaction. A comprehensive understanding of the synthetic mechanisms of various CO2-derived carbon-based nanomaterials and their applications can lay a foundation for the further development of this low-carbon-footprint process.
引用
收藏
页码:27960 / 27978
页数:19
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