Capture of CO2 during the Electrolysis Process and Its Utilization in Supercapacitor Materials

被引:1
|
作者
Hu, Mengjun [1 ]
Tan, Rui [2 ]
Jiang, Xiaojuan [1 ]
Dong, Mengyao [1 ]
Wen, Liangying [2 ]
Hu, Meilong [2 ]
机构
[1] Chongqing Ind Polytech Coll, Sch Mech Engn & Automat, Key Lab Mat Proc & Mold Technol, Chongqing 401120, Peoples R China
[2] Chongqing Univ, Sch Mat Sci & Engn, Chongqing 400044, Peoples R China
来源
ACS OMEGA | 2024年 / 9卷 / 06期
关键词
ELECTROCHEMICAL CONVERSION; MOLTEN; REDUCTION; CARBON;
D O I
10.1021/acsomega.3c07587
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
With climate change and environmental issues, the emissions of CO2 and its greenhouse effect have become a focal point. At present, the utilization of CO2 includes its synthesis into chemicals and fuels such as methane, methanol, and CO. CO2 utilization can be achieved through carbon capture and storage technologies, which involve capturing CO2 from industrial emissions and storing it to reduce the CO2 concentration in the atmosphere. However, these CO2 capture and utilization technologies still face challenges, such as technical immaturity and high costs. One of the CO2 capture and utilization technologies is the production of energy storage materials. In this study, CO2 captured by molten salt was used as the carbon source, and TiO2 nanotube arrays were used as precursors. Titanium carbide nanotube arrays(TiC-NTAs)with high specific surface area and high conductivity were prepared by electrolysis. Afterward, the electrochemical energy storage performance of TiC in different electrolytes was tested. The results show that reducing the ionic radius of the electrolyte is conducive to increasing the area-specific capacitance of the device and that the degradation of the cycle life of the quasi-solid supercapacitor may be caused by an increase in the internal resistance due to the loss of water from the electrolyte. This study provides a reference value for the low-temperature synthesis of nanometal carbides and the selection of electrolytes.
引用
收藏
页码:6888 / 6893
页数:6
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