CO2 transformed into highly active catalysts for the oxygen reduction reaction via low-temperature molten salt electrolysis

被引:0
|
作者
Remmel, Anna-Liis [1 ]
Ratso, Sander [1 ,3 ]
Liivand, Kerli [1 ]
Danilson, Mati [2 ]
Kaare, Katlin [1 ]
Mikli, Valdek [2 ]
Kruusenberg, Ivar [1 ]
机构
[1] NICPB, Akad Tee 23, EE-12618 Tallinn, Estonia
[2] Tallinn Univ Technol, Dept Mat & Environm Technol, Ehitajate tee 5, EE-19086 Tallinn, Estonia
[3] Univ Calif Berkeley, Nucl Engn Dept, 2521 Hearst Ave, Berkeley, CA 94709 USA
关键词
CARBON; IRON;
D O I
10.1016/j.elecom.2024.107781
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The implementation of a technology capable of capturing and converting CO2 into valuable products is one of the key requirements for limiting the effects of our carbon-intensive industries. At the same time, future CO2 emissions need to be reduced to combat climate change, meaning that new devices capable of storing and converting energy without CO2 emissions have to be adopted widely. In this work, we demonstrate catalysts made directly from CO2 for fuel cells and zinc-air K2CO3 and a new mixture containing 0.1 mol of LiOH in addition. The effects of the electrolyte towards the final carbon product and its electrocatalytic activity are analysed using the rotating disk electrode method, X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. The porosity of the materials is described by N2 adsorption and the best performing catalyst is compared to the activity of a commercial 20 wt% PtRu/C material in a zinc-air battery.
引用
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页数:9
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