Faradic Side Reactions at Novel Carbon Flow-Through Electrodes for Desalination Studied in a Static Supercapacitor Architecture

被引:1
|
作者
Molaei, Arman [1 ]
Crispin, Xavier [1 ]
机构
[1] Linkoping Univ, Dept Sci & Technol, Lab Organ Elect, S-60174 Norrkoping, Sweden
来源
ADVANCED ENERGY AND SUSTAINABILITY RESEARCH | 2023年 / 4卷 / 01期
基金
瑞典研究理事会;
关键词
capacitive deionization; desalination; hydrogen peroxide; oxygen reduction reactions; supercapacitors; CAPACITIVE DEIONIZATION; HYDROGEN-PEROXIDE; ENERGY RECOVERY; WATER; PERFORMANCE; SYSTEM; OXYGEN; POLARIZATION; STABILITY; NACL;
D O I
10.1002/aesr.202200119
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Desalination by capacitive deionization (CDI) is a promising technique to combine desalination and energy storage. The efficiency of charge storage process, which is equivalent to the desalination process, depends strongly on the presence of Faradic side reactions on the electrode. Herein, the performance of a new low-cost designed flow-through electrode with porous carbon nanoparticles (CP) coating on carbon-fiber paper (CFP) is evaluated. The CP layer enables high capacitance while the CFP core makes fluid dynamics along and across the electrode. The electrodes are evaluated by studying the effective operational CDI parameters, such as operational voltage, degassing of electrolyte, and salt concentration. The Faradic side reaction and its effect on charge efficiency (CE) are evaluated which are estimated to decrease to 46% by liquid flow bringing dissolved oxygen from the air-electrolyte interface to the electrode. The CE enhances to 59% with a salt concentration of 1 m. By purging N-2 gas, CE is much higher (>85%) with a maximum efficiency of 97% at 0.6 V. Three regimes of the complex kinetic of side reactions are found involving various species such as O-2, H2O2, H-2, and carbon oxidation and the implication of those regimes for real applications are discussed.
引用
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页数:14
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