Integrating battery and capacitive materials for efficient sodium and chloride capture

被引:3
|
作者
Shi, Wenhui [1 ]
Jiang, Qing [1 ]
Han, Xuran [1 ]
Dai, Runyu [1 ]
Jiang, Shengguang [1 ]
Li, Jun [2 ]
Shen, Jiangnan [1 ]
Cao, Xiehong [3 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn, Ctr Membrane Separat & Water Sci & Technol, Hangzhou 310014, Peoples R China
[2] Alphaverse Grp Ltd, Hong Kong 999077, Peoples R China
[3] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Peoples R China
基金
中国国家自然科学基金;
关键词
Dual-ion electrochemical deionization; Battery electrode materials; Capacitive electrode materials; MOF-derived carbon; Prussian blue; Bismuth oxychloride; DEIONIZATION PERFORMANCE; CARBON FRAMEWORKS; DESALINATION; ION; GRAPHENE; ENERGY; ELECTRODE; FUTURE; TECHNOLOGY; REMOVAL;
D O I
10.1007/s10008-023-05510-0
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Capacitive deionization (CDI) has been considered as a novel technology to relieve freshwater shortages. However, due to the limited physical adsorption capacity, the salt removal capacity remains low. To enhance the desalination capacity, battery type, and capacitive materials are employed to fabricate a dual-ion electrochemical deionization (DEDI) device. Herein, a Prussian blue/carbon framework (PB/CF) and BiOCl/CF were prepared by in situ conversion with a MOF-derived carbon framework as the precursor. A PB/CF composite was used as the sodium electrode, and BiOCl/CF was used as the chloride electrode. This system achieved high desalination capacity, excellent cycling stability, and rapid desalination. The maximum desalination capacity was 163 mg g(-1) at 100 mA g(-1), and the desalination rate was 0.631 mg g(-1) s(-1) at a high current density of 1000 mA g(-1). The outstanding desalination performance of this system arose from the synergistic effect of combining battery materials with a carbon framework for deionization and offers potential for future desalination designs.
引用
收藏
页码:1423 / 1431
页数:9
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