Controllable synthesis of a hollow core-shell Co-Fe layered double hydroxide derived from Co-MOF and its application in capacitive deionization

被引:69
作者
Li, Zhe [1 ]
Mao, Shudi [1 ]
Yang, Ying [1 ]
Sun, Zhuo [1 ,2 ]
Zhao, Ran [1 ,2 ]
机构
[1] East China Normal Univ, Sch Phys & Elect Sci, Minist Educ, Engn Res Ctr Nanophoton & Adv Instrument, 500 Dongchuan Rd, Shanghai 200241, Peoples R China
[2] Univ Alberta, East China Normal Univ, Joint Inst Adv Sci & Technol, 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China
关键词
Capacitive deionization; Hollow structure; Pseudocapacitance; METAL-ORGANIC FRAMEWORK; DESALINATION PERFORMANCE; WATER DESALINATION; EXCHANGE MEMBRANES; ELECTRODE MATERIAL; CARBON COMPOSITE; ACTIVATED CARBON; ANION-EXCHANGE; REMOVAL; FABRICATION;
D O I
10.1016/j.jcis.2020.11.091
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Capacitive deionization (CDI) is considered one of the most promising desalination technologies for obtaining fresh water from saline water. In this work, we synthesized a hollow core-shell Co-MOF@Fe/Co-LDH (Co-Fe-LDH) material by developing a strategy to simultaneously grow Co/Fe-LDH on the surface of a Co-MOF precursor in situ. Owing to the increase in the specific surface area of the hollow structure and the Faradaic process of a layered double hydroxide (LDH), the Co-Fe-LDH material exhibits high electrical double layer (EDL) capacitance and pseudocapacitance, which significantly improves the salt adsorption of the material during CDI (34.2 mg/g in a 600 mg/L NaCl solution at 1.2 V). The adsorption for NaCl in this work is approximately 2.5 times the maximum salt adsorption capacity (SAC) of LDH materials applied in nonmembrane CDI (NMCDI). This work may provide a promising model for the application of hollow LDH materials that exhibit pseudocapacitance in CDI. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:85 / 94
页数:10
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