Capacitive Deionization of Saline Water by Using MoS2-Graphene Hybrid Electrodes with High Volumetric Adsorption Capacity

被引:197
作者
Han, Jinlong [1 ]
Yan, Tingting [1 ]
Shen, Junjie [2 ]
Shi, Liyi [1 ]
Zhang, Jianping [1 ]
Zhang, Dengsong [1 ]
机构
[1] Shanghai Univ, Dept Chem, Coll Sci,State Key Lab Adv Special Steel, Res Ctr Nano Sci & Technol,Sch Mat Sci & Engn, Shanghai 200444, Peoples R China
[2] Univ Bath, Dept Chem Engn, Bath BA2 7AY, Avon, England
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE ELECTRODES; ELECTROCHEMICAL PERFORMANCES; CARBON POLYHEDRA; EXFOLIATED MOS2; SIO ANODES; REMOVAL; DESALINATION; BRACKISH; DESIGN; SUPERCAPACITOR;
D O I
10.1021/acs.est.9b04274
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Capacitive deionization (CDI) has received wide attention as an emerging water treatment technology because of its low energy consumption, low cost, and high efficiency. However, the conventional carbon electrode materials for CDI have low densities, which occupy large volumes and are disadvantageous for use in limited space (e.g., in household or on offshore platforms). In order to miniaturize the CDI device, it is quite urgent to develop high volumetric adsorption capacity (VAC) electrode materials. To overcome this issue, we rationally designed and originally developed high VAC MoS2-graphene hybrid electrodes for CDI. It is interesting that MoS2-graphene hybrid electrode has a much higher NaCl VAC of 14.3 mg/cm(3) with a gravimetric adsorption capacity of 19.4 mg/g. It has been demonstrated that the adsorption capacity is significantly enhanced because of the rapid ion transport of MoS2 and high electrical conductivity of graphene. In situ Raman spectra and high-angle annular dark-field scanning transmission electron microscopy tests demonstrated a favorable Faradaic reaction, which was crucial to enhancing the NaCl VAC of the MoS2-graphene hybrid electrode. This work opens a new avenue for miniaturizing future CDI devices.
引用
收藏
页码:12668 / 12676
页数:9
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