Constructing titanium carbide MXene/reduced graphene oxide superlattice heterostructure via electrostatic self-assembly for high- performance capacitive deionization

被引:45
|
作者
Xu, Huiting [1 ]
Li, Meng [1 ]
Gong, Siqi [1 ]
Zhao, Fan [1 ]
Zhao, Yang [2 ]
Li, Chunli [1 ]
Qi, Junjie [1 ]
Wang, Zhiying [1 ]
Wang, Honghai [1 ]
Fan, Xiaobin [2 ]
Peng, Wenchao [2 ]
Liu, Jiapeng [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Natl Local Joint Engn Lab Energy Conservat Chem Pr, Tianjin 300130, Peoples R China
[2] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, Sch Chem Engn & Technol, State Key Lab Chem Engn, Tianjin 300072, Peoples R China
关键词
Two-dimensional nanomaterials; Superlattice heterostructure; Electrostatic self-assembly; Capacitive deionization; DESALINATION; REMOVAL; HYBRID; IONS;
D O I
10.1016/j.jcis.2022.05.131
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 has attracted wide concern on account of its high energy efficiency, low manufacturing cost and environmental friendliness. Nevertheless, the development of capacitive deionization is still impeded because of the scarcity of suitable electrode materials with superior performance. Herein, we successfully prepared the two-dimensional (2D) titanium carbide (Ti3C2Tx) MXene/ reduced graphene oxide (rGO) superlattice heterostructure by a facile electrostatic self-assembly strategy and systematically investigated its performance as capacitive deionized electrode materials. The unique 2D/2D super lattice heterostructure not only effectively alleviates the self-stacking problem of Ti(3)C(2)T(x)MXene nanosheets, but also endows the heterostructure with superior conductivity and fast ion diffusion rate. As a result, the MXene/rGO superlattice heterostructure exhibits an outstanding salt (Na+) adsorption capacity (48 mg g-1) at 1.2 V significantly superior to pristine Ti3C2Tx MXene nanosheets, along with outstanding long-term cycling performance. Furthermore, the mechanism involved was elucidated through comprehensive characterizations. Therefore, this study offers a new pathway for designing high-performance electrode materials for capacitive deionization.(C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:233 / 241
页数:9
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