Hierarchical Co3O4/CNT decorated electrospun hollow nanofiber for efficient hybrid capacitive deionization

被引:37
|
作者
Guo, Lu [1 ]
Zhang, Jintao [1 ]
Ding, Meng [1 ]
Gu, Chengding [2 ]
Vafakhah, Sareh [1 ]
Zhang, Wang [1 ]
Li, Dong-sheng [3 ]
Alvarado, Pablo Valdivia Y. [1 ]
Yang, Hui Ying [1 ]
机构
[1] Singapore Univ Technol & Design, Pillar Engn Prod Dev, 8 Somapah Rd, Singapore 487372, Singapore
[2] Yunnan Univ, Sch Mat & Energy, Kunming 650091, Yunnan, Peoples R China
[3] China Three Gorges Univ, Coll Mat & Chem Engn, Key Lab Inorgan Nonmetall Crystalline & Energy Co, Yichang 443002, Peoples R China
关键词
Hybrid capacitive deionization; Co3O4@CNF@CNT; Electrospinning; Pseudocapacitance; Desalination; DESALINATION PERFORMANCE; ENERGY-CONSUMPTION; STORAGE ELECTRODE; GRAPHENE; WATER; COMPOSITE; NANOSHEETS; MEMBRANES; ENHANCE; TIO2;
D O I
10.1016/j.seppur.2021.118593
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Hybrid capacitive deionization (HCDI) is emerging as an energy-efficient alternative for brackish water desalination with low expenditure cost and favourable ion removal effectiveness by adopting battery-type electrodes in the traditional capacitive deionization (CDI) system. Herein, an unscalable electrospinning method is introduced to contrive cathode material for HCDI system. Co3O4 and nitrogen-doped carbon nanotube decoration are formed successfully and uniformly distributed with the hollow structure of free-standing carbon nanofibers (Co3O4@CNF@CNT). The conductive "bridges" provided by the CNF matrix significantly shorten the diffusion length of Na+ and promote the electrical conductivity of the Co3O4 nanoparticles. Moreover, benefiting from the incorporation of nitrogen-doped CNTs, the electrical conductivity is further enhanced. The as-prepared Co3O4@CNF@CNT cathode shows excellent pseudocapacitive performance of 395F g(-1) at a scan rate of 1 mV s(-1) and superior rate performance of 279F g(-1) at 100 mV s(-1). The HCDI system delivers an outstanding salt adsorption capacity (SAC) of 58.6 mg g(-1) and a highest salt adsorption rate (SAR) of 12.27 mg g(-1) min(-1) with a potential difference of 1.4 V, indicating the great potential of applying Co3O4@CNF@CNT in the practical HCDI system.
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页数:8
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