New design on Li-ion battery anode of ternary complex metal/metal oxide@CNT: A case study of hierarchical NiCo-NiCo2O4@CNTs

被引:46
作者
Ding, Chunyan [1 ,2 ]
Wang, Lijuan [1 ]
Zhou, Weiwei [1 ]
Wang, Dong [1 ,2 ]
Du, Yu [1 ]
Wen, Guangwu [1 ,2 ,3 ,4 ]
机构
[1] Harbin Inst Technol Weihai, Sch Mat Sci & Engn, Weihai 264209, Peoples R China
[2] Harbin Inst Technol, Sch Mat Sci & Engn, Harbin 150001, Heilongjiang, Peoples R China
[3] Shandong Univ Technol, Sch Mat Sci & Engn, Zibo 255000, Peoples R China
[4] Shandong Ind Ceram Res & Design Inst Co Ltd, Zibo 255000, Peoples R China
基金
中国国家自然科学基金;
关键词
Reversible SEI films; NiCo2O4; CNTs; Chemical vapor deposition; Pseudocapacitive electrode; Lithium-ion battery; LITHIUM-ION; HIGH-PERFORMANCE; HOLLOW MICROSPHERES; CARBON NANOTUBES; FACILE SYNTHESIS; STORAGE; NANOPARTICLES; COMPOSITES; ELECTRODE; CAPACITY;
D O I
10.1016/j.cej.2018.07.125
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Urgent and heavy demand of high energy/power density lithium-ion batteries (LIBs) challenges the ultimate limit of commercial anodes. Herein, enlightened by the extra capacity on transition metal oxides (TMO) anodes derived from the transition metal (TM) catalytic effect on reversible solid-electrolyte interface (SEI) films, a ternary composite consisting of TM, TMO, and carbon matrix, namely TM/TMO/carbon, is proposed as a novel and high-efficiency anode prototype. In this electrode design, TMO not only serve as active material but also pulverizes the TM nanoparticles via the conversion reaction during cycling. Pulverized TM nanoparticles can activate and/or promote the reversible transformation of SEI films more efficiently. And carbon matrix ensures the electronic conductivity and integrity of the overall electrode during multiple electrochemical reactions. As a proof-of-concept demonstration, NiCo-NiCo2O4@ carbon nanotubes (NC-NCO@CNTs) is synthesized by a bottom-up strategy via in-situ growth on a simplified chemical vapor deposition (CVD) process. As designed, the NC-NCO@CNTs keeps gaining extra capacity upon cycling, delivering an unceasingly increased capacity up to 1324 mAh g(-1) (500 mA g(-1)), splendid rate performance (945 mAh g(-1) at 1000 mA g(-1), 696 mAh g(-1) at 2000 mA g-1), and ultralong lifespan (2200 cycles). Detailed electrochemical investigation reveals a transformation of lithium storage mechanism from battery-type conversion reaction to pseudocapacitive electrochemical interfacial reaction arising from SEI films. It is believed that our work offers a novel and effective prototype for designing high energy/power density anodes for LIBs.
引用
收藏
页码:340 / 349
页数:10
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