Cyclability of binder-free β-Ni(OH)2 anodes shaped by EPD for Li-ion batteries

被引:16
|
作者
Cabanas-Polo, S. [1 ,2 ]
Gonzalez, Z. [2 ]
Sanchez-Herencia, A. J. [2 ]
Ferrari, B. [2 ]
Caballero, A. [3 ]
Hernan, L. [3 ]
Morales, J. [3 ]
机构
[1] Univ Erlangen Nurnberg, Inst Biomat, Dept Mat Sci & Engn, Erlangen, Germany
[2] CSIC, Inst Ceram & Glass, Madrid, Spain
[3] Univ Cordoba, Univ Res Inst Fine Chem & Nanochem, Cordoba, Spain
关键词
NEGATIVE-ELECTRODE MATERIALS; ELECTROPHORETIC DEPOSITION; NICKEL-HYDROXIDE; ELECTROCHEMICAL PERFORMANCE; CATHODE MATERIALS; LITHIUM; FABRICATION; NI(OH)(2); ALUMINA; FILM;
D O I
10.1016/j.jeurceramsoc.2014.08.014
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The electrochemical behaviour of beta-Ni(OH)(2) based anodes in Li-ion batteries (LIB) was analyzed. beta-Ni(OH)(2) nanoplatelests evidence an additional capacity ascribed to secondary reactions, while the high reversibility is related to the catalytic activity of the Ni nanoparticles within the nanostructure. In this manuscript we discuss the influence of the micro-architecture of the films shaped by electrophoretic deposition (EPD) in the electrochemical behaviour of the Li cell, when beta-Ni(OH)(2) has been considered as the active material. By EPD, the beta-Ni(OH)(2) nanoplatelets packed preferentially aligned parallel to their basal planes leading to a well-ordered and dense microstructure. Apart from the mesoporosity of the beta-Ni(OH)(2) nanoplatelets and its particular crystallography, the increase of packing density and connectivity are the key points affecting the electrochemical response of the anodes. A highly ordered and interconnected microstructure promotes the electrode stability during cycling and, although the additional capacity delivered due to the side reactions decreases, the electrolyte and the connectivity degradation are prevented. Microstructures of the densest structures maintain the delivered capacity of the anode at 600 mA h/g, close to the theoretical value, for more than 30 cycles. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:573 / 584
页数:12
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