Electrochemical reactivity and design of NiP2 negative electrodes for secondary Li-lon batteries

被引:223
作者
Gillot, F
Boyanov, S
Dupont, L
Doublet, ML
Morcrette, A
Monconduit, L [1 ]
Tarascon, JM
机构
[1] Univ Montpellier 2, LAMMI, UMR 5072, F-34095 Montpellier, France
[2] Univ Picardie, LRCS, UMR 6007, F-80039 Amiens, France
[3] Univ Montpellier 2, LSDSMS, UMR 5636, F-34095 Montpellier, France
关键词
D O I
10.1021/cm051574b
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
We report the electrochemical study of cubic and monoclinic NiP2 polymorphs toward Li, as a candidate for anodic applications for Li-ion batteries. We found that the monoclinic form is the most attractive one performance-wise. Monoclinic NiP2 can reversibly uptake 5 lithium per formula unit, leading to reversible capacities of 1000 mAh/g at an average potential of 0.9 V vs Li+/Li degrees. From complementary X-ray diffraction (XRD) and HRTEM (high-resolution transmission electron microscopy) measurements, it was shown that, during the first discharge, the cubic phase undergoes a pure conversion process (NiP2 + 6 Li+ + 6e(-) -> Ni degrees + 2Li(3)P) as opposed to a sequential insertion-conversion process for monoclinic NiP2. Such a different behavior rooted in subtle structural changes was explained through electronic structure calculations. Once the first discharged is achieved, both phases were shown to react with Li through a classical conversion process. More importantly, we report a novel way to design NiP2 electrodes with enhanced capacity retention and rate capabilities. It consists in growing the monoclinic NiP2 phase, through a vapor-phase transport process, on a commercial Ni-foam commonly used in Ni-based alkaline batteries. These new self-supported electrodes, based on chemically made interfaces, offer new opportunities to fully exploit the capacity gains provided by conversion reactions.
引用
收藏
页码:6327 / 6337
页数:11
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