Aqueous Synthesized Nanostructured Li4Ti5O12 for High-Performance Lithium Ion Battery Anodes

被引:21
作者
Chiu, Hsien-chieh [1 ]
Brodusch, Nicolas [1 ]
Gauvin, Raynald [1 ]
Guerfi, Abdelbast [2 ]
Zaghib, Karim [2 ]
Demopoulos, George P. [1 ]
机构
[1] McGill Univ, Dept Mat Engn, Montreal, PQ H3A 0C5, Canada
[2] Inst Rech Hydro Quebec IREQ, Varennes, PQ J3X 1S1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
SOL-GEL METHOD; SPINEL LI4TI5O12; ELECTROCHEMICAL PROPERTIES; HYDROTHERMAL SYNTHESIS; INSERTION; SURFACE; STORAGE; CHALLENGES; STABILITY; ELECTRODE;
D O I
10.1149/2.008305jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Nanostructured Li4Ti5O12 (LTO) was prepared via a novel process comprising low-temperature (<100 degrees C) aqueous synthesis and annealing of the hydrous intermediate phase Li1.81H0.19Ti2O5 center dot 2H(2)O (LTH) using only LiOH and TiCl4 as precursors. Nanosheet-structured LTH converted to either LTO nanosheets (102 m(2) . g(-1)) or LTO nanoparticles (28 m(2) . g(-1)) upon annealing at 400 and 600 degrees C respectively, each exhibiting unique electrochemical performance properties. The nanosheet-structured LTO exhibited higher initial charge capacity (228.3 vs. 187.3 mAh g(-1) at 1.0 V cutoff and C/24 rate) than the nanoparticle-structured LTO. Furthermore, the LTO nanosheets taking advantage of their short diffusion path exhibited better rate capability than the LTO nanoparticles; for example their discharge capacity at 15 C was 115 mAh . g(-1) vs. 68.4 mAh . g(-1) at 1.2 V cutoff for the LTO nanoparticles. Meanwhile, the LTO nanoparticles exhibited better cyclability than the LTO nanosheets because of their higher crystallinity. Thus after 130 1 C cycles with cut off at 1.2 V (vs. Li/Li+), the discharge capacity of the nanosheets was 132.9 mAh . g(-1) while that of nanoparticles was 150.7 mAh . g(-1), corresponding to 85 and 97% discharge capacity retention respectively. The newly synthesized nanostructured LTO material can offer a low cost scalable solution for high-performance LIB anodes. (C) 2013 The Electrochemical Society.
引用
收藏
页码:A3041 / A3047
页数:7
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