材料科学
阳极
硫黄
石墨烯
兴奋剂
电化学
阴极
锂(药物)
煅烧
扩散
纳米技术
化学工程
电极
光电子学
催化作用
物理化学
有机化学
化学
冶金
医学
热力学
物理
内分泌学
工程类
作者
Dongdong Wang,Hongxia Liu,Zhongqiang Shan,Dawei Xia,Ren Na,Haodong Liu,Baohe Wang,Jianhua Tian
标识
DOI:10.1016/j.ensm.2020.02.019
摘要
Abstract Enhancing the electron/ion transfer ability of Li4Ti5O12 materials is very important to achieve advanced high-rate and long-life anode in lithium ion batteries (LIBs). Here, for the first time, we report Li4Ti5O12/nitrogen, sulfur co-doped porous graphene composites (LTO/N, S-PG) via one-step facile calcination and activation process by using LiOH as Li source and activating agent. Mechanisms underlying the beneficial effects of N, S co-doped graphene for LTO anode were substantiated by the Density Functional Theory (DFT) calculations, revealing that co-doped N and S atoms not only significantly facilitate Li+ adsorption, but also ameliorate Li+ diffusion in graphene. Furthermore, the synergistic effects of nanosized LTO and porous graphene endow the composites with efficient Li+ diffusion channels and electron-conductive networks. Therefore, the LTO/N, S-PG can deliver extraordinarily high rate capability (e.g. 130 mA h g−1 at 80 C and 123 mA h g−1 at 100 C), and excellent cycling stability (83.1% capacity retention after 4000 cycles at 20 C). In addition, their superior electrochemical performance was also demonstrated in the full cells with LiNi0.5Mn1.5O4 cathode, which displayed 89.5% capacity retention after 500 cycles at 5 C. These results suggest the great promise of using the LTO/N, S-PG as a novel anode material for high-rate and long-life LIBs.
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