材料科学
阳极
阴极
石墨烯
密度泛函理论
锂(药物)
离子
离子键合
化学工程
范德瓦尔斯力
氧化物
面(心理学)
纳米技术
分子
计算化学
物理化学
化学
电极
医学
有机化学
内分泌学
冶金
心理学
社会心理学
人格
工程类
五大性格特征
作者
Yihui Zou,Guojing Chang,Shuai Chen,Tongchao Liu,Yanzhi Xia,Cheng‐Meng Chen,Dongjiang Yang
标识
DOI:10.1016/j.cej.2018.06.104
摘要
Abstract Li4Ti5O12/LiFePO4 (LTO/LFP) is a promising lithium ion batteries (LIBs) configuration due to its high safety and circularity. However, three factors result in the low capacity at high current density and low energy density in LTO/LFP: (i) low intrinsic electronic and ionic conductivities; (ii) long one-dimensional (1D) pathway along the [0 1 0] channel; (iii) Fe-Li antisite defect in LFP. It is still a great challenge to address the three problems simultaneously in LTO/LFP cell. Herein, we synthesized LFP ultrathin nanosheets (∼5–10 nm) with oriented (0 1 0) facet and ultralow Fe-Li antisite defects with the assistance of alginate and 2D reduced graphene oxide (LFP NS/r-GO). The novel “egg-box” structure in alginate is the key to restrain the Fe-Li antisites. The sandwich structure, which is formed by long range Van der Waals forces and hydrogen bond between the Li-Fe-P-alginate molecules and 2D r-GO nanosheets, results in the formation of ultrathin LFP NSs with oriented (0 1 0) facet. The density functional theory (DFT) calculations reveal that the tacking of LFP ultrathin NS with oriented (0 1 0) facet on the r-GO has a strong ability of Li+ ion deintercalation. When evaluating LFP NS/r-GO as cathode materials for LIBs, the sample displays outstanding rate capacity of 98.6 mA h g−1 at 100 C and its full cell with LTO anode achieves remarkable specific energy (265 W h kg−1) and power density (6.81 kW kg−1).
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