阳极
石墨烯
材料科学
电化学
化学工程
扩散
氧化物
离子
锂(药物)
异质结
纳米技术
储能
插层(化学)
电极
无机化学
化学
光电子学
物理化学
冶金
内分泌学
工程类
物理
功率(物理)
热力学
有机化学
量子力学
医学
作者
Dingrong Deng,Xueyang Cui,Qi‐Hui Wu,Mingsen Zheng,Quanfeng Dong
标识
DOI:10.1016/j.jallcom.2020.155413
摘要
Sodium ion (Na+) storage has attracted wide attention as an advanced large-scale energy storage system for our modern society. Due to the larger radius of Na+ than lithium ion, finding a suitable anode material for sodium ion batteries (SIBs) is a big challenge especially at low temperature. Here, an in-situ method which simultaneous reduction of graphene and oxidation of Ti3+ was used to synthesize a 3 dimensional (3D) TiO2@ reduced graphene oxide (TiO2@rGO) structure. The special 3D structure built with the basic structure units of TiO2@rGO heterojunctions could offer fast ion insertion/deinsertion, short diffusion distance, and lower diffusion energy barrier as well, thus enhance the Na+ intercalation pseudocapacitive process. The enhanced pseudocapacitive process could increase the kinetic reaction of the cell especially at the high current densities. The synthesized TiO2@rGO sample exhibits an outstanding electrochemistry performance as an anode material for SIBs with superior cycling and rate performance. At a current density of 7 A g−1, it showed a high capacity retention of above 90% and with a capacity decay of 0.0003% per cycle. Most importantly, owning to the fast electron exchange rate in the system, the cell shows an outstanding electrochemical performance at an ultra-low temperature of −40 °C.
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