锐钛矿
材料科学
阳极
电化学
扩散
纳米结构
化学工程
插层(化学)
氧气
析氧
钠
密度泛函理论
纳米技术
电极
无机化学
催化作用
光催化
物理化学
化学
热力学
有机化学
物理
工程类
冶金
计算化学
作者
Jun Chen,Zhiying Ding,Chao Wang,Hongshuai Hou,Yan Zhang,Chi-Wei Wang,Guoqiang Zou,Xiaobo Ji
标识
DOI:10.1021/acsami.6b01183
摘要
Nanostructured black anatase titania with oxygen vacancies (OVs) is efficiently obtained and employed as an anode in sodium-ion batteries (SIBs) for the first time. The incorporation of OVs into TiO2 is demonstrated to render considerably enhanced-rate performances, higher initial capacities, and an accelerated electrochemical activation process during cycling, derived from the boosted intrinsic electric conductivity and improved kinetics of Na uptake. Bestowed with the integrated merits of OVs and shortened Na ion diffusion length in the nanostructure, black titania delivers a reversible specific capacity of 207.6 mAh g–1 at 0.2 C, retains 99.1% over 500 cycles at 1 C stably, and still maintains 91.2 mAh g–1 even at the high rate of 20 C. Density functional theory (DFT) calculations suggest that the lower sodiation energy barrier of anatase with OVs enables a more favorable Na intercalation into black anatase. Thus, it is of great significance to introduce OVs into TiO2 to stimulate ultrafast and durable sodium-storage properties, which also offers a potential strategy to project more superior electrodes, utilizing internal defects.
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