假电容
材料科学
相(物质)
离子
动力学
储能
纳米技术
基质(化学分析)
化学工程
电极
化学
电化学
复合材料
超级电容器
功率(物理)
物理
有机化学
物理化学
量子力学
工程类
作者
Shen Liu,K. Niu,Shuailin Chen,Xin Sun,Lehao Liu,Bing Jiang,Lihua Chu,Xiaojun Lv,Meicheng Li
出处
期刊:Carbon energy
[Wiley]
日期:2022-02-27
卷期号:4 (4): 645-653
被引量:19
摘要
Abstract Bronze phase TiO 2 [TiO 2 (B)] has great research potential for sodium storage since it has a higher theoretical capacity and ion mobility compared with other phases of TiO 2 . In this case, preparing porous TiO 2 (B) nanosheets, which can provide abundant sodium insertion channels, is the most effective way to improve transport kinetics. Here, we use the strong one‐dimensional TiO 2 nanowires as the matrix for stringing these nanosheets together through a simple solvothermal method to build a bunchy hierarchical structure [TiO 2 (B)‐BH], which has fast pseudocapacitance behavior, high structural stability, and effective ion/electron transport. With the superiorities of this structure design, TiO 2 (B)‐BH has a higher capacity (131 vs. 70 mAh g −1 [TiO 2 ‐NWs] at 0.5 C). And it is worth mentioning that the reversible capacity of up to 500 cycles can still be maintained at 85 mAh g −1 at a high rate of 10 C. Meanwhile, we also further analyzed the sodium storage mechanism through the ex‐situ X‐ray powder diffraction test, which proved the high structural stability of TiO 2 (B)‐BH in the process of sodiumization/de‐sodiumization. This strategy of uniformly integrating nanosheets into a matrix can also be extended to preparing electrode material structures of other energy devices.
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