阳极
化学
锐钛矿
电解质
扩散
化学工程
相(物质)
纳米颗粒
钠离子电池
插层(化学)
钠
电池(电)
电化学
电极
热液循环
纳米技术
无机化学
法拉第效率
催化作用
材料科学
光催化
生物化学
物理
功率(物理)
有机化学
物理化学
量子力学
工程类
热力学
作者
Jintao Lv,Peidian Chong,Shiqi Huang,Yafeng Li,Mingdeng Wei
标识
DOI:10.1016/j.jelechem.2021.115687
摘要
TiO2 is considered as a potential anode with the advantages of stable structure and high safety. However, the large-scale application of TiO2 is restricted due to its low electronic conductivity and sluggish Na+ diffusion. In the present work, anatase and TiO2-B dual-phase TiO2 hollow microspheres (TiO2-MS) were designed through a universal hydrothermal reaction. These microspheres were composed of nanosheets, and the nanosheets were consisted of small nanoparticles. Benefitting from the synergistic effect of dual-phase TiO2 nanoparticles and hierarchical structure, the TiO2-MS can not only buffer the volume changes during Na+ intercalation/deintercalation process, but also provide the contact space for electrolyte − electrode. As a result, the TiO2-MS anode delivered a distinguished sodium storage performance, maintained 240 mA h g−1 at 2C (1C = 168 mA g−1) after 150 cycles. Even the current density was increased to 20C, a capacity of 159.7 mA h g−1can still be maintained after 5000 cycles.
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