材料科学
阳极
锐钛矿
电化学
锂(药物)
化学工程
纳米颗粒
二氧化钛
纳米技术
复合材料
电极
物理化学
催化作用
医学
工程类
内分泌学
化学
光催化
生物化学
作者
Chengwei Lu,Ruyi Fang,Yongping Gan,Xinping He,Zhen Xiao,Hui Huang,Jun Zhang,Xinhui Xia,Wenkui Zhang,Yang Xia
标识
DOI:10.1021/acsami.3c16525
摘要
Titanium dioxide (TiO2) has been widely used as an alternative anodic material for lithium-ion batteries (LIBs) due to its ultrahigh capacity retention and long cycle lifespan. However, the restriction of lithium insertion, intrinsically poor electronic conductivity, and sluggish lithium ionic kinetics of bulk TiO2 hinder their specific capacity and rate performance. Herein, LiTiO2 nanoparticles (NPs) are synthesized via a facile ball milling method by the reaction of anatase TiO2 with LiH. The as-prepared LiTiO2 NPs have strong structural stability and a "zero strain" effect during the repeated intercalation/deintercalation, even at low potential. As anodic materials for LIBs, LiTiO2 NPs exhibit a superior rate performance of ∼100 mA h g–1 at 10C (3350 mA g–1) with a capacity retention of 100% after 1000 cycles, which is 5 times higher than that of the original commercial anatase TiO2 powder. The higher specific capacity of LiTiO2 NPs is attributed to the increased conversion of Ti3+ to Ti2+ on the porous surface of LiTiO2 NPs, which provides a more capacitive contribution. This study not only provides a new fabrication approach toward Ti-based anodes for ultrafast LIBs but also underscores the potential importance of embedding lithium into transition metal oxides as a strategy for boosting their electrochemical performance.
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