Oxygen vacancy-modulated zeolitic Li4Ti5O12 microsphere anode for superior lithium-ion battery

被引:14
作者
Yeo, Seohyeon [1 ]
Raj, Michael Ruby [1 ]
Lee, Gibaek [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Adv Energy Mat Design Lab, Gyongsan 38541, South Korea
基金
新加坡国家研究基金会;
关键词
Lithium titanate oxide; Microspheres; Oxygen vacancies; Lithium storage mechanism; Lithium-ion batteries; SELF-DOPED LI4TI5O12; HIGH-PERFORMANCE ANODE; MOLTEN-SALT; THIN-FILMS; NANOSHEETS; NANOPARTICLES;
D O I
10.1016/j.electacta.2022.141809
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Spinel Li4Ti5O12 (LTO) is a promising anode material for state-of-the-art high-power lithium-ion batteries (LIBs) owing to its "zero strain" characteristics during fast charging/discharging, long cycle life, and high rate capability. However, the poor ionic/electronic conductivity and sluggish ionic diffusion coefficient of LTO restrict its practical utility. Porous zeolitic LTO (Z-LTO) microspheres were synthesized herein as anode materials for LIBs using TiO2 and LiOH center dot H2O via a hydrothermal method combined with Ar/H-2 thermal treatment. The increased concentration of Ti3+ self-doping-derived oxygen vacancies in as-synthesized Z-LTO and porous microspherical Z-LTO aggregates greatly improved the electronic conductivity and structural stability. These features contributed to achieving much higher discharge capacities of similar to 210 and similar to 180 mAh g(-1) at 0.5 C and 1 C rates, respectively, as well as excellent ultra-high rate capability of 45 mAh g(-1) at 50 C rate, while still maintaining the outstanding long-life cyclic stability (similar to 181 mAh g 1 at 5 C rate after 2000 cycles), with 90% capacity retention, compared to commercial LTO (C-LTO). Charge contribution kinetics analysis indicated that the lithium storage mechanisms in Z-LTO, particularly at a high rate, were dominantly diffusion-controlled due to the larger ion-diffusion ability (D-Li approximate to 4.18 x 10(-8) cm(2) s(-1)). This finding confirms that the generation of surface defects by creating Ti3+/Ti4+ pairs and oxygen vacancy engineering in LTO is an effective approach for enhancing the ion/electron mobility, which can be extended to boost the battery performance of other materials with low ionic conductivities for advanced energy storage systems.
引用
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页数:10
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