Incorporation of amorphous TiO2 into one-dimensional SnO2 nanostructures as superior anodes for lithium-ion batteries

被引:39
作者
Cheong, Jun Young [1 ]
Kim, Chanhoon [1 ]
Jung, Ji-Won [1 ]
Yun, Tae-Gwang [1 ]
Youn, Doo Young [1 ]
Cho, Su-Ho [1 ]
Yoon, Ki Ro [1 ]
Jang, Hye-Yeon [1 ]
Song, Seok Won [1 ]
Kim, Il-Doo [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, 335 Sci Rd, Daejeon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
Tin (IV) oxide; Titanium (IV) oxide; Lithium; Nanotubes; Porous; Anode; ELECTROCHEMICAL PERFORMANCE; CARBON NANOSTRUCTURES; GRAPHENE OXIDE; STORAGE; CAPACITY; NANOPARTICLES; ELECTRODES; NANOTUBES; LAYER; NANOCRYSTALS;
D O I
10.1016/j.jpowsour.2018.08.060
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium-ion batteries (LIBs) with higher energy density are necessary to meet the increasing demands of energy storage system (ESS) in near future. Tin (IV) oxide, SnO2, is one of highly promising anode candidates due to its high theoretical capacity (782 mAh g(-1)), abundance, environmental friendliness, and safety with organic electrolytes. However, a rapid capacity fading and poor rate capabilities arising from the large volume expansion and subsequent agglomeration of Sn nanoparticles have been major issues of SnO2. Here, we have synthesized one-dimensional (1D) SnO2-amorphous titanium (IV) oxide NTs (SnO2-a-TiO2 NTs), which allow both facile ionic and electron transport as well as easy penetration of electrolytes. The resultant SnO2-a-TiO2 NTs not only alleviate volume expansion by maintaining their structural integrity but also possess minimal charge transfer resistance even after a number of cycles. SnO2-a-TiO2 NTs exhibit both excellent cycle retention characteristics (1050.2 mAh g(-1) after 250 cycles) and outstanding rate capability (522.3 mAh g(-1) at a current density of 5000 mA g(-1)), which is attributed to the introduction of amorphous TiO2 that not only acts as buffer agent for volume changes of SnO2 but also allows fast surface-controlled diffusion process due to its pseudocapacitive charge storage mechanisms.
引用
收藏
页码:485 / 492
页数:8
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