Co3O4 hollow nanospheres doped with ZnCo2O4 via thermal vapor mechanism for fast lithium storage

被引:26
作者
Song, Weixin [1 ,4 ]
Ji, Kangyu [2 ]
Aguadero, Ainara [1 ,4 ]
Shearing, Paul R. [3 ]
Brett, Dan J. L. [3 ]
Xie, Fang [1 ,4 ]
Riley, D. Jason [1 ,4 ]
机构
[1] Imperial Coll London, Dept Mat, London SW7 2AZ, England
[2] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[3] UCL, Dept Chem Engn, Electrochem Innovat Lab, London WC1 E6BT, England
[4] Imperial Coll London, Ctr Nanotechnol, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
Binary metal oxide doping; metal organic frameworks; Thermal vapor transport mechanism; Lithium storage; HIGH-PERFORMANCE ANODE; ION BATTERIES; CARBON NANOFIBERS; FACILE SYNTHESIS; HIGH-CAPACITY; NANOPARTICLES; ZNO; MICROSPHERES; NANOSHEETS; GROWTH;
D O I
10.1016/j.ensm.2018.05.004
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
Binary metal oxides offer improved anode materials in lithium ion batteries owing to enhanced electrical conductivity but suffer from large volume expansion on lithiation. A novel route to hollow Co3O4 nanospheres doped with ZnCo2O4 is demonstrated that mitigates the expansion issue and shows excellent performance at high current densities. The synthetic route is based on the pyrolysis of binary metal-organic-frameworks (MOFs) with the controlled loss of zinc tuning the micro and nanostructure of the material through a thermal vapor mechanism. The optimal structures, that contain hollow Co3O4 spheres of ca. 50 nm diameter doped with ZnCo2O4, show a specific capacity of 890 mAh g(-1) at a current rate of 0.1 A g(-1) and show a similar specific capacity at 1 A g(-1) after 120 cycles at high current densities. The kinetics of lithiation/delithiation changes from diffusion-controlled to a surface-controlled process by the nanosizing of the particles. The resultant faster ion diffusion and capacitive storage for lithium ions are responsible for the extraordinary high-rate performance of the hollow structures.
引用
收藏
页码:324 / 334
页数:11
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