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Constructing Three-Dimensional Macroporous TiO 2 Microspheres with Enhanced Pseudocapacitive Lithium Storage under Deep Discharging/Charging Conditions

TiO has been intensively investigated as an anode material for lithium-ion batteries (LIBs) in 1.0-3.0 V ( Li /Li). However, it is a challenge to realize its theoretical capacity (336 mAh g ) in this limited potential range. Extending the potential range below 1.0 V would increase its capacity but u...

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Published in:ACS applied materials & interfaces 2021-04, Vol.13 (14), p.16528-16535
Main Authors: He, Ruhan, Liu, Zhenhui, He, Pan, Luo, Wen, Yu, Ruohan, Hong, Xufeng, Pan, Xuelei, Zhou, Qingqu, Mai, Liqiang, Zhou, Liang
Format: Article
Language:English
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Summary:TiO has been intensively investigated as an anode material for lithium-ion batteries (LIBs) in 1.0-3.0 V ( Li /Li). However, it is a challenge to realize its theoretical capacity (336 mAh g ) in this limited potential range. Extending the potential range below 1.0 V would increase its capacity but usually at the expense of its cyclic stability owing to the sluggish ionic diffusion and unsatisfactory structural stability. Here, three-dimensional (3D) macroporous TiO microspheres with interconnected pores and nanocrystalline thin walls have been constructed through a scalable template-assisted spray drying method to overcome these obstacles. When applied to LIBs, high and stable discharge capacity (300 mAh g at 0.1 A g ) as well as superior cyclic stability (242 mAh g after 1000 cycles at 1.0 A g ) can be achieved under deep discharging/charging conditions (0.01-3.0 V Li /Li). Furthermore, the 3D macroporous structure is well preserved under deep discharging/charging and the X-ray diffraction (XRD) patterns and Raman spectra reveal the dominant pseudocapacitive contribution at low potentials (0.01-1.0 V). This work not only develops a facile method to synthesize macroporous metal oxides but also provides insight into the lithium storage mechanism of TiO under deep discharging/charging conditions.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c02411