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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 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.1c02411 |