Conditions Extrêmes et Matériaux : Haute Température et Irradiation
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2018

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F.Lu, Q.Chen, S.Gen, M.Allix, H.Wu, Q.Huang, X.Kuang, *, 'Innovative lithium storage enhancement in cation- de fi cient anatase via layered oxide hydrothermal transformation', J. Mater. Chem. A 6 24232 (2018) doi:10.1039/c8ta07605g

The soft-chemistry synthetic routes of anatase phases for energy conversion and storage usually employ expensive and air-sensitive amorphous alkoxides, which hardly access the electrochemically active cationic vacancy defects in the cationic donor-substituted anatase compositions. Here we demonstrate an innovative way of using layered K 3 Ti 5 NbO 14 as a cost-e ff ectively crystalline precursor to synthesize cation-de fi cient Nb-doped TiO 2 (NTO, formulated as Ti 0.8 Nb 0.16 , 0.04 O 2 ) anatase by a one-pot hydrothermal route. When used as an anode in lithium ion batteries, the NTO electrode displayed initial discharge and charge capacities of 618 and 384.6 mA h g  1 at a current density of 0.2C respectively, with a remarkable discharge capacity of  246.8 mA h g  1 retained after 100 cycles, representing the highest value among those reported for Nb-doped TiO 2 anatases at low current density. A discharge capacity of 137.1 mA h g  1 was obtained even at a high current density of 2C. A full cell, fabricated using the NTO electrode as the anode and a commercial LiCoO 2 cathode, is shown to deliver a discharge capacity of 220.2 mA h g  1 after 57 cycles, which exceeds those of most previously reported full cells based on the TiO 2 anode and makes this NTO material a promising anode candidate for LIBs. These results present a practical synthetic strategy for tuning cationic vacancies through aliovalent cationic substitution to improve the electrochemical performance of actual LIBs and possibly to develop further relevant devices.