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Co-Modification of commercial TiO anode by combining a solid electrolyte with pitch-derived carbon to boost cyclability and rate capabilities
The bad electrochemical performance circumscribes the application of commercial TiO 2 (c-TiO 2 ) anodes in Li-ion batteries. Carbon coating could ameliorate the electronic conductivity of TiO 2 , but the ionic conductivity is still inferior. Herein, a co-modification method was proposed by combining...
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Published in: | Nanoscale advances 2020-06, Vol.2 (6), p.2531-2539 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | The bad electrochemical performance circumscribes the application of commercial TiO
2
(c-TiO
2
) anodes in Li-ion batteries. Carbon coating could ameliorate the electronic conductivity of TiO
2
, but the ionic conductivity is still inferior. Herein, a co-modification method was proposed by combining the solid electrolyte of lithium magnesium silicate (LMS) with pitch-derived carbon to concurrently meliorate the electronic and ionic conductivities of c-TiO
2
. The homogeneous mixtures were heated at 750 °C, and the co-modified product with suitable amounts of LMS and carbon demonstrates cycling capacities of 256.8, 220.4, 195.9, 176.4, and 152.0 mA h g
−1
with multiplying current density from 100 to 1600 mA g
−1
. Even after 1000 cycles at 500 mA g
−1
, the maintained reversible capacity was 244.8 mA h g
−1
. The superior rate performance and cyclability correlate closely with the uniform thin N-doped carbon layers on the surface of c-TiO
2
particles to favor the electrical conduction, and with the ion channels in LMS as well as the cation exchangeability of LMS to facilitate the Li
+
transfer between the electrolyte, carbon layers, and TiO
2
particles. The marginal amount of fluoride in LMS also contributes to the excellent cycling stability of the co-modified c-TiO
2
.
The bad electrochemical performance circumscribes the application of commercial TiO
2
(c-TiO
2
) anodes in Li-ion batteries. |
---|---|
ISSN: | 2516-0230 |
DOI: | 10.1039/d0na00192a |