Issue 6, 2020

Co-Modification of commercial TiO2 anode by combining a solid electrolyte with pitch-derived carbon to boost cyclability and rate capabilities

Abstract

The bad electrochemical performance circumscribes the application of commercial TiO2 (c-TiO2) anodes in Li-ion batteries. Carbon coating could ameliorate the electronic conductivity of TiO2, 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-TiO2. 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-TiO2 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 TiO2 particles. The marginal amount of fluoride in LMS also contributes to the excellent cycling stability of the co-modified c-TiO2.

Graphical abstract: Co-Modification of commercial TiO2 anode by combining a solid electrolyte with pitch-derived carbon to boost cyclability and rate capabilities

Supplementary files

Article information

Article type
Paper
Submitted
07 Mar 2020
Accepted
15 Apr 2020
First published
15 Apr 2020
This article is Open Access
Creative Commons BY-NC license

Nanoscale Adv., 2020,2, 2531-2539

Co-Modification of commercial TiO2 anode by combining a solid electrolyte with pitch-derived carbon to boost cyclability and rate capabilities

L. Kong, J. An, S. Kang, M. Huang, H. Yang, H. Zhu, Y. Qi, X. Bai, N. Lun and Y. Bai, Nanoscale Adv., 2020, 2, 2531 DOI: 10.1039/D0NA00192A

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