Issue 27, 2014

High lithium electroactivity of boron-doped hierarchical rutile submicrosphere TiO2

Abstract

We have reported a facile method to fabricate hierarchical boron-doped rutile submicrosphere TiO2 (SMT), whose primary particles are ∼20 nm in diameter. The as-synthesized boron-doped SMT shows excellent cycling performance and rate capability in comparison with undoped TiO2 as an anode material in Lithium-Ion Batteries (LIBs). It has a very stable capacity of ∼190 mA h g−1 for 500 cycles at 1C. In addition, the density functional theory (DFT) calculations are carried out to indicate that a low concentration (<1.0 at%) of boron doping could enhance the carrier mobility μ and electrical conductivity σ, and thus reveal the relationship between the electronic structure of boron-doped SMT and the performances of the boron-doped SMT anode in LIBs. Our results also clearly demonstrate the importance and advantage of the hierarchical submicrometer-sized spherical morphology of the TiO2 anode in LIBs.

Graphical abstract: High lithium electroactivity of boron-doped hierarchical rutile submicrosphere TiO2

Supplementary files

Article information

Article type
Paper
Submitted
26 Mar 2014
Accepted
01 May 2014
First published
01 May 2014

J. Mater. Chem. A, 2014,2, 10599-10606

Author version available

High lithium electroactivity of boron-doped hierarchical rutile submicrosphere TiO2

H. Tian, F. Xin, X. Tan and W. Han, J. Mater. Chem. A, 2014, 2, 10599 DOI: 10.1039/C4TA01438C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements