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Updated: Aug 28, 2025

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
Improved conductivity and ionic mobility in nanostructured thin films via aliovalent doping for ultra-high rate
Clayton T Kacica1, Pratim Biswas1
1Aerosol and Air Quality Research Laboratory, Center for Aerosol Science and Engineering, Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis 1 Brookings Drive St. Louis MO 63130 USA pbiswas@wustl.edu +1-314-935-5464 +1-314-935-5548.
Abstract:
A high-rate lithium ion battery electrode consisting of nanostructured copper-doped TiO2 films, synthesized using a single-step, template-free aerosol chemical vapor deposition technique, is reported herein. A narrowing of the band gap of the copper-doped films from 2.92 to 1.93 eV corresponds to a large increase in electronic conductivity, overcoming a major drawback of pristine TiO2 in electronic applications. Lithium-ion batteries using copper-doped films as the negative electrode exhibit improved charge retention at ultra-high charge rates, up to 50C. Additionally, over 2000 charge-discharge cycles at a rate of 10C, the copper-doped TiO2 electrodes display higher stable cycling capacities. Cyclic voltammetry (CV) and a galvanostatic intermittent titration technique (GITT) provide insight into the chemical diffusion of Li+ in the TiO2 matrix, with copper-doped TiO2 electrodes exhibiting an order of magnitude higher value in CV measurements over pristine TiO2. GITT provided the state-of-charge (SoC) resolved chemical diffusion coefficient of Li+ and suggests that a minimum value occurs at a moderate SoC of 60%, with values near the extremes being over two orders of magnitude higher. Both techniques indicate increased Li+ mobility due to copper-doping, supporting improved electrochemical performance in ultra-high rate battery testing.

