Li+ Ion Insertion in TiO2 (Anatase). 2. Voltammetry on Nanoporous Films

• Published in: The journal of physical chemistry. B Vol. 101; no. 39; pp. 7717 - 7722
• Main Authors: Lindström, Henrik, Södergren, Sven, Solbrand, Anita, Rensmo, Håkan, Hjelm, Johan, Hagfeldt, Anders, Lindquist, Sten-Eric
• Format: Journal Article
• Language: English
• Published: American Chemical Society 25-09-1997
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/jp970490q

Electrochemical properties of Li+ ion insertion in nanoporous TiO2 (anatase) electrodes were studied by voltammetry. Linear and cyclic potential scans were recorded as a function of electrolyte concentration, film thickness, and temperature. The currents were directly proportional to the inner electrode area of the electrodes. The reduction of Ti4+ and oxidation of Ti3+ are sluggish and follows irreversible kinetics. The standard rate constant was (3.5 ± 0.5) × 10-10 cm/s. The transfer coefficient was close to 0.5, indicating that the potential drop appears mainly across the Helmholtz layer. The capacitive currents govern largely the shape of the i − v curves, except within a region near the peak potential where diffusion-limited insertion and extraction of Li+ ions in the anatase lattice are dominating. The diffusion coefficient at 25 °C in the nanoporous structure was approximately 2 × 10-17 cm2/s for insertion and 4 × 10-17 cm2/s for extraction. The activation energy was 0.4 eV for insertion and 0.5 eV for extraction. The maximum obtained mole fraction of Li+ in Li x TiO2 was x = 0.47.