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

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 elect...

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Published in:The journal of physical chemistry. B 1997-09, Vol.101 (39), p.7717-7722
Main Authors: Lindström, Henrik, Södergren, Sven, Solbrand, Anita, Rensmo, Håkan, Hjelm, Johan, Hagfeldt, Anders, Lindquist, Sten-Eric
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container_end_page 7722
container_issue 39
container_start_page 7717
container_title The journal of physical chemistry. B
container_volume 101
creator Lindström, Henrik
Södergren, Sven
Solbrand, Anita
Rensmo, Håkan
Hjelm, Johan
Hagfeldt, Anders
Lindquist, Sten-Eric
description 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.
doi_str_mv 10.1021/jp970490q
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title Li+ Ion Insertion in TiO2 (Anatase). 2. Voltammetry on Nanoporous Films
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