Preferentially Oriented TiO2 Nanotubes as Anode Material for Li-Ion Batteries: Insight into Li-Ion Storage and Lithiation Kinetics
Source abstract
Abstract
Self-organized TiO 2 nanotubes (NTs) with a preferential orientation along the [001] direction are anodically grown by controlling the water content in the fluoride-containing electrolyte. The intrinsic kinetic and thermodynamic properties of the Li intercalation process in the preferentially oriented (PO) TiO 2 NTs and in a randomly oriented (RO) TiO 2 NT reference are determined by combining complementary electrochemical methods, including electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic cycling. PO TiO 2 NTs demonstrate an enhanced performance as anode material in Li-ion batteries due to faster interfacial Li insertion/extraction kinetics. It is shown that the thermodynamic properties, which describe the ability of the host material to intercalate Li ions, have a negligible influence on the superior performance of PO NTs. This work presents a straightforward approach for gaining important insight into the influence of the crystallographic orientation on lithiation/delithiation characteristics of nanostructured TiO 2 based anode materials for Li-ion batteries. The introduced methodology has high potential for the evaluation of battery materials in terms of their lithiation/delithiation thermodynamics and kinetics in general.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Extraction and Separation Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Physical Chemistry, Leopold-Franzens-University Innsbruck, Innrain 52c, Innsbruck 6020, Austria
Advanced Light Source (ALS) and Joint Center for Energy Storage Research (JCESR), Lawrence Berkeley National Laboratory, 1 Cyclotron Rd., Berkeley, California 94720, United States
Funding
Austrian Science Fund · Deutsche Forschungsgemeinschaft
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