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Li Insertion into Li4Ti5 O 12 (Spinel) Charge Capability vs. Particle Size in Thin-Film Electrodes

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In this paper, the authors present a Web of Science Record created on 2006-02-21, modified on 2017-05-12, for the LPI-ARTICLE-2003-015.
Abstract
Reference LPI-ARTICLE-2003-015doi:10.1149/1.1581262View record in Web of Science Record created on 2006-02-21, modified on 2017-05-12

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Pseudocapacitive Contributions to Electrochemical Energy Storage in TiO2 (Anatase) Nanoparticles

TL;DR: In this paper, the capacitive effects of nanostructured materials for electrochemical energy storage have been investigated over a dimensional regime where both capacitive and lithium intercalation processes contribute to the total stored charge.
Journal ArticleDOI

Porous Li4Ti5O12 Coated with N‐Doped Carbon from Ionic Liquids for Li‐Ion Batteries

TL;DR: In this paper, a uniform nitrogen-doped carbon coating layer is formed on Li4Ti5O12 particles by mixing porous Li4T2O12 powder with an ionic liquid and then treating the mixture at moderate temperature.
Journal ArticleDOI

Large Impact of Particle Size on Insertion Reactions. A Case for Anatase LixTiO2

TL;DR: The particle size dependence of insertion reactions has been investigated for lithiated anatase TiO2, revealing progressively increasing Li capacity and Li-ion solubility for decreasing particle sizes, strongly deviating from the expected Li-rich andLi-poor phase separation as occurs in the bulk material.
Journal ArticleDOI

Sub-150 °C processed meso-superstructured perovskite solar cells with enhanced efficiency

TL;DR: In this article, a low temperature route for compact TiO2, tailored for perovskite MSSC operation, was realized, and the optimized formulation was shown to achieve full sun solar power conversion efficiencies of up to 15.9% in an all low temperature processed solar cell.
Journal ArticleDOI

Sustained Lithium-Storage Performance of Hierarchical, Nanoporous Anatase TiO2 at High Rates: Emphasis on Interfacial Storage Phenomena

TL;DR: In this paper, a hierarchical, nanoporous TiO2 structure is successfully prepared by a simple in situ hydrolysis method, and it achieves a sustained high lithium storage performance especially at high charge/discharge rates due to its substantially high surface area.
References
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Journal ArticleDOI

Conversion of light to electricity by cis-X2bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) charge-transfer sensitizers (X = Cl-, Br-, I-, CN-, and SCN-) on nanocrystalline titanium dioxide electrodes

TL;DR: Cis-X 2 Bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) complexes were prepared and characterized with respct to their absorption, luminescence, and redox behavior.
Journal ArticleDOI

Zero‐Strain Insertion Material of Li [ Li1 / 3Ti5 / 3 ] O 4 for Rechargeable Lithium Cells

TL;DR: In this paper, a defect spinel-framework structure was examined in nonaqueous lithium cells and it was shown that the lattice dimension did not change during the reaction since the reaction consists of lithium ion and electron insertion into/extraction from the solid matrix without a noticeable change in lattice dimensions.
Journal ArticleDOI

Electrochemical and photoelectrochemical investigation of single-crystal anatase

TL;DR: In this article, the electrochemical and photoelectrochemical behavior of a single crystal of anatase was scrutinized for the first time, and it was shown that anatase (101) and rutile (001) electrodes differ mainly in the position of the...
Journal ArticleDOI

An Asymmetric Hybrid Nonaqueous Energy Storage Cell

TL;DR: In this paper, a nonaqueous asymmetric electrochemical cell technology is presented where the positive electrode stores charge through a reversible nonfaradaic or pseudocapacitive reaction of anions on the surface of an activated carbon positive electrode.
Journal ArticleDOI

Structure and electrochemistry of the spinel oxides LiTi2O4 and Li43Ti53O4

TL;DR: In this paper, Li/LiTi2O4 and Li 4 3 Ti 5 3 O4 cells cycle reversibly with little capacity loss for over 100 cycles, but have subtle differences in their voltage profiles.
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