<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kacica CT</submitter><funding>Division of Earth Sciences</funding><funding>Division of Materials Research</funding><pagination>2160-2169</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9419002</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2(5)</volume><pubmed_abstract>A high-rate lithium ion battery electrode consisting of nanostructured copper-doped TiO&lt;sub>2&lt;/sub> 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 TiO&lt;sub>2&lt;/sub> 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 TiO&lt;sub>2&lt;/sub> electrodes display higher stable cycling capacities. Cyclic voltammetry (CV) and a galvanostatic intermittent titration technique (GITT) provide insight into the chemical diffusion of Li&lt;sup>+&lt;/sup> in the TiO&lt;sub>2&lt;/sub> matrix, with copper-doped TiO&lt;sub>2&lt;/sub> electrodes exhibiting an order of magnitude higher value in CV measurements over pristine TiO&lt;sub>2&lt;/sub>. GITT provided the state-of-charge (SoC) resolved chemical diffusion coefficient of Li&lt;sup>+&lt;/sup> 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&lt;sup>+&lt;/sup> mobility due to copper-doping, supporting improved electrochemical performance in ultra-high rate battery testing.</pubmed_abstract><journal>Nanoscale advances</journal><pubmed_title>Improved conductivity and ionic mobility in nanostructured thin films &lt;i>via&lt;/i> aliovalent doping for ultra-high rate energy storage.</pubmed_title><pmcid>PMC9419002</pmcid><funding_grant_id>1161543</funding_grant_id><funding_grant_id>1806147</funding_grant_id><pubmed_authors>Kacica CT</pubmed_authors><pubmed_authors>Biswas P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Improved conductivity and ionic mobility in nanostructured thin films &lt;i>via&lt;/i> aliovalent doping for ultra-high rate energy storage.</name><description>A high-rate lithium ion battery electrode consisting of nanostructured copper-doped TiO&lt;sub>2&lt;/sub> 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 TiO&lt;sub>2&lt;/sub> 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 TiO&lt;sub>2&lt;/sub> electrodes display higher stable cycling capacities. Cyclic voltammetry (CV) and a galvanostatic intermittent titration technique (GITT) provide insight into the chemical diffusion of Li&lt;sup>+&lt;/sup> in the TiO&lt;sub>2&lt;/sub> matrix, with copper-doped TiO&lt;sub>2&lt;/sub> electrodes exhibiting an order of magnitude higher value in CV measurements over pristine TiO&lt;sub>2&lt;/sub>. GITT provided the state-of-charge (SoC) resolved chemical diffusion coefficient of Li&lt;sup>+&lt;/sup> 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&lt;sup>+&lt;/sup> mobility due to copper-doping, supporting improved electrochemical performance in ultra-high rate battery testing.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2026-03-31T11:21:06.865Z</modification><creation>2025-02-19T01:37:11.634Z</creation></dates><accession>S-EPMC9419002</accession><cross_references><pubmed>36132522</pubmed><doi>10.1039/d0na00160k</doi></cross_references></HashMap>