<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu B</submitter><funding>State Key Laboratory of New Ceramic and Fine Processing Tsinghua University</funding><funding>National Natural Science Foundation of China</funding><pagination>1625</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8911284</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(5)</volume><pubmed_abstract>Defect engineering is one of the effective ways to improve the electrochemical property of electrode materials for lithium-ion batteries (LIB). Herein, an organic functional molecule of p-phenylenediamine is embedded into two-dimensional (2D) layered TiO2 as the electrode for LIB. Then, the 2D carbon/TiO2 composites with the tuning defects are prepared by precise control of the polymerization and carbothermal atmospheres. Low valence titanium in metal oxide and nitrogen-doped carbon nanosheets can be obtained in the carbon/TiO2 composite under a carbonization treatment atmosphere of N2/H2 gas, which can not only increase the electronic conductivity of the material but also provide sufficient electrochemical active sites, thus producing an excellent rate capability and long-term cycle stability. The prepared composite can provide a high capacity of 396.0 mAh g-1 at a current density of 0.1 A g-1 with a high capacitive capacity ratio. Moreover, a high specific capacity of 80.0 mAh g-1 with retention rate of 85% remains after 10,000 cycles at 3.0 A g-1 as well as the Coulomb efficiency close to 100%. The good rate-capability and cycle-sustainability of the layered materials are ascribed to the increase of conductivity, the lithium-ion transport channel, and interfacial capacitance due to the multi-defect sites in the layered composite.</pubmed_abstract><journal>Materials (Basel, Switzerland)</journal><pubmed_title>Tuning the Defects of Two-Dimensional Layered Carbon/TiO2 Superlattice Composite for a Fast Lithium-Ion Storage.</pubmed_title><pmcid>PMC8911284</pmcid><funding_grant_id>21905282</funding_grant_id><funding_grant_id>KFZD202003</funding_grant_id><pubmed_authors>Gu B</pubmed_authors><pubmed_authors>Shen Z</pubmed_authors><pubmed_authors>Liu B</pubmed_authors><pubmed_authors>Li A</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Wang J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tuning the Defects of Two-Dimensional Layered Carbon/TiO2 Superlattice Composite for a Fast Lithium-Ion Storage.</name><description>Defect engineering is one of the effective ways to improve the electrochemical property of electrode materials for lithium-ion batteries (LIB). Herein, an organic functional molecule of p-phenylenediamine is embedded into two-dimensional (2D) layered TiO2 as the electrode for LIB. Then, the 2D carbon/TiO2 composites with the tuning defects are prepared by precise control of the polymerization and carbothermal atmospheres. Low valence titanium in metal oxide and nitrogen-doped carbon nanosheets can be obtained in the carbon/TiO2 composite under a carbonization treatment atmosphere of N2/H2 gas, which can not only increase the electronic conductivity of the material but also provide sufficient electrochemical active sites, thus producing an excellent rate capability and long-term cycle stability. The prepared composite can provide a high capacity of 396.0 mAh g-1 at a current density of 0.1 A g-1 with a high capacitive capacity ratio. Moreover, a high specific capacity of 80.0 mAh g-1 with retention rate of 85% remains after 10,000 cycles at 3.0 A g-1 as well as the Coulomb efficiency close to 100%. The good rate-capability and cycle-sustainability of the layered materials are ascribed to the increase of conductivity, the lithium-ion transport channel, and interfacial capacitance due to the multi-defect sites in the layered composite.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-26T10:13:43.697Z</modification><creation>2025-04-06T13:16:13.005Z</creation></dates><accession>S-EPMC8911284</accession><cross_references><pubmed>35268856</pubmed><doi>10.3390/ma15051625</doi></cross_references></HashMap>