<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jin Z</submitter><funding>National Science Foundation</funding><pagination>3533-3538</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8943886</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(12)</volume><pubmed_abstract>Redox-active two-dimensional polymers (RA-2DPs) are promising lithium battery organic cathode materials due to their regular porosities and high chemical stabilities. However, weak electrical conductivities inherent to the non-conjugated molecular motifs used thus far limit device performance and the practical relevance of these materials. We herein address this problem by developing a modular approach to construct π-conjugated RA-2DPs with a new polycyclic aromatic redox-active building block PDI-DA. Efficient imine-condensation between PDI-DA and two polyfunctional amine nodes followed by quantitative alkyl chain removal produced RA-2DPs TAPPy-PDI and TAPB-PDI as conjugated, porous, polycrystalline networks. In-plane conjugation and permanent porosity endow these materials with high electrical conductivity and high ion diffusion rates. As such, both RA-2DPs function as organic cathode materials with good rate performance and excellent cycling stability. Importantly, the improved design enables higher areal mass-loadings than were previously available, which drives a practical demonstration of TAPPy-PDI as the power source for a series of LED lights. Collectively, this investigation discloses viable synthetic methodologies and design principles for the realization of high-performance organic cathode materials.</pubmed_abstract><journal>Chemical science</journal><pubmed_title>π-Conjugated redox-active two-dimensional polymers as organic cathode materials.</pubmed_title><pmcid>PMC8943886</pmcid><funding_grant_id>DMR-2002634</funding_grant_id><pubmed_authors>Gray J</pubmed_authors><pubmed_authors>Nuckolls C</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Venkataraman L</pubmed_authors><pubmed_authors>Cheng Q</pubmed_authors><pubmed_authors>Bao ST</pubmed_authors><pubmed_authors>Wei F</pubmed_authors><pubmed_authors>Jin Z</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Evans AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>π-Conjugated redox-active two-dimensional polymers as organic cathode materials.</name><description>Redox-active two-dimensional polymers (RA-2DPs) are promising lithium battery organic cathode materials due to their regular porosities and high chemical stabilities. However, weak electrical conductivities inherent to the non-conjugated molecular motifs used thus far limit device performance and the practical relevance of these materials. We herein address this problem by developing a modular approach to construct π-conjugated RA-2DPs with a new polycyclic aromatic redox-active building block PDI-DA. Efficient imine-condensation between PDI-DA and two polyfunctional amine nodes followed by quantitative alkyl chain removal produced RA-2DPs TAPPy-PDI and TAPB-PDI as conjugated, porous, polycrystalline networks. In-plane conjugation and permanent porosity endow these materials with high electrical conductivity and high ion diffusion rates. As such, both RA-2DPs function as organic cathode materials with good rate performance and excellent cycling stability. Importantly, the improved design enables higher areal mass-loadings than were previously available, which drives a practical demonstration of TAPPy-PDI as the power source for a series of LED lights. Collectively, this investigation discloses viable synthetic methodologies and design principles for the realization of high-performance organic cathode materials.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-09T21:56:48.617Z</modification><creation>2025-04-04T13:30:54.355Z</creation></dates><accession>S-EPMC8943886</accession><cross_references><pubmed>35432867</pubmed><doi>10.1039/d1sc07157b</doi></cross_references></HashMap>