<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Myers AR</submitter><funding>Chemical Sciences, Geosciences, and Biosciences Division</funding><funding>National Renewable Energy Laboratory</funding><pagination>8190-8198</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10958597</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(11)</volume><pubmed_abstract>Innovation in optoelectronic semiconductor devices is driven by a fundamental understanding of how to move charges and/or excitons (electron-hole pairs) in specified directions for doing useful work, e.g., for making fuels or electricity. The diverse and tunable electronic and optical properties of two-dimensional (2D) transition metal dichalcogenides (TMDCs) and one-dimensional (1D) semiconducting single-walled carbon nanotubes (s-SWCNTs) make them good quantum confined model systems for fundamental studies of charge and exciton transfer across heterointerfaces. Here we demonstrate a mixed-dimensionality 2D/1D/2D MoS&lt;sub>2&lt;/sub>/SWCNT/WSe&lt;sub>2&lt;/sub> heterotrilayer that enables ultrafast photoinduced exciton dissociation, followed by charge diffusion and slow recombination. Importantly, t</pubmed_abstract><journal>ACS nano</journal><pubmed_title>Ultrafast Charge Transfer Cascade in a Mixed-Dimensionality Nanoscale Trilayer.</pubmed_title><pmcid>PMC10958597</pmcid><funding_grant_id>DE-AC36-08GO28308</funding_grant_id><pubmed_authors>Hermosilla-Palacios MA</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Myers AR</pubmed_authors><pubmed_authors>Blackburn JL</pubmed_authors><pubmed_authors>Johnson JC</pubmed_authors><pubmed_authors>Gish MK</pubmed_authors><pubmed_authors>Earley JD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultrafast Charge Transfer Cascade in a Mixed-Dimensionality Nanoscale Trilayer.</name><description>Innovation in optoelectronic semiconductor devices is driven by a fundamental understanding of how to move charges and/or excitons (electron-hole pairs) in specified directions for doing useful work, e.g., for making fuels or electricity. The diverse and tunable electronic and optical properties of two-dimensional (2D) transition metal dichalcogenides (TMDCs) and one-dimensional (1D) semiconducting single-walled carbon nanotubes (s-SWCNTs) make them good quantum confined model systems for fundamental studies of charge and exciton transfer across heterointerfaces. Here we demonstrate a mixed-dimensionality 2D/1D/2D MoS&lt;sub>2&lt;/sub>/SWCNT/WSe&lt;sub>2&lt;/sub> heterotrilayer that enables ultrafast photoinduced exciton dissociation, followed by charge diffusion and slow recombination. Importantly, t</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-22T12:55:18.889Z</modification><creation>2025-04-06T00:29:10.349Z</creation></dates><accession>S-EPMC10958597</accession><cross_references><pubmed>38465641</pubmed><doi>10.1021/acsnano.3c12179</doi></cross_references></HashMap>