<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><submitter>Baldwin A</submitter><funding>European Research Council</funding><funding>Royal Society</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>4003-4011</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8154849</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(16)</volume><pubmed_abstract>Halide perovskites are versatile semiconductors with applications including photovoltaics and light-emitting devices, having modular optoelectronic properties realizable through composition and dimensionality tuning. Layered Ruddlesden-Popper perovskites are particularly interesting due to their unique 2D character and charge carrier dynamics. However, long-range energy transport through exciton diffusion in these materials is not understood or realized. Here, local time-resolved luminescence mapping techniques are employed to visualize exciton transport in exfoliated flakes of the BA&lt;sub>2&lt;/sub>MA&lt;sub>&lt;i>n&lt;/i>-1&lt;/sub>Pb&lt;sub>&lt;i>n&lt;/i>&lt;/sub>I&lt;sub>3&lt;i>n&lt;/i>+1&lt;/sub> perovskite family. Two distinct transport regimes are uncovered, depending on the temperature range. Above 100 K, diffusion is mediated by thermally activated hopping processes between localized states. At lower temperatures, a nonuniform energy landscape emerges in which transport is dominated by downhill energy transfer to lower-energy states, leading to long-range transport over hundreds of nanometers. Efficient, long-range, and switchable downhill transfer offers exciting possibilities for controlled directional long-range transport in these 2D materials for new applications.</pubmed_abstract><journal>The journal of physical chemistry letters</journal><pubmed_title>Local Energy Landscape Drives Long-Range Exciton Diffusion in Two-Dimensional Halide Perovskite Semiconductors.</pubmed_title><pmcid>PMC8154849</pmcid><funding_grant_id>756962</funding_grant_id><funding_grant_id>UF150033</funding_grant_id><funding_grant_id>EP/R023980/1</funding_grant_id><funding_grant_id>NF170533</funding_grant_id><pubmed_authors>Galkowski K</pubmed_authors><pubmed_authors>Chahbazian R</pubmed_authors><pubmed_authors>Delport G</pubmed_authors><pubmed_authors>Stranks SD</pubmed_authors><pubmed_authors>Baldwin A</pubmed_authors><pubmed_authors>Loh KP</pubmed_authors><pubmed_authors>Leng K</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>Local Energy Landscape Drives Long-Range Exciton Diffusion in Two-Dimensional Halide Perovskite Semiconductors.</name><description>Halide perovskites are versatile semiconductors with applications including photovoltaics and light-emitting devices, having modular optoelectronic properties realizable through composition and dimensionality tuning. Layered Ruddlesden-Popper perovskites are particularly interesting due to their unique 2D character and charge carrier dynamics. However, long-range energy transport through exciton diffusion in these materials is not understood or realized. Here, local time-resolved luminescence mapping techniques are employed to visualize exciton transport in exfoliated flakes of the BA&lt;sub>2&lt;/sub>MA&lt;sub>&lt;i>n&lt;/i>-1&lt;/sub>Pb&lt;sub>&lt;i>n&lt;/i>&lt;/sub>I&lt;sub>3&lt;i>n&lt;/i>+1&lt;/sub> perovskite family. Two distinct transport regimes are uncovered, depending on the temperature range. Above 100 K, diffusion is mediated by thermally activated hopping processes between localized states. At lower temperatures, a nonuniform energy landscape emerges in which transport is dominated by downhill energy transfer to lower-energy states, leading to long-range transport over hundreds of nanometers. Efficient, long-range, and switchable downhill transfer offers exciting possibilities for controlled directional long-range transport in these 2D materials for new applications.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2024-11-12T19:42:29.621Z</modification><creation>2022-02-10T12:17:17.25Z</creation></dates><accession>S-EPMC8154849</accession><cross_references><pubmed>33877840</pubmed><doi>10.1021/acs.jpclett.1c00823</doi></cross_references></HashMap>