<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fu S</submitter><funding>Natural Science Foundation of Shandong Province (Shandong Provincial Natural Science Foundation)</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><funding>Taishan Scholar Foundation of Shandong Province</funding><pagination>1457-1464</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12404993</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(9)</volume><pubmed_abstract>Hot carriers, inheriting excess kinetic energy from high-energy photons, drive numerous optoelectronic applications reliant on non-equilibrium transport processes. Although extensively studied in inorganic materials, their potential in organic-based systems remains largely unexplored. Here we demonstrate highly mobile hot carriers in crystalline two-dimensional conjugated coordination polymer Cu&lt;sub>3&lt;/sub>BHT (BHT, benzenehexathiol) films. Leveraging a suite of ultrafast spectroscopic and imaging techniques, we map the microscopic charge transport landscape in Cu&lt;sub>3&lt;/sub>BHT films following non-equilibrium photoexcitation across temporal, spatial and frequency domains, revealing two distinct high-mobility transport regimes. In the non-equilibrium regime, hot carriers achieve an ultrahi</pubmed_abstract><journal>Nature materials</journal><pubmed_title>Unveiling high-mobility hot carriers in a two-dimensional conjugated coordination polymer.</pubmed_title><pmcid>PMC12404993</pmcid><funding_grant_id>tsqn201909047</funding_grant_id><funding_grant_id>22472085</funding_grant_id><funding_grant_id>ZR2023JQ005</funding_grant_id><funding_grant_id>22272092</funding_grant_id><pubmed_authors>Hambsch M</pubmed_authors><pubmed_authors>Fu S</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Feng X</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Kaiser U</pubmed_authors><pubmed_authors>Gao G</pubmed_authors><pubmed_authors>Li K</pubmed_authors><pubmed_authors>Dong R</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Parkin SSP</pubmed_authors><pubmed_authors>Bonn M</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>St Petkov P</pubmed_authors><pubmed_authors>Gao W</pubmed_authors><pubmed_authors>Mannsfeld SCB</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Zhu T</pubmed_authors><pubmed_authors>Wang HI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Unveiling high-mobility hot carriers in a two-dimensional conjugated coordination polymer.</name><description>Hot carriers, inheriting excess kinetic energy from high-energy photons, drive numerous optoelectronic applications reliant on non-equilibrium transport processes. Although extensively studied in inorganic materials, their potential in organic-based systems remains largely unexplored. Here we demonstrate highly mobile hot carriers in crystalline two-dimensional conjugated coordination polymer Cu&lt;sub>3&lt;/sub>BHT (BHT, benzenehexathiol) films. Leveraging a suite of ultrafast spectroscopic and imaging techniques, we map the microscopic charge transport landscape in Cu&lt;sub>3&lt;/sub>BHT films following non-equilibrium photoexcitation across temporal, spatial and frequency domains, revealing two distinct high-mobility transport regimes. In the non-equilibrium regime, hot carriers achieve an ultrahi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-29T21:45:24.359Z</modification><creation>2026-04-08T06:08:40.43Z</creation></dates><accession>S-EPMC12404993</accession><cross_references><pubmed>40360871</pubmed><doi>10.1038/s41563-025-02246-2</doi></cross_references></HashMap>