<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Landi N</submitter><funding>European Social Fund</funding><pagination>9517-9525</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9575147</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(40)</volume><pubmed_abstract>Mixed-cation lead mixed-halide perovskites are the best candidates for perovskite-based photovoltaics, thanks to their higher efficiency and stability compared to the single-cation single-halide parent compounds. TripleMix (Cs&lt;sub>0.05&lt;/sub>MA&lt;sub>0.14&lt;/sub>FA&lt;sub>0.81&lt;/sub>PbI&lt;sub>2.55&lt;/sub>Br&lt;sub>0.45&lt;/sub> with FA = formamidinium and MA = methylammonium) is one of the most efficient and stable mixed perovskites for single-junction solar cells. The microscopic reasons why triple-cation perovskites perform so well are still under debate. In this work, we investigated the structure and dynamics of TripleMix by exploiting multinuclear solid-state nuclear magnetic resonance (SSNMR), which can provide this information at a level of detail not accessible by other techniques. &lt;sup>133&lt;/sup>Cs, &lt;sup>13&lt;/sup>C, &lt;sup>1&lt;/sup>H, and &lt;sup>207&lt;/sup>Pb SSNMR spectra confirmed the inclusion of all ions in the perovskite, without phase segregation. Complementary measurements showed a peculiar longitudinal relaxation behavior for the &lt;sup>1&lt;/sup>H and &lt;sup>207&lt;/sup>Pb nuclei in TripleMix with respect to single-cation single-halide perovskites, suggesting slower dynamics of both organic cations and halide anions, possibly related to the high photovoltaic performances.</pubmed_abstract><journal>The journal of physical chemistry letters</journal><pubmed_title>Solid-State Nuclear Magnetic Resonance of Triple-Cation Mixed-Halide Perovskites.</pubmed_title><pmcid>PMC9575147</pmcid><funding_grant_id>AIM1809115-2</funding_grant_id><pubmed_authors>Landi N</pubmed_authors><pubmed_authors>Simbula A</pubmed_authors><pubmed_authors>Carignani E</pubmed_authors><pubmed_authors>Maurina E</pubmed_authors><pubmed_authors>Borsacchi S</pubmed_authors><pubmed_authors>Marongiu D</pubmed_authors><pubmed_authors>Calucci L</pubmed_authors><pubmed_authors>Geppi M</pubmed_authors><pubmed_authors>Saba M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Solid-State Nuclear Magnetic Resonance of Triple-Cation Mixed-Halide Perovskites.</name><description>Mixed-cation lead mixed-halide perovskites are the best candidates for perovskite-based photovoltaics, thanks to their higher efficiency and stability compared to the single-cation single-halide parent compounds. TripleMix (Cs&lt;sub>0.05&lt;/sub>MA&lt;sub>0.14&lt;/sub>FA&lt;sub>0.81&lt;/sub>PbI&lt;sub>2.55&lt;/sub>Br&lt;sub>0.45&lt;/sub> with FA = formamidinium and MA = methylammonium) is one of the most efficient and stable mixed perovskites for single-junction solar cells. The microscopic reasons why triple-cation perovskites perform so well are still under debate. In this work, we investigated the structure and dynamics of TripleMix by exploiting multinuclear solid-state nuclear magnetic resonance (SSNMR), which can provide this information at a level of detail not accessible by other techniques. &lt;sup>133&lt;/sup>Cs, &lt;sup>13&lt;/sup>C, &lt;sup>1&lt;/sup>H, and &lt;sup>207&lt;/sup>Pb SSNMR spectra confirmed the inclusion of all ions in the perovskite, without phase segregation. Complementary measurements showed a peculiar longitudinal relaxation behavior for the &lt;sup>1&lt;/sup>H and &lt;sup>207&lt;/sup>Pb nuclei in TripleMix with respect to single-cation single-halide perovskites, suggesting slower dynamics of both organic cations and halide anions, possibly related to the high photovoltaic performances.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-27T03:36:05.527Z</modification><creation>2025-04-06T18:55:24.912Z</creation></dates><accession>S-EPMC9575147</accession><cross_references><pubmed>36200785</pubmed><doi>10.1021/acs.jpclett.2c02313</doi></cross_references></HashMap>