<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shaek S</submitter><funding>Technion-Israel Institute of Technology</funding><funding>Horizon 2020 Framework Programme</funding><funding>Nancy and Stephen Grand Technion Energy Program</funding><funding>EuroTech alliance program</funding><funding>Israel Science Foundation</funding><funding>Russell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology</funding><pagination>9064-9072</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10653075</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(21)</volume><pubmed_abstract>Lead-free perovskite nanocrystals are of interest due to their nontoxicity and potential application in the display industry. However, engineering their optical properties is nontrivial and demands an understanding of emission from both self-trapped and free excitons. Here, we focus on tuning silver-based double perovskite nanocrystals' optical properties via two iso-valent dopants, Bi and Sb. The photoluminescence quantum yield of the intrinsic Cs&lt;sub>2&lt;/sub>Ag&lt;sub>1-&lt;i>y&lt;/i>&lt;/sub>Na&lt;sub>&lt;i>y&lt;/i>&lt;/sub>InCl&lt;sub>6&lt;/sub> perovskite increased dramatically upon doping. However, the two dopants affect the optical properties very differently. We hypothesize that the differences arise from their differences in electronic level contributions and ionic sizes. This hypothesis is validated through ab</pubmed_abstract><journal>Chemistry of materials : a publication of the American Chemical Society</journal><pubmed_title>How Does Local Strain Affect Stokes Shifts in Halide Double Perovskite Nanocrystals?</pubmed_title><pmcid>PMC10653075</pmcid><funding_grant_id>949682</funding_grant_id><funding_grant_id>890015</funding_grant_id><pubmed_authors>Dror S</pubmed_authors><pubmed_authors>Shaek S</pubmed_authors><pubmed_authors>Massasa EH</pubmed_authors><pubmed_authors>Bekenstein Y</pubmed_authors><pubmed_authors>Khalfin S</pubmed_authors><pubmed_authors>Castelli IE</pubmed_authors><pubmed_authors>Pokroy B</pubmed_authors><pubmed_authors>Lang A</pubmed_authors><pubmed_authors>Kauffmann Y</pubmed_authors><pubmed_authors>Strassberg R</pubmed_authors><pubmed_authors>Wong AB</pubmed_authors><pubmed_authors>Kortstee LTJ</pubmed_authors><pubmed_authors>Levy S</pubmed_authors><pubmed_authors>Shechter R</pubmed_authors><pubmed_authors>Lifer R</pubmed_authors><pubmed_authors>Polishchuk I</pubmed_authors><pubmed_authors>Shamaev B</pubmed_authors></additional><is_claimable>false</is_claimable><name>How Does Local Strain Affect Stokes Shifts in Halide Double Perovskite Nanocrystals?</name><description>Lead-free perovskite nanocrystals are of interest due to their nontoxicity and potential application in the display industry. However, engineering their optical properties is nontrivial and demands an understanding of emission from both self-trapped and free excitons. Here, we focus on tuning silver-based double perovskite nanocrystals' optical properties via two iso-valent dopants, Bi and Sb. The photoluminescence quantum yield of the intrinsic Cs&lt;sub>2&lt;/sub>Ag&lt;sub>1-&lt;i>y&lt;/i>&lt;/sub>Na&lt;sub>&lt;i>y&lt;/i>&lt;/sub>InCl&lt;sub>6&lt;/sub> perovskite increased dramatically upon doping. However, the two dopants affect the optical properties very differently. We hypothesize that the differences arise from their differences in electronic level contributions and ionic sizes. This hypothesis is validated through ab</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-05T09:14:17.506Z</modification><creation>2025-04-05T09:14:17.506Z</creation></dates><accession>S-EPMC10653075</accession><cross_references><pubmed>37982006</pubmed><doi>10.1021/acs.chemmater.3c01771</doi></cross_references></HashMap>