<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Wen J</submitter><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Jiangsu Province</funding><pubmed_abstract>Light-induced halide segregation constrains the photovoltaic performance and stability of wide-bandgap perovskite solar cells and tandem cells. The implementation of an intermixed two-dimensional/three-dimensional heterostructure via solution post-treatment is a typical strategy to improve the efficiency and stability of perovskite solar cells. However, owing to the composition-dependent sensitivity of surface reconstruction, the conventional solution post-treatment is suboptimal for methylammonium-free and cesium/bromide-enriched wide-bandgap PSCs. To address this, we develop a generic three-dimensional to two-dimensional perovskite conversion approach to realize a preferential growth of wider dimensionality (n ≥ 2) atop wide-bandgap perovskite layers (1.78 eV). This technique involves depositing a well-defined MAPbI&lt;sub>3&lt;/sub> thin layer through a vapor-assisted two-step process, followed by its conversion into a two-dimensional structure. Such a two-dimensional/three-dimensional heterostructure enables suppressed light-induced halide segregation, reduced non-radiative interfacial recombination, and facilitated charge extraction. The wide-bandgap perovskite solar cells demonstrate a champion power conversion efficiency of 19.6% and an open-circuit voltage of 1.32 V. By integrating with the thermal-stable FAPb&lt;sub>0.5&lt;/sub>Sn&lt;sub>0.5&lt;/sub>I&lt;sub>3&lt;/sub> narrow-bandgap perovskites, our all-perovskite tandem solar cells exhibit a stabilized PCE of 28.1% and retain 90% of the initial performance after 855 hours of continuous 1-sun illumination.</pubmed_abstract><journal>Nature communications</journal><pagination>7118</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10628126</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Heterojunction formed via 3D-to-2D perovskite conversion for photostable wide-bandgap perovskite solar cells.</pubmed_title><pmcid>PMC10628126</pmcid><pubmed_authors>Wan S</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Wen J</pubmed_authors><pubmed_authors>Zheng X</pubmed_authors><pubmed_authors>Lin R</pubmed_authors><pubmed_authors>Tan H</pubmed_authors><pubmed_authors>Wu P</pubmed_authors><pubmed_authors>Tian Y</pubmed_authors><pubmed_authors>Luo H</pubmed_authors><pubmed_authors>Li K</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterojunction formed via 3D-to-2D perovskite conversion for photostable wide-bandgap perovskite solar cells.</name><description>Light-induced halide segregation constrains the photovoltaic performance and stability of wide-bandgap perovskite solar cells and tandem cells. The implementation of an intermixed two-dimensional/three-dimensional heterostructure via solution post-treatment is a typical strategy to improve the efficiency and stability of perovskite solar cells. However, owing to the composition-dependent sensitivity of surface reconstruction, the conventional solution post-treatment is suboptimal for methylammonium-free and cesium/bromide-enriched wide-bandgap PSCs. To address this, we develop a generic three-dimensional to two-dimensional perovskite conversion approach to realize a preferential growth of wider dimensionality (n ≥ 2) atop wide-bandgap perovskite layers (1.78 eV). This technique involves depositing a well-defined MAPbI&lt;sub>3&lt;/sub> thin layer through a vapor-assisted two-step process, followed by its conversion into a two-dimensional structure. Such a two-dimensional/three-dimensional heterostructure enables suppressed light-induced halide segregation, reduced non-radiative interfacial recombination, and facilitated charge extraction. The wide-bandgap perovskite solar cells demonstrate a champion power conversion efficiency of 19.6% and an open-circuit voltage of 1.32 V. By integrating with the thermal-stable FAPb&lt;sub>0.5&lt;/sub>Sn&lt;sub>0.5&lt;/sub>I&lt;sub>3&lt;/sub> narrow-bandgap perovskites, our all-perovskite tandem solar cells exhibit a stabilized PCE of 28.1% and retain 90% of the initial performance after 855 hours of continuous 1-sun illumination.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-05T10:23:29.795Z</modification><creation>2025-04-05T10:23:29.795Z</creation></dates><accession>S-EPMC10628126</accession><cross_references><pubmed>37932289</pubmed><doi>10.1038/s41467-023-43016-5</doi></cross_references></HashMap>