Seong Yeon Park, Gayoung Seo, Taeyeon Kim, Carina Pareja-Rivera, Fabian Pino, YoonGyo Kim, Jorge Simancas, Byeongsung Kim, Ignacio Utreras-Asenjo, Jhonatan Rodriguez-Pereira, Hyeonyeong Jo, JaeHong Park, Jin Ho Bang, Sofia Masi, Seog Joon Yoon, Iván Mora-Seró, Andrés F. Gualdrón-Reyes
{"title":"热/水稳定CsPbX3@SiOx核壳量子点喷墨打印和潜在的颜色转换应用","authors":"Seong Yeon Park, Gayoung Seo, Taeyeon Kim, Carina Pareja-Rivera, Fabian Pino, YoonGyo Kim, Jorge Simancas, Byeongsung Kim, Ignacio Utreras-Asenjo, Jhonatan Rodriguez-Pereira, Hyeonyeong Jo, JaeHong Park, Jin Ho Bang, Sofia Masi, Seog Joon Yoon, Iván Mora-Seró, Andrés F. Gualdrón-Reyes","doi":"10.1002/adom.202500968","DOIUrl":null,"url":null,"abstract":"<p>Ligand-mediated surface passivation is widely used to fill defect sites and stabilize perovskite nanoparticles, keeping their photophysical properties unchanged. However, this strategy can promote the growth of agglomerates, quenching the luminescence of nanoparticles. Additionally, the presence of bulky ligands can hinder the interparticle carrier transport, difficulting the fabrication of efficient optoelectronic devices. In this work, the synthesis of SiO<i><sub>x</sub></i>-covered CsPbX<sub>3</sub> PQDs (CsPbX<sub>3</sub>@SiO<i><sub>x</sub></i>) is performed through a modified ligand-assisted reprecipitation method (LARP), by adding 3-aminopropyl-triethoxysilane (APTES) and oleic acid to the mixture reaction. Here, it is possible to suppress the aggregates formation, achieving water-stable single core–shell PQDs with a photoluminescence quantum yield of up to 99.4% and facile bandgap modulation by varying the halide content. Accordingly, CsPbX<sub>3</sub>@SiO<i><sub>x</sub></i> PQDs inks are obtained for preparing inkjet-printed QR codes and color converters, with stable luminescence up to 1.5 and 9 h of continuous operation at 2.5 V for Cl/Br- and Br-perovskites, respectively. Interestingly, a PL splitting is observed for the Br/I-perovskite along the time, indicating the emergence of halide migration to generate Br- and I-rich domains, mediating the generation of white color emission. This contribution offers a prominent alternative to producing single PQDs with suitable optical properties and stability for developing promising LED technologies.</p>","PeriodicalId":116,"journal":{"name":"Advanced Optical Materials","volume":"13 29","pages":""},"PeriodicalIF":7.2000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://advanced.onlinelibrary.wiley.com/doi/epdf/10.1002/adom.202500968","citationCount":"0","resultStr":"{\"title\":\"Thermal/Water-Stable CsPbX3@SiOx Core–Shell Quantum Dots for Inkjet Printing and Potential Color Converting Applications\",\"authors\":\"Seong Yeon Park, Gayoung Seo, Taeyeon Kim, Carina Pareja-Rivera, Fabian Pino, YoonGyo Kim, Jorge Simancas, Byeongsung Kim, Ignacio Utreras-Asenjo, Jhonatan Rodriguez-Pereira, Hyeonyeong Jo, JaeHong Park, Jin Ho Bang, Sofia Masi, Seog Joon Yoon, Iván Mora-Seró, Andrés F. Gualdrón-Reyes\",\"doi\":\"10.1002/adom.202500968\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Ligand-mediated surface passivation is widely used to fill defect sites and stabilize perovskite nanoparticles, keeping their photophysical properties unchanged. However, this strategy can promote the growth of agglomerates, quenching the luminescence of nanoparticles. Additionally, the presence of bulky ligands can hinder the interparticle carrier transport, difficulting the fabrication of efficient optoelectronic devices. In this work, the synthesis of SiO<i><sub>x</sub></i>-covered CsPbX<sub>3</sub> PQDs (CsPbX<sub>3</sub>@SiO<i><sub>x</sub></i>) is performed through a modified ligand-assisted reprecipitation method (LARP), by adding 3-aminopropyl-triethoxysilane (APTES) and oleic acid to the mixture reaction. Here, it is possible to suppress the aggregates formation, achieving water-stable single core–shell PQDs with a photoluminescence quantum yield of up to 99.4% and facile bandgap modulation by varying the halide content. Accordingly, CsPbX<sub>3</sub>@SiO<i><sub>x</sub></i> PQDs inks are obtained for preparing inkjet-printed QR codes and color converters, with stable luminescence up to 1.5 and 9 h of continuous operation at 2.5 V for Cl/Br- and Br-perovskites, respectively. Interestingly, a PL splitting is observed for the Br/I-perovskite along the time, indicating the emergence of halide migration to generate Br- and I-rich domains, mediating the generation of white color emission. This contribution offers a prominent alternative to producing single PQDs with suitable optical properties and stability for developing promising LED technologies.</p>\",\"PeriodicalId\":116,\"journal\":{\"name\":\"Advanced Optical Materials\",\"volume\":\"13 29\",\"pages\":\"\"},\"PeriodicalIF\":7.2000,\"publicationDate\":\"2025-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://advanced.onlinelibrary.wiley.com/doi/epdf/10.1002/adom.202500968\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Optical Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adom.202500968\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Optical Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adom.202500968","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Thermal/Water-Stable CsPbX3@SiOx Core–Shell Quantum Dots for Inkjet Printing and Potential Color Converting Applications
Ligand-mediated surface passivation is widely used to fill defect sites and stabilize perovskite nanoparticles, keeping their photophysical properties unchanged. However, this strategy can promote the growth of agglomerates, quenching the luminescence of nanoparticles. Additionally, the presence of bulky ligands can hinder the interparticle carrier transport, difficulting the fabrication of efficient optoelectronic devices. In this work, the synthesis of SiOx-covered CsPbX3 PQDs (CsPbX3@SiOx) is performed through a modified ligand-assisted reprecipitation method (LARP), by adding 3-aminopropyl-triethoxysilane (APTES) and oleic acid to the mixture reaction. Here, it is possible to suppress the aggregates formation, achieving water-stable single core–shell PQDs with a photoluminescence quantum yield of up to 99.4% and facile bandgap modulation by varying the halide content. Accordingly, CsPbX3@SiOx PQDs inks are obtained for preparing inkjet-printed QR codes and color converters, with stable luminescence up to 1.5 and 9 h of continuous operation at 2.5 V for Cl/Br- and Br-perovskites, respectively. Interestingly, a PL splitting is observed for the Br/I-perovskite along the time, indicating the emergence of halide migration to generate Br- and I-rich domains, mediating the generation of white color emission. This contribution offers a prominent alternative to producing single PQDs with suitable optical properties and stability for developing promising LED technologies.
期刊介绍:
Advanced Optical Materials, part of the esteemed Advanced portfolio, is a unique materials science journal concentrating on all facets of light-matter interactions. For over a decade, it has been the preferred optical materials journal for significant discoveries in photonics, plasmonics, metamaterials, and more. The Advanced portfolio from Wiley is a collection of globally respected, high-impact journals that disseminate the best science from established and emerging researchers, aiding them in fulfilling their mission and amplifying the reach of their scientific discoveries.