{"title":"钯纳米晶的硒化和黄铁矿化","authors":"Cullen T. Irvine, Joshua E. Goldberger","doi":"10.1021/acs.inorgchem.5c01121","DOIUrl":null,"url":null,"abstract":"Binary and ternary palladium selenides form many different compositions and polymorphs that are host to unique electronic and magnetic phenomena such as superconductivity, exotic spin behavior, and axis-dependent conduction polarity. The development of solution-phase routes toward nano- and micrometer-scale morphologies of these compounds would facilitate future explorations of these properties in this size regime. The selenization of colloidal metal nanocrystals is a useful strategy for preparing metal selenide nanomaterials, but it has not yet been explored to form selenium-rich palladium selenide phases. Here, we demonstrate the preparation of parallelepiped-shaped particles of the metastable, monoclinic PdSe<sub>2</sub> (M-PdSe<sub>2</sub>) phase and well-faceted, octahedral-shaped particles of the pyrite Fe<sub>0.5</sub>Pd<sub>0.5</sub>Se<sub>2</sub> phase via this method. We show that the reaction of Pd nanocrystals with Na<sub>2</sub>Se<sub>2</sub> leads to the formation of amorphous PdSe<sub><i>x</i></sub> nanoparticles as an intermediate, before conversion to M-PdSe<sub>2</sub> (selenization), or Fe<sub>0.5</sub>Pd<sub>0.5</sub>Se<sub>2</sub> when also in the presence of Fe<sup>2+</sup> (pyritization). These findings provide a better understanding of palladium nanocrystal selenization pathways and how they can be further developed for the preparation of ternary metal chalcogenide phases.","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"125 1","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Selenization and Pyritization of Palladium Nanocrystals\",\"authors\":\"Cullen T. Irvine, Joshua E. Goldberger\",\"doi\":\"10.1021/acs.inorgchem.5c01121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Binary and ternary palladium selenides form many different compositions and polymorphs that are host to unique electronic and magnetic phenomena such as superconductivity, exotic spin behavior, and axis-dependent conduction polarity. The development of solution-phase routes toward nano- and micrometer-scale morphologies of these compounds would facilitate future explorations of these properties in this size regime. The selenization of colloidal metal nanocrystals is a useful strategy for preparing metal selenide nanomaterials, but it has not yet been explored to form selenium-rich palladium selenide phases. Here, we demonstrate the preparation of parallelepiped-shaped particles of the metastable, monoclinic PdSe<sub>2</sub> (M-PdSe<sub>2</sub>) phase and well-faceted, octahedral-shaped particles of the pyrite Fe<sub>0.5</sub>Pd<sub>0.5</sub>Se<sub>2</sub> phase via this method. We show that the reaction of Pd nanocrystals with Na<sub>2</sub>Se<sub>2</sub> leads to the formation of amorphous PdSe<sub><i>x</i></sub> nanoparticles as an intermediate, before conversion to M-PdSe<sub>2</sub> (selenization), or Fe<sub>0.5</sub>Pd<sub>0.5</sub>Se<sub>2</sub> when also in the presence of Fe<sup>2+</sup> (pyritization). These findings provide a better understanding of palladium nanocrystal selenization pathways and how they can be further developed for the preparation of ternary metal chalcogenide phases.\",\"PeriodicalId\":40,\"journal\":{\"name\":\"Inorganic Chemistry\",\"volume\":\"125 1\",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-05-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.inorgchem.5c01121\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.inorgchem.5c01121","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
The Selenization and Pyritization of Palladium Nanocrystals
Binary and ternary palladium selenides form many different compositions and polymorphs that are host to unique electronic and magnetic phenomena such as superconductivity, exotic spin behavior, and axis-dependent conduction polarity. The development of solution-phase routes toward nano- and micrometer-scale morphologies of these compounds would facilitate future explorations of these properties in this size regime. The selenization of colloidal metal nanocrystals is a useful strategy for preparing metal selenide nanomaterials, but it has not yet been explored to form selenium-rich palladium selenide phases. Here, we demonstrate the preparation of parallelepiped-shaped particles of the metastable, monoclinic PdSe2 (M-PdSe2) phase and well-faceted, octahedral-shaped particles of the pyrite Fe0.5Pd0.5Se2 phase via this method. We show that the reaction of Pd nanocrystals with Na2Se2 leads to the formation of amorphous PdSex nanoparticles as an intermediate, before conversion to M-PdSe2 (selenization), or Fe0.5Pd0.5Se2 when also in the presence of Fe2+ (pyritization). These findings provide a better understanding of palladium nanocrystal selenization pathways and how they can be further developed for the preparation of ternary metal chalcogenide phases.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.