Polychromatic emission can be achieved by controlling the distribution of the rare earth activator in multi-cation lattices, which can be used in the fields of white light LED and fluorescence temperature sensing. However, it is still a challenge to control their distribution and location of the target site in a given host material because the distribution of the rare earth activator is uncertain. In this paper, we have chosen LiSrCa(SiO) as the multi-cation site host and induced the distribution of Eu ions between different cation sites through anion substitution, for the first time, to regulate the luminescence characteristics of a series of LiSrCaSiON:Eu phosphors. In LiSrCa(SiO):Eu phosphors, the substitution of O by N triggered a distinct ordered to disordered structure transition of the SiO tetrahedron and induced the remote distribution of the Eu activator, which was verified through the analysis of the XRD, EPR, FT-IR and fluorescence spectra. Due to the location of Eu ions in different cation sites (Eu and Eu), two distinguishable emission peaks with tunable color emissions and different responses to temperature were realized. The white LED that utilized blue-orange-emitting LiSrCaSiON:Eu and green-emitting BaSiON:Eu (500 nm) displayed an outstanding color rendering index () of 85.1. Based on the fluorescence intensity ratio (FIR) technique, an optical temperature measurement mechanism was hypothesized and studied in the temperature range of 293-473 K. The highest of the material was 0.086 K, and was 1.76% K based on the FIR detection technology, revealing obviously better than most inorganic optical temperature-measuring materials reported before. Our work indicates that LiSrCaSiON:Eu is a promising material for application in White LEDs and optical thermometers.
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http://dx.doi.org/10.1039/d2dt00485b | DOI Listing |
Dalton Trans
January 2025
Institut für Anorganische Chemie, University of Stuttgart, Pfaffenwaldring 55, 70550 Stuttgart, Germany.
A cationic N-heterocyclic phosphenium (NHP) iron tetracarbonyl complex was synthesised from the free cation and its behaviour towards various anionic reactants studied. Reactions with fluoride, chloride, and hydride sources proceeded under attachment of the anion at phosphorus to yield Fe(CO)-complexes of neutral diazaphospholenes, while bromide and iodide reacted under addition of the anion at the metal and decarbonylation to yield NHP iron halides. Reactions with amides and organometallics were unselective.
View Article and Find Full Text PDFSci Rep
January 2025
School of Chemical Science and Technology, Key Laboratory of Medicinal Chemistry for Natural Resource, Yunnan University, No. 2 North Cuihu Road, Kunming, China.
It has been reported some nanozymes could be used as a substitute for natural enzyme to detect HO to some extent. However, the low catalytic effect of these materials limited their further application fields. Hence, to increase the catalytic activity of nanozymes was a hot research topic and many methods have been reported.
View Article and Find Full Text PDFSci Adv
January 2025
Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA.
J Am Chem Soc
January 2025
Department of Applied Chemistry, Anhui Province Engineering Laboratory for Green Pesticide Development and Application, and Anhui Province Key Laboratory of Crop Integrated Pest Management, Anhui Agricultural University, Hefei 230036, China.
Asymmetric catalysis involving a sulfoxide electrophile intermediate presents an efficient methodology for accessing stereogenic-at-sulfur compounds, such as sulfinate esters, sulfinamides, , which have garnered increasing attention in modern pharmaceutical sciences. However, as the aza-analog of sulfoxide electrophiles, the asymmetric issues about electrophilic sulfinimidoyl species remain largely unexplored and represent a significant challenge in sulfur stereochemistry. Herein, we exhibit an anionic stereogenic-at-cobalt(III) complex-catalyzed asymmetric synthesis of chiral sulfinamides via chiral sulfinimidoyl iodide intermediates.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
School of Materials Science and Engineering, State Key Lab of Silicon and Advanced, Semiconductor Materials, Zhejiang University, Hangzhou 310027, PR China. Electronic address:
NaMnTi(PO) is a promising sodium-ion cathode material due to its relatively high specific capacity, excellent thermodynamic stability and low cost. However, unfavorable electron conductivity and slow kinetics limit its practical application. Here, a strategy of hetero and multivalent anion substitution is proposed to achieve high-rate performance and good capacity retention.
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