Recently, UV/NUV excitable RGB phosphors with precisely tunable PL emission properties have been in high demand for their suitability in the fabrication of white LEDs. In this paper, we report to have tuned the PL intensity, shade, and color temperature of the defect-mediated blue phosphorescence of ZnO nanopowders by systematic annealing at different temperatures. The ZnO nanopowder was prepared by a facile and cost-effective aqueous solution-precipitation method. The as-synthesized nanopowder was annealed at different temperatures ranging from 150 °C to 850 °C and all these samples were characterized by XRD, FESEM, EDX, BET, Raman spectroscopy, and UV-Vis spectroscopy to have insight into their microstructural, compositional, and band-structure details. Optical studies of the samples were conducted by PL and τ-PL spectroscopy. Color coordinates of the samples were obtained from the CIE plots derived from the PL spectra. The CIE coordinates were further used to calculate the CCT values of the samples. τ-PL spectroscopy was carried out to measure the life-time of the photogenerated electrons. PL studies of the samples revealed that the blue emissions have red, yellow, and blue components originating from crystalline point defects, zinc interstitial (Zn), and oxygen interstitial (O). Annealing at different temperatures triggered changes in the defect concentrations leading to the corresponding changes in the intensity, shade, and color temperature of the blue phosphorescence.
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http://dx.doi.org/10.1039/d0ra04766j | DOI Listing |
Chem Sci
March 2025
Key Laboratory of Magnetic Molecules & Magnetic Information Materials (Ministry of Education), School of Chemistry and Material Science, Shanxi Normal University Taiyuan 030031 P. R. China
Metal ion-doped organic-inorganic hybrid metal halides have emerged as promising room-temperature phosphorescence (RTP) materials owing to their tunable afterglow properties and significant potential in information security applications. However, optimizing RTP performance and achieving dynamic control over afterglow colors remain challenging in 1D hybrid systems, primarily because of the inefficient energy transfer from RTP-active organic components to external emissive sites. Herein, we report a novel 1D hybrid metal halide benchmark material, [(NBP)CdClHO] (NBP-Cd, NBP = -benzylpiperidone), and a series of Mn-doped derivatives, NBP-Cd:Mn (where represents doping levels from 1% to 50%).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
City University of Hong Kong, Department of Chemistry, Department of Materials Science and Engineering, and Center of Super-Diamond and Advanced Films (COSDAF), HONG KONG.
Through-space charge transfer (TSCT) rather than the commonly postulated metal-to-ligand charge transfer (MLCT) process was proposed in getting the lowest lying excited state of newly designed Ir(III) blue phosphors. Accordingly, two benzo[d]imidazolylidene pro-chelates L12H2+ and L13H2+, one with two cyano groups at the peri-benzo and N-aryl pendent and the other with its peri-cyano group being replaced with methyl substituent, were employed in syntheses of Ir(III) complexes f-ct12b,c and f-ct13b,c. Notably, complexes f-ct12b,c exhibited the traditional MLCT process, while f-ct13b,c were dominated by the TSCT transition, resulting in a smaller S1-T1 energy gap ΔEST.
View Article and Find Full Text PDFNew approaches to prepare rarer emitters such as those that are deep-blue are needed to advance OLED technologies. Here, we demonstrate that a series of new platinum(ii) bis(acetylide) complexes [Pt(N-N)(C[triple bond, length as m-dash]CPh)] containing sulfur-bridged dipyridyl ligands (N-N) with various sulfur oxidation states: sulfide (S), sulfoxide (SO) and sulfone (SO) give access to variable emission colors from green to deep-blue. Spectroscopic, electrochemical and computational studies show that mixed character excited states have energies which are significantly influenced by the oxidation state of sulfur and the presence of substituents.
View Article and Find Full Text PDFOrg Biomol Chem
February 2025
Department of Organic Materials Science Graduate School of Organic Materials Science, Yamagata University, Yonezawa 992-8510, Japan.
To advance the development of luminescent materials based on indazoles, a class of nitrogen-containing aromatic compounds, it is crucial to establish a reliable synthetic method for their derivatives. Five 1-indazole derivatives with a ketoaryl group at the 3-position were synthesized by a cyclisation reaction using phenyltriazene derivatives. In solution state, only 3-ketoindazole derivatives bearing 4-diphenylaminophenyl or pyrenyl groups showed fluorescence at room temperature, whereas all 3-ketoindazole derivatives showed blue, green, or red phosphorescence, depending on the substituents, at 80 K.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2025
Institute of Chemical Sciences Rennes, Dpt. de Chimie, campus de Beaulieu, 35042 Rennes cedex, Rennes, FRANCE.
Pure hydrocarbon (PHC) materials are a class of highly efficient and stable host materials for organic light-emitting diodes (OLEDs), composed solely of carbon and hydrogen atoms. Despite recent great advancements in PHC research, their applications are still mainly limited to phosphorescent OLEDs (PHOLEDs). Thus, expanding PHC materials into other types of OLEDs is critical for advancing organic electronics.
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