The long after-glow phosphorescent materials were fabricated by using "wet" method. The component materials were dissolved in water solution so that their homogeneous mix was reached at molecular level. The approach that metal nitrates and organic reductants would react spontaneously and get into combustion at a moderately low ambient temperature through oxido-reduction reaction was introduced into our fabrication of long after-glow phosphorescent samples. The ambient temperature to generate the combustion could go down to 500 degrees C, and the reaction completed within 1-2 minutes, producing a fluffy resultant with small crystal structure and even composition, which is easy to grind, and with low bulk density for its powder. UV-Vis reflective spectrophotometer was used to determine and analyze the characteristics of the sample before and after its absorption of light. The result shows that the properties of the samples fabricated from both "wet" and "dry" techniques are similar except their bulk densities, and the UV-Vis reflective spectrum was able to clearly describe the spectral characteristics of long after-glow phosphorescent materials.
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Heliyon
February 2024
Department of Mechanical and Materials Engineering, Lee Kong Chian Faculty of Engineering and Science, Universiti Tunku Abdul Rahman, Sungai Long Campus, Jalan Sungai Long, Bandar Sungai Long, 43000 Kajang, Malaysia.
For enhanced applications of solar cells, organic luminescence materials like long persistent luminescence (LPL) present one of the promising avenues for light enhancement. Currently, most existing luminescent materials are based on an inorganic system that requires rare elements such as europium and dysprosium, with a very high processing temperature. Adopting organic luminescence materials that are free from rare elements is necessary, considering the low-temperature fabrication and low material cost.
View Article and Find Full Text PDFHeliyon
June 2023
Electrical Engineering Department, College of Engineering, King Khalid University, Abha, 61421, Saudi Arabia.
In new research growth long after glow material is a potential candidate due to its physical properties, chemical stability and wide application in modern solid-state lightning (LED), display devices, dosimetry and sensors. A cerium doped strontium aluminate phosphor (SrAlO:Ce) was synthesized by conventional solid-state reaction method. The crystal structure and morphology of phosphors, while doping rare earth metal and lithium metal ion was investigated by using X-ray diffraction, Raman spectroscopy and field emission scanning electron microscopy.
View Article and Find Full Text PDFSci Rep
February 2023
Department of Physics, Dr. Harisingh Gour Vishwavidyalaya (A Central University), Sagar, Madhya Pradesh, 470003, India.
In the present study, the SrAlO:Eu (x = 0.00, 0.01, 0.
View Article and Find Full Text PDFProg Mol Biol Transl Sci
January 2022
Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam, India; Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati, Assam, India; School of Health Sciences and Technology, Indian Institute of Technology Guwahati, Guwahati, Assam, India. Electronic address:
The concept of aggregation-induced emission (AIE) in purely organic luminescent molecules has drawn wide attention in the last two decades. Despite the many challenges, AIE-probes have opened versatile opportunities in many research fields. In particular, the emerging functional properties of room temperature phosphorescence (RTP) and thermally activated delayed fluorescence (TADF) have boosted the unique features of AIE luminogens (AIEgens).
View Article and Find Full Text PDFJ Nanosci Nanotechnol
March 2018
College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China.
Metal ions (Cr, Ni, Co) doped titania (M-TiO2) coupled with the long after glow phosphor MgAl2O4:(Pr3+, Dy3+) particles were synthesized by the sol-gel method, with the best mass ratio of MgAl2O4:(Pr3+, Dy3+) to M-TiO2 as 4:6. MgAl2O4:(Pr3+, Dy3+)/M-TiO2 had the persistent methyl orange (MO) photocatalytic degradation ability and the photocatalytic degradation went on reacting more than 90 min in dark after turning off the light. MgAl2O4:(Pr3+, Dy3+) emitted the light as a light source in dark which was absorbed by M-TiO2.
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