Bifunctional ferromagnetic Eu-Gd-Bi-codoped hybrid organo-silica red emitting phosphors synthesized by a modified Pechini sol-gel method
- 1. Glass Research Department, National Research Centre (NRC), El-Buhouth Str., Dokki, 12622 Cairo (Egypt)
- 2. Spectroscopy Department, National Research Centre (NRC), El-Buhouth Str., Dokki, 12622 Cairo (Egypt)
Description
Red phosphor, composed of Eu-Gd-Bi-codoped hybrid organo-silica glass, has been synthesized via a modified Pechini sol-gel process. The synthesized hybrid glass was analyzed with powder X-ray diffraction (XRD), differential thermal analysis coupled with thermogravimetry (DTA-TG) and Fourier transform infrared (FTIR) spectroscopy. XRD and DTA-TG confirmed its amorphous structure up to 1000 °C. Magnetic behavior of the produced phosphor was investigated using vibrating specimen magnetometer (VSM) and the obtained results revealed its unsaturated ferromagnetic behavior. Photoluminescence (PL) properties of the obtained phosphor have been investigated under near-UV excitation at 395 nm. The influence of calcination temperature on the PL intensity and its decay behavior as well as on the ferromagnetic characteristics has been studied to determine the optimal reaction temperature of the phosphor. The PL emission spectra show the characteristic emission bands of Eu3+ ions in the wavelength range from 580 to 700 nm. These emission spectra have been dominated by the electric dipole 5D0→7F2 transition of the Eu3+ peaked at 610–620 nm producing the red light emission of the phosphors. It was found that the phosphor performance, expressed by its PL intensity and life time, could be significantly improved by increasing of the heat treatment temperature up to 900 °C. Also, calcination at 900 °C for 6 h greatly increased both of the magnetization and retentivity, while decreased the coercivity value. The organic phenomenon of metal citrate-ethylene glycol chelation and its degradation by calcination were well followed by FTIR spectroscopy. The obtained results are promising and could afford a basis for designing of efficient red phosphors for displays, lighting and bifunctional biosensors for biomedical applications. - Highlights: • Eu-Gd-Bi-codoped hybrid organo-silica phosphor was synthesized by sol-gel method. • Inorganic Eu-Gd-Bi-silica phosphors were obtained by calcination at 500 and 900 °C. • These phosphors showed strong red emission under n-UV excitation at 395 nm. • Hybrid and inorganic phosphors exhibited unsaturated ferromagnetic behavior. • They are promising candidates for optoelectronic and biomedical applications.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.matchemphys.2017.03.035Additional details
Identifiers
- DOI
- 10.1016/j.matchemphys.2017.03.035;
- PII
- S0254-0584(17)30240-7;
Publishing Information
- Journal Title
- Materials Chemistry and Physics
- Journal Volume
- 194
- Journal Page Range
- p. 198-205
- ISSN
- 0254-0584
- CODEN
- MCHPDR
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48073864
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- BISMUTH COMPOUNDS; COERCIVE FORCE; DIFFERENTIAL THERMAL ANALYSIS; ELECTRIC DIPOLES; EMISSION SPECTRA; EUROPIUM ADDITIONS; FERROMAGNETISM; FOURIER TRANSFORMATION; GADOLINIUM ADDITIONS; GADOLINIUM COMPOUNDS; HEAT TREATMENTS; INFRARED SPECTRA; INORGANIC PHOSPHORS; MAGNETIZATION; PHOTOLUMINESCENCE; SILICA; SOL-GEL PROCESS; THERMAL GRAVIMETRIC ANALYSIS; X-RAY DIFFRACTION
- Descriptors DEC
- ALLOYS; CHEMICAL ANALYSIS; COHERENT SCATTERING; DIFFRACTION; DIPOLES; EMISSION; EUROPIUM ALLOYS; GADOLINIUM ALLOYS; GRAVIMETRIC ANALYSIS; INTEGRAL TRANSFORMATIONS; LUMINESCENCE; MAGNETISM; MINERALS; MULTIPOLES; OXIDE MINERALS; PHOSPHORS; PHOTON EMISSION; QUANTITATIVE CHEMICAL ANALYSIS; RARE EARTH ADDITIONS; RARE EARTH ALLOYS; RARE EARTH COMPOUNDS; SCATTERING; SPECTRA; THERMAL ANALYSIS; TRANSFORMATIONS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.