Persistence Mechanisms and Applications of Long Afterglow Phosphors

2015 ◽  
Vol 361 ◽  
pp. 69-94
Author(s):  
V. Shanker ◽  
D. Haranath ◽  
G. Swati

This article presents a broad review of long persistence (LP) materials that are a special kind of photon energy storage and conversion materials. They are also known as long afterglow phosphors or long decay phosphors (LDP). These phosphors can be readily excited by any ordinary household lamp, sunlight and/or ambient room lights and glow continuously in the dark for hours together without involving any radioactive elements. It is the modifications that are made to crystalline host lattice that exhibit these unusual properties related to persistence due to effective doping of some transition or rare-earth ions. A slight variation in the processing parameters such as type of reducing atmosphere, stoichiometric excess of one or more constituents, the nature of fluxes, and the intentional addition of carbon or rare-earth halides can drastically shift the emission colors and persistence times of the LP phosphors in the visible spectrum. Historically, Cu-doped ZnS phosphor had been a traditional LP material with its afterglow time less than an hour. The emission color of these LP phosphors was confined between green and yellow-green region only. However, synthesis of blue and red-emitting phosphors with long persistence times had been always a challenging task. This review article covers the recent advances in the blue, green and red-emitting LP phosphors/nanophosphors, persistence mechanism involved and the basic problems associated with their luminescence efficiency and persistence times. Modifications to existing nanosynthesis protocols to formulate a nontoxic Green Chemistry Route are also presented.Contents of Paper1. Long Afterglow Phosphors

1986 ◽  
Vol 41 (6) ◽  
pp. 866-870 ◽  
Author(s):  
H.-D. Autenrieth ◽  
S. Kemmler-Sack

By activation of the new host lattices Ba2La2B2+Te2O12 (B = Zn, Mg) with trivalent rare earth ions Ln3+ = Pr. Sm, Eu, Tb, Dy, Ho, Tm an emission in the visible region is observed. The influence of the electronic structure and concentration on the relative emission efficiency as well as the host lattice participation in the energy transfer processes are discussed.


2016 ◽  
Vol 40 (7) ◽  
pp. 6214-6227 ◽  
Author(s):  
Gattupalli Manikya Rao ◽  
G. Seeta Rama Raju ◽  
Sk. Khaja Hussain ◽  
E. Pavitra ◽  
P. S. V. Subba Rao ◽  
...  

Sr2Gd8(SiO4)6O2 is an excellent host lattice for tunable emissions via the white-light region when co-doped with suitable trivalent rare-earth ions.


MRS Advances ◽  
2019 ◽  
Vol 4 (33-34) ◽  
pp. 1895-1904
Author(s):  
Lihong Su ◽  
Kan Chen ◽  
Yongqiang Liu ◽  
ZiAo Zou ◽  
Lihua Su

Abstract:Ultraviolet light-emitting diodes (UVLEDs) with phosphor materials have considerable advantages over traditional illumination devices. Doping with rare earth ions can modify the optical spectrum of phosphor materials, but rare earths are very expensive. Thus, replacing rare earths with a common material would provide a great potential for the wide application in the future. In this study, we discovered that a novel type of semiconductor nanometre powder, namely manganese cobalt nickel copper oxide (MCNC), is able to emit blue-green wavelength spectrum when exited by 365-400nmUVLED. In addition, MCNC shows less attenuation of luminescence efficiency than other UVLED phosphor materials doped with rare earths with temperature increase. It is thus concluded that MCNC is a promising low-cost material to replace rare earths to adjust the optical spectrum wavelength of UVLED. This is the first time that nano-scale MCNC is reported to possess the property to change the optical spectrum wavelength of UVLED. This provides a new mechanical and nanometer phosphor material without rare earth doping to shift the wavelength spectrum.


1985 ◽  
Vol 40 (5) ◽  
pp. 503-507 ◽  
Author(s):  
R. Braun ◽  
R. Otto ◽  
W. Wischert ◽  
S. Kemmler-Sack

By activation of the host lattices Sr3La2W2O12 and Ca2La0,5Na0,5WO6 with the trivalent rare earth ions Ln3+ = Pr, Sm, Eu, Tb, Dy, Ho, Er a cathodoluminescence in the visible region is obtained. The influence of the electronic structure and concentration of the activator on the relative emission efficiency as well as the host lattice participation in the energy transfer processes are discussed.


1984 ◽  
Vol 39 (5) ◽  
pp. 490-494 ◽  
Author(s):  
B. Köngeter ◽  
S. Kemmler-Sack

By activation of the cubic garnet host lattice Gd3Te2Li3O12 with trivalent rare earth ions the most intense visible emission is observed for Ln3+ = Eu, Tb. Energy transfer from Gd3+ to Sm3+, Eu3+ or Dy3+, from Tb3+ to Eu3+ and from Er3+ to Tm3+ has been found to occur. The luminescence properties are strongly influenced by the substitution of Te6+ by W6+ (systems Gd3-xLnxTe2-yWyLi3O12)


2004 ◽  
Vol 201 (14) ◽  
pp. 3109-3112 ◽  
Author(s):  
Zeming Qi ◽  
Chaoshu Shi ◽  
Miao Liu ◽  
Dongfang Zhou ◽  
Xixian Luo ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (5) ◽  
pp. 3440-3445 ◽  
Author(s):  
Yunhua Yao ◽  
Cheng Xu ◽  
Ye Zheng ◽  
Chengshuai Yang ◽  
Pei Liu ◽  
...  

Improving up-conversion luminescence efficiency of rare-earth ions is always a research hotspot because of its important applications in laser source, color display, photoelectric conversion and multiplexed biolabeling.


2014 ◽  
Vol 07 (04) ◽  
pp. 1450038 ◽  
Author(s):  
Yanwei Dong ◽  
Ming Kang ◽  
Ping Zhang ◽  
Qijun Cheng ◽  
Jie Wang

Phosphors based on calcium carbonate, co-doped with various Eu 3+ and Dy 3+ concentrations were prepared by microwave co-precipitation method. The prepared phosphors were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), thermogravimetry and differential scanning calorimetry (TG-DSC) and photoluminescence and photoluminescence excitation (PL-PLE) spectroscopy. Results showed that Dy 3+ and Eu 3+ ions were uniformly introduced into the host lattice of CaCO 3 taking the place of Ca 2+ ions. Under the excitation at 382 nm, the emission peak wavelengths were at 487 nm (4 F 9/2 → 6 H 15/2 of Dy 3+), 576 nm (4 F 9/2 → 6 H 13/2 of Dy 3+), and 614 nm (5 D 0 → 7 F 2 of Eu 3+). The luminescent intensities and emitting colors of Eu 3+- Dy 3+ co-doped CaCO 3 phosphors could be controlled by UV–violet excitations wavelengths or the rare-earth ions concentrations of Eu 3+ and Dy 3+ in phosphors. The chromaticity coordinates and photographs of samples under UV light showed the changes of the luminescence color intuitively through the varing UV–violet excitations wavelengths or the rare-earth ions concentrations of Eu 3+ and Dy 3+.


1985 ◽  
Vol 40 (7) ◽  
pp. 699-705 ◽  
Author(s):  
H.-D. Autenrieth ◽  
B. Kottmann ◽  
S. Kemmler-Sack

By activation of the new host lattice Ca3La2Te2O12 with trivalent rare earth ions an emission in the visible (Ln3+=Sm, Eu, Tb, Dy, Ho, Er, Tm) or near infrared region (Nd, Ho, Er, Tm, Yb) is observed. Energy transfer from Nd3+ to Yb3+ , from Er3+, Yb3+ to Ho3+ and from Yb3+ to Tm3+ has been found to occur. The excitation, emission and diffuse reflectance spectra are analyzed.


2005 ◽  
Vol 494 ◽  
pp. 253-258
Author(s):  
E. Antić-Fidančev

Complex emission spectra of europium doped rare earth calcium oxoborates, EuCa4O(BO3)3 - EuCOB, and GdCa4O(BO3)3: Eu3+- GdCOB: Eu3+, were finely analyzed for better understanding of some local perturbations detected in these solid media. Highlighting a “size effect” of dopant / matrix ions, the interaction between the host lattice and the embedded ion is demonstrated. The evolution of the crystal field strength of R3+ ions along the rare earth series is presented for C-type RE2O3 oxides. According to R3+ - RE3+ ionic radii difference (R3+ for a dopant ion and RE3+ for a matrix ion), two opposite standings are evidenced along a series. Effect of high concentration doping on spectral line broadening is illustrated following a half-height width of 2P1/2 level of Nd3+ ion in A-type La2O3 oxide.


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