scholarly journals Effect of Ce3+ Co-doping on GdPO4:Tb3+ Nanoparticles: Photoluminescence and Energy Transfer Studies

2021 ◽  
Vol 33 (4) ◽  
pp. 903-908
Author(s):  
N. Yaiphaba

Low temperature synthesis of Tb3+-doped GdPO4 nanoparticles sensitized with Ce3+ (Ce3+ = 0, 3, 5, 7 and 10 at.%) have been reported. Ethylene glycol was used as capping agent as well as reaction medium at 160 ºC. The as-prepared particles crystallized in a monoclinic structure with an average crystallite size of 25-46 nm. From the photoluminescence study, enhanced emission of Tb3+ with co-doping of Ce3+ was attributed to efficient energy transfer from the sensitizer to activator. The luminescence emission intensity increases upto 5 at.% of Ce3+ and then decreases. Less efficient energy transfer from sensitizer to the activator with increasing concentration of sensitizer may be attributed to critical concentration of Ce3+ with the host or dipole-quadrupole interaction amongst the Ce3+ ions. Moreover, presence of -OH group in the samples will make them a potential target for biological labeling and optical devices.

2021 ◽  
Author(s):  
Yun-Ling Yang ◽  
Jia-Yong Yuan ◽  
Yu-Ting Fan ◽  
Dongyun Wan ◽  
Qian-Li Li ◽  
...  

A serials of Bi3+ and Mn2+ co-doping CaZnOS phosphors with tunable emission color have been synthesized by high temperature solid-state reaction method. Their crystal structure, spectroscopic properties, energy transfer and...


Soft Matter ◽  
2021 ◽  
Author(s):  
Xinxian Ma ◽  
bo qiao ◽  
Jinlong Yue ◽  
JingJing Yu ◽  
yutao geng ◽  
...  

Based on a new designed acyl hydrazone gelator (G2), we developed an efficient energy transfer supramolecular organogel in glycol with two different hydrophobic fluorescent dyes rhodamine B (RhB) and acridine...


2004 ◽  
Vol 43 (15) ◽  
pp. 1976-1979 ◽  
Author(s):  
Freek J. M. Hoeben ◽  
Laura M. Herz ◽  
Clément Daniel ◽  
Pascal Jonkheijm ◽  
Albertus P. H. J. Schenning ◽  
...  

2012 ◽  
Vol 22 (21) ◽  
pp. 10816 ◽  
Author(s):  
Diana Savateeva ◽  
Dzmitry Melnikau ◽  
Vladimir Lesnyak ◽  
Nikolai Gaponik ◽  
Yury P. Rakovich

2008 ◽  
Vol 61 (8) ◽  
pp. 585 ◽  
Author(s):  
Simon Boyd ◽  
Kenneth P. Ghiggino ◽  
W. David McFadyen

The photochemistry of two anthracene-appended cobalt(iii) cyclam complexes is explored with a view to demonstrate a photoactivated ligand release process. The ligand exchange processes that occur in the complexes cis-[CoL(NO2)(ONO)]+ and trans-[CoL(NO2)(ONO)]+ in which L = 6-(anthracen-9-ylmethyl)-1,4,8,11-tetraazacyclotetradecane were monitored upon illumination of the anthracenyl chromophore at 360 nm in the presence of a large excess of thiocyanate. The trans-[CoL(NO2)(ONO)]+ complex underwent a ligand exchange reaction in the absence of light and displayed an enhancement of the reaction upon illumination. In contrast the cis-[CoL(NO2)(ONO)]+ complex was stable in the dark but displayed a significant quantum yield of photoactivated ligand release (Φ = 0.19). It is proposed that in cis-[CoL(NO2)(ONO)]+ the photoexcited anthracenyl chromophore undergoes efficient energy transfer to the cobalt(iii) cyclam before ligand exchange. Complexes based on the anthracenylcyclam–cobalt(iii) framework may be potentially useful candidates as photoactivated ligand release systems.


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