Luminescence characterization of sol-gel derived Pr3+ doped NaGd(WO4)2 phosphors for solid state lighting applications

2016 ◽  
Vol 179 ◽  
pp. 295-303 ◽  
Author(s):  
A. Durairajan ◽  
D. Thangaraju ◽  
S. Moorthy Babu ◽  
M.A. Valente
2020 ◽  
Vol 29 ◽  
pp. 876-879
Author(s):  
S.K. Ramteke ◽  
N.S. Kokode ◽  
R.L. Kohale ◽  
A.N. Yerpude ◽  
S.J. Dhoble

2007 ◽  
Vol 515 (18) ◽  
pp. 7053-7058 ◽  
Author(s):  
Suman Pokhrel ◽  
Xinglin Li ◽  
Lihua Huo ◽  
Hui Zhao ◽  
Xiaoli Cheng

2014 ◽  
Vol 787 ◽  
pp. 387-394 ◽  
Author(s):  
Yan Ni Tan ◽  
Yong Liu ◽  
Zhang Qing ◽  
Gurpreet Birdi ◽  
Liam M. Grover

Calcium silicate (CS) is a main component of Portland cement and is responsible for the strength development. Recent research has shown that dicalcium silicate cement (CSC) is bioactive and is a potential candidate for bone replacement. Traditionally, dicalcium silicate powder is synthesized by a solid state reaction or a sol-gel method. The solid-state reaction, however, usually needs a higher temperature and a longer calcination time. Furthermore, the dicalcium silicate powder made by the sol-gel method is not pure, and contains a significant quantity of CaO which is harmful to the strength and biological properties of the CSC. The Pechini technique is an alternative, low temperature polymeric precursor route for synthesis of high purity powders. In this study, purer CS powder was synthesized via the Pechini method by calcination at 800°C for 3h. DSC-TGA, XRD, SEM were used for characterization of CS powder and the hydrated cement. The DSC-TGA curves showed that the main exothermic peak was at 479°C and the total mass loss was 79.2%. The XRD patterns of CSC after hydration for 7, 14, and 35 days illustrated that dicalcium silicate hydrate (Ca1.5SiO3.5·xH2O, C-S-H) was formed in the hardened CS paste. The XRD peaks on the diffraction pattern of the C-S-H of the day 35 sample were of greater intensity than those at day 7 and day 14. This demonstrates that the hydration speed was slow and complete hydration could take more than one month. Flake-like crystals were observed on scanning electron micrographs following hardening. The degradation study result showed that there was no mass loss of CSC after the samples were soaked into phosphate buffered saline (PBS) for 40 days. The silicon assay revealed that orthosilicic acid could be released from CSC after the samples were soaked in simulated body fluid (SBF). Silicon is known to be critical to skeletal mineralization. The existence of silicon may stimulate the proliferation of bone and activate cells to produce bone. Investigation of cell attachment confirmed that the MC-3T3 cells attached well to the surfaces of CSC after seeding.


2014 ◽  
Vol 43 (26) ◽  
pp. 9860-9871 ◽  
Author(s):  
S. Som ◽  
P. Mitra ◽  
Vijay Kumar ◽  
Vinod Kumar ◽  
J. J. Terblans ◽  
...  

This paper reports on the structural, optical and photometric characterization of an Eu3+/Dy3+ doped yttrium oxysulfide phosphor (Y2O2S:Eu3+/Dy3+) for near white emission in solid state lighting.


2014 ◽  
Vol 38 (12) ◽  
pp. 5793-5800 ◽  
Author(s):  
Xiaoguang Huang ◽  
Gaël Zucchi ◽  
Jacqueline Tran ◽  
Robert B. Pansu ◽  
Arnaud Brosseau ◽  
...  

Luminescent thin films of hybrid silica-based materials were studied and an Eu-containing one was coated on a near-UV LED chip to be investigated as a red phosphor.


2004 ◽  
Vol 847 ◽  
Author(s):  
Christel Gervais ◽  
Beatriz Julián ◽  
Eloisa Cordoncillo ◽  
Purificación Escribano ◽  
Mark E. Smith ◽  
...  

ABSTRACTThe objective of this paper is to review various solid state NMR techniques that have been, or can be used for the structural characterization of siloxane—oxide hybrid systems prepared by sol-gel process, and to discuss the type of information they provide, as well as their limitations. More precisely, this paper focuses on NMR techniques to probe and quantify the different types of oxo-bridges (M–O–M of oxide network, Si–O–Si of siloxane chains and Si–O–M siloxane–MxOy interface) in siloxane-oxide nanocomposites prepared through hydrolysis and condensation of organosilanes and M(OR)n alkoxides. In addition the influence of the functionality of the silicon alkoxides and the nature of the MxOy oxides on the extent of the Si-O-M interface will be examined.


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