Color control and white upconversion luminescence of LaOF:Ln3+ (Ln = Yb, Er, Tm) nanocrystals prepared by the sol–gel Pechini method

2013 ◽  
Vol 42 (14) ◽  
pp. 5159 ◽  
Author(s):  
Kezhi Zheng ◽  
Ye Liu ◽  
Zhenyu Liu ◽  
Zhe Chen ◽  
Weiping Qin
RSC Advances ◽  
2021 ◽  
Vol 11 (49) ◽  
pp. 30926-30936
Author(s):  
Kamel Saidi ◽  
Wajdi Chaabani ◽  
Mohamed Dammak

Novel orthophosphate LiZnPO4:Yb3+–Er3+/Ho3+ with tunable luminescence have been synthesized via sol–gel/Pechini method for optical thermometry.


Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 937
Author(s):  
Katarzyna Halubek-Gluchowska ◽  
Damian Szymański ◽  
Thi Ngoc Lam Tran ◽  
Maurizio Ferrari ◽  
Anna Lukowiak

Looking for upconverting biocompatible nanoparticles, we have prepared by the sol–gel method, silica–calcia glass nanopowders doped with different concentration of Tm3+ and Yb3+ ions (Tm3+ from 0.15 mol% up to 0.5 mol% and Yb3+ from 1 mol% up to 4 mol%) and characterized their structure, morphology, and optical properties. X-ray diffraction patterns indicated an amorphous phase of the silica-based glass with partial crystallization of samples with a higher content of lanthanides ions. Transmission electron microscopy images showed that the average size of particles decreased with increasing lanthanides content. The upconversion (UC) emission spectra and fluorescence lifetimes were registered under near infrared excitation (980 nm) at room temperature to study the energy transfer between Yb3+ and Tm3+ at various active ions concentrations. Characteristic emission bands of Tm3+ ions in the range of 350 nm to 850 nm were observed. To understand the mechanism of Yb3+–Tm3+ UC energy transfer in the SiO2–CaO powders, the kinetics of luminescence decays were studied.


2016 ◽  
Vol 188 ◽  
pp. 23-27 ◽  
Author(s):  
Xing Gao ◽  
Nengli Wang ◽  
Tao Shi ◽  
Shuo Wang ◽  
Minhui Zhang ◽  
...  

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Anna Prnová ◽  
Jana Valúchová ◽  
Monika Michálková ◽  
Beáta Pecušová ◽  
Milan Parchovianský ◽  
...  

Abstract Glass microspheres with yttria-alumina eutectic composition (76.8 mol % Al2O3 and 23.2 mol % Y2O3) were prepared by sol-gel Pechini method and flame synthesis with or without subsequent milling. Prepared amorphous powders were studied by X-ray powder diffraction (XRD), particle size analysis (PSA), scanning electron microscopy (SEM) and differential thermal analysis (DTA). Hot pressing (HP), rapid hot pressing (RHP) and spark plasma sintering (SPS) were used to sinter amorphous precursor powders at 1600 °C without holding time (0 min). The preparation process including milling step resulted in amorphous powders with narrower particle size distribution and smaller particle size. All applied pressure assisted sintering techniques resulted in dense bulk samples with fine grained microstructure consisting of irregular α-Al2O3 and Y3Al5O12 (YAG) grains. Milling was beneficial in terms of final microstructure refinement and mechanical properties of sintered materials. A material with the Vickers hardness of HV = (17.1 ± 0.3) GPa and indentation fracture resistance of (4.2 ± 0.2) MPa.m1/2 was prepared from the powder milled for 12 h.


RSC Advances ◽  
2019 ◽  
Vol 9 (44) ◽  
pp. 25627-25637 ◽  
Author(s):  
Ma. Oumezzine ◽  
Herbet Bezerra Sales ◽  
Ahmed Selmi ◽  
E. K. Hlil

Bulk nanocrystalline samples of (La1−xPrx)0.67Ba0.33MnO3 (0.075 ≤ x ≤ 0.30) manganites with a fixed carrier concentration are prepared by the sol–gel based Pechini method.


2012 ◽  
Vol 229 ◽  
pp. 290-293 ◽  
Author(s):  
A.M. Huízar-Félix ◽  
T. Hernández ◽  
S. de la Parra ◽  
J. Ibarra ◽  
B. Kharisov

2009 ◽  
Vol 66 ◽  
pp. 167-170 ◽  
Author(s):  
Zhen Zhong Zhang ◽  
Ji Hong Zhang ◽  
Wei Zhou ◽  
Ming Xia Song ◽  
Wei Li ◽  
...  

Er3+/Yb3+ co-doped TiO2 nanocrystals were prepared by Sol-gel method in which titanium tetrachloride was adopted as the precursor. The structure, particle size, and optical properties of samples were characterized by X-ray diffraction(XRD), Field emission-Scanning Electron Microscopy(FE-SEM) and photoluminescence(PL) spectra. Er3+ concentration was fixed at 1.0mol%, and Yb3+ concentration was changed from 3 to 10mol%. Intense upconversion luminescence was observed when the samples were excited by 980nm laser. The dependence of upconversion luminescence on Yb3+ concentration was presented. The results show that the upconversion luminescence increases with the Yb3+ concentration and gets its peak at 5%. The ratio of red emission to green emission(R/G) was strikingly enhanced with the increase of Yb3+ concentration. Under the excitation of 980nm, the green emission in the range of 520-570nm (2H11/2, 4S3/2→4I15/2) and the red emission in the range of 640~690nm (4F9/2 →4I15/2) are both due to two photons process. The possible upconversion mechanism was discussed.


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.


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