scholarly journals Synthesis of BiVO4 nanoparticles by the co-precipitation method and study the crystal structure, optical and photocatalytic properties of them

2020 ◽  
Vol 28 (3) ◽  
pp. 797-806
Author(s):  
نسرین قزکوب ◽  
مرتضی زرگرشوشتری ◽  
ایرج کاظمی‌نژاد ◽  
سید محمد لاری بقال ◽  
◽  
...  
2019 ◽  
Vol 546 (1) ◽  
pp. 48-56
Author(s):  
Ze Wu ◽  
Yang Song ◽  
Ruonan Zhang ◽  
Lianwei Shan ◽  
Limin Dong ◽  
...  

2019 ◽  
Vol 75 (5) ◽  
pp. 589-597 ◽  
Author(s):  
Dinu Alexander ◽  
Kukku Thomas ◽  
Monu Joy ◽  
P. R. Biju ◽  
N. V. Unnikrishnan ◽  
...  

The structural features leading to the intense quenching free luminescence exhibited by europium oxalate nanocrystals, poly[[hexaaquatri-μ2-oxalato-dieuropium] 4.34-hydrate], {[Eu2(C2O4)3(H2O)6]·4.34H2O} n , is the focal point of this report. Europium oxalate nanocrystals were synthesized by a simple microwave-assisted co-precipitation method. Powder X-ray diffraction analysis revealed the monoclinic structure of the nanocrystals and the phase purity. The morphology and particle size were examined by transmission electron microscopy (TEM) analysis. Luminescence measurements on a series of samples of La2–x Eu x (C2O4)3·10H2O, with x varying in the range 0.1 to 2, established the quenching free nature exhibited by the europium oxalate nanocrystals. A single-crystal structure analysis was carried out and the quenching free luminescence is explained on the basis of the crystal structure. A detailed photoluminescence characterization was carried out using excitation and emission studies, decay analysis, and CIE coordinate and colour purity evaluation. The various spectroscopic parameters were evaluated by Judd–Ofelt theoretical analysis and the results are discussed on the basis of the crystal structure analysis.


2019 ◽  
Vol 45 (17) ◽  
pp. 21768-21772 ◽  
Author(s):  
Tien A. Nguyen ◽  
Vinh N.T. Pham ◽  
Hanh T. Le ◽  
Diem H. Chau ◽  
V.O. Mittova ◽  
...  

2014 ◽  
Vol 602-603 ◽  
pp. 110-113 ◽  
Author(s):  
Yan Juan Li ◽  
Ying Chun Zhang ◽  
Jia Xun Leng

In this paper, yttrium aluminum garnet (YAG) powders were synthesized by the normal-strike co-precipitation method (adding precipitant solution to the metal nitrate solution). Aluminum nitrate (Al (NO3)39H2O) and yttrium nitrate (Y(NO3)36H2O) were used as raw materials and ammonium hydrogen carbonate (AHC) was used as the precipitant. The precursor was calcined at the temperature of 900-1200 °C for 2 hours. The crystal structure and microstructure of YAG powders were investigated and analyzed by XRD, FESEM, TG-DTA and laser particle size analysis. The results show that the concentration of metal ion and AHC have a significant effect on crystal structure of YAG powders, and pure YAG powders were obtained at 1000 °C when the concentration of Al3+was 0.1 mol/L and the concentration of AHC was 1 mol/L. The average primary crystallites particle sizes were ranged from 50 nm to100 nm in diameter. nanosize YAG powders with excellent properties and good dispersity can be produced at the temperature of 1100 °C.


2019 ◽  
Vol 96 ◽  
pp. 105922 ◽  
Author(s):  
A.T. Nguyen ◽  
Vinh N.T. Pham ◽  
T. Tr L. Nguyen ◽  
V.O. Mittova ◽  
Q.M. Vo ◽  
...  

2014 ◽  
Vol 1033-1034 ◽  
pp. 1172-1175
Author(s):  
Li Ping Lin ◽  
Feng Hua Huang ◽  
Pei Feng Chen

The water-soluble ZnSe:Ag quantum dots were synthesized in aqueous medium by chemical co-precipitation method with L-cysteine as surface modifier. The crystal structure and optical properties of the obtained ZnSe:Ag quantum dots have been characterized by X-ray power diffraction, infrared spectrum, UV-Vis absorption spectrum and photoluminescence spectrum. Results indicate that ZnSe:Ag quantum dots belong to the cubic blende structure and have good fluorescent characteristics. The L-cysteine modified on the surface of ZnSe:Ag quantum dots renders the quantum dots water-soluble, biocompatible.


2015 ◽  
Vol 1112 ◽  
pp. 19-22
Author(s):  
Umi Nuraini ◽  
Lita Amalia ◽  
Kurniawati C. Rosyidah ◽  
M. Zainuri

Synthesis of Zn doped Barium M-Hexaferrite (BaFe12-xZnxO19) has been performed by co-precipitation method. The purified iron sand from Tulungagung is used as a precursor of Fe3O4. Synthesis of Zn doped Barium M-Hexaferrite (BaFe12-xZnxO19) with variations of x = 0.3, 0.5, and 0.7 wt % has been calcined at temperatures of 1000°C for 5 hours. Ion Zn2+ (with 0 ≤ x ≤ 0.7 wt %) does not change the crystal structure of Barium M-Hexaferrite (BaM), but give a slight displacement of the peak position of the diffraction pattern. SEM figures showed that Zn doped Barium M-Hexaferrite (BaFe12-xZnxO19) have a hexagonal structure, similar to BaM structure. Doping of Zn has changed the magnetic properties of Barium M-Hexaferrit (BaM), from hard magnetic become soft magnetic. Barium M-Hexaferrit (BaM) has a value of Coercivity Field (Hc) and Remanence Magnetization (Mr) is 0.03734 T and 8.334 emu/g. At variation x = 0.3, the Remanence Magnetization (Mr) reaches the highest value. At this point, a value of Coercivity Field (Hc) and Remanence Magnetization (Mr) is 0.0506 T and 14.782 emu/gram respectively.


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