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Preparation of nanodispersed fluorite-type Sr1-xRxF2+x(R=Er, Yb, Ho) phases from citrate solutions
被引:14
|作者:
Fedorov, Pavel P.
[1
,3
]
Luginina, Anna A.
[1
,2
]
Ermakova, Julia A.
[1
]
Kuznetsov, Sergey V.
[1
]
Voronov, Valery V.
[1
]
Uvarov, Oleg V.
[1
]
Pynenkov, Alexandr A.
[3
]
Nishchev, Konstantin N.
[3
]
机构:
[1] RAS, AM Prokhorov Gen Phys Inst, Ul Vavilova 38, Moscow 119991, Russia
[2] VINITI RAS, All Russian Inst Sci & Tech Informat, Ul Usievicha 20, Moscow 125190, Russia
[3] NP Ogarev Mordovia State Univ, Ul Bolshevistskaya 68, Saransk 430005, Russia
关键词:
Inorganic fluorides;
Nanoparticles;
Solid solutions;
Rare earths;
Chemical synthesis;
Citrate complexe;
UP-CONVERSION NANOPARTICLES;
SOL-GEL;
STRONTIUM FLUORIDE;
AQUEOUS-SOLUTIONS;
OPTICAL CERAMICS;
CITRIC-ACID;
NANOCRYSTALS;
CELLULOSE;
SURFACE;
GROWTH;
D O I:
10.1016/j.jfluchem.2016.12.003
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Fluorite-type Sr1-xRxF2+x (R = Er, Yb, Ho) phases were precipitated from aqueous citrate solutions. Compounds in the series Sr1-xRxF2+x (R = Er, Yb, Ho) formed 5-9 nm weakly-agglomerated powders and/or aqueous colloidal solutions. Surfaces of such nanoparticles were modified in situ by citrate complexes. The phase composition, morphology and size of the formed Sr1-xRxF2+x (R = Er, Yb, Ho) hanoparticles were affected by several factors, including R:citrate and Sr:citrate precursor ratios, pH and initial solution concentrations, choice of fluorinating agent (HF or NH4F), order of starting material addition, thermal treatment conditions, etc. All synthesized specimens were characterized by X-ray powder diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetry analysis (TGA), and transmission electron microscopy (TEM) techniques. (C) 2016 Elsevier B.V. All rights reserved.
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页码:8 / 15
页数:8
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