B-site modified photoferroic Cr3+-doped barium titanate nanoparticles: microwave-assisted hydrothermal synthesis, photocatalytic and electrochemical properties

被引:62
作者
Amaechi, I. C. [1 ]
Kolhatkar, G. [1 ]
Youssef, A. Hadj [1 ]
Rawach, D. [2 ]
Sun, S. [1 ]
Ruediger, A. [1 ]
机构
[1] Inst Natl Rech Sci, Ctr Enegie Mat Telecommun INRS EMT, 1650 Blvd Lionel Boulet, Varennes, PQ J3X 1S2, Canada
[2] Univ Sherbrooke, Fac Sci, Dept Chim, 2500 Blvd Univ, Sherbrooke, PQ J1K 2R1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
BATIO3; FERROELECTRICS; PARTICLES; COMPOSITE; EVOLUTION; PRESSURE; WATER; SIZE; CR;
D O I
10.1039/c9ra03439k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report on the synthesis of photoferroic Cr3+-doped BaTiO3 nanoparticles with nominal Cr content ranging from 2-8 mol% by a microwave-assisted hydrothermal method. The absorption properties of the doped systems are significantly enhanced due to the d-d band transition of Cr3+/4+. The structural properties of the materials are examined on the basis of lattice distortions given by the tolerance factor and microstrain. Raman scattering provides complementary information on the lattice vibrations indicating a softening of the longitudinal optic (LO) phonon mode located at 716 cm(-1) with increasing Cr concentration. The charge transport properties investigated through electrochemical impedance spectroscopy (EIS) demonstrate that there is a reduction in the charge transfer resistance from 5.2 omega to 4.3 omega for the undoped and 4 mol% Cr3+-doped respectively, which favors the degradation kinetics. The photo-oxidation ability of the systems is evaluated by time evolution of photodegradation of methyl orange under standardized solar irradiation. The experimental results confirm that the best photocatalytic performance is achieved with the 4 mol% Cr3+-doped BaTiO3 nanoparticles, which is similar to 2.7 times higher than for the undoped sample. Evidence of superoxide radical being the dominant active species is provided by in situ reactive oxide species (ROS) capture experiments.
引用
收藏
页码:20806 / 20817
页数:12
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