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Magnetic and photocatalytic properties of nano-sized sulfur-doped trirutile oxide, CuSb2O6
被引:10
作者:
Atri, Shalu
[1
]
Uma, Sitharaman
[1
]
Nagarajan, Rajamani
[1
]
机构:
[1] Univ Delhi, Mat Chem Grp, Dept Chem, Delhi 110007, India
关键词:
Semiconductors;
Chemical synthesis;
X-ray diffraction;
Raman spectroscopy;
Magnetic properties;
HYDROTHERMAL SYNTHESIS;
ELECTRONIC-STRUCTURE;
CRYSTAL-STRUCTURE;
SOLID-STATE;
LIGHT;
NANOPARTICLES;
NANOCRYSTALS;
DEGRADATION;
CONVERSION;
EVOLUTION;
D O I:
10.1016/j.mssp.2020.105226
中图分类号:
TM [电工技术];
TN [电子技术、通信技术];
学科分类号:
0808 ;
0809 ;
摘要:
Sulfur-doped trirutile-structured CuSb2O6 was realized by single-step oxidation of Chalcostibite (CuSbS2) with the hydrogen peroxide solution. Its powder X-ray diffraction pattern confirmed the alpha-polymorphic form of CuSb2O6, with a crystallite size of 6 nm, corroborating well with tetragonal symmetry observed in lattice fringes and SAED pattern. The TEM-EDS analysis indicated sulfur doping in the sample. The dopant amount quantified using thermogravimetric and XPS analysis. The sulfide doping caused the reduction of some amounts of Cu2+ to Cu+ with a noticeable decrease in the bandgap as compared to undoped beta-CuSb2O6. The positive slope in the Williamson-Hall plot of sulfur-doped sample implied tensile strain. The short-range antiferromagnetic interaction of Cu2+ was absent in the magnetic measurements of the sample. Instead, it displayed a paramagnetic behavior down to 2 K. Change in electronic structure coupled with the high surface area of 203 m(2)/g introduced catalytic property in the sample for the photodegradation of carcinogenic rhodamine 6G (Rh 6G) spanning four cycles consecutively. During these experiments, no alteration of catalyst structure was visible.
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页数:9
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