Synthesis and characterization of low dimensional ZnS- and PbS-semiconductor particles on a montmorillonite template

被引:17
作者
Jankovic, Lubos [1 ,2 ]
Dimos, Konstantinos [2 ]
Bujdak, Juraj [1 ]
Koutselas, Ioannis [2 ,3 ]
Madejova, Jana [1 ]
Gournis, Dimitrios [2 ]
Karakassides, Michael A. [2 ]
Komadel, Peter [1 ]
机构
[1] Slovak Acad Sci, Inst Inorgan Chem, SK-84536 Bratislava, Slovakia
[2] Univ Ioannina, Dept Mat Sci & Engn, GR-45110 Ioannina, Greece
[3] Univ Patras, Dept Mat Sci, GR-26504 Patras, Greece
关键词
SOCIETY SOURCE CLAYS; CADMIUM-SULFIDE; MAGNETIC-PROPERTIES; OPTICAL-PROPERTIES; LAYERED CLAYS; BASE-LINE; CDS; MINERALS; NANOCOMPOSITES; NANOPARTICLES;
D O I
10.1039/c002891f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Low dimensional metal sulfide particles have been prepared in the interlayers of montmorillonites via reactions of the metal ion-exchanged clay minerals in aqueous dispersions with gaseous hydrogen sulfide. The montmorillonites separated from the Wyoming (USA) and Jelsovy Potok (Slovakia) bentonites were saturated with Pb2+ or Zn2+. In the final nanohybrids, the smectite mineral can be incorporated with metal sulfide pillars and/or nanoparticles. Properties of the prepared materials were investigated by various analytical techniques. The formation of metal sulfide nanoparticles in the interlayer galleries was indicated by X-ray diffraction and energy dispersive X-ray analysis. About 50% of Pb2+ or Zn2+ present in montmorillonite has formed metal sulfide semiconducting units. Infrared spectroscopy and thermogravimetric analysis were used for characterization of starting materials and products. Ultraviolet-visible absorption and photoluminescence spectroscopies confirmed that final composite systems acquired the optical properties of the incorporated quantum low dimensional systems exhibiting blue shift of the energy gap and higher oscillator strength excitonic peaks. Larger amounts of metal sulfide nanoparticles were formed in montmorillonite Jelsovy Potok probably as a consequence of its higher cation exchange capacity.
引用
收藏
页码:14236 / 14244
页数:9
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