Use of ionic liquids in the synthesis of nanocrystals and nanorods of semiconducting metal chalcogenides

被引:126
作者
Biswas, Kanishka
Rao, C. N. R.
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, DST Unit Nanosci, Bangalore 560064, Karnataka, India
[2] Jawaharlal Nehru Ctr Adv Sci Res, CSIR, Ctr Excellence Chem, Bangalore 560064, Karnataka, India
[3] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
关键词
ionic liquids; metal chalcogenides; nanocrystals; nanorods; nanostructures;
D O I
10.1002/chem.200601733
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have synthesized nanoparticles of hexagonal US in the diameter range 3-13 nm by the reaction of cadmium acetate dihydrate with thioacetamide in imidazolium [BMIM]-based ionic liquids. We have obtained three different particle sizes of CdS by changing the anion of the ionic liquid. Addition of trioctylphosphine oxide (TOPO) to the reaction mixture causes greater monodispersity as well as smaller particle size, while addition of ethylenediamine produces nanorods of 7 nm average diameter. Hexagonal ZnS and cubic PbS nanoparticles with average diameters of 3 and 10 nm, respectively, have been prepared by the reaction of the metal acetates with thioacetamide in [BMIM][BF4]. Hexagonal CdSe nanoparticles with an average diameter 12 nm were obtained by the reaction of cadmium acetate dihydrate with dimethylselenourea in [BMIM][BF4]. In this case also we observe the same effect of the addition of TOPO as in the case of CdS. Addition of ethylenediamine to the reaction mixture gives rise to nanorods. ZnSe nanowires with a cubic structures, possible diameters in the range 70-100 nm by the reaction of zinc acetate dihydrate with dimethylselenourea in [BMIM][MeSO4]. The nanostructures obtained are single crystalline in all the cases. Most of the nanostructures show characteristic UV/Vis absorption and photoluminescence emission spectra. The thermodynamically most stable structures are generally produced in the synthesis carried out in ionic liquids.
引用
收藏
页码:6123 / 6129
页数:7
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