Metal selenobenzoate complexes: Novel single source precursors for the synthesis of metal selenide semiconductor nanomaterials

被引:13
|
作者
Khan, Malik Dilshad [1 ,3 ]
Aamir, Muhammad [2 ]
Akhtar, Javeed [2 ]
Malik, Mohammad Azad [3 ]
Revaprasadu, Neerish [1 ]
机构
[1] Univ Zululand, Dept Chem, Private Bag X1001, ZA-3880 Kwa Dlangezwa, South Africa
[2] Mirpur Univ Sci & Technol, Dept Chem, Mat Lab, Allama Iqbal Rd, Mirpur Ajk, Pakistan
[3] Univ Manchester, Sch Mat, Oxford Rd, Manchester M13 9PL, Lancs, England
基金
新加坡国家研究基金会;
关键词
Silver and Gold nanoparticles; CHEMICAL-VAPOR-DEPOSITION; THIN-FILMS; ELECTRONIC-STRUCTURE; TIN SELENIDE; PHASE; SULFIDE; NANOPARTICLES; NANOCRYSTALS; BI2S3; SHAPE;
D O I
10.1016/j.matpr.2019.02.190
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nanomaterials synthesis using single source precursors is a fascinating development in material science. The shape and size dependent properties offer countless opportunities for interesting discoveries, but also poses challenges to the scientific community to control the shape and size of these materials. Selenocarboxylate complexes are difficult to synthesize, due to the instability of selenocarboxylic acids. In this study, we have developed an efficient one-pot synthesis of the selenobenzoate ligand and its three new metal complexes, tris(selenobenzoato) antimony(III), tris(selenobenzoato) bismuth(III) and bis(selenobenzoato) dibutyltin(IV). The complexes were used as single source precursors to synthesize Sb2Se3 nanorods, Bi2Se3 and SnSe nanosheets by colloidal thermolysis using the hot injection method. The as-synthesized nanomaterials were characterized by p-XRD, TEM, SAED and HRTEM techniques. The complexes were synthesized by a facile method with high yields and are stable at room temperature for period of several months, We believe that the selenobenzoate complexes with other metals can also be synthesized by using our method and those complexes can be useful precursors for metal selenide thin films or nanoparticles. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:66 / 74
页数:9
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