The assembly of semiconductor sulfide nanocrystallites with organic reagents as templates

被引:35
作者
Lu, QY [1 ]
Gao, F [1 ]
Zhao, DY [1 ]
机构
[1] Fudan Univ, Dept Chem, Mol Catalysis & Innovat Mat Lab, Shanghai 200433, Peoples R China
关键词
D O I
10.1088/0957-4484/13/6/309
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
An organic reagent-assisted method has been developed for the synthesis and assembly of copper sulfide, cadmium sulfide and silver sulfide nanocrystallites at low temperature under hydro- or solvothermal conditions. Nanowire-like aggregates (with an average diameter of 120 nm and length of 2 mum) assembled by digenite phase copper sulfide nanoparticles, nanotube-like aggregates (with diameters ranging from 40 to 200 nm and lengths from 400 nm to 4 mum) and nanovesicle-like aggregates (with size ranging from 50 to 180 nm) assembled using djurleite phase copper sulfide nanoparticles have been obtained using triethylenediamine, tramethylethylenediamine and di-n-butylamine as the linking agents, respectively. A cetyltrimethyl-ammonium bromide-assisted solvothermal process with CdCl2, and thiourea as the reactants and ethylenediamine as the solvent has been proposed to control the length of the US nanorods from 300 nm to 4.5 mun and construct novel US nanorod-based structures, including polydentate wire-like architectures and polydentate sphere-like architectures composed of dozens of US nanorods of 10 nm in width and 100 nm in length. A CH3(CH2)(11) SH-template method has been adopted to realize the synthesis and the simultaneous assembly of silver sulfide nanocrystallites with AgNO3 and Na2S as reactants. By changing the reaction temperature and the dodecylthiol concentration, two-dimensional orthogonal and hexagonal-like ordered silver sulfide nanoparticle arrays and quasi-orthogonal silver sulfide nanorod arrays can be obtained. This organic reagent-assisted route is very simple and can be extended to the synthesis and assembly of other semiconductor sulfide nanocrystals.
引用
收藏
页码:741 / 745
页数:5
相关论文
共 44 条
[1]   Self-assembly of a two-dimensional superlattice of molecularly linked metal clusters [J].
Andres, RP ;
Bielefeld, JD ;
Henderson, JI ;
Janes, DB ;
Kolagunta, VR ;
Kubiak, CP ;
Mahoney, WJ ;
Osifchin, RG .
SCIENCE, 1996, 273 (5282) :1690-1693
[2]   Structure and dynamics in alkanethiolate monolayers self-assembled on gold nanoparticles: A DSC, FT-IR, and deuterium NMR study [J].
Badia, A ;
Cuccia, L ;
Demers, L ;
Morin, F ;
Lennox, RB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (11) :2682-2692
[3]  
Brinker CJ, 1999, ADV MATER, V11, P579, DOI 10.1002/(SICI)1521-4095(199905)11:7<579::AID-ADMA579>3.0.CO
[4]  
2-R
[5]   Controlled growth of gold nanoparticles during ligand exchange [J].
Brown, LO ;
Hutchison, JE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (04) :882-883
[6]   NOVEL GOLD-DITHIOL NANO-NETWORKS WITH NONMETALLIC ELECTRONIC-PROPERTIES [J].
BRUST, M ;
BETHELL, D ;
SCHIFFRIN, DJ ;
KIELY, CJ .
ADVANCED MATERIALS, 1995, 7 (09) :795-&
[7]   Fabrication and alignment of wires in two dimensions [J].
Chung, SW ;
Markovich, G ;
Heath, JR .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (35) :6685-6687
[8]   Bacterial templating of ordered macrostructures in silica and silica-surfactant mesophases [J].
Davis, SA ;
Burkett, SL ;
Mendelson, NH ;
Mann, S .
NATURE, 1997, 385 (6615) :420-423
[9]   Highly oriented molecular Ag nanocrystal arrays [J].
Harfenist, SA ;
Wang, ZL ;
Alvarez, MM ;
Vezmar, I ;
Whetten, RL .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (33) :13904-13910
[10]   Infrared spectroscopy of three-dimensional self-assembled monolayers: N-alkanethiolate monolayers on gold cluster compounds [J].
Hostetler, MJ ;
Stokes, JJ ;
Murray, RW .
LANGMUIR, 1996, 12 (15) :3604-3612