Branched wires of CdTe nanocrystals using amphiphilic molecules as templates

被引:35
作者
Zhang, L
Gaponik, N
Müller, J
Plate, U
Weller, H
Erker, G
Fuchs, H
Rogach, AL
Chi, LF
机构
[1] Univ Munster, Inst Phys, D-48149 Munster, Germany
[2] Ctr Nanotechnol CeNTech, D-48149 Munster, Germany
[3] Univ Hamburg, Inst Phys Chem, D-20146 Hamburg, Germany
[4] Univ Munster, Organ Chem Inst, D-48149 Munster, Germany
[5] Klin & Poliklin Mund & Kiefer Gesichtschirurg, D-48129 Munster, Germany
[6] Univ Munich, Dept Phys, D-80799 Munich, Germany
[7] Univ Munich, CeNS, D-80799 Munich, Germany
关键词
chirality; interfaces; monolayers; nanocrystals; nanowires;
D O I
10.1002/smll.200400148
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The preparation of branched wires comprised of luminescent CdTe nanocrystals (NC) by Langmuir-monolayer-guided self-assembly using C12-(L)Cys-(L)Cys-C18 molecular aggregates as templates was analyzed. This process exemplifies the ability of NCs to self-organize into a superstructure due to intrinsic anisotropy of inter-nanocrystal interactions. Due to the availability of SH groups in the hydrophilic heads of the C12-(L)Cys-(L)Cys-C18 molecule, it was anticipated that possibility of using molecular aggregates as templates to assemble NCs into wires. The separated rigid wires of approximate 10 nm in width and up to 2 μm in length was observed at low surface pressure. The use of self-patterned molecular aggregates as templates for interfacial assembly can provide general method to organize metal or semiconductor NCs in a pre-designed way. The results show that the formation of rigid, single wires at higher surface density is presumed to be caused by cooperative molecule-to-molecule.
引用
收藏
页码:524 / 527
页数:4
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