Ultra long Copper Phthalocyanine Nanowires with New Crystal Structure and Broad Optical Absorption

被引:56
作者
Wang, Hai [3 ,4 ]
Mauthoor, Soumaya [1 ,2 ]
Din, Salahud [1 ,2 ]
Gardener, Jules A. [3 ,4 ]
Chang, Rio [1 ,2 ]
Warner, Marc [3 ,4 ]
Aeppli, Gabriel [3 ,4 ]
McComb, David W. [1 ,2 ]
Ryan, Mary P. [1 ,2 ]
Wu, Wei [3 ,4 ]
Fisher, Andrew J. [3 ,4 ]
Stoneham, Marshall [3 ,4 ]
Heutz, Sandrine [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, London Ctr Nanotechnol, London SW7 2AZ, England
[3] UCL, Dept Phys & Astron, London WC1E 6BT, England
[4] UCL, London Ctr Nanotechnol, London WC1E 6BT, England
基金
英国工程与自然科学研究理事会;
关键词
nanowire; phthalocyanine; organic vapor phase deposition; polymorph; molecular magnetism; molecular optoelectronics; TRANSISTORS; GROWTH; SPECTRA; FILMS;
D O I
10.1021/nn100782w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of molecular nanostructures plays a major role in emerging organic electronic applications, as it leads to improved performance and is compatible with our increasing need for miniaturization. In particular, nanowires have been obtained from solution or vapor phase and have displayed high conductivity or large interfacial areas in solar cells. In all cases however, the crystal structure remains as in films or bulk, and the exploitation of wires requires extensive postgrowth manipulation as their orientations are random. Here we report copper phthalocyanine (CuPc) nanowires with diameters of 10-100 nm, high directionality, and unprecedented aspect ratios. We demonstrate that they adopt a new crystal phase, designated eta-CuPc, where the molecules stack along the long axis. The resulting high electronic overlap along the centimeter length stacks achieved in our wires mediates antiferromagnetic couplings and broadens the optical absorption spectrum. The ability to fabricate ultralong, flexible metal phthalocyanine nanowires opens new possibilities for applications of these simple molecules.
引用
收藏
页码:3921 / 3926
页数:6
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