Fabrication of chiral plasmonic oligomers using cysteine-modified gold nanorods as monomers

被引:40
作者
Hou, Shuai [1 ,2 ]
Wen, Tao [1 ,2 ]
Zhang, Hui [1 ,2 ]
Liu, Wenqi [1 ,2 ]
Hu, Xiaona [1 ,2 ]
Wang, Rongyao [3 ]
Hu, Zhijian [1 ]
Wu, Xiaochun [1 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Key Lab Standardizat & Measurement Nanotechno, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Beijing Inst Technol, Minist Educ, Sch Phys, Key Lab Cluster Sci, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
chiral nanostructures; circular dichroism; gold nanorods; plasmon coupling; self-assembly; CIRCULAR-DICHROISM; OPTICAL-ACTIVITY; NANOPARTICLES; ASSEMBLIES; NANOSTRUCTURES; NANOCRYSTALS; DISCRETE; DIMERS;
D O I
10.1007/s12274-014-0530-z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Generation of circular dichroism (CD) beyond the UV region is of great interest in developing chiral sensors and chiroptical devices. Herein, we demonstrate a simple and versatile method for fabrication of plasmonic oligomers with strong CD response in the visible and near IR spectral range. The oligomers were fabricated by triggering the side-by-side assembly of cysteine-modified gold nanorods. The modified nanorods themselves did not exhibit obvious plasmonic CD signals; however, the oligomers show strong CD bands around the plasmon resonance wavelength. The sign of the CD band was dictated by the chirality of the absorbed cysteine molecules. By adjusting the size of the oligomers, the concentration of chiral molecules, and/or the aspect ratio of the nanorods, the CD intensity and spectral range were readily tunable. Theoretical calculations suggested that CD of the oligomers originated from a slight twist of adjacent nanorods within the oligomer. Therefore, we propose that the adsorbed chiral molecules are able to manipulate the twist angles between the nanorods and thus modulate the CD response of the oligomers.
引用
收藏
页码:1699 / 1705
页数:7
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