Circular Gold Nanodisks with Synthetically Tunable Diameters and Thicknesses

被引:63
作者
Cui, Ximin [1 ]
Qin, Feng [1 ]
Ruan, Qifeng [1 ]
Zhuo, Xiaolu [1 ]
Wang, Jianfang [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R China
关键词
anisotropic oxidation; dimers; gold nanodisks; plasmon coupling; plasmon resonance; PLASMON RESONANCES; NANOPARTICLE SYNTHESIS; NANORODS; NANOSTRUCTURES; SHAPE; SCATTERING; ARRAYS; NANOSPHERES; DEVICES; DIMERS;
D O I
10.1002/adfm.201705516
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
2D or pseudo-2D plasmonic Au nanocrystals, such as circular Au nanodisks, possess unique plasmonic properties. Circular Au nanodisks not only possess two large surfaces with circular symmetry but also exhibit the wide tunability for their plasmon resonance. However, the lack of effective synthetic methods for producing size-tunable and monodispersed circular Au nanodisks hinders further studies on their properties and applications. Herein, the synthesis of uniformly sized circular Au nanodisks with synthetically tunable diameters and thicknesses is reported. By performing mild anisotropic oxidation on pregrown Au nanoplates with different thicknesses, the thicknesses of the obtained nanodisks are varied from approximate to 10 nm to approximate to 50 nm. The nanodisk diameters are tailored from approximate to 50 nm to approximate to 150 nm by controlling the oxidation time. Moreover, both homodimers and heterodimers made of circular Au nanodisks are constructed using molecular linkers. They exhibit rich plasmon modes. In particular, dark multipolar plasmon resonance modes can be excited and observed in the asymmetric heterodimers. Such circular Au nanodisks with controllable sizes, large atomically flat surfaces, and a dominant dipolar plasmon mode are ideal building blocks for constructing plasmonic assemblies and plasmon-coupled systems with desired plasmonic properties and functions.
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页数:13
相关论文
共 56 条
[1]   Fluorescence Enhancement at Docking Sites of DNA-Directed Self-Assembled Nanoantennas [J].
Acuna, G. P. ;
Moeller, F. M. ;
Holzmeister, P. ;
Beater, S. ;
Lalkens, B. ;
Tinnefeld, P. .
SCIENCE, 2012, 338 (6106) :506-510
[2]   Polarization Selective Electromagnetic-Induced Transparency in the Disordered Plasmonic Quasicrystal Structure [J].
Amin, Muhammad ;
Khan, Adnan D. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (37) :21633-21638
[3]  
Armelles G, 2013, ADV OPT MATER, V1, P10, DOI [10.1002/adom.201370002, 10.1002/adom.201200011]
[4]   Strongly interacting plasmon nanoparticle pairs: From dipole-dipole interaction to conductively coupled regime [J].
Atay, T ;
Song, JH ;
Nurmikko, AV .
NANO LETTERS, 2004, 4 (09) :1627-1631
[5]  
Atwater HA, 2010, NAT MATER, V9, P205, DOI [10.1038/nmat2629, 10.1038/NMAT2629]
[6]   Encapsulated Annealing: Enhancing the Plasmon Quality Factor in Lithographically-Defined Nanostructures [J].
Bosman, Michel ;
Zhang, Lei ;
Duan, Huigao ;
Tan, Shu Fen ;
Nijhuis, Christian A. ;
Qiu, Cheng-Wei ;
Yang, Joel K. W. .
SCIENTIFIC REPORTS, 2014, 4
[7]   Collective plasmon modes in a compositionally asymmetric nanoparticle dimer [J].
Chen, Fuyi ;
Alemu, Negash ;
Johnston, Roy L. .
AIP ADVANCES, 2011, 1 (03)
[8]   Gold nanoparticles in biomedical applications: recent advances and perspectives [J].
Dykman, Lev ;
Khlebtsov, Nikolai .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (06) :2256-2282
[9]  
Edwardson TGW, 2016, NAT CHEM, V8, P162, DOI [10.1038/NCHEM.2420, 10.1038/nchem.2420]
[10]   CONTROLLED NUCLEATION FOR REGULATION OF PARTICLE-SIZE IN MONODISPERSE GOLD SUSPENSIONS [J].
FRENS, G .
NATURE-PHYSICAL SCIENCE, 1973, 241 (105) :20-22