Browsing by Author "Zhang, Huanan"

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    Chiral plasmonics of self-assembled nanorod dimers
    (Nature Publishing Group, 2013) Ma, Wei; Kuang, Hua; Wang, Libing; Xu, Liguang; Chang, Wei-Shun; Zhang, Huanan; Sun, Maozhong; Zhu, Yinyue; Zhao, Yuan; Liu, Liqiang; Xu, Chuanlai; Link, Stephan; Kotov, Nicholas A.
    Chiral nanoscale photonic systems typically follow either tetrahedral or helical geometries that require four or more different constituent nanoparticles. Smaller number of particles and different chiral geometries taking advantage of the self-organization capabilities of nanomaterials will advance understanding of chiral plasmonic effects, facilitate development of their theory, and stimulate practical applications of chiroplasmonics. Here we show that gold nanorods self-assemble into side-by-side orientated pairs and ‘‘ladders’’ in which chiral properties originate from the small dihedral angle between them. Spontaneous twisting of one nanorod versus the other one breaks the centrosymmetric nature of the parallel assemblies. Two possible enantiomeric conformations with positive and negative dihedral angles were obtained with different assembly triggers. The chiral nature of the angled nanorod pairs was confirmed by 4p full space simulations and the first example of single-particle CD spectroscopy. Self-assembled nanorod pairs and ‘‘ladders’’ enable the development of chiral metamaterials, (bio)sensors, and new catalytic processes.
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    Circular Differential Scattering of Single Chiral Self-Assembled Gold Nanorod Dimers
    (American Chemical Society, 2015) Wang, Lin-Yung; Smith, Kyle W.; Dominiquez-Medina, Sergio; Moody, Nicole; Olson, Jana M.; Zhang, Huanan; Chang, Wei-Shun; Kotov, Nicholas; Link, Stephan; Laboratory for Nanophotonics
    Circular dichroism spectroscopy is essential for structural characterization of proteins and chiral nanomaterials. Chiral structures from plasmonic materials have extraordinary strong circular dichroism effects compared to their molecular counterparts. While being extensively investigated, the comprehensive account of circular dichroism effects consistent with other plasmonic phenomena is still missing. Here we investigated the circular differential scattering of a simple chiral plasmonic system, a twisted side-by-side Au nanorod dimer, using single-particle circular dichroism spectroscopy complimented with electromagnetic simulations. This approach enabled us to quantify the effects of structural symmetry breaking, namely, size-mismatch between the constituent Au nanorods and large twist angles on the resulting circular differential scattering spectrum. Our results demonstrate that, if only scattering is considered as measured by dark-field spectroscopy, a homodimer of Au nanorods with similar sizes produces a circular differential scattering line shape that is different from the bisignate response of the corresponding conventional CD spectrum, which measures extinction, that is, the sum of scattering and absorption. On the other hand, symmetry breaking in a heterodimer with Au nanorods with different sizes yields a bisignate circular differential scattering line shape. In addition, we provide a general method for correcting linear dichroism artifacts arising from slightly elliptically polarized light in a typical dark-field microscope, as is necessary especially when measuring highly anisotropic nanostructures, such as side-by-side nanorods. This work lays the foundation for understanding absorption and scattering contributions to the CD line shape of single chiroplasmonic nanostructures free from ensemble-averaging, especially important for self-assembled chiral nanostructures that usually exist as both enantiomers.