Ma, WeiKuang, HuaWang, LibingXu, LiguangChang, Wei-ShunZhang, HuananSun, MaozhongZhu, YinyueZhao, YuanLiu, LiqiangXu, ChuanlaiLink, StephanKotov, Nicholas A.2013-06-192013-06-192013Ma, Wei, Kuang, Hua, Wang, Libing, et al.. "Chiral plasmonics of self-assembled nanorod dimers." <i>Scientific Reports,</i> 3, (2013) Nature Publishing Group: 1934. http://dx.doi.org/10.1038/srep01934.https://hdl.handle.net/1911/71340Chiral 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.engArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.Journal articlehttp://dx.doi.org/10.1038/srep01934