TY - JOUR
T1 - Fano Resonance in Asymmetric Plasmonic Nanostructure
T2 - Separation of Sub-10 nm Enantiomers
AU - Cao, Tun
AU - Mao, Libang
AU - Qiu, Yimei
AU - Lu, Li
AU - Banas, Agnieszka
AU - Banas, Krzysztof
AU - Simpson, Robert E.
AU - Chui, Hsiang Chen
N1 - Funding Information:
This work was supported by International Science & Technology Cooperation Program of China (Grant No. 2015DFG12630), A-Star Singapore–China Joint Research Program (1420200046), and Program for Liaoning Excellent Talents in University (Grant No. LJQ2015021). L.L. acknowledges his Ministry of Education (MoE) studentship. The authors acknowledge the Singapore Synchrotron Light Source (SSLS) for providing the facility necessary for conducting the research. The laboratory is a National Research Infrastructure under the National Research Foundation Singapore.
Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/2/5
Y1 - 2019/2/5
N2 - Separating enantiomers is vital in chemical syntheses, life sciences, and physics. However, the usual chemical processes are inefficient. Recently, plasmonic nanostructures have drawn considerable attention for manipulating nanoparticles; however, only a few approaches are proposed to discriminate between entities that differ in terms of their handedness. This is because the chiral polarizability is much smaller than the electric polarizability, and therefore the non-chiral gradient force dominates over the chiral gradient force. This limit means that the enantioselective sorting of chiral nanoparticles is a formidable challenge. A plasmonic nanostructure consisting of a disc-double split ring resonator exhibiting a dipole–octupole (DO) Fano resonance (FR) is designed and fabricated. It is theoretically demonstrated that such a DO-FR can markedly enhance the chiral gradient force on the paired enantiomers. The coaxial channel of the resonator possessing high chirality density gradients around the DO-FR is derived. This provides an enhanced chiral gradient force that dominates over the non-chiral gradient forces on sub-10 nm chiral nanoparticles. Enantiomeric pairs can thus experience distinct potential wells in terms of signs. This proposed structure may advance the techniques of enantiopurification and enantioseparation, bringing a new perspective to state-of-the-art all-optical enantiopure synthesis.
AB - Separating enantiomers is vital in chemical syntheses, life sciences, and physics. However, the usual chemical processes are inefficient. Recently, plasmonic nanostructures have drawn considerable attention for manipulating nanoparticles; however, only a few approaches are proposed to discriminate between entities that differ in terms of their handedness. This is because the chiral polarizability is much smaller than the electric polarizability, and therefore the non-chiral gradient force dominates over the chiral gradient force. This limit means that the enantioselective sorting of chiral nanoparticles is a formidable challenge. A plasmonic nanostructure consisting of a disc-double split ring resonator exhibiting a dipole–octupole (DO) Fano resonance (FR) is designed and fabricated. It is theoretically demonstrated that such a DO-FR can markedly enhance the chiral gradient force on the paired enantiomers. The coaxial channel of the resonator possessing high chirality density gradients around the DO-FR is derived. This provides an enhanced chiral gradient force that dominates over the non-chiral gradient forces on sub-10 nm chiral nanoparticles. Enantiomeric pairs can thus experience distinct potential wells in terms of signs. This proposed structure may advance the techniques of enantiopurification and enantioseparation, bringing a new perspective to state-of-the-art all-optical enantiopure synthesis.
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U2 - 10.1002/adom.201801172
DO - 10.1002/adom.201801172
M3 - Article
AN - SCOPUS:85057747431
SN - 2195-1071
VL - 7
JO - Advanced Optical Materials
JF - Advanced Optical Materials
IS - 3
M1 - 1801172
ER -