Silver nanowires (Ag NWs) present prominent waveguiding properties of subwavelength light due to their nanoconfinement with propagating surface plasmons, which is of great importance for on-chip integration of nanophotonic devices and optical computation. Such propagating plasmons also exert plasmonic forces, which can be utilized to manipulate nanoparticles (NPs) beyond the diffraction limit. However, such controllability is spatially limited to the near fields, whereas a large portion of uncontrolled particles are randomly deposited on the chips, which could be detrimental to the integrated optical devices. Herein we shine continuous wave laser at one end of the Ag NW immersed in AgNO3 solution to launch the propagating surface plasmons. The laser irradiation also induces the photoreduction of Ag+ ions to locally generate tiny Ag NPs, which evolve into large Ag flake branches closer to the other end of the Ag NW. Such a peculiar growth is due to the synergistic effect of plasmonic forces and the thermophoretic/thermo-osmosis forces induced by temperature gradient. These branched Ag NWs with sharp angles are intrinsically chiral, which can be partially controlled by changing the irradiation location, forming plasmonic chiral enantiomers. The circular differential scattering (CDS) response of these branched Ag NWs can be as large as 40%, which can be used for chiral enantiomer sensing with spectral dissymmetric factor up to 4 nm induced by phenylalanine. This plasmon-directed on-wire growth not only offers a facile approach for generating plasmonic chiral nanostructures with remote controllability, but also provides significant insights on the synergistic effect of plasmonic forces and thermal-induced forces, which has great implications for self-assembly and integration of on-chip optics.
Keywords: chirality; circular differential scattering; plasmonic forces; surface plasmon polaritons; thermophoretic forces.