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Unidirectionally propagated electromagnetic waves are rare in nature but heavily sought after due to their potential applications in backscatter-free optical information processing setups. It was theoretically shown that the distinct bulk optical band topologies of a gyrotropic metal and an isotropic metal can enable topologically protected unidirectional surface plasmon polaritons (SPPs) at their interface. Here, we experimentally identify such interfacial modes at terahertz frequencies. Launching the interfacial SPPs via a tailored grating coupler, the far-field spectroscopy data obtained reveals strongly nonreciprocal SPP dispersions that are highly consistent with the theoretical predictions. The directionality of the interfacial SPPs studied here is flexibly tunable by either varying the external field or adjusting the metallic characteristics of the bulk materials. The experimental realization of actively tunable unidirectional SPPs sets the foundation for developing nanophotonic information processing devices based on topologically protected interfacial waves.
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Controlled orientation and alignment of rod‐shaped plasmonic nanoparticles are of great interest for many applications. Herein, it is demonstrated that the nonlinear optical response of gold nanorod suspensions is dynamically controlled by electric field‐induced orientation. Merely by switching incident light polarization, the longitudinal and transverse surface plasmon resonance (SPR) absorption peaks are modulated with opposite trends, and the resulting optical nonlinearity is revealed from self‐trapping of plasmonic resonant solitons. Moreover, even with a very low concentration of fluorescent molecules, a significant increase in the fluorescent signal is observed with a transmittance‐type volume detection scheme. Such an enhancement is attributed to a combined action of optical force‐induced nonlinearity and electric field‐induced nanorod orientation, as explained by the theoretical analyses. Herein, new possibilities for engineering nonlinear plasmonic soft matter and detecting low‐concentration (yet a large total number of moleculesas needed) fluorescent samples are brought out.
