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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. 

It was demonstrated recently that the nano-optical and nanoelectronic properties of VO₂can be spatially programmed through the local injection of oxygen vacancies by atomic force microscope writing. In this work, we study the dynamic evolution of the patterned domain structures as a function of the oxygen vacancy concentration and the time. A threshold doping level is identified that is critical for both the metal–insulator transition and the defect stabilization. The diffusion of oxygen vacancies in the monoclinic phase is also characterized, which is directly responsible for the short lifetimes of sub-100 nm domain structures. This information is imperative for the development of oxide nanoelectronics through defect manipulations. 

Abstract Multiferroics are a unique class of materials where magnetic and ferroelectric orders coexist. The research on multiferroics contributes significantly to the fundamental understanding of the strong correlations between different material degrees of freedom and provides an energy‐efficient route toward the electrical control of magnetism. While multiple ABO₃oxide perovskites are identified as being multiferroic, their magnetoelectric coupling strength is often weak, necessitating the material search in different compounds. Here, the observation of room‐temperature multiferroic orders in multi‐anion SrNbO_3−xN_xthin films is reported. In these samples, the multi‐anion state enables the room‐temperature ferromagnetic ordering of the Nb d‐electrons. Simultaneously, ferroelectric responses that originate from the structural symmetry breaking associated are found with both the off‐center displacements of Nb and the geometric displacements of Sr, depending on the relative O‐N arrangements within the Nb‐centered octahedra. The findings not only diversify the available multiferroic material pool but also demonstrate a new multiferroism design strategy via multi‐anion engineering.