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The terahertz (THz) frequency range is key to studying collective excitations in many crystals and organic molecules. However, due to the large wavelength of THz radiation, the local probing of these excitations in smaller crystalline structures or few-molecule arrangements requires sophisticated methods to confine THz light down to the nanometer length scale, as well as to manipulate such a confined radiation. For this purpose, in recent years, taking advantage of hyperbolic phonon polaritons (HPhPs) in highly anisotropic van der Waals (vdW) materials has emerged as a promising approach, offering a multitude of manipulation options, such as control over the wavefront shape and propagation direction. Here, we demonstrate the THz application of twist-angle-induced HPhP manipulation, designing the propagation of confined THz radiation between 8.39 and 8.98 THz in the vdW material α-molybdenum trioxide (α-MoO3), hence extending twistoptics to this intriguing frequency range. Our images, recorded by near-field optical microscopy, show the frequency- and twist-angle-dependent changes between hyperbolic and elliptic polariton propagation, revealing a polaritonic transition at THz frequencies. As a result, we are able to allocate canalization (highly collimated propagation) of confined THz radiation by carefully adjusting these two parameters, i.e. frequency and twist angle. Specifically, we report polariton canalization in α-MoO3at 8.67 THz for a twist angle of 50°. Our results demonstrate the precise control and manipulation of confined collective excitations at THz frequencies, particularly offering possibilities for nanophotonic applications.

Advances in the field of nanoplasmonics are hindered by the limited capabilities of simulation tools in dealing with realistic systems comprising regions that extend over many light wavelengths. We show that the optical response of unprecedentedly large systems can be accurately calculated by using a combination of surface integral equation (SIE) method of moments (MoM) formulation and an expansion of the electromagnetic fields in a suitable set of spatial wave functions viafast multipole methods. We start with a critical review of volume versussurface integral methods, followed by a short tutorial on the key features that render plasmons useful for sensing (field enhancement and confinement). We then use the SIE-MoM to examine the plasmonic and sensing capabilities of various systems with increasing degrees of complexity, including both individual and interacting gold nanorods and nanostars, as well as large random and periodic arrangements of ∼1000 gold nanorods. We believe that the present results and methodology raise the standard of numerical electromagnetic simulations in the field of nanoplasmonics to a new level, which can be beneficial for the design of advanced nanophotonic devices and optical sensing structures.

Here we report the synthesis of PLGA/DOXO-core Au-branched shell nanostructures (BGNSHs) functionalized with a human serum albumin/indocyanine green/folic acid complex (HSA-ICG-FA) to configure a multifunctional nanotheranostic platform. First, branched gold nanoshells (BGNSHs) were obtained through a seeded-growth surfactant-less method. These BGNSHs were loaded during the synthetic process with the chemotherapeutic drug doxorubicin, a DNA intercalating agent and topoisomerase II inhibitior. In parallel, the fluorescent near-infrared (NIR) dye indocyanine green (ICG) was conjugated to the protein human serum albumin (HSA) by electrostatic and hydrophobic interactions. Subsequently, folic acid was covalently attached to the HSA-ICG complex. In this way, we created a protein complex with targeting specificity and fluorescent imaging capability. The resulting HSA-ICG-FA complex was adsorbed to the gold nanostructures surface (BGNSH-HSA-ICG-FA) in a straightforward incubation process thanks to the high affinity of HSA to gold surface. In this manner, BGNSH-HSA-ICG-FA platforms were featured with multifunctional abilities: the possibility of fluorescence imaging for diagnosis and therapy monitoring by exploiting the inherent fluorescence of the dye, and a multimodal therapy approach consisting of the simultaneous combination of chemotherapy, provided by the loaded drug, and the potential cytotoxic effect of photodynamic and photothermal therapies provided by the dye and the gold nanolayer of the hybrid structure, respectively, upon NIR light irradiation of suitable wavelength. The combination of this trimodal approach was observed to exert a synergistic effect on the cytotoxicity of tumoral cells in vitro. Furthermore, FA was proved to enhance the internalization of nanoplatform. The ability of the nanoplatforms as fluorescence imaging contrast agents was tested by preliminary analyzing their biodistribution in vivoin a tumor-bearing mice model.

A route to produce single crystals of ε-Fe2O3individually wrapped in a silica shell is presented. Formation of ε-Fe2O3/silica nanospheres was achieved by controlled recrystallization of maghemite particles confined in silica shells viacalcination in air. Phase transition was monitored by X-ray diffraction, magnetometry, and transmission electron microscopy. Core−shell nanocomposite particles can be dispersed as a colloidal suspension in several polar liquids enlarging the processability spectrum of the material and thus facilitating the use of ε-Fe2O3in technological applications and its integration in devices.