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This Perspective surveys the state-of-the-art and future prospects of science and technology employing nanoconfined light (nanophotonics and nanoplasmonics) in combination with magnetism. We denote this field broadly as nanoscale magnetophotonics. We include a general introduction to the field and describe the emerging magneto-optical effects in magnetoplasmonic and magnetophotonic nanostructures supporting localized and propagating plasmons. Special attention is given to magnetoplasmonic crystals with transverse magnetization and the associated nanophotonic non-reciprocal effects and to magneto-optical effects in periodic arrays of nanostructures. We also give an overview of the applications of these systems in biological and chemical sensing, as well as in light polarization and phase control. We further review the area of nonlinear magnetophotonics, the semiconductor spin-plasmonics, and the general principles and applications of opto-magnetism and nano-optical ultrafast control of magnetism and spintronics. [ABSTRACT FROM AUTHOR]

Electron energy-loss spectroscopy, interband, plasmons, self-coupling, strong coupling Keywords: electron energy-loss spectroscopy; interband; plasmons; self-coupling; strong coupling EN electron energy-loss spectroscopy interband plasmons self-coupling strong coupling 1 1 1 01/23/23 20230115 NES 230115 In nickel, which is both a ferromagnet and a catalyst, electronic interband transitions (pictured in green) couple strongly to both propagating (in nanofilms) and localized (in nanostructures, controlled by their size) surface plasmons (pictured as red/blue charge oscillations), creating new hybrid matter states - plasmon-interband polaritons - with potentially very intriguing properties and applications in photocatalysis and magneto-optics. For further information, see article number 2201971 by Alexandre Dmitriev, Søren Raza, and co-workers. [Extracted from the article]

Nanophotonic chiral antennas exhibit orders of magnitude higher circular dichroism (CD) compared to molecular systems. When the structural chirality is merged with magnetism at the nanoscale, efficient magnetic control over the dichroic response is achieved, bringing exciting prospects to active nanophotonic devices. Here, we devise macroscopic enantiomeric magnetophotonic metasurfaces of plasmonic-ferromagnetic spiral antennas assembled on large areas via hole-mask colloidal lithography. The simultaneous presence of 3D- and 2D-features in chiral nanoantennas induces large CD response, where we identify reciprocal and non-reciprocal contributions, respectively. Exploring further this type of magnetophotonic metasurfaces might allow the realization of high-sensitivity chiral sensors and prompts the design of advanced macroscopic optical devices operating with polarized light. [ABSTRACT FROM AUTHOR]

Structured solid targets are widely investigated to increase the energy absorption of high-power laser pulses so as to achieve efficient ion acceleration. Here we report the first experimental study of the maximum energy of proton beams accelerated from sub-micrometric foils perforated with holes of nanometric size. By showing the lack of energy enhancement in comparison to standard flat foils, our results suggest that the high contrast routinely achieved with a double plasma mirror does not prevent damaging of the nanostructures prior to the main interaction. Particle-in-cell simulations support that even a short scale length plasma, formed in the last hundreds of femtoseconds before the peak of an ultrashort laser pulse, fills the holes and hinders enhanced electron heating. Our findings reinforce the need for improved laser contrast, as well as for accurate control and diagnostics of on-target plasma formation. [ABSTRACT FROM AUTHOR]

Active nanophotonics can be realized by controlling the optical properties of materials with external magnetic fields. Here, we explore the influence of optical anisotropy on the magneto-optical activity in nonmagnetic hyperbolic nanoparticles. We demonstrate that the magneto-optical response is driven by the hyperbolic dispersion via the coupling of metallic-induced electric and dielectric-induced magnetic dipolar optical modes with static magnetic fields. Magnetic circular dichroism experiments confirm the theoretical predictions and reveal tunable magneto-optical activity across the visible and near infrared spectral range. [ABSTRACT FROM AUTHOR]

The nonreciprocal magnetoelectric effect, also known as the Tellegen effect, promises a number of groundbreaking phenomena connected to fundamental (e.g., electrodynamics of axion and relativistic matter) and applied physics (e.g., magnetless isolators). We propose a three-dimensional metamaterial with an isotropic and resonant Tellegen response in the visible frequency range. The metamaterial is formed by randomly oriented bi-material nanocylinders in a host medium. Each nanocylinder consists of a ferromagnet in a single-domain magnetic state and a high-permittivity dielectric operating near the magnetic Mie-type resonance. The proposed metamaterial requires no external magnetic bias and operates on the spontaneous magnetization of the nanocylinders. By leveraging the emerging magnetic Weyl semimetals, we further show how a giant bulk effective magnetoelectric effect can be achieved in a proposed metamaterial, exceeding that of natural materials by almost four orders of magnitude., (© 2024. The Author(s).)

Molecular polaritons are hybrid light-matter states that emerge when a molecular transition strongly interacts with photons in a resonator. At optical frequencies, this interaction unlocks a way to explore and control new chemical phenomena at the nanoscale. Achieving such control at ultrafast timescales, however, is an outstanding challenge, as it requires a deep understanding of the dynamics of the collectively coupled molecular excitation and the light modes. Here, we investigate the dynamics of collective polariton states, realized by coupling molecular photoswitches to optically anisotropic plasmonic nanoantennas. Pump-probe experiments reveal an ultrafast collapse of polaritons to pure molecular transition triggered by femtosecond-pulse excitation at room temperature. Through a synergistic combination of experiments and quantum mechanical modelling, we show that the response of the system is governed by intramolecular dynamics, occurring one order of magnitude faster with respect to the uncoupled excited molecule relaxation to the ground state., (© 2023. The Author(s).)

In this work we report on plasma oxidation of palladium (Pd) to form reliable palladium/palladium oxide (Pd/PdO x ) core-shell sensor for ppb level H 2 S detection and its performance improvement through nanostructuring using hole-mask colloidal lithography (HCL). The plasma oxidation parameters and the sensor operating conditions are optimized to arrive at a sensor device with high sensitivity and repeatable response for H 2 S. The plasma oxidized palladium/palladium oxide sensor shows a response of 43.1% at 3 ppm H 2 S at the optimum operating temperature of 200 °C with response and recovery times of 24 s and 155 s, respectively. The limit of detection (LoD) of the plasma oxidised beam is 10 ppb. We further integrate HCL, a bottom-up and cost-effective process, to create nanodiscs of fixed diameter of 100 nm and varying heights (10, 15 and 20 nm) on 10 nm thin Pd beam which is subsequently plasma oxidized to improve the H 2 S sensing characteristics. The nanostructured Pd/PdO x sensor with nanodiscs of 100 nm diameter and 10 nm height shows an enhancement in sensing performance by 11.8% at same operating temperature and gas concentration. This nanostructured sensor also shows faster response and recovery times (15 s and 100 s, respectively) compared to the unstructured Pd/PdO x counterpart together with an experimental LoD of 10 ppb and the estimated limit going all the way down to 2 ppb. Material characterization of the fabricated Pd/PdO x sensors is done using UV-vis spectroscopy and x-ray photoemission spectroscopy.

We report on the fabrication of disordered nanostructures by combining colloidal lithography and silicon etching. We show good control of the short-range ordered colloidal pattern for a wide range of bead sizes from 170 to 850 nm. The inter-particle spacing follows a Gaussian distribution with the average distance between two neighboring beads (center to center) being approximately twice their diameter, thus enabling the nanopatterning with dimensions relevant to the light wavelength scale. The disordered nanostructures result in a lower integrated reflectance (8.1%) than state-of-the-art random pyramid texturing (11.7%) when fabricated on 700 µm thick wafers. When integrated in a 1.1 µm thin crystalline silicon slab, the absorption is enhanced from 24.0% up to 64.3%. The broadening of resonant modes present for the disordered nanopattern offers a more broadband light confinement compared to a periodic nanopattern. Owing to its simplicity, versatility and the degrees of freedom it offers, this potentially low-cost bottom-up nanopatterning process opens perspectives towards the integration of advanced light-trapping schemes in thin solar cells.

We present a compact platform for biochemosensing based on the combination of a vertical-cavity surface-emitting laser (VCSEL) light source, microelectromechanical systems (MEMS)-based microoptics, a specially designed nanoplasmonic sensing chip, and charge-coupled device (CCD) detector. The platform does not require any spectral analyzer for signal evaluation, showing good promise for facile integration, neither does it use any microscope setup for the signal collection or imaging. The analytical capabilities of the developed biochemosensing platform are demonstrated by evaluation of the protein-substrate (biotinylated bovine serum albumin-gold) and the protein-protein (biotin-NeutrAvidin) binding kinetics, which is further compared to detection based on conventional optical extinction spectroscopy. The instrument is able to detect low femtomoles of adsorbed proteins with the limit of detection comparable to the state-of-the-art research and commercial optical label-free biochemosensors.

Hydrogen-bond formation between ionic adsorbates on an Ag(111) surface under ultrahigh vacuum was studied by scanning tunneling microscopy/spectroscopy (STM/STS), X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS), and molecular dynamics calculations. The adsorbate, 1,3,5-benzenetricarboxylic acid (trimesic acid, TMA), self-assembles at low temperatures (250-300 K) into the known open honeycomb motif through neutral hydrogen bonds formed between carboxyl groups, whereas annealing at 420 K leads to a densely packed quartet structure consisting of flat-lying molecules with one deprotonated carboxyl group per molecule. The resulting charged carboxylate groups form intermolecular ionic hydrogen bonds with enhanced strength compared to the neutral hydrogen bonds; this represents an alternative supramolecular bonding motif in 2D supramolecular organization.

We present a comprehensive investigation of the modular assembly of surface-supported metal-organic coordination systems with specific topologies and high structural stability formed by vapor deposition of 1,4-benzenedicarboxylic acid molecules and iron atoms on a Cu(100) surface under ultra-high vacuum conditions. By making use of the two carboxylate moieties available for lateral linkage to Fe atoms, we succeeded in the fabrication of distinct Fe-carboxylate coordination architectures at the surface by carefully adjusting the ligand and metal concentration ratio and the temperature of the post-deposition annealing treatment. The mononuclear, 1D-polymeric and fully 2D-reticulated metallosupramolecular arrangements obtained were characterized in situ at the single-molecule level by scanning tunneling microscopy.