Chiromagnetic Plasmonic Nanoassemblies with Magnetic Field Modulated Chiral Activity

Chiral plasmonic nanoassemblies, which exhibit outstanding chiroptical activity in the visible or near‐infrared region, are popular candidates in molecular sensing, polarized nanophotonics, and biomedical applications. Their optical chirality can be modulated by manipulating chemical molecule stimuli or replacing the building blocks. However, instead of irreversible chemical or material changes, real‐time control of optical activity is desired for reversible and noninvasive physical regulating methods, which is a challenging research field. Here, the directionally and reversibly switching optical chirality of magneto‐plasmonic nanoassemblies is demonstrated by the application of an external magnetic field. The gold‐magnetic nanoparticles core–satellite (Au@Fe₃O₄) nanostructures exhibit chiral activity in the UV–visible range, and the circular dichroism signal is 12 times greater under the magnetic field. Significantly, the chiral signal can be reversed by regulating the direction of the applied magnetic field. The attained magnetic field‐regulated chirality is attributed to the large contributions of the magnetic dipole moments to polarization rotation. This magnetic field‐modulated optical activity may be pivotal for photonic devices, information communication, as well as chiral metamaterials.     

Seed‐Induced Growth of Flower‐Like Au–Ni–ZnO Metal–Semiconductor Hybrid Nanocrystals for Photocatalytic Applications

The combination of metal and semiconductor components in nanoscale to form a hybrid nanocrystal provides an important approach for achieving advanced functional materials with special optical, magnetic and photocatalytic functionalities. Here, a facile solution method is reported for the synthesis of Au–Ni–ZnO metal–semiconductor hybrid nanocrystals with a flower‐like morphology and multifunctional properties. This synthetic strategy uses noble and magnetic metal Au@Ni nanocrystal seeds formed in situ to induce the heteroepitaxial growth of semiconducting ZnO nanopyramids onto the surface of metal cores. Evidence of epitaxial growth of ZnO{0001} facets on Ni {111} facets is observed on the heterojunction, even though there is a large lattice mismatch between the semiconducting and magnetic components. Adjustment of the amount of Au and Ni precursors can control the size and composition of the metal core, and consequently modify the surface plasmon resonance (SPR) and magnetic properties. Room‐temperature superparamagnetic properties can be achieved by tuning the size of Ni core. The as‐prepared Au–Ni–ZnO nanocrystals are strongly photocatalytic and can be separated and re‐cycled by virtue of their magnetic properties. The simultaneous combination of plasmonic, semiconducting and magnetic components within a single hybrid nanocrystal furnishes it multifunctionalities that may find wide potential applications.     

Interfacial Capillary‐Force‐Driven Self‐Assembly of Monolayer Colloidal Crystals for Supersensitive Plasmonic Sensors

Colloidal lithography technology based on monolayer colloidal crystals (MCCs) is considered as an outstanding candidate for fabricating large‐area patterned functional nanostructures and devices. Although many efforts have been devoted to achieve various novel applicatons, the quality of MCCs, a key factor for the controllability and reproducibility of the patterned nanostructures, is often overlooked. In this work, an interfacial capillary‐force‐driven self‐assembly strategy (ICFDS) is designed to realize a high‐quality and highly‐ordered hexagonal monolayer MCCs array by resorting the capillary effect of the interfacial water film at substrate surface as well as controlling the zeta potential of the polystyrene particles. Compared with the conventional self‐assembly method, this approach can realize the reself‐assembly process on the substrate surface with few colloidal aggregates, vacancy, and crystal boundary defects. Furthermore, various typical large‐scale nanostructure arrays are achieved by combining reactive ion etching, metal‐assisted chemical etching, and so forth. Specifically, benefiting from the as‐fabricated high‐quality 2D hexagonal colloidal crystals, the surface plasmon resonance (SPR) sensors achieve an excellent refractive index sensitivity value of 3497 nm RIU^?1, which is competent for detecting bovine serum albumin with an ultralow concentration of 10^?8 m . This work opens a window to prepare high‐quality MCCs for more potential applications.     

Large Photothermal Effect in Sub‐40 nm h‐BN Nanostructures Patterned Via High‐Resolution Ion Beam

The controlled nanoscale patterning of 2D materials is a promising approach for engineering the optoelectronic, thermal, and mechanical properties of these materials to achieve novel functionalities and devices. Herein, high‐resolution patterning of hexagonal boron nitride (h‐BN) is demonstrated via both helium and neon ion beams and an optimal dosage range for both ions that serve as a baseline for insulating 2D materials is identified. Through this nanofabrication approach, a grating with a 35 nm pitch, individual structure sizes down to 20 nm, and additional nanostructures created by patterning crystal step edges are demonstrated. Raman spectroscopy is used to study the defects induced by the ion beam patterning and is correlated to scanning probe microscopy. Photothermal and scanning near‐field optical microscopy measure the resulting near‐field absorption and scattering of the nanostructures. These measurements reveal a large photothermal expansion of nanostructured h‐BN that is dependent on the height to width aspect ratio of the nanostructures. This effect is attributed to the large anisotropy of the thermal expansion coefficients of h‐BN and the nanostructuring implemented. The photothermal expansion should be present in other van der Waals materials with large anisotropy and can lead to applications such as nanomechanical switches driven by light.     

Tracking the Fate of Surface Plasmon Resonance‐Generated Hot Electrons by In Situ SERS Surveying of Catalyzed Reaction

Plasmonic catalysis is an emerging process that utilizes surface plasmon resonance (SPR) process to harnesses solar energy for the promotion of catalyzed reactions. In most cases, SPR generated hot electrons (HEs) play an indispensable role in this solar‐chemical energy shift process. Therefore, understanding the effectiveness of the HEs in promoting chemical reactions, and identifying the key factors that contribute to this utilization efficiency is of profound importance. Herein, the authors outline an in situ surface enhanced Raman spectroscopy protocol to track the fate of HEs. This is based on the unheeded HEs‐acceleration nature of the p‐nitirothiophenol hydrogenation reaction. By this way, the authors discover that unlike Au@Pd nanostructures which experience a 20‐fold increase in rate constant, HEs primary leak to surrounding H⁺/O species through Ag pinholes in Ag@Pd. This work sheds light on why Ag is seldom employed as a plasmonic cocatalyst, and provides a new viewpoint to design plasmonic nanocatalysts with efficient light utilization.     

Designable Luminescence with Quantum Dot–Silver Plasmon Coupler

We explore a strongly interacting QDs/Ag plasmonic coupling structure that enables multiple approaches to manipulate light emission from QDs. Group II–VI semiconductor QDs with unique surface states (SSs) impressively modify the plasmonic character of the contiguous Ag nanostructures whereby the localized plasmons (LPs) in the Ag nanostructures can effectively extract the non‐radiative SSs of the QDs to radiatively emit via SS–LP resonance. The SS–LP coupling is demonstrated to be readily tunable through surface‐state engineering both during QD synthesis and in the post‐synthesis stage. The combination of surface‐state engineering and band‐tailoring engineering allows us to precisely control the luminescence color of the QDs and enables the realization of white‐light emission with single‐size QDs. Being a versatile metal, the Ag in our optical device functions in multiple ways: as a support for the LPs, for optical reflection, and for electrical conduction. Two application examples of the QDs/Ag plasmon coupler for optical devices are given, an Ag microcavity + plasmon‐coupling structure and a new QD light‐emitting diode. The new QDs/Ag plasmon coupler opens exciting possibilities in developing novel light sources and biomarker detectors.     

Theoretical and experimental study of the surface plasmon resonance effect on a recordable compact disk

The surface plasmon resonance (SPR) effect on noble-metal surfaces has been explored by several investigators for the development of chemical and biological sensors as well as for the design of optical devices for other applications. The effect can be observed by use of prism couplers, diffraction gratings, and specially configured optical fibers. In an attempt to seek a new configuration that minimizes costs of fabricating media that support SPR in conjunction with designing a new format suitable for large-scale chemical and biological sensing, I have investigated the feasibility of using a commercially available, gold-type, recordable compact disk for observation of the SPR phenomenon. Experimental and theoretical results of this investigation are reported.     

Plasmonic ZnO/Ag Embedded Structures as Collecting Layers for Photogenerating Electrons in Solar Hydrogen Generation Photoelectrodes

A new fabrication strategy in which Ag plasmonics are embedded in the interface between ZnO nanorods and a conducting substrate is experimentally demonstrated using a femtosecond‐laser (fs‐laser)‐induced plasmonic ZnO/Ag photoelectrodes. This fs‐laser fabrication technique can be applied to generate patternable plasmonic nanostructures for improving their effectiveness in hydrogen generation. Plasmonic ZnO/Ag nanostructure photoelectrodes show an increase in the photocurrent of a ZnO nanorod photoelectrodes by higher than 85% at 0.5 V. Both localized surface plasmon resonance in metal nanoparticles and plasmon polaritons propagating at the metal/semiconductor interface are available for improving the capture of sunlight and collecting charge carriers. Furthermore, in‐situ X‐ray absorption spectroscopy is performed to monitor the plasmonic‐generating electromagnetic field upon the interface between ZnO/Ag nanostructures. This can reveal induced vacancies on the conduction band of ZnO, which allow effective separation of charge carriers and improves the efficiency of hydrogen generation. Plasmon‐induced effects enhance the photoresponse simultaneously, by improving optical absorbance and facilitating the separation of charge carriers.     

Parallel Preparation of Densely Packed Arrays of 150‐nm Gold‐Nanocrescent Resonators in Three Dimensions

Metallic nanostructures show interesting optical properties due to their plasmonic resonances, and when arranged in three‐dimensional (3D) arrays hold promise for optical metamaterials with negative refractive index. Towards this goal a simple, cheap, and parallel method to fabricate large‐area, ordered arrays of 150‐nm gold nanocrescents supporting plasmonic resonances in the near‐infrared spectral range is demonstrated. In this process hexagonally ordered monolayers of monodisperse colloids are prepared by a simple floating technique, and subsequently the individual particles are size‐reduced in a plasma process and used as a shadow mask with the initial lattice spacing. The resulting two‐dimensional array of plasmonic resonators is coated with a transparent silica layer, which serves as a support for a second layer prepared by the identical process. The mutual orientation of the nanostructures between the individual layers can be freely adjusted, which determines the polarization‐dependent absorption of the array and opens the possibility to introduce chirality in this type of 3D metamaterial. The iteration of this simple and efficient methodology yields 3D arrays with optical features as sharp as those of the individual nanocrescents, and shows strong potential for large‐scale production of high‐quality optical metamaterials.     

Metallic film optimization in a surface plasmon resonance biosensor by the extended Rouard method

The extended Rouard method is applied to the computation of a multi-absorbing-layer system for the optimization of surface plasmon resonance (SPR) sensors. Specifically, the effect of the properties of a metallic layer on the shape of the reflectivity and sensitivity curve is demonstrated in the case of a Kretschmann configuration. This theoretical investigation allows us to establish the best optical properties of the metal to obtain a localized SPR, given the illuminating beam properties. Toward the development of a sensitive biosensor based on SPR, we quantify the changes in reflectivity of such an optical biosensor induced by the deposition of a nanometric biochemical film as a function of the metal film characteristics and the illumination operating conditions. The sensitivity of the system emphasizes the potential of such biophotonic technology using metallic multilayer configurations, especially with envisioned metamaterials.     

Acousto-optical Transducer with Surface Plasmons

The surface plasmon resonance (SPR) is a sensitive technique for the detection of changes in dielectric parameters in close proximity to a metal film supporting surface plasmon waves. Here we study the application of the SPR effect to an efficient conversion of an acoustic signal into an optical one. Such a transducer potentially has a large bandwidth and good sensitivity. When an acoustic wave is incident onto a receiving plate positioned within the penetration depth of the surface plasmons, it creates displacements of the surface of the plate and, thus, modulates the dielectric properties in the proximity of the gold film. This modulation, in turn, modifies the light reflection under surface plasmon resonance conditions. We simulate characteristics of this acousto-optical transducer with surface plasmons and provide sets of parameters at the optical wavelength of 800 nm and 633 nm for its realization.     

DNA‐Origami‐Based Assembly of Anisotropic Plasmonic Gold Nanostructures

Precise control over the assembly of anisotropic plasmonic gold nanostructures with relative spatial directionality and sequence asymmetry remains a major challenge and offers great fundamental insight and optical application possibilities. Here, a novel strategy is developed to anisotropically functionalize gold nanorods (AuNRs) by using a DNA‐origami‐based precise machine to transfer essential DNA sequence configurations to the surface of the AuNRs through an intentionally designed toehold‐initiated displacement reaction. Different AuNR products are examined via hybridization with DNA‐AuNPs that display distinct elements of regiospecificity. These assembled anisotropic plasmonic gold nanostructures based on the DNA‐origami precise machine inherit the encoded information from the parent platform with high fidelity and show fixed orientation and bonding anisotropy, thereby generating discrete plasmonic nanostructures with enhanced Raman resonance.     

Luminescence of a Transition Metal Complex Inside a Metamaterial Nanocavity

Modification of the local density of optical states using metallic nanostructures leads to enhancement in the number of emitted quanta and photocatalytic turnover of luminescent materials. In this work, the fabrication of a metamaterial is presented that consists of a nanowire separated from a metallic mirror by a polymer thin film doped with a luminescent organometallic iridium(III) complex. The large spin–orbit coupling of the heavy metal atom results in an excited state with significant magnetic‐dipole character. The nanostructured architecture supports two distinct optical modes and their assignment achieved with the assistance of numerical simulations. The simulations show that one mode is characterized by strong confinement of the electric field and the other by strong confinement of the magnetic field. These modes elicit drastic changes in the emitter's photophysical properties, including dominant nanocavity‐derived modes observable in the emission spectra along with significant increases in emission intensity and the total decay rate. A combination of simulations and momentum‐resolved spectroscopy helps explain the mechanism of the different interactions of each optical mode supported by the metamaterial with the excited state of the emitter.     

Progressive Design of Plasmonic Metal–Semiconductor Ensemble toward Regulated Charge Flow and Improved Vis–NIR‐Driven Solar‐to‐Chemical Conversion

Surface plasmon resonance (SPR)‐mediated photocatalysis without the bandgap limitations of traditional semiconductor has aroused significant attention in solar‐to‐chemical energy conversion. However, the photocatalytic efficiency barely initiated by the SPR effects is still challenged by the low concentration and ineffective extraction of energetic hot electrons, slow charge migration rates, random charge diffusion directions, and the lack of highly active sites for redox reactions. Here, the tunable, progressive harvesting of visible‐to‐near infrared light (vis–NIR, λ > 570 nm) by designing plasmonic Au nanorods and metal (Au, Ag, or Pt) nanoparticle codecorated 1D CdS nanowire (1D CdS NW) ensemble is reported. The intimate integration of these metal nanostructures with 1D CdS NWs promotes the extraction and manipulated directional separation and migration of hot charge carriers in a more effective manner. Such cooperative synergy with tunable control of interfacial interaction, morphology optimization, and cocatalyst strategy results in the distinctly boosted performance for vis–NIR‐driven plasmonic photocatalysis. This work highlights the significance of rationally progressive design of plasmonic metal–semiconductor‐based composite system for boosting the regulated directional flow of hot charge carrier and thus the more efficient use of broad‐spectrum solar energy conversion.     

Reflection and Absorption Techniques for Optical Characterization of Chemically Assembled Nanomaterials

This review discusses recent developments in the areas of fabrication, certain types of optical characterization, and applications of a selected class of chemically assembled nanomaterials, namely i) gold and silver nanoparticles deposited onto optically transparent glass substrates; ii) thiol‐functionalized self‐assembled monolayers (SAMs); iii) chemically stabilized gold and silver nanoparticles (monolayer protected clusters, MPCs); and iv) MPCs linked to metallic substrates and adsorbates. Six linear optical techniques for the characterization of these materials are discussed: transmission localized surface plasmon resonance spectroscopy, T‐LSPR; propagating surface plasmon resonance spectroscopy, P‐SPR; polarization‐selective Fourier transform infrared reflection absorption spectroscopy, PS‐FTIRRAS; polarization‐modulation Fourier transform infrared reflection absorption spectroscopy, PM‐FTIRRAS; surface‐enhanced infrared reflection absorption spectroscopy, SEIRRAS; and infrared ellipsometry. The review focuses particularly on providing a unified treatment of these six optical techniques by using a relatively simple stratified multilayer model.     

Small-angle measurement based on surface-plasmon resonance and the use of magneto-optical modulation

A new, to our knowledge, optical method for small-angle measurement based on surface-plasmon resonance (SPR) is presented. In this method the high sensitivity of the phase of SPR to the angle of incidence is employed to improve the resolution of the measurement of the angle. Small-angle measurement is performed by the monitoring of the phase shift resulting from the minute change of the angle of incidence with the use of magneto-optical modulation. The validity of this method is demonstrated, and a measurement resolution of 0.2 arc sec is achieved experimentally.     

Quartz crystal microbalance with integrated surface plasmon grating coupler

We have integrated a surface plasmon grating coupler into a quartz crystal microbalance (QCM) for studying surface association/dissociation reactions. In the integrated system only QCM measurement is needed to record both the optical and the acoustic signals in the same association/dissociation reaction. This integration considerably simplifies a conventional combination instrument of a grating-coupled surface plasmon resonance (SPR) spectrometer and a quartz crystal microbalance by eliminating a number of SPR components. Moreover, in the integrated system detection of the light reflections is not needed by which one bypasses the interference problem caused by two coherent light reflections off the glass window used to seal the fluid sample and off the sensor surface. The utility of the integrated system is demonstrated using a layer-by-layer polyelectrolyte multilayer deposition protocol, in which the complete features of a conventional grating-coupled SPR/QCM combination instrument are retained, including detection of optical and acoustic changes, as well as monitoring of adsorption kinetics.     

Colloid‐Interface‐Assisted Laser Irradiation of Nanocrystals Superlattices to be Scalable Plasmonic Superstructures with Novel Activities

High‐efficient charge and energy transfer between nanocrystals (NCs) in a bottom‐up assembly are hard to achieve, resulting in an obstacle in application. Instead of the ligands exchange strategies, the advantage of a continuous laser is taken with optimal wavelength and power to irradiate the film‐scale NCs superlattices at solid–liquid interfaces. Owing to the Au‐based NCs' surface plasmon resonance (SPR) effect, the gentle laser irradiation leads the Au NCs or Au@CdS core/shell NCs to attach each other with controlled pattern at the interfaces between solid NCs phase and liquid ethanol/ethylene glycol. A continuous wave 532 nm laser (6.68–13.37 W cm^?2), to control Au‐based superlattices, is used to form the monolayer with uniformly reduced interparticle distance followed by welded superstructures. Considering the size effect to Au NCs' melting, when decreasing the Au NCs size to ≈5 nm, stronger welding nanostructures are obtained with diverse unprecedented shapes which cannot be achieved by normal colloidal synthesis. With the help of facile scale‐up and formation at solid–liquid interfaces, and a good connection of crystalline between NCs, the obtained plasmonic superstructured films that could be facilely transferred onto different substrates exhibit broad SPR absorption in the visible and near‐infrared regime, enhanced electric conductivities, and wide applications as surface enhanced Raman scattering (SERS)‐active substrates.     

Optical properties and instrumental performance of thin gold films near the surface plasmon resonance

The optical properties of very thin gold films have been evaluated by Fresnel analysis, with optical boundary conditions pertaining to the surface plasmon resonance (SPR) at the gold-water interface. The experimental SPR characteristic was evaluated in the angular interrogation mode. Film morphology was characterized by high resolution transmission electron microscopy. The magnitude of the resonance, i.e., the SPR signal, sensitively depends on, and is affected by film thickness and morphology. A sharply defined thickness of 55 ± 5 nm is required, to achieve optimum SPR excitation conditions, and instrumental sensitivity. With decreasing film thickness, below 40 nm, the resonance angle starts to shift to larger values. A substantial increase of the intrinsic resonance broadening parameter is observed below 70 nm, associated with an increasingly asymmetric SPR line shape. A similar effect occurs in the presence of a very thin chromium adhesion layer. Surface roughness and film thickness modulations determine the experimentally observed line broadening parameter. Instrumental noise levels largely depend on accuracy and quality at which the resonance angle can be determined. Substantial improvement and instrumental sub-pixel resolution is achievable by optimum fitting routines, accounting for drastic noise reduction and improved instrumental sensitivity, up to two orders of magnitude over the inherent geometric sensor pixel resolution.