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.     

Surface Assembly and Plasmonic Properties in Strongly Coupled Segmented Gold Nanorods

An assembly strategy is reported such that segmented nanorods fabricated through template‐assisted methods can be robustly transferred and tethered to a pre‐functionalized substrate with excellent uniformity over large surface areas. After embedding the rods, sacrificial nickel segments were selectively etched leaving behind strongly coupled segmented gold nanorods with gaps between rods below 40 nm and as small as 2 nm. Hyper‐spectral imaging is utilized to measure Rayleigh scattering spectra from individual and coupled nanorod elements in contrast to common bulk measurements. This approach discerns the effects of not only changing segment and gap size but also the presence of characteristic defects on the plasmonic coupling between closely spaced nanorods. Polarized hyper‐spectral measurements are conducted to provide direct observation of the anisotropic plasmonic resonance modes in individual and coupled nanorods, which are close to those predicted by computer simulations for nanorods with ideal shapes. Some common deviations from ideal shape such as non‐flat facets and asymmetric tails are demonstrated to result in the appearance of characteristic plasmon resonances, which have not been considered before. The large‐scale assembly of coupled noble nanostructures with fine control over geometry and high uniformity provides means to strongly tune the scattering, absorption, and near‐field plasmonic properties through the geometric arrangement of precisely controlled nanorod segments.     

Lateral Magnetic Near‐Field Imaging of Plasmonic Nanoantennas With Increasing Complexity

The design of many promising, newly emerging classes of photonic metamaterials and subwavelength confinement structures requires detailed knowledge and understanding of the electromagnetic near‐field interactions between their building blocks. While the electric field distributions and, respectively, the electric interactions of different nanostructures can be routinely measured, for example, by scattering near‐field microscopy, only recently experimental methods for imaging the magnetic field distributions became available. In this paper, we provide direct experimental maps of the lateral magnetic near‐field distributions of variously shaped plasmonic nanoantennas by using hollow‐pyramid aperture scanning near‐field optical microscopy (SNOM). We study both simple plasmonic nanoresonators, such as bars, disks, rings and more complex antennas. For the studied structures, the magnetic near‐field distributions of the complex resonators have been found to be a superposition of the magnetic near‐fields of the individual constituting elements. These experimental results, explained and validated by numerical simulations, open new possibilities for engineering and characterization of complex plasmonic antennas with increased functionality.     

Target‐Triggered Assembly of Nanogap Antennas to Enhance the Fluorescence of Single Molecules and Their Application in MicroRNA Detection

Nanogap antennas are plasmonic nanostructures with a strong electromagnetic field generated at the gap region of two neighboring particles owing to the coupling of the collective surface plasmon resonance. They have great potential for improving the optical properties of fluorophores. Herein, nanogap antennas are constructed using an aqueous solution‐based method to overcome the defects of weak fluorescence and photobleaching associated with traditional organic dyes, and a highly sensitive nanogap antenna‐based sensing strategy is presented for the detection of low‐abundance nucleic acid biomarkers via a target‐triggered strand displacement amplification (SDA) reaction between two DNA hairpins that are tagged to the tips of gold nanorods (Au NRs). In the presence of targets, end‐to‐end Au NR dimers gradually form, and the fluorophores quenched by the Au NRs exhibit a dramatic fluorescence enhancement due to the plasmon‐enhanced fluorescence effect of nanogap antennas. Meanwhile, the SDA reaction results in secondary amplification of fluorescence signals. Combined with single‐molecule counting, this method applied in miRNA‐21 detection can achieve a low detection limit of 97.2 × 10^?18 m . Moreover, accurate discrimination between different cells through miRNA‐21 imaging demonstrates the potential of this method in monitoring the expression level of low‐abundance nucleic acid biomarkers.     

Experimental and theoretical investigation of silver-coated ZnO nanorod arrays as antennas for the visible and near-IR spectral range

A new design of optical antennas consisting of zinc oxide (ZnO) nanorods covered by a thin metal film is proposed. Arrays of highly oriented ZnO nanorods perpendicular to a substrate and covered by a thin silver film have been obtained using methods of carbothermal synthesis and magnetron sputtering. The problems of electromagnetic wave diffraction on a single metal/dielectric nanovibrator (situated at the interface of dielectrics) and on a two-dimensional periodic array of these nanovibrators have been solved. The results of calculations of the electrodynamic characteristics of optical antennas with various lengths have been compared to experimental data.     

Label-free plasmonic detection of biomolecular binding by a single gold nanorod

We report the use of individual gold nanorods as plasmonic transducers to detect the binding of streptavidin to individual biotin-conjugated nanorods in real time on a surface. Label-free detection at the single-nanorod level was performed by tracking the wavelength shift of the nanorod-localized surface plasmon resonant scattering spectrum using a dark-field microspectroscopy system. The lowest streptavidin concentration that was experimentally measured was 1 nM, which is a factor of 1000-fold lower than the previously reported detection limit for streptavidin binding by biotinylated single plasmonic nanostructures. We believe that the current optical setup is able to reliably measure wavelength shifts as small as 0.3 nm. Binding of streptavidin at 1 nM concentration induces a mean resonant wavelength shift of 0.59 nm suggesting that we are currently operating at close to the limit of detection of the system.     

On chip plasmonic monopole nano-antennas and circuits

Analogues of many radio frequency (RF) antenna designs such as the half-wave dipole and Yagi-Uda have been successfully adapted to the optical frequency regime, opening the door for important advances in biosensing, photodetection, and emitter control. Examples of monopole antennas, however, are conspicuously rare given the element's extensive use in RF applications. Monopole antennas are attractive as they represent an easy to engineer, compact geometry and are well isolated from interference due the ground plane. Typically, however, the need to orient the antenna element perpendicular to a semi-infinite ground plane requires a three-dimensional structure and is incompatible with chip-based fabrication techniques. We propose and demonstrate here for the first time that monopole antenna elements can be fashioned out of single element nanoparticles fabricated in conventional planar geometries by using a small nanorod as a wire reflector. The structure offers a compact geometry and the reflector element provides a measure of isolation analogous to the RF counterpart. This isolation persists in the conductive coupling regime, allowing multiple monopoles to be combined into a single nanoparticle, yet still operate independently. This contrasts with several previous studies that observed dramatic variations in the spectral response of conductively coupled particles. We are able to account for these effects by modeling the system using circuit equations from standard RF antenna theory. Our model accurately describes this behavior as well as the detailed resonance tuning of the structure. As a specific practical application, the monopole resonances are precisely tuned to desired protein absorption bands, thereby enhancing their spectroscopic signatures. Furthermore, the accurate modeling of conductive coupling and demonstrated electronic isolation should be of general interest to the design of complex plasmonic circuits incorporating multiple antennas and other current carrying elements.     

Plasmonic Luneburg and Eaton lenses

Plasmonics takes advantage of the properties of surface plasmon polaritons, which are localized or propagating quasiparticles in which photons are coupled to the quasi-free electrons in metals. In particular, plasmonic devices can confine light in regions with dimensions that are smaller than the wavelength of the photons in free space, and this makes it possible to match the different length scales associated with photonics and electronics in a single nanoscale device. Broad applications of plasmonics that have been demonstrated to date include biological sensing, sub-diffraction-limit imaging, focusing and lithography and nano-optical circuitry. Plasmonics-based optical elements such as waveguides, lenses, beamsplitters and reflectors have been implemented by structuring metal surfaces or placing dielectric structures on metals to manipulate the two-dimensional surface plasmon waves. However, the abrupt discontinuities in the material properties or geometries of these elements lead to increased scattering of surface plasmon polaritons, which significantly reduces the efficiency of these components. Transformation optics provides an alternative approach to controlling the propagation of light by spatially varying the optical properties of a material. Here, motivated by this approach, we use grey-scale lithography to adiabatically tailor the topology of a dielectric layer adjacent to a metal surface to demonstrate a plasmonic Luneburg lens that can focus surface plasmon polaritons. We also make a plasmonic Eaton lens that can bend surface plasmon polaritons. Because the optical properties are changed gradually rather than abruptly in these lenses, losses due to scattering can be significantly reduced in comparison with previously reported plasmonic elements.     

Miniature Hollow Gold Nanorods with Enhanced Effect for In Vivo Photoacoustic Imaging in the NIR‐II Window

The miniaturization of gold nanorods exhibits a bright prospect for intravital photoacoustic imaging (PAI) and the hollow structure possesses a better plasmonic property. Herein, miniature hollow gold nanorods (M‐AuHNRs) (≈46 nm in length) possessing strong plasmonic absorbance in the second near‐infrared (NIR‐II) window (1000–1350 nm) are developed, which are considered as the most suitable range for the intravital PAI. The as‐prepared M‐AuHNRs exhibit 3.5 times stronger photoacoustic signal intensity than the large hollow Au nanorods (≈105 nm in length) at 0.2 optical density under 1064 nm laser irradiation. The in vivo biodistribution measurement shows that the accumulation in tumor of miniature nanorods is twofold as high as that of the large counterpart. After modifying with a tumor‐targeting molecule and fluorochrome, in living tumor‐bearing mice, the M‐AuHNRs group gives a high fluorescence intensity in tumors, which is 3.6‐fold that of the large ones with the same functionalization. Moreover, in the intravital PAI of living tumor‐bearing mice, the M‐AuHNRs generate longer‐lasting and stronger photoacoustic signal than the large counterpart in the NIR‐II window. Overall, this study presents the fabrication of M‐AuHNRs as a promising contrast agent for intravital PAI.     

Thermo-responsive plasmonic nanohybrids with tunable optical properties

In this paper, we study the temperature-dependent optical properties of gold–silver core–shell (Au@Ag) nanorods coated by a thermo-responsive polymer poly (N-isopropylacrylamide) (PNIPAM). The wavelength of the plasmonic resonant absorption of the nanohybrids changes with temperature due to the combination effects of the plasmon resonance of the core and the thermal response of the shell. Using effective medium theory, we find that with increase of temperature, the absorption peak red-shifts due to the competition effects from the changes of the thickness and the effective refractive index of the polymer shell. The working wavelength can be tuned by the aspect ratio of nanorods. Moreover, the temperature sensitivity of plasmon resonance increases with the increase of the aspect ratio. Our studies provide a proof-of-concept design of thermal responsive plasmonic smart material.     

Strong enhancement of the radiative decay rate of emitters by single plasmonic nanoantennas

We demonstrate a strong, 5-fold enhancement of the radiative decay rate from highly efficient fluorescent dye molecules around resonant optical nanoantennas. The plasmonic modes of individual gold dimer antennas are tuned by the particle length and the antenna gap, providing control over both the spectral resonance position and the near-field mode profile of the nanoantenna. Resonant enhancement of the radiative and nonradiative decay rates of a fluorescent dye is observed, resulting in an increase of the internal quantum efficiency from 40% up to 53% for single antennas, and up to 59% for antenna clusters. This improvement of the already high quantum efficiency of the dye molecules is in agreement with electrodynamic model calculations that predict a maximum attainable efficiency around 80% due to nonradiative losses in the metal.     

Templating of self-alignment patterns of anisotropic gold nanoparticles on ordered SWNT macrostructures

We report a simple and versatile technique for oriented assembly of gold nanorods on aligned single-walled carbon nanotube (SWNT) macrostructures, such as thin nanotube films and nanotube fibers. The deposition and assembly is accomplished via drop drying of dilute gold nanorod suspensions on SWNT macrostructures under ambient conditions. Guided by anisotropic interactions, gold nanorods, and polygonal platelets spontaneously align with SWNTs, resulting in macroscopic arrays of locally ordered nanorods supported on aligned SWNT substrates. SEM reveals that the scalar order parameter of rods relative to the local average SWNT alignment is 0.7 for rods on SWNT films and 0.9 for rods on SWNT fibers. This self-alignment is enabled by anisotropic gold nanoparticle-SWNT interactions and is observed for a wide range of nanoparticles, including nanorods with aspect ratios ranging from 2-35, thin gold triangular and other polygonal platelets. The plasmonic properties of aligned gold nanorods together with superior electronic, chemical and mechanical properties of SWNTs make these hybrid nanocomposites valuable for the design of self-assembled multifunctional optoelectronic materials and optical metamaterials.     

Encoding Random Hot Spots of a Volume Gold Nanorod Assembly for Ultralow Energy Memory

Data storage with ultrahigh density, ultralow energy, high security, and long lifetime is highly desirable in the 21st century and optical data storage is considered as the most promising way to meet the challenge of storing big data. Plasmonic coupling in regularly arranged metallic nanoparticles has demonstrated its superior properties in various applications due to the generation of hot spots. Here, the discovery of the polarization and spectrum sensitivity of random hot spots generated in a volume gold nanorod assembly is reported. It is demonstrated that the two‐photon‐induced absorption and two‐photon‐induced luminescence of the gold nanorods adjacent to such hot spots are enhanced significantly because of plasmonic coupling. The polarization, wavelength, and spatial multiplexing of the hot spots can be realized by using an ultralow energy of only a few picojoule per pulse, which is two orders of magnitude lower than the value in the state‐of‐the‐art technology that utilizes isolated gold nanorods. The ultralow recording energy reduces the cross‐talk between different recording channels and makes it possible to realize rewriting function, improving significantly both the quality and capacity of optical data storage. It is anticipated that the demonstrated technology can facilitate the development of multidimensional optical data storage for a greener future.     

Self-organized silver nanoparticles for three-dimensional plasmonic crystals

Metal nanostructures that support surface plasmons are compelling as plasmonic circuit elements and as the building blocks for metamaterials. We demonstrate here the spontaneous self-assembly of shaped silver nanoparticles into three-dimensional plasmonic crystals that display a frequency-selective response in the visible wavelengths. Extensive long-range order mediated by exceptional colloid monodispersity gives rise to optical passbands that can be tuned by particle volume fraction. These metallic supercrystals present a new paradigm for the fabrication of plasmonic materials, delivering a functional, tunable, completely bottom-up optical element that can be constructed on a massively parallel scale without lithography.     

Langmuir-Blodgett films of gold/silica core/shell nanorods

We report the preparation of Langmuir- and Langmuir-Blodgett films of mesoporous silica coated gold nanorods. The silica coating on the gold nanorods was found to prevent the aggregation of the plasmonic particles trapped at the air/water interface. Due to the small aspect ratio of the gold core and the presence of the silica shell, the orientational alignment of the nanorods in the Langmuir-Blodgett film is hindered. After particle deposition, no plasmon coupling was observed, which enables the design of the resulting film's optical property at the particle level. By using mesoporous silica as the shell material, the accessibility of the metal core's surface is preserved. Organic dye (Rhodamine 6G) was found to be able to penetrate into the mesoporous shell of the gold nanorods, resulting in a red shift of the longitudinal plasmon mode.     

Directed assembly of gold nanorods using aligned electrospun polymer nanofibers for highly efficient SERS substrates

Nonspherical metal nanoparticles are very attractive plasmonic nanostructures owing to the facile tunability of the plasmonic properties and the presence of sharp corners and edges, which act as electromagnetic hot spots for surface enhanced Raman scattering (SERS). However, such anisotropic nanostructures exhibit strong polarization dependence in their plasmonic properties, exhibiting significantly higher SERS intensity in certain orientations. In this paper, we demonstrate a facile strategy to achieve directed assembly of aligned gold nanorods using highly aligned electrospun nanofibers. We believe that the interstices between the nanofibers act as micro-and nanochannels, resulting in hydrodynamic drag forces on the gold nanorods, thus inducing massive alignment of the same on the nanofibers. Apart from exhibiting nearly 50 times higher SERS intensity compared to a planar SERS substrate with randomly oriented nanorods, our results highlight the importance of the orientation of anisotropic nanostructures. Finite difference time domain (FDTD) simulations employed to understand the electromagnetic field distribution around an aligned nanorod array showed excellent agreement with the experimental observations.     

All-optical control of a single plasmonic nanoantenna-ITO hybrid

We demonstrate experimentally picosecond all-optical control of a single plasmonic nanoantenna embedded in indium tin oxide (ITO). We identify a picosecond response of the antenna-ITO hybrid system, which is distinctly different from transient bleaching observed for gold antennas on a nonconducting SiO(2) substrate. Our experimental results can be explained by the large free-carrier nonlinearity of ITO, which is enhanced by plasmon-induced hot-electron injection from the gold nanoantenna into the conductive oxide. The combination of tunable antenna-ITO hybrids with nanoscale plasmonic energy transfer mechanisms, as demonstrated here, opens a path for new ultrafast devices to produce nanoplasmonic switching and control.     

Enhancing single-nanoparticle surface-chemistry by plasmonic overheating in an optical trap

Surface-chemistry of individual, optically trapped plasmonic nanoparticles is modified and accelerated by plasmonic overheating. Depending on the optical trapping power, gold nanorods can exhibit red shifts of their plasmon resonance (i.e., increasing aspect ratio) under oxidative conditions. In contrast, in bulk exclusively blue shifts (decreasing aspect ratios) are observed. Supported by calculations, we explain this finding by local temperatures in the trap exceeding the boiling point of the solvent that cannot be achieved in bulk.     

High-Speed Parallel Plasmonic Direct-Writing Nanolithography Using Metasurface-Based Plasmonic Lens

Simple and efficient nanofabrication technology with low cost and high flexibility is indispensable for fundamental nanoscale research and prototyping. Lithography in the near field using the surface plasmon polariton (i.e., plasmonic lithography) provides a promising solution. The system with high stiffness passive nanogap control strategy on a high-speed rotating substrate is one of the most attractive high-throughput methods. However, a smaller and steadier plasmonic nanogap, new scheme of plasmonic lens, and parallel processing should be explored to achieve a new generation high resolution and reliable efficient nanofabrication. Herein, a parallel plasmonic direct-writing nanolithography system is established in which a novel plasmonic flying head is systematically designed to achieve around 15 nm minimum flying-height with high parallelism at the rotating speed of 8–18 m·s⁻¹. A multi-stage metasurface-based polarization insensitive plasmonic lens is proposed to couple more power and realize a more confined spot compared with conventional plasmonic lenses. Parallel lithography of the nanostructures with the smallest (around 26 nm) linewidth is obtained with the prototyping system. The proposed system holds great potential for high-freedom nanofabrication with low cost, such as planar optical elements and nano-electromechanical systems.