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Alexander O. Govorov

Publications and source records attributed to Alexander O. Govorov.

At least 19 recordsLinked to original sources

Plasmon-interband hybridization and anomalous production of hot electrons in aluminum nanoantennas

Strong coupling typically occurs between two separate objects or between an object and its environment (such as an atom and a cavity). However, it can also occur between two different excitations within the same object, a situation that has been much less studied. In this study, we observe strong coupling between localized surface plasmon resonances and the interband transition in aluminum nanorods, as evidenced by optical spectroscopy and electron energy loss spectroscopy, and corroborated with numerical simulations. Strong coupling is observed between the interband transition and multiple orders of the surface plasmon mode, including dark ones. We also obtain experimental maps of the hybrid modes at the nanoscale. In each case, the associated Rabi energy, which corresponds to the energy splitting between the two polaritonic branches, is obtained. Finally, a dedicated numerical model was employed to calculate the hot electron generation rate in the nanorods. The calculations demonstrate that efficient generation of hot electrons can be achieved in the near-infrared region, when the interband transition is strongly coupled with a plasmon resonance. This high generation rate stems from the hybrid nature of the mode, as its plasmonic component provides a high absorption cross-section, while the IT part ensures efficient conversion to hot electrons. Consequently, aluminum nanorods represent an efficient source of hot electrons in the visible and near-infrared regions, with potential applications in local photochemistry, photodetection, and solar energy harvesting.

physics.optics

Hot electrons and electromagnetic effects in the broadband Au, Ag, and Ag-Au nanocrystals: The UV, visible, and NIR plasmons

Energetic and optical properties of plasmonic nanocrystals strongly depend on their sizes, shapes, and composition. Whereas using plasmonic nanoparticles in biotesting has become routine, applications of plasmonics in energy are still early in development. Here, we investigate hot electron (HE) generation and related electromagnetic effects in both mono- and bi-metallic nanorods (NRs) and focus on one promising type of bi-metallic nanocrystals - core-shell Au-Ag nanorods. The spectra of the NRs are broadband, highly tunable with their geometry, and have few plasmon resonances. In this work, we provide a new quantum formalism describing the HE generation in bi-metallic nanostructures. Interestingly, we observe that the HE generation rate at the UV plasmon resonance of Au-Ag NRs appears to be very high. These HEs are highly energetic and suitable for carbon-fuel reactions. Simultaneously, the HE generation at the longitudinal plasmon (L-plasmon) peaks, which can be tuned from the yellow to near-IR, depends on the near-field and electromagnetic Mie effects, limiting the HE efficiencies for the long and large NRs. These properties of the L-plasmon relate to all kinds of NRs (Au, Ag, and Au-Ag). We also consider the generation of the interband d-holes in Au and Ag, since the involvement of the d-band is crucial for the energetic properties of UV plasmons. The proposed formalism is an important development for the description of bi-metallic (or tri-metallic, or more complex) nanostructures, and it paves the way to the efficient application of the plasmonic HEs and hot holes in sensing, nanotechnology, photocatalysis, and electrophotochemistry.

cond-mat.mes-hall

Mie Sensing with Neural Networks: Recognition of Nano-Object Parameters, the Invisibility Point, and Restricted Models

In this work, we use artificial neural networks (ANNs) to recognize the material composition, sizes of nanoparticles and their concentrations in different media with high accuracy, solely from the absorbance spectrum of a macroscopic sample. We construct ANNs operating in the following two schemes. The first scheme is designed to recognize the dimensions and refractive indices of dielectric scatterers in mixed ensembles. The second ANN model simultaneously recognizes the dimensions of gold nanospheres in a mixture and the refractive index of a matrix. A challenge in the first scheme arises at and near the invisibility point, i.e., when the refractive index of nanoparticles is close to that of the medium. Of course, particle recognition in this regime faces fundamental physical limitations. However, such recognition near the invisibility point is possible, and our study reveals its unique properties. Interestingly, the recognition process for the refractive index in the vicinity of the invisibility point shows very small errors. In contrast, the errors for the recognition of the radius grow strongly near this point. Another regime with limited recognition occurs when the extinction spectra are not unique and can correspond to different realizations of nanoparticle mixtures. Regarding multi-particle or polydisperse solutions, the ML-based models should in such cases be rationally restricted to maintain the feasibility of the recognition process. Overall, the recognition schemes proposed and investigated by us can find their applications in the field of sensing.

physics.optics

Universal imprinting of chirality with chiral light by employing plasmonic metastructures

Chirality, either of light or matter, has proved to be very practical in biosensing and nanophotonics. However, the fundamental understanding of its temporal dynamics still needs to be discovered. A realistic setup for this are the so-called metastructures, since they are optically active and are built massively, hence rendering an immediate potential candidate. Here we propose and study the electromagnetic-optical mechanism leading to chiral optical imprinting on metastructures. Induced photothermal responses create anisotropic permittivity modulations, different for left or right circularly polarized light, leading to temporal-dependent chiral imprinting of hot-spots, namely imprinting of chirality. The above effect has not been observed yet, but it is within reach of modern experimental approaches. The proposed nonlinear chiroptical effect is general and should appear in any anisotropic material; however, we need to design a particular geometry for this effect to be strong. These new chiral time-dependent metastructures may lead to a plethora of applications.

physics.optics

Colloidal Titanium Nitride Nanobars for Broadband Inexpensive Plasmonics and Photochemistry from Visible to Mid-IR Wavelengths

Developing colloidal plasmonic nanomaterials with high carrier density that show optical resonances and photochemical activity extending from the visible to the mid-infrared (MIR) ranges remains a challenging pursuit. Here, we report the fabrication of titanium nitride (TiN) nanobars obtained using a two step procedure based on a wet chemical route synthesis of TiO2 nanowires and their subsequent high temperature annealing in ammonia flow. Electromagnetic simulations of the resulting TiN nanobars reveal a rich set of optical resonances featuring transverse, longitudinal and mixed transverse longitudinal plasmonic modes that cover energies from the visible to MIR region. TiN nanobars decorated with Pt co catalyst nanocrystals show enhanced photocatalytic hydrogen evolution activity in comparison to both isotropic TiN nanospheres of similar size and TiN nanocubes under near infrared excitation at 940 nm due to the enhanced hot electron generation. We also demonstrate that plasmonic TiN nanobars can be used for the detection of furfural molecular vibrations by providing a strong surface enhanced infrared absorption (SEIRA) effect in the MIR region.

physics.optics

Plasmonic nanocrystals with complex shapes for photocatalysis and growth: Contrasting anisotropic hot-electron generation with the photothermal effect

In plasmonics, and particularly in plasmonic photochemistry, the effect of hot-electron generation is an exciting phenomenon driving new fundamental and applied research. However, obtaining a microscopic description of the hot-electron states represents a challenging problem, limiting our capability to design efficient nanoantennas exploiting these excited carriers. This paper addresses this limitation and studies the spatial distributions of the photophysical dynamic parameters controlling the local surface photochemistry on a plasmonic nanocrystal. We found that the generation of energetic electrons and holes in small plasmonic nanocrystals with complex shapes is strongly position-dependent and anisotropic, whereas the phototemperature across the nanocrystal surface is nearly uniform. Our formalism includes three mechanisms for the generation of excited carriers: the Drude process, the surface-assisted generation of hot-electrons in the sp-band, and the excitation of interband d-holes. Our computations show that the hot-carrier generation originating from these mechanisms reflects the internal structure of hot spots in nanocrystals with complex shapes. The injection of energetic carriers and increased surface phototemperature are driving forces for photocatalytic and photo-growth processes on the surface of plasmonic nanostructures. Therefore, developing a consistent microscopic theory of such processes is necessary for designing efficient nanoantennas for photocatalytic applications.

cond-mat.mes-hall

On the origin of chirality in plasmonic meta-molecules

Chirality is a fundamental feature in all domains of nature, ranging from particle physics over electromagnetism to chemistry and biology. Chiral objects lack a mirror plane and inversion symmetry and therefore cannot be spatially aligned with their mirrored counterpart, their enantiomer. Both natural molecules and artificial chiral nanostructures can be characterized by their light-matter interaction, which is reflected in circular dichroism (CD). Using DNA origami, we assemble model meta-molecules from multiple plasmonic nanoparticles, representing meta-atoms accurately positioned in space. This allows us to reconstruct piece by piece the impact of varying macromolecular geometries on their surrounding optical near fields. Next to the emergence of CD signatures in the instance that we architect a third dimension, we design and implement sign flipping signals through addition or removal of single particles in the artificial molecules. Our data and theoretical modelling reveal the hitherto unrecognized phenomenon of chiral plasmonic-dielectric coupling, explaining the intricate electromagnetic interactions within hybrid DNA-based plasmonic nanostructures.

physics.optics

A light-driven three-dimensional plasmonic nanosystem that translates molecular motion into reversible chiroptical function

Nature has developed striking light-powered proteins such as bacteriorhodopsin, which can convert light energy into conformational changes for biological functions. Such natural machines are a great source of inspiration for creation of their synthetic analogues. However, synthetic molecular machines typically operate at the nanometre scale or below. Translating controlled operation of individual molecular machines to a larger dimension, for example, to 10-100 nm, which features many practical applications, is highly important but remains challenging. Here we demonstrate a light-driven plasmonic nanosystem that can amplify the molecular motion of azobenzene through the host nanostructure and consequently translate it into reversible chiroptical function with large amplitude modulation. Light is exploited as both energy source and information probe. Our plasmonic nanosystem bears unique features of optical addressability, reversibility and modulability, which are crucial for developing all-optical molecular devices with desired functionalities.

physics.optics

Chiral Plasmonic Nanostructures Enabled by Bottom-Up Approaches

We present a comprehensive review of recent developments in the field of chiral plasmonics. Significant advances have been made recently in understanding the working principles of chiral plasmonic structures. With advances in micro- and nanofabrication techniques, a variety of chiral plasmonic nanostructures have been experimentally realized; these tailored chiroptical properties vastly outperform those of their molecular counterparts. We focus on chiral plasmonic nanostructures created using bottom-up approaches, which not only allow for rational design and fabrication but most intriguingly in many cases also enable dynamic manipulation and tuning of chiroptical responses. We first discuss plasmon-induced chirality, resulting from the interaction of chiral molecules with plasmonic excitations. Subsequently, we discuss intrinsically chiral colloids, which give rise to optical chirality owing to their chiral shapes. Finally, we discuss plasmonic chirality, achieved by arranging achiral plasmonic particles into handed configurations on static or active templates. Chiral plasmonic nanostructures are very promising candidates for real-life applications owing to their significantly larger optical chirality than natural molecules. In addition, chiral plasmonic nanostructures offer engineerable and dynamic chiroptical responses, which are formidable to achieve in molecular systems. We thus anticipate that the field of chiral plasmonics will attract further widespread attention in applications ranging from enantioselective analysis to chiral sensing, structural determination, and in situ ultrasensitive detection of multiple disease biomarkers, as well as optical monitoring of transmembrane transport and intracellular metabolism.

physics.optics

Hot electron generation through near-field excitation of plasmonic nanoresonators

We theoretically study hot electron generation through the emission of a dipole source coupled to a nanoresonator on a metal surface. In our hybrid approach, we solve the time-harmonic Maxwell's equations numerically and apply a quantum model to predict the efficiency of hot electron generation. Strongly confined electromagnetic fields and the strong enhancement of hot electron generation at the metal surface are predicted and are further interpreted with the theory of quasinormal modes. In the investigated nanoresonator setup, both the emitting source and the acceptor resonator are localized in the same volume, and this configuration looks promising to achieve high efficiencies of hot electron generation. By comparing with the efficiency calculated in the absence of the plasmonic nanoresonator, that is, the dipole source is located near a flat, unstructured metal surface, we show that the effective excitation of the modes of the nanoresonator boosts the generation efficiency of energetic charge carriers. The proposed scheme can be used in tip-based spectroscopies and other optoelectronic applications.

physics.optics

Comments on "Recent Developments in Plasmon-Assisted Photocatalysis -- a Personal Perspective"

The authors of preprint arXiv:2009.00286 and paper Appl. Phys. Lett. 117, 130501 (2020), Y. Sivan and Y. Dubi, made several wrong and inconsistent comments on our papers [J. Phys. Chem. C 117, 16616-16631 (2013), ACS Photonics 4 (11), 2759-2781 (2017)]. Moreover, the authors of arXiv:2009.00286 addressed in their comments features that were not present in our paper [ACS Photonics 4 (11), 2759-2781 (2017)]. In this document we go through the comments made in arXiv:2009.00286, which we found to be wrong and misleading.

cond-mat.mtrl-sci

Long- and Short-Ranged Chiral Interactions in DNA Assembled Plasmonic Chains

Molecular chirality plays a crucial role in innumerable biological processes. The chirality of a molecule can typically be identified by its characteristic optical response, the circular dichroism (CD). CD signals have thus long been used to identify the state of molecules or to follow dynamic protein configurations. In recent years, the focus has moved towards plasmonic nanostructures, as they show potential for applications ranging from pathogen sensing to novel optical materials. The plasmonic coupling of the individual elements of such chiral metallic structures is a crucial prerequisite to obtain sizeable CD signals. We here identified and implemented various coupling entities - chiral and achiral - to obtain chiral transfer over distances close to 100 nm. The coupling is realized by an achiral nanosphere situated between a pair of gold nanorods that are arranged far apart but in a chiral fashion. We synthesized these structures with nanometer precision using DNA origami and obtained sample homogeneity that allowed us to directly demonstrate efficient chiral energy transfer between the distant nanorods. The transmitter particle causes a strong enhancement in amplitude of the CD response, the emergence of an additional chiral feature at the resonance frequency of the nanosphere, and a redshift of the longitudinal plasmonic resonance frequency of the nanorods. Numerical simulations closely match our experimental observations and give insights in the intricate behavior of chiral optical fields and the transfer of plasmons in complex architectures.

physics.optics

Comments on ""Hot" electrons in metallic nanostructures -- non-thermal carriers or heating?" and "Assistance of metal nanoparticles to photo-catalysis -- nothing more than a classical heat source"

The authors of preprint arXiv:1810.00565 and paper in Light: Science & Applications (2019), Y. Dubi and Y. Sivan, made several wrong and inconsistent comments on several of our papers. In addition, the paper in Faraday Discuss. 214, 215-233 (2018) by the same authors also contains several wrong statements in relationship with our work. Moreover, the authors address in their comments features that were in fact not present in our work. In what follows we present correction to a number of specific points in which they either misrepresented or erroneously interpreted our published work.

cond-mat.mes-hall

Temporal plasmonics: Fano and Rabi regimes in the time domain in metal nanostructures

The Fano and Rabi models represent remarkably common effects in optics. Here we study the coherent time dynamics of plasmonic systems exhibiting Fano and Rabi resonances. We demonstrate that these systems show fundamentally different dynamics. A system with a Fano resonance displays at most one temporal beat under pulsed excitation, whereas a system in the Rabi regime may have any number of beats. Remarkably, the Fano-like systems show time dynamics with very characteristic coherent tails despite the strong decoherence that is intrinsic for such systems. The coherent Fano and Rabi dynamics that we predicted can be observed in plasmonic nanocrystal dimers in time-resolved experiments. Our study demonstrates that such coherent temporal plasmonics includes nontrivial and characteristic relaxation behaviors and presents an interesting direction to develop with further research.

cond-mat.mes-hall

Strong Quantum Confinement Effects and Chiral Excitons in Bio-Inspired ZnO-Amino Acid Co-Crystals

Elucidating the underlying principles behind band gap engineering is paramount for the successful implementation of semiconductors in photonic and optoelectronic devices. Recently it has been shown that the band gap of a wide and direct band gap semiconductor, such as ZnO, can be modified upon co-crystallization with amino acids, with the role of the biomolecules remaining unclear. Here, by probing and modeling the light emitting properties of ZnO-amino acid co-crystals, we identify the amino acids role on this band gap modulation and demonstrate their effective chirality transfer to the inter-band excitations in ZnO. Our 3D quantum model suggests that the strong band edge emission blue shift in the co-crystals can be explained by a quasi-periodic distribution of amino acid potential barriers within the ZnO crystal lattice. Overall, our findings indicate that biomolecule co-crystallization can be used as a truly bio-inspired means to induce chiral quantum confinement effects in quasi-bulk semiconductors.

cond-mat.mtrl-sci

Broadband mid-infrared perfect absorber using fractal Gosper curve

Designing broadband metamaterial perfect absorbers is challenging due to the intrinsically narrow bandwidth of surface plasmon resonances. Here, the paper reports an ultra-broadband metamaterial absorber by using space filling Gosper curve. The optimized result shows an average absorptivity of 95.78% from 2.64 to 9.79 μm across the entire mid-infrared region. Meanwhile, the absorber shows insensitivity to the polarization angle and the incident angle of the incident light. The underlying physical principles, used in our broadband absorber, involve a fractal geometry with multiple scales and a dissipative plasmonic crystal. The broadband perfect absorption can be attributed to multiple electric resonances at different wavelengths supported by a few segments in the defined Gosper curve.

physics.optics

Circular Dichroism of Chiral Molecules in DNA- Assembled Plasmonic Hotspots

The chiral state of a molecule plays a crucial role in molecular recognition and biochemical reactions. Because of this and owing to the fact that most modern drugs are chiral, the sensitive and reliable detection of the chirality of molecules is of great interest to drug development. The majority of naturally occurring biomolecules exhibit circular dichroism (CD) in the UV-range. Theoretical studies and several experiments have demonstrated that this UV-CD can be transferred into the plasmonic frequency domain when metal surfaces and chiral biomolecules are in close proximity. Here, we demonstrate that the CD transfer effect can be drastically enhanced by placing chiral molecules, here double-stranded DNA, inside a plasmonic hotspot. By using different particle types (gold, silver, spheres and rods) and by exploiting the versatility of DNA origami we were able to systematically study the impact of varying particle distances on the CD transfer efficiency and to demonstrate CD transfer over the whole optical spectrum down to the near infrared. For this purpose, nanorods were also placed upright on our DNA origami sheets, this way forming strong optical antennas. Theoretical models, demonstrating the intricate relationships between molecular chirality and achiral electric fields, support our experimental findings.

cond-mat.mes-hall

Mid-infrared Plasmonic Circular Dichroism Generated by Graphene Nanodisk Assemblies

It is very interesting to bring plasmonic circular dichroism spectroscopy to the mid-infrared spectral interval, and there are two reasons for this. This spectral interval is very important for thermal bio-imaging and, simultaneously, this spectral range includes vibrational lines of many chiral biomolecules. Here we demonstrate that graphene plasmons indeed offer such opportunity. In particular, we show that chiral graphene assemblies consisting of a few graphene nanodisks can generate strong circular dichroism (CD) in the mid-infrared interval. The CD signal is generated due to the plasmon-plasmon coupling between adjacent nanodisks in the specially designed chiral graphene assemblies. Because of the large dimension mismatch between the thickness of a graphene layer and the incoming light's wavelength, three-dimensional configurations with a total height of a few hundred nanometers are necessary to obtain a strong CD signal in the mid-infrared range. The mid-infrared CD strength is mainly governed by the total dimensions (total height and helix scaffold radius) of the graphene nanodisk assembly, and by the plasmon-plasmon interaction strength between its constitutive nanodisks. Both positive and negative CD bands can be observed in the graphene assembly array. The frequency interval of the plasmonic CD spectra overlaps with the vibrational modes of some important biomolecules, such as DNA and many different peptides, giving rise to the possibility of enhancing the vibrational optical activity of these molecular species by attaching them to the graphene assemblies. Simultaneously the spectral range of chiral mid-infrared plasmons in our structures appears near the typical wavelength of the human-body thermal radiation and, therefore, our chiral metastructures can be potentially utilized as optical components in thermal imaging devices.

cond-mat.mtrl-sci