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Register a new userAtomic Response in the Near-field of Nanostructured Plasmonic Metamaterial
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Added by
Syed Abdullah Aljunid
Publication date
2016
fields
Physics
and research's language is
English
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We report on reflection spectra of caesium atoms in close vicinity of a nanostructured metallic meta-surface. We show that the hyperfine sub-Doppler spectrum of the $6S_{1/2} - 6P_{3/2}$ resonance transition at 852 nm is strongly affected by the coupling to the plasmonic resonance of the nanostructure. Fine tuning of dispersion and positions of the atomic lines in the near-field of plasmonic metamaterials could have uses and implications for the atom-based metrology, sensing and the development of atom-on-a-chip devices.
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Silver, especially in the form of nanostructures, is widely employed as an antimicrobial agent in a large range of commercial products. The origin of the biocidal mechanism has been elucidated in the last decades, and most likely originates from silver cation release due to oxidative dissolution followed by cellular uptake of silver ions, a process that causes a severe disruption of bacterial metabolism and eventually leads to eradication. Despite the large number of works dealing with the effects of nanosilver shape/size on the antibacterial mechanism and on the (bio)physical chemistry pathways that drive bacterial eradication, little effort has been devoted to the investigation of the silver NPs plasmon response upon interaction with bacteria. Here we present a detailed investigation of the bacteria-induced changes of the plasmon spectral and dynamical features after exposure to one of the most studied bacterial models, Escherichia Coli. Ultrafast pump-probe measurements indicate that the dramatic changes on particle size/shape and crystallinity, which stem from a bacteria-induced oxidative dissolution process, translate into a clear modification of the plasmon spectral and dynamical features. This study may open innovative new avenues in the field of biophysics of bio-responsive materials, with the aim of providing new and reliable biophysical signatures of the interaction of these materials with complex biological environments.
We propose a new approach to understand the time-dependent temperature increasing process of gold-silica core-shell nanoparticles injected into chicken tissues under near-infrared laser irradiation. Gold nanoshells strongly absorb near-infrared radiations and efficiently transform absorbed energy into heat. Temperature rise given by experiments and numerical calculations based on bioheat transfer are in good agreement. Our work improves the analysis of a recent study [Richardson et al., Nano Lett. 9, 1139 (2009)] by including effects of the medium perfusion on temperature increase. The theoretical analysis can also be used to estimate the distribution of nanoparticles in experimental samples and provide a relative accuracy prediction for the temperature profile of new systems. This methodology would provide a novel and reliable tool for speeding up photothermal investigations and designing state-of-the-art photothermal devices.
Contrary to classical predictions, the optical response of few-nm plasmonic particles depends on particle size due to effects such as nonlocality and electron spill-out. Ensembles of such nanoparticles (NPs) are therefore expected to exhibit a nonclassical inhomogeneous spectral broadening due to size distribution. For a normal distribution of free-electron NPs, and within the simple nonlocal Hydrodynamic Drude Model (HDM), both the nonlocal blueshift and the plasmon linewidth are shown to be considerably affected by ensemble averaging. Size-variance effects tend however to conceal nonlocality to a lesser extent when the homogeneous size-dependent broadening of individual NPs is taken into account, either through a local size-dependent damping (SDD) model or through the Generalized Nonlocal Optical Response (GNOR) theory. The role of ensemble averaging is further explored in realistic distributions of noble-metal NPs, as encountered in experiments, while an analytical expression to evaluate the importance of inhomogeneous broadening through measurable quantities is developed. Our findings are independent of the specific nonclassical theory used, thus providing important insight into a large range of experiments on nanoscale and quantum plasmonics.
The interplay of spin angular momentum and thermal radiation is a frontier area of interest to nanophotonics as well as topological physics. Here, we show that a thick planar slab of a nonreciprocal material, despite being at thermal equilibrium with its environment, can exhibit nonzero photon spin angular momentum and nonzero radiative heat flux in its vicinity. We identify them as the persistent thermal photon spin (PTPS) and the persistent planar heat current (PPHC) respectively. With a practical example system, we reveal that the fundamental origin of these phenomena is connected to spin-momentum locking of thermally excited evanescent waves. We also discover spin magnetic moment of surface polaritons in nonreciprocal photonics that further clarifies these features. We then propose a novel thermal photonic imaging experiment based on Brownian motion that allows one to witness these surprising features by directly looking at them using a lab microscope. We further demonstrate the universal behavior of these near-field thermal radiation phenomena through a comprehensive analysis of gyroelectric, gyromagnetic and magneto-electric nonreciprocal materials. Together, these results expose a surprisingly little explored research area of thermal spin photonics with prospects for new avenues related to non-Hermitian topological photonics and radiative heat transport.
In this work we study the strong confinement effects on the electromagnetic response of metallic nanoparticles. We calculate the field enhancement factor for nanospheres of various radii by using optical constants obtained from both classical and quantum approaches and compare their size-dependent features. To evaluate the scattered near-field, we solve the electromagnetic wave equation within a finite element framework. When quantization of electronic states is considered for the input optical functions, a significant blue-shift in the resonance of the enhanced field is observed, in contrast to the case in which functions obtained classically are used. Furthermore, a noticeable underestimation of the field amplification is found in the calculation based on a classical dielectric function. Our results are in good agreement with available experimental reports and provide relevant information on the cross-over between classical and quantum regime, useful in potentiating nanoplasmonics applications.
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