Nanophotonic Chiral Sensing: How Does It Actually Work?

Nanophotonic chiral sensing has recently attracted a lot of attention. The idea is to exploit the strong light-matter interaction in nanophotonic resonators to determine the concentration of chiral molecules at ultralow thresholds, which is highly attractive for numerous applications in life science and chemistry. However, a thorough understanding of the underlying interactions is still missing. The theoretical description relies on either simple approximations or on purely numerical approaches. We close this gap and present a general theory of chiral light-matter interactions in arbitrary resonators. Our theory describes the chiral interaction as a perturbation of the resonator modes, also known as resonant states or quasi-normal modes. We observe two dominant contributions: A chirality-induced resonance shift and changes in the modes' excitation and emission efficiencies. Our theory brings deep insights for tailoring and enhancing chiral light-matter interactions. Furthermore, it allows us to predict spectra much more efficiently in comparison to conventional approaches. This is particularly true, as chiral interactions are inherently weak and therefore perturbation theory fits extremely well for this problem.

Highly Sensitive Refractive Index Sensors with Plasmonic Nanoantennas-Utilization of Optimal Spectral Detuning of Fano Resonances.

We analyze and optimize the performance of coupled plasmonic nanoantennas for refractive index sensing. The investigated structure supports a sub- and super-radiant mode that originates from the weak coupling of a dipolar and quadrupolar mode, resulting in a Fano-type spectral line shape. In our study, we vary the near-field coupling of the two modes and particularly examine the influence of the spectral detuning between them on the sensing performance. Surprisingly, the case of matched resonance frequencies does not provide the best sensor. Instead, we find that the right amount of coupling strength and spectral detuning allows for achieving the ideal combination of narrow line width and sufficient excitation strength of the subradiant mode, and therefore results in optimized sensor performance. Our findings are confirmed by experimental results and first-order perturbation theory. The latter is based on the resonant state expansion and provides direct access to resonance frequency shifts and line width changes as well as the excitation strength of the modes. Based on these parameters, we define a figure of merit that can be easily calculated for different sensing geometries and agrees well with the numerical and experimental results.

Chiral plasmonics.

We present a comprehensive overview of chirality and its optical manifestation in plasmonic nanosystems and nanostructures. We discuss top-down fabricated structures that range from solid metallic nanostructures to groupings of metallic nanoparticles arranged in three dimensions. We also present the large variety of bottom-up synthesized structures. Using DNA, peptides, or other scaffolds, complex nanoparticle arrangements of up to hundreds of individual nanoparticles have been realized. Beyond this static picture, we also give an overview of recent demonstrations of active chiral plasmonic systems, where the chiral optical response can be controlled by an external stimulus. We discuss the prospect of using the unique properties of complex chiral plasmonic systems for enantiomeric sensing schemes.

Analytic Optimization of Near-Field Optical Chirality Enhancement.

We present an analytic derivation for the enhancement of local optical chirality in the near field of plasmonic nanostructures by tuning the far-field polarization of external light. We illustrate the results by means of simulations with an achiral and a chiral nanostructure assembly and demonstrate that local optical chirality is significantly enhanced with respect to circular polarization in free space. The optimal external far-field polarizations are different from both circular and linear. Symmetry properties of the nanostructure can be exploited to determine whether the optimal far-field polarization is circular. Furthermore, the optimal far-field polarization depends on the frequency, which results in complex-shaped laser pulses for broadband optimization.

A Switchable Mid-Infrared Plasmonic Perfect Absorber with Multispectral Thermal Imaging Capability.

A switchable perfect absorber with multispectral thermal imaging capability is presented. Aluminum nanoantenna arrays above a germanium antimony telluride (GST) spacer layer and aluminum mirror provide efficient wavelength-tunable absorption in the mid-infrared. Utilizing the amorphous-to-crystalline phase transition in GST, this device offers switchable absorption with strong reflectance contrast at resonance and large phase-change-induced spectral shifts.

Active Chiral Plasmonics.

Active control over the handedness of a chiral metamaterial has the potential to serve as key element for highly integrated polarization engineering approaches, polarization sensitive imaging devices, and stereo display technologies. However, this is hard to achieve as it seemingly involves the reconfiguration of the metamolecule from a left-handed into a right-handed enantiomer and vice versa. This type of mechanical actuation is intricate and usually neither monolithically realizable nor viable for high-speed applications. Here, enabled by the phase change material Ge3Sb2Te6 (GST-326), we demonstrate a tunable and switchable mid-infrared plasmonic chiral metamaterial in a proof-of-concept experiment. A large tunability range of the circular dichroism response from λ = 4.15 to 4.90 µm is achieved, and we experimentally demonstrate that the combination of a passive bias-type chiral layer with the active chiral metamaterial allows for switchable chirality, that is, the reversal of the circular dichroism sign, in a fully planar, layered design without the need for geometrical reconfiguration. Because phase change materials can be electrically and optically switched, our designs may open up a path for highly integrated mid-IR polarization engineering devices that can be modulated on ultrafast time scales.

Quantitative angle-resolved small-spot reflectance measurements on plasmonic perfect absorbers: impedance matching and disorder effects.

Plasmonic devices with absorbance close to unity have emerged as essential building blocks for a multitude of technological applications ranging from trace gas detection to infrared imaging. A crucial requirement for such elements is the angle independence of the absorptive performance. In this work, we develop theoretically and verify experimentally a quantitative model for the angular behavior of plasmonic perfect absorber structures based on an optical impedance matching picture. To achieve this, we utilize a simple and elegant k-space measurement technique to record quantitative angle-resolved reflectance measurements on various perfect absorber structures. Particularly, this method allows quantitative reflectance measurements on samples where only small areas have been nanostructured, for example, by electron-beam lithography. Combining these results with extensive numerical modeling, we find that matching of both the real and imaginary parts of the optical impedance is crucial to obtain perfect absorption over a large angular range. Furthermore, we successfully apply our model to the angular dispersion of perfect absorber geometries with disordered plasmonic elements as a favorable alternative to current array-based designs.

Yttrium hydride nanoantennas for active plasmonics.

A key challenge for the development of active plasmonic nanodevices is the lack of materials with fully controllable plasmonic properties. In this work, we demonstrate that a plasmonic resonance in top-down nanofabricated yttrium antennas can be completely and reversibly turned on and off using hydrogen exposure. We fabricate arrays of yttrium nanorods and optically observe, in extinction spectra, the hydrogen-induced phase transition between the metallic yttrium dihydride and the insulating trihydride. Whereas the yttrium dihydride nanostructures exhibit a pronounced particle plasmon resonance, the transition to yttrium trihydride leads to a complete vanishing of the resonant behavior. The plasmonic resonance in the dihydride state can be tuned over a wide wavelength range by simply varying the size of the nanostructures. Furthermore, we develop an analytical diffusion model to explain the temporal behavior of the hydrogen loading and unloading trajectories observed in our experiments and gain information about the thermodynamics of our device. Thus, our nanorod system serves as a versatile basic building block for active plasmonic devices ranging from switchable perfect absorbers to active local heating control elements.

Interpreting chiral nanophotonic spectra: the plasmonic Born-Kuhn model.

One of the most intuitive ways to classically understand the generation of natural optical activity in chiral media is provided by the coupled oscillator model of Born and Kuhn consisting of two identical, vertically displaced, coupled oscillators. We experimentally realize and discuss its exact plasmonic analog in a system of corner-stacked gold nanorods. In particular, we analyze the arising circular dichroism and optical rotatory spectra in terms of hybridized electromagnetic modes and retardation. Specifically, we demonstrate how tuning the vertical distance between the nanorods can lead to a selective excitation of the occurring bonding and antibonding chiral plasmonic modes.

Large-area 3D chiral plasmonic structures.

We manufacture large-area plasmonic structures featuring 3-dimensional chirality by colloidal nanohole lithography. By varying the polar rotating speed of the samples during gold evaporation, we can fabricate spiral-type ramp nanostructures. The optical properties show chiroptical resonances in the 100 to 400 THz frequency region (750 to 3000 nm), with circular dichroism values of up to 13%. Our method offers a simple low-cost manufacturing method of cm(2)-sized chiral plasmonic templates for chiroptical applications such as stereochemical enantiomer sensors.

Plasmonic diastereomers: adding up chiral centers.

We construct chiral plasmonic molecules by assembling two individual chiral centers. Interestingly, depending on the exact arrangement of the centers, all combinations result in a chiral compound with a strong chiral optical response. Furthermore, we demonstrate that the overall circular dichrosim (CD) is determined by the response of the individual chiral centers. We find that the CD spectra of the composite molecules are then simply given as the sum of the CD spectra of the constituting building blocks. Interestingly, as soon as strong near-field coupling takes place between chiral centers, we find strong deviation from the simple additive chiral behavior. Most importantly, we demonstrate that the optical response of complex chiral plasmonic systems can be decomposed and understood in terms of fundamental building blocks, offering simple and straightforward design rules for future applications such as chiral optical elements and enantiomer sensors.

Formation of chiral fields in a symmetric environment.

Chiral fields, i. e., electromagnetic fields with nonvanishing optical chirality, can occur next to symmetric nanostructures without geometrical chirality illuminated with linearly polarized light at normal incidence. A simple dipole model is utilized to explain this behavior theoretically. Illuminated with circularly polarized light, the chiral near-fields are still dominated by the distributions found for the linear polarization but show additional features due to the optical chirality of the incident light. Rotating the angle of linear polarization introduces more subtle changes to the distribution of optical chirality. Using our findings, we propose a novel scheme to obtain chiroptical far-field response using linearly polarized light, which could be utilized for applications such as optical enantiomer sensing.

Optical properties of chiral three-dimensional plasmonic oligomers at the onset of charge-transfer plasmons.

We demonstrate strong chiral optical response in three-dimensional chiral nanoparticle oligomers in the wavelength regime between 700 and 3500 nm. We show in experiment and simulation that this broad-band response occurs at the onset of charge transfer between the individual nanoparticles. The ohmic contact causes a strong red shift of the fundamental mode, while the geometrical shape of the resulting fused particles still allows for an efficient excitation of higher order modes. Calculated spectra and field distributions confirm our interpretation and show a number of interacting plasmonic modes. Our results deepen the understanding of the chiral optical response in complex chiral plasmonic nanostructures and pave the road toward broad-band chiral optical devices with strong responses, for example, for chiral plasmon rulers or sensing applications.

Three-dimensional chiral plasmonic oligomers.

The living world is chiral. Chirality or the handedness of a structure or molecule is at the heart of life itself. Recently, it has been shown that plasmonic structures exhibit unprecedented and gigantic chiral optical responses. Here we show that truly three-dimensional arrangements of plasmonic "meta-atoms" only exhibit a chiral optical response if similar plasmonic "atoms" are arranged in a handed fashion as we require resonant plasmonic coupling. Moreover, we demonstrate that such particle groupings, similarly to molecular systems, possess the capability to encode their three-dimensional arrangement in unique and well-modulated spectra making them ideal candidates for a three-dimensional chiral plasmon ruler. Our results are crucial for the future design and improvement of plasmonic chiral optical systems, for example, for ultrasensitive enantiomer sensing on the single molecule level.