Circular extinction of plasmonic silver nanocaps and gas sensing

2016 ◽  
Vol 186 ◽  
pp. 345-352 ◽  
Author(s):  
Jun Li ◽  
Nicholas. A. Kotov

Chiral plasmonic nanostructures exhibit strong rotatory optical activity and are expected to enrich the field of metaoptical materials. Potential applications of chiroplasmonic nanostructures include circular polarizers, optical polarization detectors, asymmetric catalysts, and sensors. However, chiral plasmonic materials require subwavelength structural control and involve laborious chemical or lithographic procedures for their manufacturing. Moreover, strong rotatory activity of subwavelength structures whose chirality was imparted by microfabrication, has been obtained for the red and infrared parts of the spectrum but faces new challenges for the blue and violet spectral ranges even with plasmonic materials with plasmonic bands in the 200–400 nm window. In this study, we address this problem by preparing chiral subwavelength nanostructures by glancing angle sputtering of metallic silver on ZnO nanopillar arrays. Silver deposition in two different planes is a convenient method for preparation of silver chiroplasmonic nanocaps (Ag CPNCs) with controlled asymmetry. Circular dichroism spectroscopy was used to examine the circular extinction for the left-handed nanocaps (L-CPNCs) with understanding that not only circular dichroism but also many other optical effects contribute to the amplitude of these bands. The pillared silver films exhibit circular extinction in the violet area of the electromagnetic spectrum. Partial oxidation of Ag to AgxO causes the absorption and corresponding circular extinction band obtained using a conventional CD spectrometer at 400–525 nm to increase and shift. This optical material may be used to detect oxygen and extends the spectrum of application of chiroplasmonic materials to gas sensing.

Small ◽  
2016 ◽  
Vol 13 (1) ◽  
pp. 1601115 ◽  
Author(s):  
Xiaoli Wang ◽  
Zhiyong Tang

Nanophotonics ◽  
2020 ◽  
Vol 9 (10) ◽  
pp. 3419-3434 ◽  
Author(s):  
Shao-Ding Liu ◽  
Jun-Yan Liu ◽  
Zhaolong Cao ◽  
Jin-Li Fan ◽  
Dangyuan Lei

AbstractEnhancing the circular dichroism signals of chiral plasmonic nanostructures is vital for realizing miniaturized functional chiroptical devices, such as ultrathin wave plates and high-performance chiral biosensors. Rationally assembling individual plasmonic metamolecules into coupled nanoclusters or periodic arrays provides an extra degree of freedom to effectively manipulate and leverage the intrinsic circular dichroism of the constituent structures. Here, we show that sophisticated manipulation over the geometric parameters of a plasmonic stereo-metamolecule array enables selective excitation of its surface lattice resonance mode either by left- or right-handed circularly polarized incidence through diffraction coupling, which can significantly amplify the differential absorption and hence the intrinsic circular dichroism. In particular, since the diffraction coupling requires no index-matching condition and its handedness can be switched by manipulating the refractive index of either the superstrate or the substrate, it is therefore possible to achieve dynamic tuning and active control of the intrinsic circular dichroism response without the need of modifying structure parameters. Our proposed system provides a versatile platform for ultrasensitive chiral plasmonics biosensing and light field manipulation.


2018 ◽  
Vol 6 (14) ◽  
pp. 1800153 ◽  
Author(s):  
Joel T. Collins ◽  
Xuezhi Zheng ◽  
Nuno V. S. Braz ◽  
Eli Slenders ◽  
Shuai Zu ◽  
...  

2022 ◽  
Author(s):  
Vikas Yadav ◽  
Soumik Siddhanta

Circular dichroism (CD) from plasmonic nanostructures yields fascinating insights into their chiroptical properties, however, the weak signals make their investigations profoundly challenging. We have demonstrated a method for significantly improving...


2019 ◽  
Author(s):  
Won Jin Choi ◽  
Gong Cheng ◽  
Zhengyu Huang ◽  
Shuai Zhang ◽  
Theodore B. Norris ◽  
...  

ABSTRACTSTerahertz circular dichroism (TCD) offers spectroscopic capabilities for understanding mesoscale chiral architecture and low-energy vibrations of macromolecules in (bio)materials1–5. However, the lack of dynamic polarization modulators comparable to polarization optics for other parts of electromagnetic spectrum impedes proliferation of TCD spectroscopy6–10. Here we show that tunable optical elements fabricated from patterned plasmonic sheets with periodic kirigami cuts make possible polarization modulation of THz radiation under application of mechanical strain. A herringbone pattern of microscale metal stripes enables dynamic range of polarization rotation modulation exceeding 80° over thousands of cycles. Upon out-of-plane buckling, the plasmonic stripes function as reconfigurable semi-helices of variable pitch aligned along the THz propagation direction. Several biomaterials, exemplified by elytrons of Chrysina gloriosa beetles, revealed distinct TCD fingerprints associated with the helical substructure in the biocomposite. Analogous kirigami modulators will also enable other applications in THz optics, such as polarization-based terahertz imaging and phase-encrypted telecommunication.


2015 ◽  
Vol 112 (46) ◽  
pp. 14206-14211 ◽  
Author(s):  
Tingting Fan ◽  
Patrik Grychtol ◽  
Ronny Knut ◽  
Carlos Hernández-García ◽  
Daniel D. Hickstein ◽  
...  

We demonstrate, to our knowledge, the first bright circularly polarized high-harmonic beams in the soft X-ray region of the electromagnetic spectrum, and use them to implement X-ray magnetic circular dichroism measurements in a tabletop-scale setup. Using counterrotating circularly polarized laser fields at 1.3 and 0.79 µm, we generate circularly polarized harmonics with photon energies exceeding 160 eV. The harmonic spectra emerge as a sequence of closely spaced pairs of left and right circularly polarized peaks, with energies determined by conservation of energy and spin angular momentum. We explain the single-atom and macroscopic physics by identifying the dominant electron quantum trajectories and optimal phase-matching conditions. The first advanced phase-matched propagation simulations for circularly polarized harmonics reveal the influence of the finite phase-matching temporal window on the spectrum, as well as the unique polarization-shaped attosecond pulse train. Finally, we use, to our knowledge, the first tabletop X-ray magnetic circular dichroism measurements at the N4,5 absorption edges of Gd to validate the high degree of circularity, brightness, and stability of this light source. These results demonstrate the feasibility of manipulating the polarization, spectrum, and temporal shape of high harmonics in the soft X-ray region by manipulating the driving laser waveform.


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