scholarly journals Subwavelength imaging at infrared frequencies using an array of metallic nanorods

2007 ◽  
Vol 75 (3) ◽  
Author(s):  
Mário G. Silveirinha ◽  
Pavel A. Belov ◽  
Constantin R. Simovski
2015 ◽  
Author(s):  
Yoshiro Ohashi ◽  
Bikas Ranjan ◽  
Yuika Saito ◽  
Prabhat Verma

2019 ◽  
Vol 31 (45) ◽  
pp. 1804958 ◽  
Author(s):  
Yanhong Ma ◽  
Wenyu Jiang ◽  
Yuanqing Xu ◽  
Yong Zhang

2008 ◽  
Author(s):  
Kevin J. Webb ◽  
Huikan Liu ◽  
Alon Ludwig ◽  
S. Schivanand

1989 ◽  
Vol 134 ◽  
pp. 197-198
Author(s):  
D. M. Worrall ◽  
B. J. Wilkes

Quasars with similar core-compact radio properties can be classified by their differences at optical and infrared frequencies. Their X-ray properties might be expected to be similar if the synchrotron self-Compton mechanism relates their radio and X-ray emission. We have compared the 0.2–3.5 keV mean power-law energy spectral indices, , for 4 quasar classes: 12 Highly Polarized QSOs (HPQs), 19 Flat Radio Spectrum, core-compact, low-polarization, QSOs (FRS QSOs), 24 radio-selected BL Lac objects, and 7 X-ray-selected BL Lac objects.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Michał Dudek ◽  
Rafał Kowerdziej ◽  
Alessandro Pianelli ◽  
Janusz Parka

AbstractGraphene-based hyperbolic metamaterials provide a unique scaffold for designing nanophotonic devices with active functionalities. In this work, we have theoretically demonstrated that the characteristics of a polarization-dependent tunable hyperbolic microcavity in the mid-infrared frequencies could be realized by modulating the thickness of the dielectric layers, and thus breaking periodicity in a graphene-based hyperbolic metamaterial stack. Transmission of the tunable microcavity shows a Fabry–Perot resonant mode with a Q-factor > 20, and a sixfold local enhancement of electric field intensity. It was found that by varying the gating voltage of graphene from 2 to 8 V, the device could be self-regulated with respect to both the intensity (up to 30%) and spectrum (up to 2.1 µm). In addition, the switching of the device was considered over a wide range of incident angles for both the transverse electric and transverse magnetic modes. Finally, numerical analysis indicated that a topological transition between elliptic and type II hyperbolic dispersion could be actively switched. The proposed scheme represents a remarkably versatile platform for the mid-infrared wave manipulation and may find applications in many multi-functional architectures, including ultra-sensitive filters, low-threshold lasers, and photonic chips.


2006 ◽  
Vol 140 (1) ◽  
pp. 9-13 ◽  
Author(s):  
Hui Liu ◽  
Xiaopeng Zhao ◽  
Quanhong Fu

2007 ◽  
Vol 90 (19) ◽  
pp. 191904 ◽  
Author(s):  
Hui Liu ◽  
Xiaopeng Zhao
Keyword(s):  

1962 ◽  
Vol 18 (12) ◽  
pp. 1603-1613 ◽  
Author(s):  
J.J. Shipman ◽  
V.L. Folt ◽  
S. Krimm

1987 ◽  
Vol 41 (5) ◽  
pp. 809-820 ◽  
Author(s):  
James Grainger ◽  
Leslie T. Gelbaum

Reference infrared vapor-phase spectra of the 22 tetrachlorodibenzo-dioxin (TCDD) isomers were recorded at low microgram concentrations. These reference spectra of synthetic mixture components separated chromatographically or by spectral subtraction exhibit distinct infrared spectra for each isomer. The infrared frequencies are delineated in correlation tables and are interpreted in terms of substitution patterns which determine the strength of the ether linkage. Absorbance values in the 1330–1280 cm−1 (C-O-C asymmetric stretch) region correlate with specific substitution patterns and molecular geometry. Relative electron-withdrawing capacities for chlorinated aromatic rings in TCDD isomers were estimated on the basis of relative capacities determined for model compounds. Qualitative correlations were established between electron-withdrawing capacities and the effects of resonance and field interactions on the ether linkage absorption frequencies of individual TCDD isomers. Gas chromatography Fourier transform infrared (GC/FT-IR) isomer assignments are generally consistent with those obtained by proton Fourier transform nuclear magnetic resonance (1H FT/NMR) and flame ionization gas chromatography (GC/FID). A chromatographically independent method of assigning TCDD isomer structures on the basis of ether linkage asymmetric stretching frequencies was established by utilization of valence-bond approximations. GC/FT-IR assignments for several TCDD isomers differ from isomer assignments in previously published results. A user-generated, vapor-phase reference library, containing individual TCDD spectra and spectra of isomer pairs that are incompletely resolved on chromatographic columns, correctly identified each isomer in variety of mixtures by means of a software algorithm.


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