scholarly journals Active narrowband filter based on 2.5D metasurface from Ge2Sb2Te5

2021 ◽  
Vol 2015 (1) ◽  
pp. 012147
Author(s):  
A I Solomonov ◽  
O M Kushchenko ◽  
D A Yavsin ◽  
M V Rybin ◽  
A D Sinelnik

Abstract We propose a new concept of an active narrowband filter based on a 2.5D metasurface from Ge2Sb2Te5 (GST). In this paper, we present a numerical calculation of the transmission spectrum from a structure of ellipsoids of revolution. For this 2.5D metasurface, modulation of narrow peaks in the IR range for s- and p-polarization is shown. A manufacturing technique using two-photon lithography and laser electrodispersion is proposed.

2012 ◽  
Vol 590 ◽  
pp. 411-415
Author(s):  
Ying Ying Zhang

In this paper, a new structure with square metal hole arrays was devised for SPR sense, and it was optimized by numerical calculation based on finite element analysis. After optimization, a very narrow SPR peak, which is just tenth of the conventional SPR sensor, can be obtained in the transmission spectrum. Besides, the linear measuring range is more than 0.4 RIU. Consequently, the newly designed structure will be benefit for the ability of resist noise and resolution.


2020 ◽  
Vol 54 (3 (253)) ◽  
pp. 165-171
Author(s):  
H.L. Margaryan ◽  
N.H. Hakobyan ◽  
V.K. Abrahamyan ◽  
P.K. Gasparyan ◽  
A.S. Yeremyan ◽  
...  

The manufacturing technique of a millimetric sizes cantilever from photo-driven azobenzene polymer is described. The cantilever oscillations under the influence of laser radiation are studied. The possibility of making a micron-sized cantilever by a femtosecond laser initiated two-photon polymerization technique is shown. Such cantilever can become the basis for a high sensitive sensor, controlled directly by light.


Author(s):  
David W. Piston ◽  
Brian D. Bennett ◽  
Robert G. Summers

Two-photon excitation microscopy (TPEM) provides attractive advantages over confocal microscopy for three-dimensionally resolved fluorescence imaging and photochemistry. Two-photon excitation arises from the simultaneous absorption of two photons in a single quantitized event whose probability is proportional to the square of the instantaneous intensity. For example, two red photons can cause the transition to an excited electronic state normally reached by absorption in the ultraviolet. In practice, two-photon excitation is made possible by the very high local instantaneous intensity provided by a combination of diffraction-limited focusing of a single laser beam in the microscope and the temporal concentration of 100 femtosecond pulses generated by a mode-locked laser. Resultant peak excitation intensities are 106 times greater than the CW intensities used in confocal microscopy, but the pulse duty cycle of 10-5 maintains the average input power on the order of 10 mW, only slightly greater than the power normally used in confocal microscopy.


Author(s):  
David W. Piston

Two-photon excitation fluorescence microscopy provides attractive advantages over confocal microscopy for three-dimensionally resolved fluorescence imaging. Two-photon excitation arises from the simultaneous absorption of two photons in a single quantitized event whose probability is proportional to the square of the instantaneous intensity. For example, two red photons can cause the transition to an excited electronic state normally reached by absorption in the ultraviolet. In our fluorescence experiments, the final excited state is the same singlet state that is populated during a conventional fluorescence experiment. Thus, the fluorophore exhibits the same emission properties (e.g. wavelength shifts, environmental sensitivity) used in typical biological microscopy studies. In practice, two-photon excitation is made possible by the very high local instantaneous intensity provided by a combination of diffraction-limited focusing of a single laser beam in the microscope and the temporal concentration of 100 femtosecond pulses generated by a mode-locked laser. Resultant peak excitation intensities are 106 times greater than the CW intensities used in confocal microscopy, but the pulse duty cycle of 10−5 maintains the average input power on the order of 10 mW, only slightly greater than the power normally used in confocal microscopy.


1996 ◽  
Vol 43 (9) ◽  
pp. 1765-1771 ◽  
Author(s):  
M. W. HAMILTON and D. S. ELLIOTT

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