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1.
Micromachines (Basel) ; 13(6)2022 Jun 18.
Artigo em Inglês | MEDLINE | ID: mdl-35744578

RESUMO

The proposed reconfigurable radiating antenna design is based on the integration of a reconfigurable fractal antenna and electro-optic substrate material. This antenna can be adjusted to achieve either re-configurability or tunability in the desired frequency range for wireless systems. The electromagnetic characteristics of the fractal antenna are manipulated at both the level of fractal geometry, electrical length and dielectric substrate. The designed antenna features multiband responses, in which the geometry and length change create a large frequency shift and the dielectric change using polymer dispersed liquid crystal (PDLC) creates fine and/or continuous tuning. The far field and scattering properties of the antenna are analyzed using the Computer Simulation Technology (CST) Microwave Studio Suite. The proposed approach has successfully demonstrated reconfigurable switching for up to four frequency bands between 0.2 and 0.6 THz. The dielectric constant change in the PDLC substrate shows fine and continuous frequency tuning with an 8% maximum frequency shift when operating around 0.54 THz and a high directivity of 7.35 dBi at 0.54 THz and 8.43 dBi at 0.504 THz. The antenna can also realize a peak gain of 4.29 dBi at 0.504 THz in the extraordinary polarization state of PDLC. The designed antenna can be readily integrated in the current communication devices, such as satellites, smart phones, laptops, and other portable electronic devices, due to its compact geometry and IC compatible design. In satellite applications, the proposed antenna can play a significant role in terms of security. The antenna could be extremely useful for satellites that want to keep their information secret; by constantly switching their operating frequency, spy satellites can evade detection and data collection from enemy ears.

2.
Sci Rep ; 12(1): 6096, 2022 Apr 12.
Artigo em Inglês | MEDLINE | ID: mdl-35414703

RESUMO

Developing a polarization insensitive, omnidirectional, and ultra-wideband (UWB) antenna is highly desired for improving the utilization of freely available electromagnetic (EM) radiation energy. In this study, we have designed an UWB antenna based on tapered flower petals and numerically analyzed to show that it is a promising candidate for energy harvesting applications in the infrared (IR) to UV-visible regime. The impacts of design strategy and parameters on the absorption performance are studied numerically. The antenna shows a high performance in both bandwidth and absorptivity (average absorption of 84.5% spanning a broad range from 25 to 800 THz) under normal incidence of plane waves. To get a better understanding behind such high and UWB absorption mechanism, we investigated the electric field (E-field) distribution over the structure. The antenna also generates less than 5% absorption deviation between normal to 45° incident angle and 0.05% absorption deviation between 0° and 90° polarizations for both transverse electric (TE) and transverse magnetic (TM) modes. This new design aspect and the numerical findings unfolds the new direction for numerous EM wideband applications such as THz technology, photo detection, bolometric sensing, camouflaging, spectral imaging, and ambient EM energy harvesting applications.

3.
RSC Adv ; 8(38): 21210-21213, 2018 Jun 08.
Artigo em Inglês | MEDLINE | ID: mdl-35539957

RESUMO

In this paper, we developed a high-performance solid-state pH sensor using a Ce0.9Sr0.1(Zr0.53Ti0.47)O4 (CSZT) membrane through a very simple sol-gel spin-coating process. The structural properties of the CSZT membrane are correlated with its sensing characteristics. The CSZT based EIS sensor exhibited a high pH sensitivity of 92.48 mV pH-1, which is beyond the Nernst limit (59.4 mV pH-1), and good reliability in terms of a low hysteresis voltage of 1 mV and a small drift rate of 0.15 mV h-1. This behaviour is attributed to the incorporation of Sr in the CSZT sensing membrane, which promotes change in the Ce oxidation state from Ce4+ to Ce3+.

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