Slotline‐based frequency‐reconfigurable quadrature coupler with wide tunable range and simple tuning mechanism

Author(s):  
Yu Fei Pan ◽  
Wing Shing Chan
2020 ◽  
Author(s):  
Egle Maximowitsch ◽  
Tatiana Domratcheva

Photoswitching of phytochrome photoreceptors between red-absorbing (Pr) and far-red absorbing (Pfr) states triggers light adaptation of plants, bacteria and other organisms. Using quantum chemistry, we elucidate the color-tuning mechanism of phytochromes and identify the origin of the Pfr-state red-shifted spectrum. Spectral variations are explained by resonance interactions of the protonated linear tetrapyrrole chromophore. In particular, hydrogen bonding of pyrrole ring D with the strictly conserved aspartate shifts the positive charge towards ring D thereby inducing the red spectral shift. Our MD simulations demonstrate that formation of the ring D–aspartate hydrogen bond depends on interactions between the chromophore binding domain (CBD) and phytochrome specific domain (PHY). Our study guides rational engineering of fluorescent phytochromes with a far-red shifted spectrum.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Se-Hwan Kim ◽  
Kimleng Chuon ◽  
Shin-Gyu Cho ◽  
Ahreum Choi ◽  
Seanghun Meas ◽  
...  

AbstractMicrobial rhodopsins are distributed through many microorganisms. Heliorhodopsins are newly discovered but have an unclear function. They have seven transmembrane helices similar to type-I and type-II rhodopsins, but they are different in that the N-terminal region of heliorhodopsin is cytoplasmic. We chose 13 representative heliorhodopsins from various microorganisms, expressed and purified with an N-terminal His tag, and measured the absorption spectra. The 13 natural variants had an absorption maximum (λmax) in the range 530–556 nm similar to proteorhodopsin (λmax = 490–525 nm). We selected several candidate residues that influence rhodopsin color-tuning based on sequence alignment and constructed mutants via site-directed mutagenesis to confirm the spectral changes. We found two important residues located near retinal chromophore that influence λmax. We also predict the 3D structure via homology-modeling of Thermoplasmatales heliorhodopsin. The results indicate that the color-tuning mechanism of type-I rhodopsin can be applied to understand the color-tuning of heliorhodopsin.


Crystals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 268
Author(s):  
Jeong-Hoon Ko ◽  
Jun-Chan Choi ◽  
Dong-Jin Lee ◽  
Jae-Won Lee ◽  
Hak-Rin Kim

In liquid crystal (LC) displays, deriving an optimum resistance level of an LC alignment polyimide (PI) layer is important because of the trade-off between the voltage holding and surface-discharging properties. In particular, to apply a power-saving low-frequency operation scheme to fringe-field switching (FFS) LC modes with negative dielectric LC (n-LC), delicate material engineering is required to avoid surface-charge-dependent image flickering and sticking problems, which severely degrade with lowering operation frequency. Therefore, this paper proposes a photocontrolled variable-resistivity PI layer in order to systematically investigate the voltage holding and discharging properties of the FFS n-LC modes, according to the PI resistivity (ρ) levels. By doping fullerene into the high-ρ PI as the photoexcited charge-generating nanoparticles, the ρ levels of the PI were continuously controllable with a wide tunable range (0.95 × 1015 Ω∙cm to 5.36 × 1013 Ω∙cm) through Ar laser irradiation under the same LC and LC alignment conditions. The frequency-dependent voltage holding and discharge behaviors were analyzed with photocontrolled ρ variation. Thus, the proposed experimental scheme is a feasible approach in PI engineering for a power-saving low-frequency FFS n-LC mode without the image flickering and image sticking issues.


2009 ◽  
Vol 82 (9) ◽  
pp. 1140-1148 ◽  
Author(s):  
Kazuhiro Fujimoto ◽  
Jun-ya Hasegawa ◽  
Hiroshi Nakatsuji

2014 ◽  
Vol 126 (13) ◽  
pp. 3450-3454 ◽  
Author(s):  
Sabrina Buchini ◽  
François-Xavier Gallat ◽  
Ian R. Greig ◽  
Jin-Hyo Kim ◽  
Soichi Wakatsuki ◽  
...  

2010 ◽  
Vol 31 (2) ◽  
pp. 108-110 ◽  
Author(s):  
Cong Huang ◽  
P.J. Zampardi ◽  
K. Buisman ◽  
C. Cismaru ◽  
M. Sun ◽  
...  
Keyword(s):  

Nano Energy ◽  
2021 ◽  
pp. 106741
Author(s):  
Yizhan Yang ◽  
Wanli Yang ◽  
Yunbo Wang ◽  
Xiangbin Zeng ◽  
Yuantai Hu

2018 ◽  
Vol 5 (7) ◽  
pp. 172010 ◽  
Author(s):  
Jonathan E. Barnsley ◽  
Elliot J. Tay ◽  
Keith C. Gordon ◽  
Daniel B. Thomas

Variation in animal coloration is often viewed as the result of chemically distinct pigments conferring different hues. The role of molecular environment on hue tends to be overlooked as analyses are mostly performed on free pigments extracted from the integument. Here we analysed psittacofulvin pigments within parrot feathers to explore whether the in situ organization of pigments may have an effect on hue. Resonance Raman spectra from a red region of a yellow-naped amazon Amazona auropalliata tail feather show frequency dispersion, a phenomenon that is related to the presence of a range of molecular conformations (and multiple chromophores) in the pigment, whereas spectra from a yellow region on the same feather do not show the same evidence for multiple chromophores. Our findings are consistent with non-isomeric psittacofulvin pigments behaving as a single chromophore in yellow feather barbs, which implies that psittacofulvins are dispersed into a structurally disordered mixture in yellow feathers compared with red feathers. Frequency dispersion in red barbs may instead indicate that pigments are structurally organized through molecule–molecule interactions. Major differences in the hues of parrot feathers are thus associated with differences in the organization of pigments within feathers.


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