Post-Synthetic Color Tuning of the Ultra-Effective and Highly Stable Surface-Confined Electrochromic Monolayer: Shades of Green for Camouflage Materials

Author(s):  
Nadia O. Laschuk ◽  
Iraklii I. Ebralidze ◽  
E. Bradley Easton ◽  
Olena V. Zenkina
Keyword(s):  
2019 ◽  
Author(s):  
Ji Liu ◽  
Michael Nolan

<div>In the atomic layer deposition (ALD) of Cobalt (Co) and Ruthenium (Ru) metal using nitrogen plasma, the structure and composition of the post N-plasma NHx terminated (x = 1 or 2) metal surfaces are not well known but are important in the subsequent metal containing pulse. In this paper, we use the low-index (001) and (100) surfaces of Co and Ru as models of the metal polycrystalline thin films. The (001) surface with a hexagonal surface structure is the most stable surface and the (100) surface with a zigzag structure is the least stable surface but has high reactivity. We investigate the stability of NH and NH2 terminations on these surfaces to determine the saturation coverage of NHx on Co and Ru. NH is most stable in the hollow hcp site on (001) surface and the bridge site on the (100) surface, while NH2 prefers the bridge site on both (001) and (100) surfaces. The differential energy is calculated to find the saturation coverage of NH and NH2. We also present results on mixed NH/NH2-terminations. The results are analyzed by thermodynamics using Gibbs free energies (ΔG) to reveal temperature effects on the stability of NH and NH2 terminations. Ultra-high vacuum (UHV) and standard ALD</div><div>operating conditions are considered. Under typical ALD operating conditions we find that the most stable NHx terminated metal surfaces are 1 ML NH on Ru (001) surface (350K-550K), 5/9 ML NH on Co (001) surface (400K-650K) and a mixture of NH and NH2 on both Ru (100) and Co (100) surfaces.</div>


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.


2021 ◽  
pp. 2104923
Author(s):  
Qian Li ◽  
Bin Xu ◽  
Zhongwei Chen ◽  
Jiang Han ◽  
Li Tan ◽  
...  

1981 ◽  
Vol 17 (10) ◽  
pp. 344 ◽  
Author(s):  
J.M. Saurel ◽  
J. Lassale ◽  
W. Shahab ◽  
G. Cambon ◽  
J. Attal

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

2000 ◽  
Vol 19 (1) ◽  
pp. 82-93 ◽  
Author(s):  
Christoph D. Matthaei ◽  
Chris J. Arbuckle ◽  
Colin R. Townsend
Keyword(s):  

2007 ◽  
Vol 125 (1-2) ◽  
pp. 85-91 ◽  
Author(s):  
M. Godlewski ◽  
M. Skrobot ◽  
E. Guziewicz ◽  
M.R. Phillips

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