Unique optical and electronic properties of thin film, non-polymeric compounds for device applications

1983 ◽  
Vol 12 (6) ◽  
pp. 989-1001 ◽  
Author(s):  
M. L. Kaplan ◽  
S. R. Forrest ◽  
P. H. Schmidt ◽  
T. Venkatesan ◽  
A. J. Lovinger
Keyword(s):  
Thin Film ◽  
Electronic Properties ◽  
Optical And Electronic Properties ◽  
Polymeric Compounds ◽  
Device Applications

Nonlinear optical and electronic properties of SiC/PMMA/Ge/Fe waveguide for device applications

2007 ◽  
Author(s):  
Abdalla Darwish ◽  
Brent Koplitz ◽  
Nickolai Kukhtarev ◽  
Xiaodong Zhang ◽  
Robet Combs ◽  
...  
Keyword(s):  
Electronic Properties ◽  
Nonlinear Optical ◽  
Optical And Electronic Properties ◽  
Device Applications

Electrochemical polymerization of 1,4-di(aryl)cyclopentadienes: thin-film optical and electronic properties

RSC Advances ◽  
2015 ◽  
Vol 5 (67) ◽  
pp. 54727-54734 ◽  
Author(s):  
M. E. Vega ◽  
L. Chen ◽  
M. R. Khoshi ◽  
C. Casseus ◽  
A. Pietrangelo
Keyword(s):  
Thin Film ◽  
Comparative Study ◽  
Electronic Properties ◽  
Electrochemical Polymerization ◽  
Electrochemical Generation ◽  
Optical And Electronic Properties

A comparative study on the electrochemical generation and properties of (co)polymers prepared from 1,4-di(aryl)-5,5-dimethylcyclopentadienes is reported.

Effect of indium incorporation, stimulated by UHV treatment, on the chemical, optical and electronic properties of ZnO thin film

2020 ◽  
pp. 110560
Author(s):  
Mahmoud Bedrouni ◽  
Bachir Kharroubi ◽  
Abdellah Ouerdane ◽  
M'hammed Bouslama ◽  
M'hamed Guezzoul ◽  
...  
Keyword(s):  
Thin Film ◽  
Electronic Properties ◽  
Zno Thin Film ◽  
Optical And Electronic Properties

Unique nonlinear optical and electronic properties of SiC:Ge waveguide for device applications

2003 ◽  
Author(s):  
Abdalla M. Darwish ◽  
Brent D. Koplitz ◽  
Nicholai V. Kukhtarev ◽  
Oliva Mitchell ◽  
R. Haydel ◽  
...  
Keyword(s):  
Electronic Properties ◽  
Nonlinear Optical ◽  
Optical And Electronic Properties ◽  
Device Applications

1,1’-Biaceanthrylene and 2,2'-Biaceanthrylene: Models for Linking Larger Polycyclic Aromatic Hydrocarbons via Five-Membered Rings

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Electronic Properties ◽  
Aromatic Hydrocarbons ◽  
Model Systems ◽  
Redox Potentials ◽  
Dimer Model ◽  
Optical And Electronic Properties ◽  
Polycyclic Aromatic

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>

1,1’-Biaceanthrylene and 2,2'-Biaceanthrylene: Models for Linking Larger Polycyclic Aromatic Hydrocarbons via Five-Membered Rings

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Electronic Properties ◽  
Aromatic Hydrocarbons ◽  
Model Systems ◽  
Redox Potentials ◽  
Dimer Model ◽  
Optical And Electronic Properties ◽  
Polycyclic Aromatic

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>

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