Vibrational excitation in

1986 ◽  
Vol 64 (12) ◽  
pp. 1657-1663 ◽  
Author(s):  
Tom G. Slanger
Keyword(s):  
Charge Transfer ◽  
Vibrational Excitation ◽  
Transfer Mechanism ◽  
Charge Transfer Mechanism ◽  
Vibrational Distribution ◽  
Vibrational Levels ◽  
Excitation Processes ◽  
Oxygen Atoms

Excitation processes for [Formula: see text] in aurorae, in the nightglow, and in laboratory sources are discussed. It is shown that the observed vibrational distribution in aurorae is consistent with the [Formula: see text] + NO charge-transfer mechanism. Arguments are presented for the case that quenching of O2(b) in vibrational levels above ν′ = 1 is rapid, and that therefore the auroral source is much larger than previously supposed. It is suggested that oxygen atoms are an efficient quencher for O2(b) levels above ν′ = 1.

A 2D/2D S-scheme photo-Fenton catalyst based on ultrathin Bi2MoO6 and Fe2O3 hexagonal nanosheets for efficient tetracycline degradation

2021 ◽  
Vol 11 (8) ◽  
pp. 2948-2956
Author(s):  
Wenliang Wang ◽  
Wenli Zhao ◽  
Huimin Huang ◽  
Ruyao Chen ◽  
Haifeng Shi
Keyword(s):  
Charge Transfer ◽  
Transfer Mechanism ◽  
Charge Transfer Mechanism ◽  
Fenton Catalyst ◽  
Tetracycline Degradation ◽  
Degradation Activity

Fe2O3/Bi2MoO6 heterojunctions exhibit an observably improved photo-Fenton catalytic tetracycline degradation activity, which is accredited to an 2D/2D S-scheme charge transfer mechanism.

Oxidation mode on charge transfer mechanism in formation of Mn–Co–Ni–O spinel films by RF sputtering

2017 ◽  
Vol 28 (18) ◽  
pp. 13659-13664 ◽  
Author(s):  
Qin Shi ◽  
Wei Ren ◽  
Wenwen Kong ◽  
Lei Wang ◽  
Chao Ma ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Rf Sputtering ◽  
Transfer Mechanism ◽  
Charge Transfer Mechanism

Theoretical study on the charge transfer mechanism at donor/acceptor interface: Why TTF/TCNQ is inadaptable to photovoltaics?

2016 ◽  
Vol 145 (24) ◽  
pp. 244705 ◽  
Author(s):  
Shuang-Bao Li ◽  
Yun Geng ◽  
Yu-Ai Duan ◽  
Guang-Yan Sun ◽  
Min Zhang ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Theoretical Study ◽  
Transfer Mechanism ◽  
Charge Transfer Mechanism ◽  
Donor Acceptor

Altitude dependence of the vibrational distribution of in the nightglow and the possible effects of vibrational excitation in the formation of O(1S)

1984 ◽  
Vol 62 (8) ◽  
pp. 780-788 ◽  
Author(s):  
I. C. McDade ◽  
E. J. Llewellyn ◽  
R. G. H. Greer ◽  
G. Witt
Keyword(s):  
Vibrational Relaxation ◽  
Vibrational Excitation ◽  
Relaxation Model ◽  
Terrestrial Atmosphere ◽  
Transfer Step ◽  
Vibrational Distribution ◽  
Altitude Dependence ◽  
Vibrational Levels ◽  
The Individual

A simple vibrational relaxation model that reproduces the observed vibrational distribution of the [Formula: see text] Herzberg II bands in the terrestrial nightglow is used to derive the altitude profiles of the fractional populations in the individual vibrational levels. Through consideration of these profiles it is shown that if [Formula: see text] is the Barth precursor of O(1S) in the nightglow then, at least in the terrestrial atmosphere, the higher vibrational levels appear to be more effective in the Barth transfer step than the lower vibrational levels.

A charge transfer mechanism for the colour of rose quartz

1978 ◽  
Vol 46 (2) ◽  
pp. K135-K140 ◽  
Author(s):  
G. Smith ◽  
E. R. Vance ◽  
Z. Hasan ◽  
A. Edgar ◽  
W. A. Runciman
Keyword(s):  
Charge Transfer ◽  
Transfer Mechanism ◽  
Charge Transfer Mechanism ◽  
A Charge

Interfacial charge transfer events of BODIPY molecules: single molecule spectroelectrochemistry and substrate effects

2014 ◽  
Vol 16 (42) ◽  
pp. 23150-23156 ◽  
Author(s):  
Jia Liu ◽  
Caleb M. Hill ◽  
Shanlin Pan ◽  
Haiying Liu
Keyword(s):  
Charge Transfer ◽  
Single Molecule ◽  
Single Molecules ◽  
Transfer Mechanism ◽  
Substrate Effects ◽  
Interfacial Charge Transfer ◽  
Charge Transfer Mechanism ◽  
Nanostructured Substrates ◽  
Interfacial Charge

BODIPY dye single molecules on nanostructured substrates are studied with a single molecule spectroelectrochemistry technique to reveal the heterogeneous charge transfer mechanism.

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