scholarly journals Kinetics of cluster growth in expanding rare-gas jet

1999 ◽  
Vol 25 (4) ◽  
pp. 266-273 ◽  
Author(s):  
M. A. Ratner
Keyword(s):  
Gas Jet ◽  
Rare Gas ◽  
1992 ◽  
Vol 97 (5) ◽  
pp. 3325-3332 ◽  
Author(s):  
M. Mantel ◽  
M. Schumann ◽  
A. Giez ◽  
H. Langhoff ◽  
W. Hammer ◽  
...  

2012 ◽  
Vol 175 ◽  
pp. 4-11 ◽  
Author(s):  
T.V. Tropin ◽  
N. Jargalan ◽  
M.V. Avdeev ◽  
O.A. Kyzyma ◽  
R.A. Eremin ◽  
...  

2007 ◽  
Vol 37 (11) ◽  
pp. 1060-1064 ◽  
Author(s):  
I L Beigman ◽  
V E Levashov ◽  
K N Mednikov ◽  
A S Pirozhkov ◽  
E N Ragozin ◽  
...  

2005 ◽  
Vol 237-240 ◽  
pp. 689-694 ◽  
Author(s):  
Yuri S. Kaganovsky ◽  
E. Mogilko ◽  
A. Ofir ◽  
A.A. Lipovskii ◽  
M. Rosenbluh

Annealing in a hydrogen atmosphere of silicate glass plates doped by Ag+ ions leads to the reduction of silver to a metallic state (Ag0) and to the formation of silver nanoclusters. The kinetics of clustering during hydrogen diffusion into the glass and diffusion of Ag0 atoms in the glass matrix have been studied in a temperature ranging from 160 to 200oC by SEM, AFM and optical spectrometry. The absorption spectra have a peak near 410 nm corresponding to the surface plasmon resonance in Ag clusters. The position of the peak moves as the clusters grow. A theoretical analysis of the absorption spectra allowed us to estimate the cluster size as a function of time, as well as the thickness of the layer filled by clusters, which also changes with time. From AFM data we could measure the kinetics of cluster growth on the surface. We have theoretically analyzed the kinetics of cluster growth during reactive hydrogen diffusion, the kinetics of bulk cluster growth, surface cluster growth, and thickening of the layer filled by clusters.


Soft Matter ◽  
2017 ◽  
Vol 13 (6) ◽  
pp. 1276-1290 ◽  
Author(s):  
Suman Majumder ◽  
Johannes Zierenberg ◽  
Wolfhard Janke

1979 ◽  
Vol 9 (5) ◽  
pp. 593-597 ◽  
Author(s):  
N G Basov ◽  
V A Danilychev ◽  
V A Dolgikh ◽  
O M Kerimov ◽  
Vladimir S Lebedev ◽  
...  

1977 ◽  
Vol 55 (11) ◽  
pp. 2133-2143 ◽  
Author(s):  
James K. Baird

We present a theory of the rate constant for electron capture by SF6 when it is dissolved in liquid hydrocarbon and condensed rare gas solvents. The theory includes the effects of diffusion and solvation on the observed rate. Also included is the effect of the long-range polarization force acting between the electron and the SF6 molecule. The role of the solvent molecules in modifying this force is taken into account by use of a dielectric screening function. The theory is applied with semiquantitative success to electron capture data in the solvents: methane, ethane, propane, butane, n-pentane, neopentane, n-hexane, cyclohexane, isooctane, tetramethylsilane, argon, and xenon.


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