Phosphorescence Spectroscopy as a Probe of the Glassy State in Amorphous Solids

Author(s):  
Richard Ludescher
1992 ◽  
Vol 89 ◽  
pp. 2073-2089 ◽  
Author(s):  
GP Johari
Keyword(s):  

1991 ◽  
Vol 01 (C7) ◽  
pp. C7-439-C7-442 ◽  
Author(s):  
N. V. GRUZDEV ◽  
E. G. SIL'KIS ◽  
V. D. TITOV ◽  
Yu. G. VAINER

1981 ◽  
Vol 42 (C6) ◽  
pp. C6-125-C6-127
Author(s):  
R. Vacher ◽  
J. Pelous
Keyword(s):  

1985 ◽  
Vol 46 (C8) ◽  
pp. C8-281-C8-286 ◽  
Author(s):  
C. Tête ◽  
D. Boumazouza ◽  
G. Marchal ◽  
Ph. Mangin ◽  
J. Bouillot ◽  
...  

MRS Advances ◽  
2020 ◽  
Vol 5 (61) ◽  
pp. 3141-3152
Author(s):  
Alma C. Chávez-Mejía ◽  
Génesis Villegas-Suárez ◽  
Paloma I. Zaragoza-Sánchez ◽  
Rafael Magaña-López ◽  
Julio C. Morales-Mejía ◽  
...  

AbstractSeveral photocatalysts, based on titanium dioxide, were synthesized by spark anodization techniques and anodic spark oxidation. Photocatalytic activity was determined by methylene blue oxidation and the catalytic activities of the catalysts were evaluated after 70 hours of reaction. Scanning Electron Microscopy and X Ray Diffraction analysis were used to characterize the catalysts. The photocatalyst prepared with a solution of sulfuric acid and 100 V presented the best performance in terms of oxidation of the dye (62%). The electric potential during the synthesis (10 V, low potential; 100 V, high potential) affected the surface characteristics: under low potential, catalyst presented smooth and homogeneous surfaces with spots (high TiO2 concentration) of amorphous solids; under low potential, catalyst presented porous surfaces with crystalline solids homogeneously distributed.


2019 ◽  
Author(s):  
Ketan Khare ◽  
Frederick R. Phelan Jr.

<a></a><a>Quantitative comparison of atomistic simulations with experiment for glass-forming materials is made difficult by the vast mismatch between computationally and experimentally accessible timescales. Recently, we presented results for an epoxy network showing that the computation of specific volume vs. temperature as a function of cooling rate in conjunction with the time–temperature superposition principle (TTSP) enables direct quantitative comparison of simulation with experiment. Here, we follow-up and present results for the translational dynamics of the same material over a temperature range from the rubbery to the glassy state. Using TTSP, we obtain results for translational dynamics out to 10<sup>9</sup> s in TTSP reduced time – a macroscopic timescale. Further, we show that the mean squared displacement (MSD) trends of the network atoms can be collapsed onto a master curve at a reference temperature. The computational master curve is compared with the experimental master curve of the creep compliance for the same network using literature data. We find that the temporal features of the two data sets can be quantitatively compared providing an integrated view relating molecular level dynamics to the macroscopic thermophysical measurement. The time-shift factors needed for the superposition also show excellent agreement with experiment further establishing the veracity of the approach</a>.


1972 ◽  
Vol 7 (4) ◽  
pp. 467-471 ◽  
Author(s):  
Cristina Catana ◽  
J. S. Colligon ◽  
G. Carter

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