Mechanism of Stress-Enhanced Solid-Phase Epitaxy

1991 ◽  
Vol 237 ◽  
Author(s):  
T. K. Chaki
Keyword(s):  
Hydrostatic Pressure ◽  
Point Defects ◽  
Solid Phase ◽  
Amorphous Solid ◽  
Amorphous Layer ◽  
Crystalline Phases ◽  
Self Diffusion ◽  
Bending Stresses ◽  
Enhanced Mobility ◽  
The Difference

ABSTRACTEnhancement of solid-phase epitaxial growth (SPEG) due to hydrostatic pressures and bending stresses is explained by stress-enhanced mobility of point defects in the amorphous solid. The crystallization is by the adjustment of atomic positions in the vicinity of the crystallization/amorphous (c-a) interface due to self-diffusion in the amorphous phase, assisted by a free energy decrease equal to the difference in free energies between the amorphous and crystalline phases. Due to a mismatch in the bulk moduli between the amorphous and crystalline phases, the application of a hydrostatic pressure can develop tensile stresses in the amorphous layer near the c-a interface. Non-hydrostatic stresses in the amorphous layer enhance the mobility of point defects in the amorphous layer and, therefore, an enhancement of the SPEG rate. In the cases of both hydrostatic pressure and bending, the enhancement occurs in the tensile side, indicating that vacancy-like mechanism is predominant in SPEG.

Solid-Phase Epitaxy - Role of Point Defects in Amorphous Solids

1993 ◽  
Vol 319 ◽  
Author(s):  
T.K. Chaki
Keyword(s):  
Epitaxial Growth ◽  
Point Defects ◽  
Solid Phase ◽  
Ion Irradiation ◽  
Amorphous Solid ◽  
Amorphous Layer ◽  
Amorphous Solids ◽  
Solid Phase Epitaxy ◽  
Self Diffusion

AbstractA model of solid-phase epitaxial growth (SPEG), explaining enhancing effects of ion-irradiation and dopants, is presented. The crystallization is by the adjustment of atomic positions in the amorphous side of the crystalline/amorphous (c-a) interface due to self-diffusion in the amorphous solid, assisted by a freeenergy decrease associated with the transformation from the amorphous (a) to crystalline (c) phase. Irradiation and electrically active dopants increase the selfdiffusivity of a-phase by generating point defects in the amorphous layer and thus enhance crystallization. An expression for the velocity of epitaxial growth is derived. The low activation energy of ion-induced SPEG is due to recombination of point defects in the a-phase.

Diffusion in Gallium Arsenide and GaAs-Based Layered Structures

1989 ◽  
Vol 163 ◽  
Author(s):  
U. Gösele ◽  
T. Y. Tan ◽  
Shaofeng Yu
Keyword(s):  
Gallium Arsenide ◽  
Equilibrium Point ◽  
Point Defects ◽  
Layered Structures ◽  
Diffusion Behavior ◽  
Self Diffusion ◽  
Diffusion Mechanisms ◽  
The Difference ◽  
Positively Charged ◽  
Non Equilibrium

AbstractThe mechanisms of Ga self-diffusion can be derived from interdiffusion experiments in intrinsic and doped GaAs-based superlattices. These experiments allow to conclude that Ga self-diffusion in intrinsic and n-doped GaAs is carried by triply negatively charged gallium vacancies whereas in p-doped GaAs positively charged gallium self-interstitials dominate Ga self-diffusion. The diffusion mechanisms of Zn and Be are discussed with special emphasis on the difference between their in- and out-diffusion behavior which is due to diffusion-induced non-equilibrium point defects.

scholarly journals Changes in Phenols, Polysaccharides and Volatile Profiles of Noni (Morinda citrifolia L.) Juice during Fermentation

Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2604
Author(s):  
Zhulin Wang ◽  
Rong Dou ◽  
Ruili Yang ◽  
Kun Cai ◽  
Congfa Li ◽  
...  
Keyword(s):  
Octanoic Acid ◽  
Solid Phase ◽  
Principal Component ◽  
Hexanoic Acid ◽  
Morinda Citrifolia ◽  
Gas Chromatography Mass Spectrometry ◽  
Aroma Characteristics ◽  
Volatile Profiles ◽  
The Difference ◽  
Aroma Components

The change in phenols, polysaccharides and volatile profiles of noni juice from laboratory- and factory-scale fermentation was analyzed during a 63-day fermentation process. The phenol and polysaccharide contents and aroma characteristics clearly changed according to fermentation scale and time conditions. The flavonoid content in noni juice gradually increased with fermentation. Seventy-three volatile compounds were identified by solid-phase microextraction coupled with gas chromatography–mass spectrometry (SPME-GC-MS). Methyl hexanoate, 3-methyl-3-buten-1-ol, octanoic acid, hexanoic acid and 2-heptanone were found to be the main aroma components of fresh and fermented noni juice. A decrease in octanoic acid and hexanoic acid contents resulted in the less pungent aroma in noni juice from factory-scale fermentation. The results of principal component analysis of the electronic nose suggested that the difference in nitrogen oxide, alkanes, alcohols, and aromatic and sulfur compounds, contributed to the discrimination of noni juice from different fermentation times and scales.

Trapping Effect on the Kinetic Critical Radius in Nucleation and Growth Processes

2014 ◽  
Vol 790-791 ◽  
pp. 97-102
Author(s):  
Zoltán Erdélyi ◽  
Zoltán Balogh ◽  
Gabor L. Katona ◽  
Dezső L. Beke
Keyword(s):  
Critical Nucleus ◽  
Solid Phase ◽  
Kinetic Monte Carlo ◽  
Mean Field ◽  
Transformation Process ◽  
Nucleus Size ◽  
Critical Nucleus Size ◽  
Acta Mater ◽  
Order Of Magnitude ◽  
The Difference

The critical nucleus size—above which nuclei grow, below dissolve—during diffusion controlled nucleation in binary solid-solid phase transformation process is calculated using kinetic Monte Carlo (KMC). If atomic jumps are slower in an A-rich nucleus than in the embedding B-rich matrix, the nucleus traps the A atoms approaching its surface. It doesn’t have enough time to eject A atoms before new ones arrive, even if it would be favourable thermodynamically. In this case the critical nucleus size can be even by an order of magnitude smaller than expected from equilibrium thermodynamics or without trapping. These results were published in [Z. Erdélyi et al., Acta Mater. 58 (2010) 5639]. In a recent paper M. Leitner [M. Leitner, Acta Mater. 60 (2012) 6709] has questioned our results based on the arguments that his simulations led to different results, but he could not point out the reason for the difference. In this paper we summarize our original results and on the basis of recent KMC and kinetic mean field (KMF) simulations we show that Leitner’s conclusions are not valid and we confirm again our original results.

Pulsed Field Gradient NMR Investigation of Molecular Mobility of Trimethoxymethane in Nafion Membranes

1997 ◽  
Vol 496 ◽  
Author(s):  
Y. Wu ◽  
T. A. Za Wodzinski ◽  
M. C. Smart ◽  
S. G. Greenbaum ◽  
G.K.S. Prakash ◽  
...  
Keyword(s):  
Field Gradient ◽  
Molecular Mobility ◽  
Alternative Fuels ◽  
Direct Oxidation ◽  
Effective Distance ◽  
Pulsed Field ◽  
Self Diffusion ◽  
Lower Extent ◽  
The Difference ◽  
Nmr Signals

ABSTRACTMolecular mobility of water and trimethoxymethane (TMM) in NAFION membranes of two different equivalent weights (EW), 1100 and 1500, were investigated. Self-diffusion coefficients were determined by the NMR pulsed field gradient method, using the water and methyl protons NMR signals, in saturated NAFION samples containing concentrations of TMM in water varying between 0.5 and 14 M, and at temperatures varying from 30°C to 80°C. Diffusion of molecular species containing methyl protons is more than a factor of two slower in the 1500 EW membrane than in the 1100 EW membrane at 30°C and 1 M concentration. The difference rises to about a factor of four at 80°C and 14 M concentration. These differences are attributed to the lower extent of plasticization of the higher EW material as well as the greater effective distance between acid functional groups. NAFION samples containing methanol/water mixtures were also investigated. Comparison with the methanol results and the permeation behavior, as characterized by gas Chromatographie methods, show that more than half of the TMM is hydrolyzed to methanol as it passes through the acidic membrane. The implications of these findings for alternative fuels in direct oxidation fuel cells are discussed.

scholarly journals Predicting the glass transition temperature and viscosity of secondary organic material using molecular composition

2018 ◽  
Vol 18 (9) ◽  
pp. 6331-6351 ◽  
Author(s):  
Wing-Sy Wong DeRieux ◽  
Ying Li ◽  
Peng Lin ◽  
Julia Laskin ◽  
Alexander Laskin ◽  
...  
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Chemical Composition ◽  
Organic Compounds ◽  
Molar Mass ◽  
Solid Phase ◽  
Amorphous Solid ◽  
Semi Solid ◽  
Oxygen Atoms

Abstract. Secondary organic aerosol (SOA) accounts for a large fraction of submicron particles in the atmosphere. SOA can occur in amorphous solid or semi-solid phase states depending on chemical composition, relative humidity (RH), and temperature. The phase transition between amorphous solid and semi-solid states occurs at the glass transition temperature (Tg). We have recently developed a method to estimate Tg of pure compounds containing carbon, hydrogen, and oxygen atoms (CHO compounds) with molar mass less than 450 g mol−1 based on their molar mass and atomic O : C ratio. In this study, we refine and extend this method for CH and CHO compounds with molar mass up to ∼ 1100 g mol−1 using the number of carbon, hydrogen, and oxygen atoms. We predict viscosity from the Tg-scaled Arrhenius plot of fragility (viscosity vs. Tg∕T) as a function of the fragility parameter D. We compiled D values of organic compounds from the literature and found that D approaches a lower limit of ∼ 10 (±1.7) as the molar mass increases. We estimated the viscosity of α-pinene and isoprene SOA as a function of RH by accounting for the hygroscopic growth of SOA and applying the Gordon–Taylor mixing rule, reproducing previously published experimental measurements very well. Sensitivity studies were conducted to evaluate impacts of Tg, D, the hygroscopicity parameter (κ), and the Gordon–Taylor constant on viscosity predictions. The viscosity of toluene SOA was predicted using the elemental composition obtained by high-resolution mass spectrometry (HRMS), resulting in a good agreement with the measured viscosity. We also estimated the viscosity of biomass burning particles using the chemical composition measured by HRMS with two different ionization techniques: electrospray ionization (ESI) and atmospheric pressure photoionization (APPI). Due to differences in detected organic compounds and signal intensity, predicted viscosities at low RH based on ESI and APPI measurements differ by 2–5 orders of magnitude. Complementary measurements of viscosity and chemical composition are desired to further constrain RH-dependent viscosity in future studies.

scholarly journals The influence of high pressure on the properties of natural alumino-silicates

2002 ◽  
Vol 34 (2) ◽  
pp. 163-168
Author(s):  
N. Susic
Keyword(s):  
High Pressure ◽  
Thermal Behaviour ◽  
Amorphous Layer ◽  
New Materials ◽  
Crystalline Phases ◽  
Amorphous Phases ◽  
Long Period ◽  
Two Samples ◽  
Mineral Compositions

The effect of the application of high-pressure (up to 12 GPa) on natural alumino-silicates has been studied. Chemical and mineral compositions and thermal behaviour have been analyzed of two samples of alumino-silicates. Results obtained indicate that the application of high pressure causes notable changes. A particularly significant one is the formation of amorphous phases on account of crystalline phases. An amorphous layer formed on particle surfaces with its diverse physical, mechanical, chemical, and other properties, especially over a long period of time, can influence the processes provoking or activating land slides or soil settlements. This enables derivation of many new materials with entirely new properties important for use in the ceramic and brick industries.

scholarly journals Critical energy landscape of linear soft spheres

2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Silvio Franz ◽  
Antonio Sclocchi ◽  
Pierfrancesco Urbani
Keyword(s):  
Critical Exponents ◽  
Solid Phase ◽  
Energy Landscape ◽  
Amorphous Solid ◽  
Critical Energy ◽  
Contact Network ◽  
Stable States ◽  
Potential Energy Landscape ◽  
Soft Spheres ◽  
Non Linear System

We show that soft spheres interacting with a linear ramp potential when overcompressed beyond the jamming point fall in an amorphous solid phase which is critical, mechanically marginally stable and share many features with the jamming point itself. In the whole phase, the relevant local minima of the potential energy landscape display an isostatic contact network of perfectly touching spheres whose statistics is controlled by an infinite lengthscale. Excitations around such energy minima are non-linear, system spanning, and characterized by a set of non-trivial critical exponents. We perform numerical simulations to measure their values and show that, while they coincide, within numerical precision, with the critical exponents appearing at jamming, the nature of the corresponding excitations is richer. Therefore, linear soft spheres appear as a novel class of finite dimensional systems that self-organize into new, critical, marginally stable, states.

Sign in / Sign up

Export Citation Format

Share Document