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Using small crystallization volumes (nano-crystallization), the likelihood of nucleation is further reduced [5], because the number of nuclei is proportional to the volume of crystallization solution [6].
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This phenomenon can be explained by more amorphous silicon (a-Si) is involved in precipitation and crystallization, as a result, higher crystallization volume of crystallized-Si can be achieved.
We found that the bending strength increases rapidly with crystallization at crystal volume fractions below 10% and reaches a value 2.5 times greater than that of the original glass.
After crystallization the volume structure was imaged by nanotomography.
The atoms in the surface monolayer of the drop prematurely pack into a long-range ordered structure prior to volume crystallization, whereas diffusion dynamics maintains characteristic liquid-like features until the onset of volume crystallization.
In blends with PA domains of small volume, crystallization of PA was delayed.
The narrow band gap, sufficient crystallization, enough pore volume and large specific surface area resulted in the best photocatalytic activity of CaTa0.8Zr0.2O2.2N0.8.
Liquid crystallization stopped before volume filling the whole space, and the liquid crystalline phase and isotropic phase coexisted.
Results indicate that the magnetic field treatment increases the degree of crystallization and the volume resistivity of the composites.
While crystallization in small volume droplets is usually characterized by a low nucleation probability and correspondingly low number of crystals, we did not observe this in our experiments.
The high density crystalline nature of the surface does not thermodynamically favor volume crystallization, which occurs separately via homogeneous nucleation in the interior with further decreasing temperature.
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