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Crystal growth

About: Crystal growth is a research topic. Over the lifetime, 24571 publications have been published within this topic receiving 486898 citations.


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Journal ArticleDOI
15 Dec 1995-Science
TL;DR: In this article, a solution-liquid-solid mechanism for the growth of InP, InAs, and GaAs is described that uses simple, low-temperature (≤203°C), solution-phase reactions.
Abstract: Until now, micrometer-scale or larger crystals of the III-V semiconductors have not been grown at low temperatures for lack of suitable crystallization mechanisms for highly covalent nonmolecular solids. A solution-liquid-solid mechanism for the growth of InP, InAs, and GaAs is described that uses simple, low-temperature (≤203°C), solution-phase reactions. The materials are produced as polycrystalline fibers or near-single-crystal whiskers having widths of 10 to 150 nanometers and lengths of up to several micrometers. This mechanism shows that processes analogous to vapor-liquid-solid growth can operate at low temperatures; similar synthesis routes for other covalent solids may be possible.

1,024 citations

Journal ArticleDOI
TL;DR: In this article, the authors provide a simple narrative explaining the physical principles behind crystallization for those who are completely new to the topic, a few basic equations governing nucleation and growth, and an overview of some recent molecularscale studies that have revealed new insights into the control of crystal growth by small molecules, both organic and inorganic.
Abstract: In the most general sense, biomineralization is a process by which organisms produce materials solutions for their own functional requirements. Because so many biomineral products are derived from an initial solution phase and are either completely crystalline or include crystalline components, an understanding of the physical principles of crystallization from solutions is an important tool for students of biomineralization. However, crystal growth is a science of great breadth and depth, about which many extensive texts have been written. In addition, there are already other thorough reviews that specifically address the crystal growth field of study as it relates to biomineral formation. Consequently, the goals of this chapter are both modest and specific. It is intended to provide: 1) a simple narrative explaining the physical principles behind crystallization for those who are completely new to the topic, 2) a few basic equations governing nucleation and growth for those who wish to apply those principles—at least in a semi-quantitative fashion—to experimental observations of mineralization, and 3) an overview of some recent molecular-scale studies that have revealed new insights into the control of crystal growth by small molecules, both organic and inorganic. This last topic gets to the heart of what makes crystallization in biological systems unique. Every day, many tons of crystals are produced synthetically in non-biological processes, but by-and-large, the degree of control over nucleation and growth achieved by deterministic additions of growth modifiers or the presence of a controlling matrix is very minor. More commonly, crystal growers view modifying agents as unwanted impurities and work extremely hard to eliminate them from the starting materials. Indeed, the degree to which living organisms are able to control the crystallization process is most striking when contrasted to the products of such synthetic crystallization processes. This contrast applies to both the compositional differences that …

1,016 citations

Journal ArticleDOI
TL;DR: In this article, the growth rate of homoepitaxial diamond films reached 1 μm/h at 1000°C; film properties were identical to those of bulk crystals.

981 citations

Journal ArticleDOI
TL;DR: In this paper, high-resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD) peak broadening (Scherer) analysis were used to study coarsening and morphology development of nanocrystals.

940 citations

Journal ArticleDOI
25 May 2012-Science
TL;DR: High-resolution transmission electron microscopy using a fluid cell to directly observe oriented attachment of iron oxyhydroxide nanoparticles shows strong, highly direction-specific interactions drive crystal growth via oriented attachment.
Abstract: The oriented attachment of molecular clusters and nanoparticles in solution is now recognized as an important mechanism of crystal growth in many materials, yet the alignment process and attachment mechanism have not been established. We performed high-resolution transmission electron microscopy using a fluid cell to directly observe oriented attachment of iron oxyhydroxide nanoparticles. The particles undergo continuous rotation and interaction until they find a perfect lattice match. A sudden jump to contact then occurs over less than 1 nanometer, followed by lateral atom-by-atom addition initiated at the contact point. Interface elimination proceeds at a rate consistent with the curvature dependence of the Gibbs free energy. Measured translational and rotational accelerations show that strong, highly direction-specific interactions drive crystal growth via oriented attachment.

930 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023204
2022397
2021488
2020668
2019684
2018671