AFM investigation of step kinetics and hillock morphology of the {1 0 0} face of KDP

Step velocities and hillock slopes on the {1 0 0} face of KDP were measured over a supersaturation range of 0< σ

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Veröffentlicht in:Journal of crystal growth 2004-01, Vol.260 (3), p.566-579
Hauptverfasser: Thomas, T.N., Land, T.A., Martin, T., Casey, W.H., DeYoreo, J.J.
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container_end_page 579
container_issue 3
container_start_page 566
container_title Journal of crystal growth
container_volume 260
creator Thomas, T.N.
Land, T.A.
Martin, T.
Casey, W.H.
DeYoreo, J.J.
description Step velocities and hillock slopes on the {1 0 0} face of KDP were measured over a supersaturation range of 0< σ
doi_str_mv 10.1016/j.jcrysgro.2003.08.054
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The formation of macrosteps and their evolution with distance from the hillock top were also observed. Hillock slope depended linearly on supersaturation and hillock geometry. The two non-equivalent sectors exhibited different slopes and step velocities. AFM shows an elementary step height of 3.7 Å, or half the unit cell height, whereas previous interferometric experiments assumed the elementary step was a unit cell. Values of the step edge energy ( α), the kinetic coefficients for the slow and fast directions ( β S and β F), and the activation energies for slow and fast step motion ( E a,S and E a,F) were calculated to be 24.0 erg/cm 2, 0.071 cm/s, 0.206 cm/s, 0.26 eV/molecule, and 0.21 eV/molecule, respectively. Analysis of macrostep evolution including the dependence of step height on time and terrace width on distance were performed and compared to predictions of published models. 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The formation of macrosteps and their evolution with distance from the hillock top were also observed. Hillock slope depended linearly on supersaturation and hillock geometry. The two non-equivalent sectors exhibited different slopes and step velocities. AFM shows an elementary step height of 3.7 Å, or half the unit cell height, whereas previous interferometric experiments assumed the elementary step was a unit cell. Values of the step edge energy ( α), the kinetic coefficients for the slow and fast directions ( β S and β F), and the activation energies for slow and fast step motion ( E a,S and E a,F) were calculated to be 24.0 erg/cm 2, 0.071 cm/s, 0.206 cm/s, 0.26 eV/molecule, and 0.21 eV/molecule, respectively. Analysis of macrostep evolution including the dependence of step height on time and terrace width on distance were performed and compared to predictions of published models. 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Atomic force microscopy</topic><topic>A1. Characterization</topic><topic>A1. Crystal morphology</topic><topic>A1. Supersaturated solutions</topic><topic>B1. Phosphates</topic><topic>Condensed matter: electronic structure, electrical, magnetic, and optical properties</topic><topic>Condensed matter: structure, mechanical and thermal properties</topic><topic>Dielectric, piezoelectric, ferroelectric and antiferroelectric materials</topic><topic>Dielectrics, piezoelectrics, and ferroelectrics and their properties</topic><topic>Electron, ion, and scanning probe microscopy</topic><topic>Exact sciences and technology</topic><topic>Kdp- and tgs-type crystals</topic><topic>Physics</topic><topic>Scanning probe microscopy: scanning tunneling, atomic force, scanning optical, magnetic force, etc</topic><topic>Structure of solids and liquids; crystallography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomas, T.N.</creatorcontrib><creatorcontrib>Land, T.A.</creatorcontrib><creatorcontrib>Martin, T.</creatorcontrib><creatorcontrib>Casey, W.H.</creatorcontrib><creatorcontrib>DeYoreo, J.J.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of crystal growth</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomas, T.N.</au><au>Land, T.A.</au><au>Martin, T.</au><au>Casey, W.H.</au><au>DeYoreo, J.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AFM investigation of step kinetics and hillock morphology of the {1 0 0} face of KDP</atitle><jtitle>Journal of crystal growth</jtitle><date>2004-01-01</date><risdate>2004</risdate><volume>260</volume><issue>3</issue><spage>566</spage><epage>579</epage><pages>566-579</pages><issn>0022-0248</issn><eissn>1873-5002</eissn><coden>JCRGAE</coden><abstract>Step velocities and hillock slopes on the {1 0 0} face of KDP were measured over a supersaturation range of 0&lt; σ&lt;0.15, where σ is the supersaturation. The formation of macrosteps and their evolution with distance from the hillock top were also observed. Hillock slope depended linearly on supersaturation and hillock geometry. The two non-equivalent sectors exhibited different slopes and step velocities. AFM shows an elementary step height of 3.7 Å, or half the unit cell height, whereas previous interferometric experiments assumed the elementary step was a unit cell. Values of the step edge energy ( α), the kinetic coefficients for the slow and fast directions ( β S and β F), and the activation energies for slow and fast step motion ( E a,S and E a,F) were calculated to be 24.0 erg/cm 2, 0.071 cm/s, 0.206 cm/s, 0.26 eV/molecule, and 0.21 eV/molecule, respectively. Analysis of macrostep evolution including the dependence of step height on time and terrace width on distance were performed and compared to predictions of published models. The results do not allow us to distinguish between a shock wave model and a continuous step-doubling model. Analysis within the latter model leads to a characteristic adsorption time for impurities ( λ −1) of 0.0716 s.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jcrysgro.2003.08.054</doi><tpages>14</tpages></addata></record>
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subjects A1. Atomic force microscopy
A1. Characterization
A1. Crystal morphology
A1. Supersaturated solutions
B1. Phosphates
Condensed matter: electronic structure, electrical, magnetic, and optical properties
Condensed matter: structure, mechanical and thermal properties
Dielectric, piezoelectric, ferroelectric and antiferroelectric materials
Dielectrics, piezoelectrics, and ferroelectrics and their properties
Electron, ion, and scanning probe microscopy
Exact sciences and technology
Kdp- and tgs-type crystals
Physics
Scanning probe microscopy: scanning tunneling, atomic force, scanning optical, magnetic force, etc
Structure of solids and liquids
crystallography
title AFM investigation of step kinetics and hillock morphology of the {1 0 0} face of KDP
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