2004
DOI: 10.1016/j.susc.2004.03.004
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Study of the orientation and frequency of occurrence of elementary steps on the (010) cleavage face of potassium acid phthalate single crystals

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Cited by 18 publications
(18 citation statements)
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“…In the present study we follow this way, using the highly ordered cleavage plane of potassium hydrogen phthalate -KAP(010) -as organic template for the growth study. This surface is molecularly flat and shows phenyl rings pointing out of the crystal [15]. Furthermore, it displays two distinct directions of surface corrugations running along <101> and [001].…”
Section: Introductionmentioning
confidence: 99%
“…In the present study we follow this way, using the highly ordered cleavage plane of potassium hydrogen phthalate -KAP(010) -as organic template for the growth study. This surface is molecularly flat and shows phenyl rings pointing out of the crystal [15]. Furthermore, it displays two distinct directions of surface corrugations running along <101> and [001].…”
Section: Introductionmentioning
confidence: 99%
“…It is common that multilayer and monolayer straight steps arrange jumbly while arrays of elementary steps are seldom seen. The orientations of the multilayer steps observed by AFM are usually different from those of elementary ones on the cleavage faces of potassium bichromate crystals [8] and potassium acid phthalate crystals [9]. Here for LAA crystals, multilayer and monolayer steps have the same orientation.…”
Section: Resultsmentioning
confidence: 89%
“…2c illustrates examples of cleavage steps whose figures are V-shaped steps and all the steps are of elementary height. V-shaped were often observed on the cleaved surfaces [8][9][10]. The formation is thought to result from cutting of dislocation loop lying in the slip plane by crack front propagating obliquely to the loop.…”
Section: Resultsmentioning
confidence: 99%
“…All these cleavage surfaces are characterized by the presence of phenyl rings arranged in a zig-zag fashion parallel to the shortest and polar lattice vector. 46 The outermost H atoms of the phenyl rings protrude out of the surface and give rise to the aforementioned molecular scale furrows. While periodicity parallel to the hydrogen bond chains is almost constant (increasing by 1.3% and 0.6% on moving from KAP to RbAP and CsAP, respectively), a major lengthening occurs for the orthogonal direction, namely, +4.7% for RbAP and +11.6% for CsAP compared to KAP.…”
Section: Discussionmentioning
confidence: 99%