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In situ X-ray studies of adlayer-induced crystal nucleation at the liquid-liquid interface.


ABSTRACT: Crystal nucleation and growth at a liquid-liquid interface is studied on the atomic scale by in situ Å-resolution X-ray scattering methods for the case of liquid Hg and an electrochemical dilute electrolyte containing Pb(2+), F(-), and Br(-) ions. In the regime negative of the Pb amalgamation potential ?(rp) = -0.70 V, no change is observed from the surface-layered structure of pure Hg. Upon potential-induced release of Pb(2+) from the Hg bulk at ? > ?(rp), the formation of an intriguing interface structure is observed, comprising a well-defined 7.6-Å-thick adlayer, decorated with structurally related 3D crystallites. Both are identified by their diffraction peaks as PbFBr, preferentially aligned with their axis along the interface normal. X-ray reflectivity shows the adlayer to consist of a stack of five ionic layers, forming a single-unit-cell-thick crystalline PbFBr precursor film, which acts as a template for the subsequent quasiepitaxial 3D crystal growth. This growth behavior is assigned to the combined action of electrostatic and short-range chemical interactions.

SUBMITTER: Elsen A 

PROVIDER: S-EPMC3637733 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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In situ X-ray studies of adlayer-induced crystal nucleation at the liquid-liquid interface.

Elsen Annika A   Festersen Sven S   Runge Benjamin B   Koops Christian T CT   Ocko Benjamin M BM   Deutsch Moshe M   Seeck Oliver H OH   Murphy Bridget M BM   Magnussen Olaf M OM  

Proceedings of the National Academy of Sciences of the United States of America 20130403 17


Crystal nucleation and growth at a liquid-liquid interface is studied on the atomic scale by in situ Å-resolution X-ray scattering methods for the case of liquid Hg and an electrochemical dilute electrolyte containing Pb(2+), F(-), and Br(-) ions. In the regime negative of the Pb amalgamation potential Φ(rp) = -0.70 V, no change is observed from the surface-layered structure of pure Hg. Upon potential-induced release of Pb(2+) from the Hg bulk at Φ > Φ(rp), the formation of an intriguing interfa  ...[more]

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