In-situ surface x-ray scattering of metal monolayers adsorbed at solid-liquid interfaces

Author(s):  
Michael F. Toney ◽  
Joseph G. Gordon II ◽  
Owen R. Melroy
2020 ◽  
Vol 124 (43) ◽  
pp. 23949-23963
Author(s):  
Jiayang Hu ◽  
Evan W. C. Spotte-Smith ◽  
Brady Pan ◽  
Roy J. Garcia ◽  
Carlos Colosqui ◽  
...  

2009 ◽  
Vol 43 (1) ◽  
pp. 110-121 ◽  
Author(s):  
U-Ser Jeng ◽  
Chiu Hun Su ◽  
Chun-Jen Su ◽  
Kuei-Fen Liao ◽  
Wei-Tsung Chuang ◽  
...  

At the National Synchrotron Radiation Research Center, a small/wide-angle X-ray scattering (SAXS/WAXS) instrument has been installed at the BL23A beamline with a superconducting wiggler insertion device. This beamline is equipped with double Si(111) crystal and double Mo/B4C multilayer monochromators, and an Si-based plane mirror that can selectively deflect the beam downwards for grazing-incidence SAXS (GISAXS) studies of air–liquid or liquid–liquid interfaces. The SAXS/WAXS instrument, situated in an experimental hutch, comprises collimation, sample and post-sample stages. Pinholes and slits have been incorporated into the beam collimation system spanning a distance of ∼5 m. The sample stage can accommodate various sample geometries for air–liquid interfaces, thin films, and solution and solid samples. The post-sample section consists of a 1 m WAXS section with two linear gas detectors, a vacuum bellows (1–4 m), a two-beamstop system and the SAXS detector system, all situated on a motorized optical bench for motion in six degrees of freedom. In particular, the vacuum bellows of a large inner diameter (260 mm) provides continuous changes of the sample-to-detector distance under vacuum. Synchronized SAXS and WAXS measurements are realizedviaa data-acquisition protocol that can integrate the two linear gas detectors for WAXS and the area detector for SAXS (gas type or Mar165 CCD); the protocol also incorporates sample changing and temperature control for programmable data collection. The performance of the instrument is illustratedviaseveral different measurements, including (1) simultaneous SAXS/WAXS and differential scanning calorimetry for polymer crystallization, (2) structural evolution with a large ordering spacing of ∼250 nm in a supramolecular complex, (3) SAXS for polymer blends underin situdrawing, (4) SAXS and anomalous SAXS for unilamellar lipid vesicles and metalloprotein solutions, (5) anomalous GISAXS for oriented membranes of Br-labeled lipids embedded with peptides, and (6) GISAXS for silicate films formedin situat the air–water interface.


1994 ◽  
Vol 375 ◽  
Author(s):  
Ronald P. Chiarello ◽  
Neil C. Sturchio

AbstractSynchrotron X-ray scattering techniques provide a powerful tool for the in situ study of atomic scale processes occurring at solid-liquid interfaces. We have applied these techniques to characterize and study reactions at mineral-water interfaces. Here we present two examples. The first is the characterization of the calcite (CaCO3) (1014) cleavage surface, in equilibrium with deionized water, by crystal truncation rod measurements. The second is the in situ study of the heteroepitaxial growth of otavite (CdCO3) on the calcite (1014) cleavage surface. The results of such studies will lead to significant progress in understanding mineral-water interface geochemistry.


2013 ◽  
Vol 765 ◽  
pp. 102-106 ◽  
Author(s):  
Adam Brown ◽  
Hong Biao Dong ◽  
Paul Howes ◽  
Chris Nicklin

A synchrotron X-Ray scattering method has been explored to probe the interactions at the interface between liquid Al and α-Al2O3. Melting and solidification behaviour has been observed in-situ in Al via collection and indexing of scattering generated at the solid-liquid interface.


2019 ◽  
Author(s):  
Christian Prehal ◽  
Aleksej Samojlov ◽  
Manfred Nachtnebel ◽  
Manfred Kriechbaum ◽  
Heinz Amenitsch ◽  
...  

<b>Here we use in situ small and wide angle X-ray scattering to elucidate unexpected mechanistic insights of the O2 reduction mechanism in Li-O2 batteries.<br></b>


2019 ◽  
Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Siqi Meng ◽  
Matthew Tirrell

We have directly observed the <i>in situ</i> self-assembly kinetics of polyelectrolyte complex (PEC) micelles by synchrotron time-resolved small-angle X-ray scattering, equipped with a stopped-flow device that provides millisecond temporal resolution. This work has elucidated one general kinetic pathway for the process of PEC micelle formation, which provides useful physical insights for increasing our fundamental understanding of complexation and self-assembly dynamics driven by electrostatic interactions that occur on ultrafast timescales.


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