TY - JOUR
T1 - Formation and Evolution of Ultrathin Silica Polymorphs on Ru(0001) Studied with Combined in Situ, Real-Time Methods
AU - Klemm, Hagen W.
AU - Prieto, Mauricio J.
AU - Peschel, Gina
AU - Fuhrich, Alexander
AU - Madej, Ewa
AU - Xiong, Feng
AU - Menzel, Dietrich
AU - Schmidt, Thomas
AU - Freund, Hans Joachim
N1 - Publisher Copyright:
Copyright © 2018 American Chemical Society.
PY - 2019/4/4
Y1 - 2019/4/4
N2 - Silica mono-and bilayer films on Ru(0001) can be physisorbed or chemisorbed, with ordered or vitreous structures, depending on the particular preparation procedures applied. Using the SMART spectro-microscope at BESSY-II with its capabilities for μ-spectroscopy, μ-diffraction, and LEEM imaging with lateral resolution below 5 nm, in situ and in real time and applied to identical areas, we have investigated the formation of these layers, defined and characterized their properties and their connected morphology, and followed their evolution. Two distinct chemisorbed monolayers and three bilayers (physisorbed crystalline and vitreous, and chemisorbed zigzag phases), and some transitions between them, have been studied. We found that, apart from the deposited silicon amount, the most important parameter for steering the evolution to a particular well-defined layer is the oxygen content at the Ru interface. Nucleation and growth of all layers are homogeneous on the scale of our resolution, leading to rather small domains (20-40 nm), mostly of the same phase, separated by defect lines. We discuss these and other basic findings in context and point out open questions. We also offer alternative recipes for the preparation of some phases, to obtain more homogeneous layers on a mesoscopic scale.
AB - Silica mono-and bilayer films on Ru(0001) can be physisorbed or chemisorbed, with ordered or vitreous structures, depending on the particular preparation procedures applied. Using the SMART spectro-microscope at BESSY-II with its capabilities for μ-spectroscopy, μ-diffraction, and LEEM imaging with lateral resolution below 5 nm, in situ and in real time and applied to identical areas, we have investigated the formation of these layers, defined and characterized their properties and their connected morphology, and followed their evolution. Two distinct chemisorbed monolayers and three bilayers (physisorbed crystalline and vitreous, and chemisorbed zigzag phases), and some transitions between them, have been studied. We found that, apart from the deposited silicon amount, the most important parameter for steering the evolution to a particular well-defined layer is the oxygen content at the Ru interface. Nucleation and growth of all layers are homogeneous on the scale of our resolution, leading to rather small domains (20-40 nm), mostly of the same phase, separated by defect lines. We discuss these and other basic findings in context and point out open questions. We also offer alternative recipes for the preparation of some phases, to obtain more homogeneous layers on a mesoscopic scale.
UR - http://www.scopus.com/inward/record.url?scp=85064010312&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.8b08525
DO - 10.1021/acs.jpcc.8b08525
M3 - Article
AN - SCOPUS:85064010312
SN - 1932-7447
VL - 123
SP - 8228
EP - 8243
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 13
ER -