% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Schwartzkopf:292942,
author = {Schwartzkopf, Matthias and Santoro, Gonzalo and Brett,
Calvin and Rothkirch, André and Polonskyi, Oleksandr and
Hinz, Alexander and Metwalli, Ezzeldin and Yao, Yuan and
Strunskus, Thomas and Faupel, Franz and Müller-Buschbaum,
Peter and Roth, Stephan V.},
title = {{R}eal-{T}ime {M}onitoring of {M}orphology and {O}ptical
{P}roperties during {S}putter {D}eposition for {T}ailoring
{M}etal–{P}olymer {I}nterfaces},
journal = {ACS applied materials $\&$ interfaces},
volume = {7},
number = {24},
issn = {1944-8252},
address = {Washington, DC},
publisher = {Soc.},
reportid = {PUBDB-2016-00172},
pages = {13547 - 13556},
year = {2015},
abstract = {The reproducible low-cost fabrication of functional
metal–polymer nanocomposites with tailored optoelectronic
properties for advanced applications remains a major
challenge in applied nanotechnology. To obtain full control
over the nanostructural evolution at the metal–polymer
interface and its impact on optoelectronic properties, we
employed combined in situ time-resolved microfocus grazing
incidence small angle X-ray scattering (μGISAXS) with in
situ UV/vis specular reflectance spectroscopy (SRS) during
sputter deposition of gold on thin polystyrene films. On the
basis of the temporal evolution of the key scattering
features in the real-time μGISAXS experiment, we directly
observed four different growth regimes: nucleation, isolated
island growth, growth of larger aggregates via partial
coalescence, and continuous layer growth. Moreover, their
individual thresholds were identified with subnanometer
resolution and correlated to the changes in optical
properties. During sputter deposition, a change in optical
reflectivity of the pristine gray-blue PS film was observed
ranging from dark blue color due to the presence of isolated
nanoclusters at the interface to bright red color from
larger Au aggregates. We used simplified geometrical
assumptions to model the evolution of average real space
parameters (distance, size, density, contact angle) in
excellent agreement with the qualitative observation of key
scattering features. A decrease of contact angles was
observed during the island-to-percolation transition and
confirmed by simulations. Furthermore, a surface diffusion
coefficient according to the kinetic freezing model and
interfacial energy of Au on PS at room temperature were
calculated based on a real-time experiment. The
morphological characterization is complemented by X-ray
reflectivity, optical, and electron microscopy. Our study
permits a better understanding of the growth kinetics of
gold clusters and their self-organization into complex
nanostructures on polymer substrates. It opens up the
opportunity to improve nanofabrication and tailoring of
metal–polymer nanostructures for optoelectronic
applications, organic photovoltaics, and plasmonic-enhanced
technologies.},
cin = {FS-PE},
ddc = {540},
cid = {I:(DE-H253)FS-PE-20120731},
pnm = {6214 - Nanoscience and Materials for Information Technology
(POF3-621) / 6G3 - PETRA III (POF3-622) / RO4638/1-1 -
In-situ Untersuchungen zu Kondensation, Nukleation und
Wachstum von Metallfilmen und Nanostrukturen auf organischen
Oberflächen während Sputterbeschichtung (238058777)},
pid = {G:(DE-HGF)POF3-6214 / G:(DE-HGF)POF3-6G3 /
G:(GEPRIS)238058777},
experiment = {EXP:(DE-H253)P-P03-20150101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000357063200051},
pubmed = {pmid:26030314},
doi = {10.1021/acsami.5b02901},
url = {https://bib-pubdb1.desy.de/record/292942},
}