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@ARTICLE{Birkel:16640,
author = {Birkel, C. S. and Claudio, T. and Panthöfer, M. and
Birkel, A. and Koll, D. and Kieslich, G. and Schmidt, J. and
Hermann, R. and Tremel, W.},
title = {{P}roperties of spark plasma sintered nanostructured {Z}n1
x{S}b},
journal = {Physica status solidi / A},
volume = {208},
issn = {0031-8965},
address = {Weinheim},
publisher = {Wiley-VCH},
reportid = {PreJuSER-16640},
pages = {1913 - 1919},
year = {2011},
note = {The Advanced Photon Source APS Argonne/Chicago is
acknowledged for synchrotron radiation beam time. The DFG
priority program SPP1386 "Nanostructured Thermoelectrics" is
acknowledged for the support of this study. C.S.B. is a
recipient of a fellowship from MATCOR, the Graduate School
of Excellence of the State of Rhineland-Palatinate. R.H.
acknowledges support from the Helmholtz-University Young
Investigator Group "Lattices Dynamics in Emerging Functional
Materials".},
abstract = {Engineering materials with specific physical properties has
recently focused on the effect of nanoscopic inhomogeneities
at the 10 nm scale. Such features are expected to scatter
medium and long-wavelength phonons lowering thereby the
thermal conductivity of the system without simultaneously
decreasing the charge transport (phonon-glass
electron-crystal concept). A new Zn1+xSb nanophase obtained
by a wet chemical approach was densified by spark plasma
sintering (SPS). Investigations on compounds subsumed as
"Zn4Sb3" always suffer from its low thermal stability and
the contamination of the nanoparticles with solvents and
additives used in the synthesis. In order to gain insight
into this compound's electronic properties we investigated a
material free from remnants of the synthesis but
contaminated with a small amount of well-characterized
decomposition product, i.e., ZnSb. To investigate the
influence of the sintering process on the densified samples,
different SPS conditions were applied. Four different
conditions were used with heating rates between 160 degrees
and 230 degrees C/min, sintering temperatures between 130
and 190 degrees C and sintering times between 3 and 6 min.
Powders from the surface of the pellets were subject to
powder X-ray diffraction (XRD) yielding information about
the surface composition. Small pieces of the pellets were
also characterized using high-energy synchrotron radiation
scattering in order to reveal the phase compositions inside
the pellets. Small changes in the sintering conditions of
the samples were found to have a large influence on the
resulting sample compositions. In addition, the phase
compositions on the surface differ significantly from the
ones inside the pellets which show a much higher grade of
decomposition. The density and morphology of the obtained
pellets have been investigated by means of laser microscopy
and scanning electron microscopy (SEM). The low density and
porosity of the different pellets is a result of the
graphite pressing tool which has to be used to ensure the
temperature control during the SPS process. (C) 2011
WILEY-VCH Verlag GmbH $\&$ Co. KGaA, Weinheim},
keywords = {J (WoSType)},
cin = {JARA-FIT / JCNS-2 / PGI-4},
ddc = {530},
cid = {$I:(DE-82)080009_20140620$ / I:(DE-Juel1)JCNS-2-20110106 /
I:(DE-Juel1)PGI-4-20110106},
pnm = {Grundlagen für zukünftige Informationstechnologien /
Großgeräte für die Forschung mit Photonen, Neutronen und
Ionen (PNI)},
pid = {G:(DE-Juel1)FUEK412 / G:(DE-Juel1)FUEK415},
shelfmark = {Materials Science, Multidisciplinary / Physics, Applied /
Physics, Condensed Matter},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000294619600032},
doi = {10.1002/pssa.201026665},
url = {https://juser.fz-juelich.de/record/16640},
}