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@INPROCEEDINGS{Schuck:154844,
author = {Schuck, Martin and Riess, Sally and Schreiber, Marcel and
Mussler, Gregor and Mennicken, Max and Grützmacher, Detlev
and Hardtdegen, Hilde},
title = {{MOVPE} of crystalline {G}e1{S}b2{T}e4 ({GST})},
school = {RWTH Aachen},
reportid = {FZJ-2014-04107},
year = {2014},
abstract = {Chalcogenide phase change materials show significant
promise on the road to an ideal memory. Ge-Sb-Te alloys
(GST) are considered to be one of the most suitable
compounds for this application and are already widely used
as non-volatile phase change memory in optical data storage
and in first PRAM (Phase-change Random Access Memory)
devices today [1, 2]. The reason is the rapid and reversible
change between its amorphous and crystalline phase with
orders of magnitude differences in reflectivity and
electrical resistivity. To this end the compounds along the
Sb2Te3 - GeTe pseudobinary line are the most widely used.
Nearly all GST layers are deposited in the amorphous phase
by sputtering. However, if nanostructures are to be achieved
without (reactive ion) etching and its detrimental side
effects, a bottom-up approach of single crystalline material
is more appropriate [3]. Also a CMOS compatible approach
should be adopted, which should be free of catalysts such as
Au. Starting point for the investigations are growth
conditions in MOVPE at which flat homogeneous coalesced
crystalline layers are deposited with only one composition.
A special challenge is the incorporation of Germanium. In
future the conditions are to be applied to selective area
growth of nanostructures such as nanowires, with which a
high scalability of structures can be ensured.Deposition was
performed in a horizontal low-pressure MOCVD reactor on 2”
Si (111) wafers, which were deoxidized by hydrofluoric acid
prior to the growth. Pure N2 carrier gas transported the
source compounds triethylantimony (TESb) and
diethyltelluride (DETe) as metal-organic precursors into the
reactor. The hydride digermane (Ge2H6) was chosen as the as
the Ge source. The partial pressures of the sources (Ge2H6:
1.46 x 10-2 mbar, TESb: 4.77 x 10-3 mbar, DETe: 1.32 x 10-1
mbar), the total gas flow of 2500 ml/min and the growth time
of 60 min were held constant. The reactor pressure was
varied between 50 mbar and 350 mbar and growth temperatures
in the range of 425°C up to 475°C. The influence of an
in-situ treatment of the substrate at growth-temperature
prior to deposition was investigated. To this end the
substrates were pre-treated with various sources and source
combinations for 1 min to 15 min. The influence of a
stabilizing pause between the in-situ pre-treatment and the
successive GST growth was also studied. The deposited
material was characterized by means of scanning electron
microscopy, Raman spectroscopy, atomic force microscopy,
energy dispersive X-Ray spectroscopy and X-Ray Diffraction
to determine topography, crystal structure and composition
of the grown layers.It was found that a lower reactor
pressure led to a more pronounced growth of flat layers. At
lower pressures, the growth temperature needed to be
increased slightly on account of the poorer decomposition of
the sources. While at a reactor pressure of 250 mbar and T =
420°C the deposited material consists of triangularly
shaped crystals with a height of about 1 µm, the samples
grown at 50 mbar consisted of nearly coalesced layers of GST
with a height around 100 nm and flat surfaces (Figure 1).
The samples deposited at 50 mbar exhibit a high
crystallinity. Their structure was determined to be
Ge1Sb2Te4, crystallized in the hexagonal phase (hcp) (Figure
2).An in-situ deposition of germanium in an antimony
atmosphere prior to the growth of GST promotes the growth of
flat layers by improving the coverage of the substrate
without disturbing the crystallinity or composition on the
Si (111) substrate. This is in accordance to the results
found for the growth of GST on SiN and SiO2 surfaces [4].},
month = {Jul},
date = {2014-07-13},
organization = {17th International Conference on
Metalorganic Vapor Phase Epitaxy,
Lausanne (Switzerland), 13 Jul 2014 -
18 Jul 2014},
subtyp = {Other},
cin = {PGI-9},
cid = {I:(DE-Juel1)PGI-9-20110106},
pnm = {421 - Frontiers of charge based Electronics (POF2-421) /
SYNAPSE - SYnthesis and functionality of chalcogenide
NAnostructures for PhaSE change memories (310339)},
pid = {G:(DE-HGF)POF2-421 / G:(EU-Grant)310339},
typ = {PUB:(DE-HGF)6},
url = {https://juser.fz-juelich.de/record/154844},
}