Accurate SIMS Doping Profiling of Aluminum-Doped
Solid-Phase Epitaxy Silicon Islands
Yann Civale,
a,z
Lis K. Nanver,
a
Stefano G. Alberici,
b
Andrew Gammon,
b
and
Ian Kelly
b
a
Laboratory of Electronic Components, Technology, and Materials, Delft Institute of Microsystems
and Nanoelectronics-DIMES, Delft University of Technology, 2628 CT Delft, The Netherlands
b
Evans Analytical Group, Brunel University, Uxbridge UB8 3PH, United Kingdom
A procedure has been implemented for a quantitative aluminum-doping profiling of m-scale aluminum-induced solid-phase-
epitaxy SPE Si islands formed at 400°C. The aluminum concentration was measured to be 1–2 10
19
cm
-3
, which is about 10
times higher than previously reported electrical activation levels. The elemental concentration was measured by secondary-ion-
mass-spectroscopy SIMS on arrays of SPE Si islands grown by a recently developed process that allows control of the island
geometry.
© 2008 The Electrochemical Society. DOI: 10.1149/1.2836739 All rights reserved.
Manuscript submitted November 8, 2007; revised manuscript received December 26, 2007.
Available electronically January 28, 2008.
Low-temperature Si crystallization techniques
1,2
are attracting
wide attention due to their many potential applications, such as
semiconducting nanowires,
3-5
thin-film transistors,
6
interconnects,
7
and shallow-junction formation.
8
One method that has proven itself
in actual device fabrication is the use of metals like nickel and
aluminum to mediate the transport of Si and thus lower the crystal-
lization temperature of Si.
9
The doping of the resulting monocrys-
talline Si c-Si by the metal is an important factor for understanding
and predicting the device performance, but up until now little quan-
titative information has been available on this subject. In the case of
Al, substitutionally incorporated dopants will act as acceptors. This
means that the Al-mediated Si crystallization also offers a low-
temperature means of creating p-doped regions. In the literature, the
incorporated Al-concentration is often assumed to be above the
equilibrium Al solid solubility in Si that is extremely low at tem-
peratures below 500°C, slightly above 10
18
cm
-3
.
10
In principle, the
concentration of Al in Si can be profiled by secondary-ion-mass-
spectroscopy SIMS analysis. However, in the Al-mediated c-Si
material the size of the crystals is typically smaller than the SIMS
analysis area and the dimensional control is poor.
11,12
Moreover, in
systems where large c-Si areas are grown, the surface is usually not
uniform enough to allow an accurate SIMS analysis.
In this article, the Al-doping concentration in a recently devel-
oped sub-500°C aluminum-/amorphous-Si -Si solid-phase epi-
taxy SPE process is extracted. This SPE process has been demon-
strated to provide high-quality, ultra-abrupt, Al-doped p
+
-n elevated
junctions down to nanoscale dimensions.
13
Moreover, both the
height and lateral dimensions of the crystallized regions can be well
controlled by adjusting the layer-stack geometry and the thermal
processing parameters. Information on the Al-doping level was ac-
quired in our past work through the fabrication and electrical char-
acterization of simple SPE-Si-based devices such as p
+
contacts,
p
+
-n diodes, or p-n-p bipolar junction transistors. From these stud-
ies, the electrically active part of the Al doping in the bulk-Si of the
islands was found to be about 2 10
18
cm
-3
. In the present work,
the high degree of controllability of the growth mechanism has been
used to create areas of SPE-Si islands that are suitable for a quanti-
tatively correct SIMS profiling of the elemental Al concentration in
the islands. A detailed description of the fabrication of the SPE-Si
islands and the SIMS measurement procedure is given. The results
show that the elemental concentration of Al in SPE-Si grown at
400°C is about 1–2 10
19
cm
-3
, which suggests that not all the
incorporated Al dopants are electrically active.
Experimental
Fabrication of SIMS analysis area.— The process flow used for
fabricating an SPE Si-island array with a total area of about 60
60 m
2
and containing 90 similar islands, each approximately
1.4 1.4 m
2
in size, is presented in Fig. 1. First, 1.4 m wide
contact windows were opened by conventional lithography through
a 30 nm thick thermal silicon dioxide SiO
2
to the 100 Si sub-
strate by using buffered hydrofluoric acid HF 1:7. Then, the native
SiO
2
was removed from the Si surface by dip-etching in HF 0.55%
immediately followed by the physical vapor deposition PVD of
first 200 nm Al containing 1% Si and then 20 nm -Si. Both layers
were deposited by using an argon flow of 100 sccm at room tem-
perature and without vacuum break in order to prevent the formation
of an aluminum oxide Al
2
O
3
interface. The Al /-Si layer stack
was then patterned using reactive-ion etching to form 5 5 m
2
large islands around the contact windows, in order to provide the
optimal supply of Si for exactly filling the whole contact window
with SPE-Si. In this manner, a practically ideal SPE-Si growth se-
lectivity can be achieved with respect to the competing process of Si
nucleation on the SiO
2
in which the windows are etched.
14
The
epitaxy itself is induced by a thermal anneal at 400°C for 40 min in
aN
2
/H
2
10:1 mixture at atmospheric pressure. After the growth,
the aluminum transport layer was removed in a solution of diluted
z
E-mail: y.civale@dimes.tudelft.nl
Figure 1. SPE process flow: a thermal oxidation, b contact window defi-
nition, c Al /-Si PVD deposition, d Al /-Si layer-stack patterning, e
SPE-Si island growth and transport layer removal, and f oxide removal.
Electrochemical and Solid-State Letters, 11 4 H74-H76 2008
1099-0062/2008/114/H74/3/$23.00 © The Electrochemical Society
H74
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