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Characterization of Epitaxially Grown MnAs Films Using AFM and MFM Equipment
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Content
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Introduction and Sample Description
Experimental Details
Data Analysis
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(Nanowerk NanoBusiness Article) Park Systems is an Atomic Force Microscope (AFM) technology
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Boasting the longest history in the AFM industry, Park
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our customers.
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Introduction and Sample Description
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Because of its ferromagnetic properties with well-oriented
interfaces at room temperature, epitaxially grown MnAs film on
GaAs substrate is one of the most promising systems for
future spintronic applications despite the large lattice
mismatch between the epitaxial film and its substrate
material. The bulk MnAs shows a phase transition from the
ferromagnetic (FM) α-MnAs to the paramagnetic orthorhombic
β-MnAs at the critical temperature of about 45°C. In the MnAs
thin film systems, the two phases coexist in the form of selforganized
periodic stripes at room temperature, occurring via
strain stabilization. The periodic length of the two coexisting
phase stripes depends strongly on the film thickness. In this
note, MnAs films with varying thickness are observed in
various magnetization states.
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The MnAs films investigated herein were grown on GaAs(001)
substrates at 270°C by molecular beam epitaxy with varying
thickness of 10, 20, 50, 100, 250, and 500 nm, respectively.
At room temperature the strain-stabilized coexistence of the
two phases was confirmed by X-ray diffraction experiments.
By using a superconducting quantum interface device
magnetometer (SQUID) the magnetic properties were also
investigated. Also Atomic Force Microscopy (AFM) and Magnetic Force Microscopy (MFM) data show that the a-MnAs
and β-MnAs stripes are aligned along the MnAs[0001] and
perpendicular to the magnetic easy axis MnAs[1120].
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The MFM images were acquired by using an XE-100 AFM with
MFM option and a magnetic cantilever (Nanosensors). A
magnetic field generator was used to apply magnetic field to
the samples, which generates magnetic fields up to 600 Oe.
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Experimental Details
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For the characterization of magnetic samples such as
epitaxially grown MnAs films, measurement of their local
magnetic property is crucial. Though SQUID gives quantitative
magnetic data about the sample under investigation, the lack
of spatial resolution does not give structural analysis regarding
the material. MFM data, on the contrary, reveals local
magnetic properties of the samples along with well-defined
topographic data.
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A vital requirement for these precise measurements by MFM is
the explicit separation of the magnetic signal from the
topographic data. While the MFM signal is collected from the
instrument, the cantilever is positioned at a certain distance
from the sample surface, so that the van-der-Waals force do
not interfere the magnetic force. To maintain this condition,
the position of the cantilever is controlled very accurately. In
conventional piezo electric tube based AFM systems, the Z
direction movement (which corresponds to the height data) is
coupled with the XY direction scanner movement due to its
geometrical design limitation. The crosstalk between XY and Z
movement introduces topographic error signal to the magnetic
signal, and it needs accurate and stable calibration to obtain
realistic results. On the contrary, XE-series AFM introduces a
perfectly decoupled XY and Z-scanners to prevent the
interference of the movement crosstalk. The separated
movement of XE-series AFM secures the real MFM data which
is decoupled from the topographic signal.
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Data Analysis
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Figure 1 shows the MFM images of the MnAs films with various
thicknesses of 25 nm, 50 nm, 100 nm, 250 nm, and 500 nm,
respectively, at (a) saturated state and (b) demagnetized
state. In these images, the easy axis of each film is
perpendicular to the stripe direction, and the observed area is
5 µm in each direction. As shown in Figure 1(a), all the
ferromagnetic (FM) stripes in each saturated film are in a
single domain state, where MFM contrast in each stripe is
ascribed to the stray field from the boundary between the
neighboring stripes. Also it is observed that the periodic length
and the widths of the a and β phase stripes decrease as the
film thickness decreases, which correlates well with strain
relaxation effects.
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| Figure 1. MFM images of epitaxially grown MnAs films with various film thicknesses of 500 nm, 250 nm, 100 nm, 50 nm, and 25 nm, respectively at (a) the saturated state and (b) the demagnetized state. Observed area is 5 µm in each direction, and the magnetic easy axis of each film is perpendicular to the FM stripes.
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In Figure 1(b), change in the domain structure of the
demagnetized films is observed, as the film thickness
decreases. In the image of the 500-nm-thick sample, the
domain structure within the FM stripes can be described as
head-on domains, which are expressed as the spin
configurations in which the magnetization directions of two
domains meet head-on as demonstrated in the rectangular box
of the MFM images. In the image of 250-nm-thick sample, two kinds of domain structures are observed, head-on domains
and simple domains. The simple domains are defined as the
spin configurations having a single spin direction along the
width of the FM stripe, as demonstrated in the rectangular box
of the MFM image. The existence of head-on domains in 250
and 500-nm-thick samples indicates the formation of a closed
domain configuration inside the film, which is expected
considering that the domain wall length of the MnAs film is
about 100 nm.9 Also, the simple domains in the films whose
thicknesses are less than 100 nm appear because the film
thickness is less than the domain wall length.
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When the film thickness is less than 100 nm, the correlation
between the spin directions in the domains of the neighboring
FM stripes becomes significant. In the MFM image of the
demagnetized 100-nm-thick sample, the stripes in the
rectangular box indicate that the spin directions of the stripes
are aligned in the same direction due to the dipolar
interactions between the neighboring stripes.
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Especially, in the image of the demagnetized 250- nm-thick
sample, the two types of domain structures are found despite
of its uniform thickness. This indicates that there may be
another major origin for the change of the domain structure in
the FM stripe in addition to the film thickness. For further
understanding, the AFM and MFM images of the 250-nm-thick
MnAs film were investigated on the area with a large
fluctuation in the stripe width, as in Figures 2(a) and (b). In
these images, simple domains are observed where the width of
stripes is relatively narrow, whereas the head-on domains
appear where the width is relatively wide. This can be
explained by the difference in the demagnetizing factor, which
can be estimated by width over thickness (w/t) stripes ratio.
From the images shown in Figure 1(b), the w/t ratio of the
500-nm-thick sample is 3.1±0.1, whereas 5.8±2.0 is
measured for the 100-nm-thick sample. Considering this, the
change of the domain structure from the head-on domain to
the simple domain can be ascribed to the increase in the
demagnetizing factor which is due to the change in the stripe
width as well as in the film thickness. In Figure 2(b), the
simple domain structure is observed where the width of the
stripe is relatively wide. On the other hand, the head-on
domain structure is observed where the width is relatively
narrow.
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| Figure 2. (a) AFM and (b) MFM image of the 250-nm-thick MnAs film on an area with a large fluctuation in the FM stripe width.
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The demagnetizing factor also can be influenced by the change
in the gap distance between the stripes. As shown in the
circular box of the Figure 2(b), the estimated demagnetizing
factor of this area is 4.0, which is lower than the average
demagnetizing factor of the FM stripes in the film, 4.7±1.3.
This indicates that the increased dipolar interaction between
neighboring stripes due to the narrow gap induces a simple
domain structure despite the small w/t ratio in this particular
area.
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Source: Characterization of Epitaxially Grown MnAs Films Using AFM and
MFM - Application Note by Park Systems. Download as pdf.
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For more information on this source please visit Park Systems.
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