We present the first experimental imaging of the internal DW structure in 55 and 85 nm diameter Ni nanocylinders, using electron holography combined with micromagnetic calculations. We demonstrate the magnetic transition from a hybrid magnetic state with both vortex and transverse DW in 85 nm diameter Ni nanocylinders to a pure transverse wall in thinner nanowires. This is particularly important as DWs in nanocylinders are model systems to go beyond the classical Walker limit.
We present the first experimental imaging of the internal DW structure in 55 and 85 nm diameter Ni nanocylinders, using electron holography combined with micromagnetic calculations. We demonstrate the magnetic transition from a hybrid magnetic state with both vortex and transverse DW in 85 nm diameter Ni nanocylinders to a pure transverse wall in thinner nanowires. This is particularly important as DWs in nanocylinders are model systems to go beyond the classical Walker limit.
The determination
of the shape of domain walls (DW) in magnetic nanocylinders has become
a very important topic in magnetism both for theoretical
and technological issues. Indeed magnetic nanocylinders are expected
to show a magnetic transition from vortex to transverse
wall as the diameter is reduced,[1,2] reflecting the competition
between dipolar and exchange energy. Moreover,
their cylindrical symmetry prevents any change in the demagnetizing
energy as the spins rotate during propagation[3,4] and
should lead to a suppression of the Walker breakdown.[5−7] This has been predicted in particular in the case of a transverse
wall in a nanocylinder. The latter point is of particular interest
for technological applications
such as logic circuit or data storage,[8−10] manipulating the walls
by means of magnetic fields[11−14] or electric current,[15−19] and for which the Walker breakdown is the main limitation
on the
DW velocities. Imaging and understanding the fine structure of the
DW in nanocylinders is then of major importance to make these systems
an interesting
alternative to the usual flat nanostripes produced by lithography.While magnetic DW have been almost exclusively studied experimentally
in nanostripes, most of the research on nanocylinders has been carried
out by means of micromagnetic calculations, and
very few experimental studies of these structures have been performed
up to now.[20,21] There are two major issues. The
first is the difficulty to grow cylindrical
magnetic nanostructures of good quality, and the second is the difficulty
of studying the DW structure inside the object with sufficient spatial
resolution. We bypass these two limitations by using template synthesis
to grow high-quality Ni nanocylinders, and we use high spatial resolution
off-axis electron holography
to study the magnetic configuration of the DW. The internal structure
of the DW is recovered, comparing the experimental magnetic phase
shift image of the electron beam with the one calculated from micromagnetic
simulations, taking into account the structural properties of the
wire deduced from the transmission electron microscopy (TEM) studies.
As the electrons cross the whole sample, electron holography offers
direct information on the internal magnetic structure with a spatial
resolution of about 5 nm as compared to other techniques such as magnetic
force microscopy (MFM), for which the magnetic state is observed via
its stray field, or magneto-optic Kerr effect (MOKE) or scanning electron
microscopy with polarization analyzer (SEMPA)[22−24] which are sensitive
to surface
magnetization and present spatial resolution of few tens of nanometers.
Moreover, as compared to previous electron holography experiments
on nanocylinders (ref (21)) showing
the stray field of the DW, we optimize the observation conditions
(see below) to study at higher magnification the magnetic state inside
the wire.Ni nanocylinders with diameters around 80 nm ±25
nm are grown by electro deposition in commercial 6 μm thick
polycarbonate membranes.[25−27] The membranes are then dissolved
in CH2Cl2, and the Ni nanowires are recovered
on a carbon foil for
structural and magnetic TEM imaging. Figure 1a shows a TEM image of one of these Ni nanowires of about 90 nm in
diameter with its corresponding diffraction pattern in Figure 1b. They both clearly demonstrate the polycrystalline
structure of the wire with randomly oriented grains, leading to a
random distribution of crystalline anisotropy and grain sizes roughly
equal to the wire diameter.
Figure 1
(a) TEM images of Ni nanocylinders grown by
electrodeposition. Triangular shape crystalline domains
are observed revealing a randomly distributed crystal orientation.
(b) Diffraction pattern of the same area presented in a.
(a) TEM images of Ni nanocylinders grown by
electrodeposition. Triangular shape crystalline domains
are observed revealing a randomly distributed crystal orientation.
(b) Diffraction pattern of the same area presented in a.Off-axis electron holography experiments performed
in a spherical
aberration-corrected Tecnai F20 microscope are used to image the remanent
magnetic configuration of single nanocylinders. Electron holography
allows recovery of the phase of the electron
beam that has been modified by interaction with magnetic and electrostatic
fields inside and outside a nanostructure. The magnetic and the electrostatic
contributions to the total phase shift are separated by subtracting
two holograms where the sample has been inverted[28] (see Supporting Information).
The magnetic phase shift can then be written as:where z is the direction
of the electron beam (perpendicular to the wire axis), r is a direction perpendicular to z, and B⊥ is the amplitude of the magnetic induction perpendicular
to both r and z. The isophase contour
of the phase image then gives a direct representation of the projected
induction field lines. However, as the phase shift is integrated over
the entire path of the electron, the 2D recorded image contains all
of the information about the internal structure of the domain wall
projected along the z direction.Before imaging
at the remanence, a 2 T magnetic field was applied perpendicular to
the nanowire axis (same
direction than the electron path) using the electromagnetic objective
lens of the microscope. We apply the field perpendicularly to the
wire axis in order to favor transverse walls nanowires of smallest
diameter. Then a single nanowire lying far from its neighbors is chosen
in order to avoid magnetic interaction between them. We present in
Figure 2a and b the amplitude image and magnetic
phase image obtained from a 70 nm diameter Ni nanocylinder and few
micrometers
long in an area where no DW shows up. The induction field lines
corresponding to the magnetic isophase contours are plotted inside
the wire. They run parallel to the wire axis, meaning that the magnetization
is uniformly aligned along the wire, without any stray field visible
at this scale. This is the simplest magnetic configuration in such
1D structure as the shape anisotropy stabilizes the magnetization
along the long axis. Figure 2c and d reports
respectively a quantitative analysis of the amplitude of the projected
induction field and the magnetic phase shift calculated for a uniform
magnetic state (see details below). We observe a very good quantitative
agreement between the experiment and the simulation. The small oscillations
of the intensity in the magnetic induction profile on the edge of
the wire come from the Fourier filtering used to reconstruct the phase
images. This demonstrates the capabilities of electron holography
coupled with micromagnetic simulations to obtain quantitative mapping
of magnetic states in nanowires.
Figure 2
Magnetic phase shift of a uniformly magnetized
nanocylinder.
Amplitude (a) and (b) magnetic phase shift images in a piece of nanocylinder
of 70 nm in diameter without DW. The lines in b corresponds to the
isocontour of the phase shift and then to the induction field lines.
(d) Calculated magnetic phase shift and isocontour from micromagnetic
simulation. The isophase lines in b and d are separated by 0.6 rad.
(c) Profile of the modulus of the projected induction in the cross
section delimited by the dashed line in b and d.
Magnetic phase shift of a uniformly magnetized
nanocylinder.
Amplitude (a) and (b) magnetic phase shift images in a piece of nanocylinder
of 70 nm in diameter without DW. The lines in b corresponds to the
isocontour of the phase shift and then to the induction field lines.
(d) Calculated magnetic phase shift and isocontour from micromagnetic
simulation. The isophase lines in b and d are separated by 0.6 rad.
(c) Profile of the modulus of the projected induction in the cross
section delimited by the dashed line in b and d.In contrast we show in Figure 3b and
e the
experimental magnetic phase shift image induced by DWs appearing in
two nanocylinders of 55 and 85 nm diameter. Magnetic domain walls
are evidenced by
the stray field leaking outside the wire in each side of the DWs.
Inside the wire, the magnetic flux at the DW position is found to
be asymmetric as compared to the uniform case. Moreover, two different
DW structures are found for two wires of different diameters. For
the smaller one (Figure 3b), field lines are
symmetric with respect to both the X and Y axis, and no magnetic induction is observed at the very
center of the domain wall. It indicates that the magnetization at
this location is either parallel to the +Z or −Z direction (the electron phase shift is only sensitive
to the Bx and By components perpendicular to the e– beam).
This is the magnetic configuration expected for a pure
transverse wall with the spins pointing in the direction of the saturation
field (+Z). For the larger diameter wire (Figure 3e), the situation is different. Field lines are
symmetric with respect to a (X,Y) plane tilted at about 45° from the Y direction.
Once again it indicates that the spins within this plane are pointing
in the ±Z direction. Note that such a magnetic
DW configuration does
not correspond to a vortex state as in such a case, the magnetic flux
should be confined within the wire, with a perfect symmetry around
the Y axis, and no stray field should be observed.
Figure 3
Transverse
DW and hybrid magnetic state in 55 and 85 nm nanocylinders. (a and
d) Amplitude image of 55 and 85 nm nanocylinders,
respectively. (b and e) Experimental magnetic phase shift
and corresponding induction field lines. (c and f) Magnetic phase
shift and corresponding induction field lines calculated from micromagnetic
simulation. The difference of isophase contour is the same for the
experiment and simulation, showing the quantitative agreement, and
is set to 0.6 and 0.3 rad for 55 and 85 nm, respectively. The color
bars on the
right give the amplitude of the phase shift in radian. The dashed
lines are a guide for the eye to position the wires. The arrows on
the scheme represent a simplified view of the magnetization within
the wire.
Transverse
DW and hybrid magnetic state in 55 and 85 nm nanocylinders. (a and
d) Amplitude image of 55 and 85 nm nanocylinders,
respectively. (b and e) Experimental magnetic phase shift
and corresponding induction field lines. (c and f) Magnetic phase
shift and corresponding induction field lines calculated from micromagnetic
simulation. The difference of isophase contour is the same for the
experiment and simulation, showing the quantitative agreement, and
is set to 0.6 and 0.3 rad for 55 and 85 nm, respectively. The color
bars on the
right give the amplitude of the phase shift in radian. The dashed
lines are a guide for the eye to position the wires. The arrows on
the scheme represent a simplified view of the magnetization within
the wire.For a better understanding of
these magnetic states, micromagnetic
3D calculations have been performed using the OOMMF code[29] to map the DW configuration for the two wires.
To fit the electron holography experiments, we have calculated the
electron beam phase shift images induced by the resulting magnetic
state in the whole (X, Y, Z) space. The nanowire diameters used for calculation were
deduced from the TEM amplitude images. As for the experiment, in the
micromagnetic calculations, the magnetization is first saturated in
the +Z direction (perpendicular to the wire axis)
applying a magnetic field of 1 T. The polycrystalline structure has
been implemented in homemade OOMMF
script in order to be as close as possible to the real system (see
methods for more details). The total area size is 600 × 600 ×
4800 nm3, and the unit cell size is 2.5 × 2.5 ×
2.5 nm3. The length of the wires was limited to 3.6 μm
in order to limit the number of cells. Parameters used for the calculation
are μ0Ms = 0.485 T, magnetocrystalline anisotropy
constant K1 = −5.7 e–3 J/m3, and exchange constant A = 9 e–12 J/m. From the remanent magnetic
configuration we calculated the magnetic induction B =
μ0(Hd + M) and
deduced
the magnetic phase shift from eq 1 in all of
the simulated space. Results of
the 3D micromagnetic calculations are shown in Figure 4 where only the part including the DW is reported as the rest
of the wire is uniformly magnetized. The color representation depicts
only the Mz component of the magnetization. The snapshots show the
magnetization orientation in three different planes perpendicular
to the wire.
Figure 4
3D micromagnetic
simulations for the 55 and 85 nm diameter nanocylinders. The snapshots
present the magnetization at the different planes
denoted on the 3D picture.
For the 55 nm diameter wire, micromagnetic calculations
indicate
a head to head transverse wall. The snapshots 1, 2, and 3 show that
the spins at the center of the wall are aligned
in the +Z direction, which result of the initial
saturation of the sample. The corresponding calculated phase shift
is reported in Figure 3c and is in very good
agreement with the experimental one (Figure 3b). The shape of the field lines at the center of the wall indicates
a slight tilt of the spins at the ±X edges of
the wire, which point in opposite directions. The qualitative and
quantitative agreements between simulation and experiment clearly
prove the appearance of a transverse DW in the 55 nm nanowire.Micromagnetic simulation indicates a more complex head-to-head
DW in the 85 nm diameter wire. Snapshots 1′, 2′, and
3′
in Figure 4 show that at the start (1′)
and the end (3′) of the DW, the spins rotate on the edge of
the cylinder (as for
a vortex), while at the center (2′) the spins are almost aligned
parallel to +Z (i.e., in the direction of the saturation
field) as for transverse wall.
This “pseudo transverse wall” with spins roughly aligned
in the +Z direction (red and yellow part in the 3D
simulation) however lies at about 45° of the Y axis. The presence
of such a “pseudo” transverse wall implies that the
cores of the vortices are not centered along the wire axis as observed
in 1′ and 3′. It also induces clockwise and anticlockwise
rotation of the vortices on each side of it. As for the 55 nm diameter
case, the phase shift calculated from this magnetic state (Figure 3f) is in perfect agreement with the experimental
result (Figure 3e). As the cores of the vortices
are not aligned with the Y axis, the resulting uncompensated
flux closure induces the appearance of a stray field as experimentally
observed. To our knowledge it is the first evidence of a magnetic
transition in a cylindrical nanostructure from a pure transverse wall
to a hybrid magnetic configuration whose fine structure has been clearly
elucidated. It is different from previous works[18] which showed that, for a field applied in the direction
of the wire axis, a pure vortex state arises for wires diameter above
60 nm. We assume that such hybrid state strongly depends on the magnetic
history of the nanostructure. In addition, we performed simulations
for diameters up to 110 nm for which this hybrid state persists.3D micromagnetic
simulations for the 55 and 85 nm diameter nanocylinders. The snapshots
present the magnetization at the different planes
denoted on the 3D picture.We must emphasize that saturating the magnetization perpendicular
to the wire axis does not lead systematically to the pinning of a
DW. As already stated, shape anisotropy tends to align all of the
spins in the direction of the wire axis to stabilize a uniform magnetic
state. We experimentally observed that most (∼60%) of the wires
are uniformly magnetized and micromagnetic simulations also confirmed
it is the most stable configuration since without considering the
polycrystalline structure, DW nucleate but move and collapse at the
edge of the wire leading to a uniform magnetic state. We then assume
that the polycrystalline structure is responsible for the DW pinning
most probably on grain boundaries as already reported in stripes.[30]In conclusion, we developed a method combining
high-resolution
electron holography with micromagnetism to obtain unprecedented resolution
of the 3D structure of DW in a cylindrical ferromagnetic nanowire.
We apply our method to demonstrate the occurrence of a magnetic transition
at remanence from a transverse wall to a hybrid magnetic state as
a function of the nanocylinder diameter. As transverse walls can be
easily nucleated by saturating
the sample perpendicular to the wire axis, they are perfect objects
to test the massless DW concept which could be an important breakthrough
to develop future spintronics devices.
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