We report an application of low-temperature Raman scattering on in-plane CuO nanowires, in which an overview of the characteristic parameter of spin-phonon coefficient, the interaction of incident light with the spin degrees of freedom, and size effects will be given. The appearance of spin-phonon coefficient decrease reflects the existence of finite size effect.
We report an application of low-temperature Raman scattering on in-plane CuO nanowires, in which an overview of the characteristic parameter of spin-phonon coefficient, the interaction of incident light with the spin degrees of freedom, and size effects will be given. The appearance of spin-phonon coefficient decrease reflects the existence of finite size effect.
Low-dimensional nanosized effects in CuO systems, especially their different physical
properties such as spin-spin [1,2], electron–phonon [3], spin-phonon interactions [4], and giant negative thermal expansion have recently received a lot of
attention [5]. The spin-spin superexchange interaction occurs via the oxygen orbital [4,6]. The magnetic interactions and Néel transition temperature
(TN) of the CuO system are strongly dependent on the exchange
interaction and the number of neighboring atoms. A transition from a first-order
transition to a commensurate antiferromagnetic state near TN ~
213 K reported for bulk CuO from neutron scattering experiments [7,8] is well understood. Controlling the size of CuO nanocrystals resulted in
short-range correlation and commensurate antiferromagnetic (AFM) ordering, where the
TN decreased from the bulk value of 213 K [9-11], with decreasing particle size, down to 40 K for 6.6-nm nanoparticles [1,2] and 13 K for 2- to 3-nm nanorods [12]. It is known that spin-phonon coupling is usually weak and undetectable
because symmetric vibrations of relevant atoms will cancel the contributions from
negative and positive displacements. The main feature of cupric oxide is the
low-symmetry monoclinic lattice, which differs from the other transition metal
monoxides, e.g., MnO, FeO, CoO, and NiO with rock salt structure [13]. The low symmetry of the CuO lattice and the anisotropic dispersion curves
indicated lattice vibration which caused a modulation of the spin-phonon interaction.
This originated from slight changes in the inter-ionic distances and bond angles,
leading to spin-phonon coupling that can be detected in the Raman spectrum, to produce a
weak feature at about 230 cm−1 below TN[14,15]. The discovery of spin-phonon coupling in CuO nanocrystals has led to renewed
interest in this phenomenon. Up to now, there have been few experimental alternatives
for the determination of the size effect of spin-phonon coupling of CuO nanowires. In
this study, low-temperature Raman spectroscopy is employed to investigate the size
effects of spin-phonon coupling in in-plane CuO nanowires. Low-temperature Raman
spectroscopy has the high spatial resolution and sensitivity necessary for probing the
local atomic vibrations of nanowires. Our results reveal that below Néel
temperature there is a ready shift of the spin-phonon coefficient
λsp decreases as the mean diameter of in-plane CuO nanowire
decreases, exhibiting a long- to short-range spin-phonon coupling that can be nicely
described with the expected theoretical order parameter as due to antiferromagnetic
ordering in in-plane CuO nanowires.
Methods
A series of in-plane CuO nanowires with various diameters were fabricated. The samples
were prepared by a process where a pure copper grid was placed in a ceramic boat inside
a quartz tube, which was then evacuated to about 10−3 Torr using a
mechanical pump. They were then heated in a tube furnace at about 200°C for
2 h for degassing, after which the samples were heated to various temperatures
ranging from 300°C to 600°C for 2 h under mixed argon (100 sccm) and
oxygen (10 sccm) gas. Details of specimen preparation and characterization have been
described in a previous paper [16]. Transmission electron microscopy (TEM) and high-resolution transmission
microscopy (HRTEM) images from a JEM-3010 transmission electron microscope (JEOL Ltd.,
Tokyo, Japan) were obtained to study the crystalline structure. The results of an early
study show that the prepared nanowires are crystalline [16], revealing a monoclinic unique Y structure with lattice parameters of
a = 4.63 Å, b = 3.55 Å, c =
5.16 Å, and β = 99°52′. The morphology of the
prepared nanowires was characterized using field-emission scanning electron microscopy
(FESEM; JEOL JSM-6500 F). The SEM images in Figure 1a,b,c,d show the morphology of the CuO nanowires with various diameters which
were synthesized at T = 600°C, 500°C, 400°C, and 300°C,
respectively. It can be seen that the in-plane CuO grew homogeneously on the copper grid
substrate to form straight nanowires. Observation of uniform nanowires (with lateral
dimensions in the nanoscale order of tens to hundreds nanometers) shows that they grew
up to a few microns in length. Figure 1e shows that the
distribution of the nanowires was quite asymmetric. The solid lines represent the
fitting curves assuming the log-normal functiona. The mean diameters obtained
from the fits of log-normal distribution are = 210 ± 15 nm,
120 ± 8 nm, 52 ± 3 nm, and 15 ± 1 nm, respectively. The
value obtained for the standard deviation of the distribution profile σ
reveals that the increase with broadening was presumably due to the crystalline
effects.
Figure 1
Morphology of the in-plane CuO nanowires. SEM images of the in-plane CuO
nanowires synthesized at various temperatures (a, b, c, d). The
distributions of the mean diameter of the nanowires obtained from a portion of the
SEM image (e). The solid lines represent the fitting curves assuming the
log-normal function, where is the mean diameter of the
nanowires.
Morphology of the in-plane CuO nanowires. SEM images of the in-plane CuO
nanowires synthesized at various temperatures (a, b, c, d). The
distributions of the mean diameter of the nanowires obtained from a portion of the
SEM image (e). The solid lines represent the fitting curves assuming the
log-normal function, where is the mean diameter of the
nanowires.
Results and discussion
All low-temperature Raman spectra were measured using a Jobin Yvon 64000 Raman
microscope (HORIBA, Minami-ku, Kyoto, Japan) equipped with a Linkam optical DSC system
(THMS600; Linkam Scientific Instruments, Surrey, UK). The results were utilized to
investigate the spectroscopic properties of CuO nanowire at various temperatures. The
specimens were mounted on a non-background sample holder fixed to a cold head in a
high-vacuum (<10−3 Torr), low-temperature (approximately
80 K) chamber. The CuO nanowire was excited by focusing a 514.5-nm Ar ion laser
(Coherent Inc., Santa Clara, CA, USA) with a 5-mW laser power on the sample to form a
spot size of approximately 1 μm in diameter, giving a power density of
102 W/cm2. From the factor group analysis of the zone
center modes for the monoclinic structure, given by Rousseau et al. [17], there are three Raman active modes (Ag,
Bg1, and Bg2) predicted
in the spectra of CuO nanowires. Figure 2 shows an example of
a series of Raman spectra taken at various temperatures, covering the antiferromagnetic
transition temperature, with a mean diameter of 120 ± 8 nm. There are two
phonon modes revealed in the Raman spectra taken of the CuO nanowires at T =
193 K at 300.2 and 348.8 cm−1[18], which are related to Ag and
Bg1 symmetries [19,20]. The peak position is lower than the value of the bulk CuO
(Ag = 301 cm−1 and
Bg1 = 348 cm−1) [21], reflecting the size effect which acts to confine the lattice vibration in
the radial directions resulting in a shift in the Ag and
Bg1 symmetries. As the temperature decreases to
83 K, it can be clearly seen that the peak positions of the Ag
and Bg1 modes around 301.8 and
350.9 cm−1, shown at the top of Figure 2, shifted toward higher Raman frequencies. While the temperature increased
from 83 to 193 K, the peak position of the Ag mode softened by
0.7%. Since the frequency of the phonon mode is related to Cu-O stretching, it is
expected that the frequency will downshift with increasing temperature, primarily due to
the softening of the force constants that originate from the thermal expansion of the
Cu-O bonds, resulting from the change in vibrational amplitude [22,23]. In the study, the high resolution of our spectrometer allowed detection of
relative change as small as 0.5 cm−1, and the vibrational
frequency of a phonon mode can be used to determine the spin-phonon interaction. A
phonon-phonon effect originates from the dynamical motion of lattice displacements,
which are strongly coupled to the spin degrees of freedom dynamically below the magnetic
ordering temperature. This coupling between the lattice and the spin degrees of freedom
is named as spin-phonon. As shown in Figure 2, with
decreasing temperature, a well-defined peak developed at 231 cm−1
signifying the spin-phonon coupling [8,19] which shows that a noticeable shift to lower frequency is sensitive to the
temperature variation.
Figure 2
Series of Raman spectra taken at various temperatures of CuO nanowires with a
mean average diameter <> = 120 ± 8 nm.
Two main phonon modes corresponding to the Ag and
Bg1 symmetries, respectively, are revealed. As
the temperature was reduced to143 K, a well-defined peak at
238 cm−1 developed, signifying the spin-phonon
coupling.
Series of Raman spectra taken at various temperatures of CuO nanowires with a
mean average diameter <> = 120 ± 8 nm.
Two main phonon modes corresponding to the Ag and
Bg1 symmetries, respectively, are revealed. As
the temperature was reduced to143 K, a well-defined peak at
238 cm−1 developed, signifying the spin-phonon
coupling.Figure 3 shows the temperature dependence of the spin-phonon
mode for in-plane CuO nanowires of various diameters. Typical examples for bulk CuO are
shown in Figure 3, indicated by open and solid squares [8]. It has been suggested in previous reports that the temperature dependence of
the spin-phonon mode (the origin of the peak at 228 cm−1) might be
associated with magnetic ordering, the frequency shift corresponding to the
spin-correlation function times a spin-phonon coupling coefficient
λsp. The temperature dependence of the spin-phonon peak can
be represented as , where is the Raman shift in the absence of spin-phonon coupling
at TN and ϕ(T) is the order parameter
estimated from the mean field theory [24]. The order parameter can be described as ϕ(T) = 1
− (T/T), where
the order parameter γ varied from 3.4 ± 0.2 to 20 ± 5. The solid curves
indicate the theoretical fitting, and the corresponding parameters are presented in
Table 1. The size effect acts to confine the spin-phonon
coupling by increasing the TN from 210 to 88 K, as shown in
Figure 4a, when the size is reduced from bulk to 15 ±
1 nm (see for comparison TN = 213 K for CuO single crystal
and powder [8,16]). The obtained spin-phonon coupling coefficient λsp
also tends to decrease with decreased phonon amplitudes as the diameter decreased, as
shown in Figure 4b, revealing the existence of short-range
coupling. This result is consistent with past reports which state that the magnetic
transition temperature of Cr2O3[25,26] and CuO nanoparticles (open square) is reduced [12], which can be attributed to the fact that the ground state fails to develop
long-range antiferromagnetic ordering. This occurs because of quantum lattice
fluctuations and being energetically favorable to some kinds of short-range order state,
resulting in a lower spin-phonon coefficient with reduced size [27,28]. The magnitudes of these obtained λsp values are
intermediate compared to approximately 1 cm−1 for FeF2
and MnF2[24], and approximately 50 cm−1 for bulk CuO [8], indicating that the size effects could result in a tendency to weaken the
strong spin-phonon coupling. A minimum spin-phonon coefficient of
λsp = 10 cm−1 was obtained in
= 15 ± 1 nm in-plane CuO nanowires, which was found to be
weaker by a factor of 0.018 than the nearest neighbor spin-spin coupling strength of
J = 552 cm−1 for one-dimensional antiferromagnetic
Heisenberg chain [29]. In general, the spin-orbit interaction will induce a small orbital moment,
which couples the magnetic moment to crystalline axes of the phonon vibration.
Anharmonic effects are expected and caused the phonon and spin contribution to mix
because the λsp decreases as the diameter of the CuO nanowires
decreases.
Figure 3
Temperature variations of the spin-phonon modes of CuO nanowires with various
mean diameters. The solid line represents the fit by the ordering
parameter.
Table 1
Summary of the fitting results of the in-plane CuO nanowires
Size (nm)
TN(K)
ωspo(cm−1)
λsp(cm−1)
γ
Bulka
210
228
50
3.4 ± 0.2
210 ± 15
148
231
28
4.5 ± 0.5
120 ± 8
143
232.6
22
5.1 ± 0.2
52 ± 3
122
233.8
12.48
8 ± 1
15 ± 1
88
234.5
10
20 ± 5
aFrom [8,15].
Figure 4
Size effects of Néel temperature and spin-phonon coupling
coefficients. The obtained Néel temperature (a) and spin-phonon
coupling coefficients (b) as a function of mean diameter, which showed a
tendency to decrease with reduction in diameter.
Temperature variations of the spin-phonon modes of CuO nanowires with various
mean diameters. The solid line represents the fit by the ordering
parameter.Size effects of Néel temperature and spin-phonon coupling
coefficients. The obtained Néel temperature (a) and spin-phonon
coupling coefficients (b) as a function of mean diameter, which showed a
tendency to decrease with reduction in diameter.Summary of the fitting results of the in-plane CuO nanowiresaFrom [8,15].
Conclusions
In conclusion, we investigate the size dependence of CuO nanowires and the nanosized
spin-phonon effects. Raising the temperature and decreasing the diameter of CuO
nanowires result in the weakening of spin-phonon coupling. The temperature variations of
the spin-phonon mode at various diameters are in good agreement with the theoretical
results. We found that the spin-phonon mode varies with the size of the CuO nanowires
and in corroboration with the strength of spin-phonon coupling. Our result reveals that
low-temperature Raman scattering techniques are a useful tool to probe the short-range
spin-phonon coupling and exchange energy between antiferromagnetic next-nearest
neighboring magnons in nanocrystals below the Néel temperature. The application of
low-temperature Raman spectroscopy on magnetic nanostructures represents an extremely
active and exciting field for the benefit of science and technology at the nanoscale.
The rising new phenomena and technical possibilities open new avenues in the
characterization of short-range spin-phonon interactions but also for the understanding
of the fundamental process of magnetic correlation growth in nanomaterials.
Endnote
a The log-normal distribution is defined as follows: , where is the mean value and
σ is the standard deviation of the function.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
SYW wrote, conceived of, and designed the experiments. PHS grew the samples and analyzed
the data. CLC contributed the Raman experimental facility and valuable discussions. All
authors discussed the results, contributed to the manuscript text, commented on the
manuscript, and approved its final version.