January 23, 2008
Thermal Surface Displacement of an
CdS Nanoparticle in an GeO2 Matrix


The thermal motion of the surface of a spherical CdS nanoparticle embedded in a GeO2 matrix is calculated, and compared to experimental measurements of low frequency polarized and depolarized Raman scattering.

   Features of the low frequency Raman spectrum of metal (Ag, Au) and semiconductor (Si, CdS, CdSe) nanoparticles embedded in a solid glass matrix are qualitatively explained in terms of the free vibration spectrum of an isolated elastic sphere. In particular, the frequencies vary as (1/d) where d is the nanoparticle diameter. However, a number of experiments give Raman peak locations that are lower than the predicted free vibration frequencies. Some earlier calculations have incorporated the elastic properties of the matrix, but these have usually calculated the frequency and the damping, but have not provided the shape of the Raman spectrum.
   Details of the calculation are reported elsewhere. Here is a summary: The system under consideration is a single nanosphere of CdS embedded in an infinite GeO2 glass matrix. Raman scattering detects fluctuations in the polarizability tensor. It is assumed here that these fluctuations are as a result of bulk thermal vibrations of the system. Ignoring quantum corrections, every phonon mode should have the same average energy (kBT). Assuming a temperature of 300 K, this energy is kBT = 4×10-21 J. The quantum spacing between levels of a phonon mode is hf, where h is Planck's constant and f is the frequency of the mode. The average occupation number of a phonon mode is approximately kBT / (hf). For a phonon of frequency 20 cm-1, this is 10, which is large enough for the mode to be treated classically.
   The incoming amplitude of the wave, A, at frequency ω has been calculated based on this (md30.htm).
   The boundary value problem is then solved (using Borland Turbo C++ programs scp78d.c, scp79d.c, scp80d.c) to get the amplitude of the vibration inside the sphere. There are two amplitudes inside the sphere for the case of spheroidal vibrations: B and C. Otherwise there is a single amplitude inside the sphere, B. These amplitudes are complex numbers. What is plotted is the displacement of the surface of the nanoparticle. This displacement has r, θ and φ components, plotted in different colors in the figures below. The angular dependence of the displacement is not shown.
   This same approach has also been applied to the cases of Si nanoparticles in a SiO2 matrix and Cd(S,Se) nanoparticles in a glass matrix.
   A separate problem which I do not address here is how to calculate the actual Raman spectrum. This is not straightforward since the polarizability of the nanoparticle will change as the nanoparticle vibrates, but it is not clear quantitatively how much.
   The same vertical scale is used in all of these figures.

Figure 1.   l = 2 spheroidal mode
The incident amplitudes A calculated in md30.htm were used.
(a) The incident wave is longitudinal spheroidal with amplitude A, where
A2 = dω kBT (2 l + 1)
-------------------
 π2 ρm clm ω2
(scp78.c, 32b.gif)
(b) The incident wave is transverse spheroidal with amplitude A where
A2 =    dω kBT (2 l + 1)
-----------------------
l(l+1) π2 ρm ctm ω2
(scp78d.c 32d.gif)

Figure 2.   l = 0 spheroidal      ("breathing")
The incident wave is longitudinal spheroidal with amplitude A where
A2 = dω kBT (2 l + 1)
-------------------
 π2 ρm clm ω2
(scp79d.c 32a.gif)

Figure 3(a).   l = 1 torsional      (Rigid rotational oscillation)
The incident wave is transverse (torsional) with amplitude A where
A2 = dω kBT (2 l + 1)
-------------------
l(l+1) π2 μm ctm
(scp80d.c 32c.gif)
What is being plotted?    The displacement field is u(r,t),
with components ur, uθ and uφ.
For l = 1 torsional modes:
ur = uθ = 0.
uφ = eiωt f(r) sin(θ)
where f(r) is a complex valued function. The green curve at left is
||f(Rp)|| where Rp is the radius of the nanoparticle.

Figure 3(b).   l = 1 torsional      (Rigid rotational oscillation)
The incident wave is transverse (torsional) with amplitude A where
A2 = dω kBT (2 l + 1)
-------------------
l(l+1) π2 μm ctm
(scp80d.c 32e.gif)
What is being plotted?    The displacement field is u(r,t),
with components ur, uθ and uφ.
For l = 1 torsional modes:
ur = uθ = 0.
uφ = eiωt f(r) sin(θ)
where f(r) is a complex valued function. The green curve at left is
||f(Rp)|| where Rp is the radius of the nanoparticle.



Daniel Murray
Associate Professor
Math, Stats & Physics Unit
University of British Columbia - Okanagan
Kelowna, BC, Canada
daniel "dot" murray "at" ubc "dot" ca

For a list of related articles click here.


"Microscopic calculations on Raman scattering from acoustic phonons confined in Si nanocrystals" Jian Zi, Kaiming Zhang, Xide Xie Phys. Rev. B, Aug. 15, 1998 arXiv:cond-mat/9807293 v1 22 Jul 1998 arxiv.org/pdf/cond-mat/9807293 - c:\cofrest\9807293.pdf [email protected] http://www.fudan.edu.cn/index_ch.php
Ding Haojiang and Chen Weiqiu, "Nonaxisymmetric free vibrations of a spherically isotropic spherical shell embedded in an elastic medium"
Int. J. Solids Structures Vol. 33, No. 18, pp. 2575-2590, 1996 ::
M. Montagna and R. Dusi, "Raman scattering from small spherical particles" Phys. Rev. B 52, 10080 (1995) - about matrix effect, small influences.
"Raman scattering from fractals. Simulation on large structures by the method of moments" G.Viliani, R.Dell'Anna, O.Pilla, M.Montagna, G.Ruoco, G.Signorelli, V.Mazzacurati http://arxiv.org/pdf/cond-mat/9504039 ::
Transverse acoustic nature of the excess of vibrational states in vitreous silica http://arxiv.org/pdf/cond-mat/0209519 ::
Lingjun Wang, Guanghong Wei, Jian Zi "A planar force-constant model for phonons in wurtzite GaN and AlN: Application to hexagonal GaN/AlN superlattices" http://arxiv.org/pdf/cond-mat/9812293 ::
Raman scattering by electron-hole excitations in silver nanocrystals Authors: H. Portales, E. Duval, L. Saviot, M. Fujii, M. Sumitomo, S. Hayashi To be pub.in PRB cond-mat/0101471 http://arxiv.org/pdf/cond-mat/0101471 :: "Phonons in a nanoparticle mechanically connected to a substrate" K. Patton and M. Geller (Dec. 30, 2002 version) :: V. L. Gurevich and H. R. Schober, Phys. Rev. B 57, 11295 (1998).
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