Based on the Chapter wrirtten by Prof. Dr. Jan K. Kruger:
"Brillouin Spectroscopy and its Application to Polymers"
Appeared in the book:Optical Techniques to Characterize Polymer Systems (Edited by Heinz Bässler) Elsevier 1989
BRIEF INTRODUCTION TO CLASSICAL BRILLOUIN SPECTROSCOPY
Brillouin
spectroscopy (BS) applied to polymers primarily concerns inelastic light
scattering on thermally excited sound waves (phonons) at hypersonic frequencies
(~10 MHz to ~100 GHz). The Brillouin scattering effect was predicted first by
Brillouin [1] and Mandelshtam [2] and for the first time experimentally verified
by Gross [3]. The kinematics of this light scattering process are governed by
energy conservation and momentum conservation
hws
= hwi
± hw
(1)
hks
= hki ± hq
(2)
wi
/2p,
ws
/2p
and W
/2p
= f are the frequencies of the incident laser light, of the scattered light and
of the involved sound wave respectively. ki and ks
are the wave vectors of the Incident laser light and the scattered light with
the sample, and q Is the wave vector of the sound wave Involved. Within
the scattering process phonons of energy hW
are either created (WS
= W-,
Stokes scattering) or annihilated (WAS
= W+,
Anti-Stokes scattering). Generally In solids three orthogonal polarized acoustic
modes of different frequencies W
(p, q) are related to each wave vector q (p = l, 2, 3) A typical BS
spectrum of a solid is shown in fig. 1.
Fig. 1 Brillouin spectrum (of Hexatriacontane at room temperature). The lines denoted by QL and QT represent the quasilongitudinal and quasitransverse acoustic phonons (seen as Stokes [-f] and anti-Stokes [+f] lines) at phonon frequency f. The quantity 2G measures the acoustic losses. R denotes the Rayleigh line which is due to elastic light scattering. For display purposes, the Rayleigh line has been reduced in height by a factor of 300 compared to the phonon lines.
It
consists of three pairs of Brillouin lines which are shifted away from the
frequency wl of the exciting laser light by the frequency W(p)
. The line width G(p,
q)
(half width at half maximum, HWHM) measures the temporal attenuation of the
acoustic modes. G(p,
q)
is inversely proportional to the life time of the phonons Involved In the
scattering process. For moderate sound attenuation (G(p,
q)
< W
(p, q)) the sound velocity v(p, q) is related to the measured
frequency W
(p, q) by
v(p,
q) = W
(p, q) / q = f (p, q) L
with p = 1, 2, 3
(3)
where
L
is the hypersonic wavelength.
The
elastic stiffness coefflcient is related to the sound velocity and the mass
density of the material by
c
(p, q) = r
v2 (p, q)
(4)
To
account for energy disipation effects complex quantities are chosen for the
elastic stiffness coefficients [c*(p, q) = c’(p, q) - ic”(p, q)].
c*(p, q) Is related to the complex phonon frequency W
*(p,
q) = W
’(p,
q) - i W
"(p, q) = W
’(p,
q) + i2G(p,
q) by
W
’(p,
q) = W
0
[c’(p, q) / c(p, q)]1/2 = [q2 c’(p, q)
/r]1/2
(5a)
with
W
0(p,
q) = q [c(p, q) /r]1/2
(5b)
and
W
"(p, q) = G(p,
q) ≈ W
’(p,
q) [c”(p, q) / 2 c’(p, q)]
(5c)
Eq.
5a and eq. 5b have been derived assuming that the elastic properties are
independent of frequency. The Influence of dispersion on c’(p, q) and
c"(p, q) is often small but can be taken into account in a formal
way [4]. It should be noticed that in contrast to ultrasonic experiments where
dispersion is reflected by the frequency dependence of the complex stiffness
coefficient and in which the wave vector q(W)
becomes the complex quantity, dispersion in Brillouin experiments is reflected
by the variation of the elastic stiffness coefficient as a function of changes
in magnitude of the wave vector. The consequences have been discussed by Evans
et al. [5].
In isotropic solids the two transversely polarized sound modes degenerate
and in neat, non-viscous (isotropic) liquids only the longitudinally polarized
sound mode can propagate. For isotropic and cubic materials the following
relation holds between the magnitude of the acoustic wave vector q = |q|
and the scattering angle Φ ¢ (ki, ks)
q
= 2 ki sin(Φ
/2) = (4pn/l0)
sin(Φ /2)
(6)
where
l0is
the wave length of the laser light and n is the refractive index of the sample.
The case of less symmetric becomes more complicated and is treated in section
II.2 of the chapter.
[1] L. Brillouin, Ann. De Physique, 17, 88
(1922)
[2] L. I. Mandelshtam, Zh. Russ. Fiz. Khim. Obs.,
58, 381 (1926)
[3] E. Gross, Nature, 126, 201,400,630
(1930)
[4] C. J. Montrose, V. A. Solovyev, T. A.
Litivitz, J. Acoust. Soc. Am., 43,117 (1968)
[5] W. A. B. Evans, J. G. Powels. J. Phys. A, 7,
1944 (1974)