International
Tables for Crystallography Volume D Physical properties of crystals Edited by A. Authier © International Union of Crystallography 2013 |
International Tables for Crystallography (2013). Vol. D. ch. 1.11, pp. 275-276
Section 1.11.6.1. Tensor atomic factors: internal symmetry
a
A. V. Shubnikov Institute of Crystallography, Leninsky pr. 59, Moscow 119333, Russia,bSteinmann Institut der Universität Bonn, Poppelsdorfer Schloss, Bonn, D-53115, Germany, and cFaculty of Physics, M. V. Lomonosov Moscow State University, Leninskie Gory, Moscow 119991, Russia |
Different types of tensors transform under the action of the extended orthogonal group (Sirotin & Shaskolskaya, 1982) as
where the coefficients
depend on the kind of tensor (see Table 1.11.6.1
) and
are coefficients describing proper rotations.
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Various parts of the resonant scattering factor (1.11.6.3) possess different kinds of symmetry with respect to: (1) space inversion
or parity, (2) rotations
and (3) time reversal
. Both dipole–dipole and quadrupole–quadrupole terms are parity-even, whereas the dipole–quadrupole term is parity-odd. Thus, dipole–quadrupole events can exist only for atoms at positions without inversion symmetry.
It is convenient to separate the time-reversible and time-non-reversible terms in the contributions to the atomic tensor factor (1.11.6.3). The dipole–dipole contribution to the resonant atomic factor can be represented as a sum of an isotropic, a symmetric and an antisymmetric part, written as (Blume, 1994
)
where
,
and
and
;
means the probability of the time-reversed state
. If, for example,
has a magnetic quantum number m, then
has a magnetic quantum number
.
In non-magnetic crystals, the probability of states with is the same, so that
and
; in this case
is symmetric under permutation of the the indices.
Similarly, the dipole–quadrupole atomic factor can be represented as (Blume, 1994)
where
with
. In (1.11.6.10)
the first plus (
) corresponds to the non-magnetic case (time reversal) and the minus (
) corresponds to the time-non-reversal magnetic term, while the second
corresponds to the symmetric and antisymmetric parts of the atomic factor. We see that
can contribute only to scattering, while
can contribute to both resonant scattering and resonant X-ray propagation. The latter term is a source of the so-called magnetochiral dichroism, first observed in Cr2O3 (Goulon et al., 2002
, 2003
), and it can be associated with a toroidal moment in a medium possessing magnetoelectric properties. The symmetry properties of magnetoelectic tensors are described well by Sirotin & Shaskolskaya (1982
), Nye (1985
) and Cracknell (1975
). Which magnetoelectric properties can be studied using X-ray scattering are widely discussed by Marri & Carra (2004
), Matsubara et al. (2005
), Arima et al. (2005
) and Lovesey et al. (2007
).
It follows from (1.11.6.8) and (1.11.6.10)
that
and the dipole–quadrupole term can be represented as a sum of the symmetric
and antisymmetric
parts. From the physical point of view, it is useful to separate the dipole–quadrupole term into
and
, because only
works in conventional optics where
. The dipole–quadrupole terms are due to the hybridization of excited electronic states with different spacial parities, i.e. only for atomic sites without an inversion centre.
The pure quadrupole–quadrupole term in the tensor atomic factor is equal towith the fourth-rank tensor
given by
This fourth-rank tensor has the following symmetries:
We can definewith
, where
We see that
vanishes in time-reversal invariant systems, which is true for non-magnetic structures.
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