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Symmetry transformations parity

If parity is not broken spontaneously, we have (La) = (Ra) = fS3, where we choose the condensate to be in the 3rd direction of color. The order parameters are singlets under the 517 (2) x SUr(2) flavor transformations while possessing baryon charge. The vev leaves invariant the following symmetry group ... [Pg.157]

Within the Hohenberg-Kohn approach [17, 18], the possibility of transforming density functional theory into a theory fully equivalent to the Schrodinger equation hinges on whether the elusive universal energy functional can ever be found. Unfortunately, the Hohenberg-Kohn theorem, being just an existence theorem, does not provide any indication of how one should proceed in order to find this functional. Moreover, the contention that such a functional should exist - and that it should be the same for systems that have neither the same number of particles nor the same symmetries (for an atom, for example, those symmetries are defined by U, L, S, and the parity operator ft) -certainly opens the door to dubious speculation. [Pg.171]

Here d is the z projection of the dipole matrix elements for the spinless S PZ transition of an outer electron. The factor (— )sw in equation (38) characterizes the symmetry in the arrangement of atomic dipoles in mixed S-P atomic states. Spin S and parity w of a molecular state are relevant either to the exchange of electrons (with atomic orbital fixed at nuclei) or to the exchange both of electrons and atomic orbitals. The exchange of orbitals (with atomic electrons attached to corresponding nuclei) is accomplished by the product of these two transformations. This explains the appearance of the spin quantum number in (38). [Pg.337]

Space inversion (or parity transformation), x —> —x This symmetry is equivalent to the reflection in a plane (i.e. mirror symmetry), as one can be obtained from the other by combination with rotation through angle 7r. [Pg.5]

The symmetry of an isolated atom is that of the full rotation group R+ (3), whose irreducible representations (IRs) are D where j is an integer or half an odd integer. An application of the fundamental matrix element theorem [22] tells that the matrix element (5.1) is non-zero only if the IR DW of Wi is included in the direct product x of the IRs of ra and < f. The components of the electric dipole transform like the components of a polar vector, under the IR l)(V) of R+(3). Thus, when the initial and final atomic states are characterized by angular momenta Ji and J2, respectively, the electric dipole matrix element (5.1) is non-zero only if D(Jl) is contained in Dx D(j 2 ) = D(J2+1) + T)(J2) + )(J2-i) for j2 > 1 This condition is met for = J2 + 1, J2, or J2 — 1. However, it can be seen that a transition between two states with the same value of J is allowed only for J 0 as DW x D= D( D(°) is the unit IR of R+(3)). For a hydrogen-like centre, when an atomic state is defined by an orbital quantum number , this can be reduced to the Laporte selection rule A = 1. This is of course formal, as it will be shown that an impurity state is the weighted sum of different atomic-like states with different values of but with the same parity P = ( —1) These states are represented by an atomic spectroscopy notation, with lower case letters for the values of (0, 1, 2, 3, 4, 5, etc. correspond to s, p, d, f, g, h, etc.). The impurity states with P = 1 and -1 are called even- and odd-parity states, respectively. For the one-valley EM donor states, this quasi-atomic selection rule determines that the parity-allowed transitions from Is states are towards np (n > 2), n/ (n > 4), nh (n > 6), or nj (n > 8) states. For the acceptor states in cubic semiconductors, the even- and odd-parity states labelled by the double IRs T of Oh or Td are indexed by + or respectively, and the parity-allowed transition take place between Ti+ and... [Pg.127]

In the above discussion of the electronic structure of the donor levels, the electron spin has been neglected. It has been, however, proven necessary to introduce the spin-orbit coupling to explain the observation of parity-forbidden transitions for donors with relatively deep ls(Ai) ground states. Using the double group representation of Td, it is found (see Table B.4 of appendix B) that the simple representations Ai and E transform into the T6 and Tg double representations, respectively and that T2 transforms into T7 + Eg. Electric-dipole transitions are symmetry-allowed between A (Tg) and the two T2 (Ty) and T2 (r8) levels. [Pg.144]

For Csv symmetry, the z component of the dipole moment transforms as Ti and the x and y components as T3. As a consequence, for E//c(z component), the parity-allowed transitions from 15 (r2) are toward the odd-parity states belonging to the T2 IR from 15 3), they are toward the odd-parity states belonging to the T3 IR. For ELc (x and y components), the parity-allowed transitions from 15 (r2) are toward the odd-parity states belonging to the r3 IR, and from 15 3) toward the odd-parity states belonging to the Ti, r2 and T3 IRs. Evidently, symmetry-allowed transitions are also possible from the 15 states toward the even-parity states with appropriate symmetry. [Pg.145]

A property that transforms like Eq. (11.5.19) is said to have definite parity and is called the parity of the property. Let us now investigate the consequences of this kind of symmetry. Again we proceed by proving a certain set of theorems. These theorems apply to the set A only if all the A have definite parity. [Pg.292]

An obvious solution to minimize the number of grid points NK is to introduce symmetry. Consider for example an inversion point such as the point x = 0 in the harmonic oscillator. The eigenfunctions can be classified as being either even or odd with respect to parity i j(<7) = i i(— < ) one restricts the calculation to one class of functions the computational effort can be reduced by a factor of 2 by using a fast cosine transform for even functions and a fast sine transform for odd functions (52). The same symmetry considerations should work for other types of grids. [Pg.212]

Nuclear states are described in quantum mechanics by eigenvalues and eigenfunctions of the Hamilton operator, to which definite quantum numbers belong. The parity of the wave function is its symmetry property under inversion through the origin of the coordinate system, i.e., when the coordinates x, y, zare transformed into —x, —y, —z. This transformation turns a right-handed coordinate system into a left-handed one or vice versa. [Pg.60]

After the discovery of parity violation the CP symmetry, i.e., the invariance of the physical laws against the simultaneous transformation of charge and space reflection, was still assumed to be exact. However, in 1964 Cronin and Fitch (Nobel Prize 1980) discovered (Christenson et al. 1964) that the weak interaction violates that as well, although this violation is tiny, not maximal, like that of the P invariance. CP violation makes it possible to differentiate between a world and an antiworld and may be related to the matter - antimatter asymmetry. [Pg.469]

Table 3> Symmetry species in some common point groups of functions transforming like the spherical harmonics of ranks 0 to under proper rotations and having even (g) or odd (u) parity under inversion. Table 3> Symmetry species in some common point groups of functions transforming like the spherical harmonics of ranks 0 to under proper rotations and having even (g) or odd (u) parity under inversion.
We can now determine the symmetry contributions from the spin functions. The So function clearly transforms according to Tq. The rotational symmetry of the triplet spin functions follows from their properties as / = 1 angular momentum functions. In addition we need to consider the effect of inversion. But the product of two spin functions must always be of even, or gerade, parity. Thus the symmetrized spin basis... [Pg.164]

The selection rules associated with single-photon absorption stem from its dependence on the transition dipole moment, which must be non-zero for absorption to occur. To satisfy this fundamental requirement, the direct product symmetry species of the initial and final wavefunctions must contain the symmetry species of the dipole operator - the latter transforming like the translation vectors x, y and z. Probably the most familiar aspect is the Laporte selection rule for centrosymmetric molecules, which allows transitions only between states of opposite parity, gerade ( ) ungerade (u). [Pg.1155]


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See also in sourсe #XX -- [ Pg.245 ]




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Parity transformation

Transformation symmetry

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