A formalism is presented that describes the time behavior of the spin density matrix of a nuclear spin system with arbitrary spin in terms of fictitious spin −(1/2) operators. This formalism is an extension of that used earlier for nuclei with spin I=1. For a spin system with n eigenstates we define for every pair of eigenstates ‖i〉 and ‖j〉 three operators Ii−jp, with p=x, y, and z, according to the three 2×2 Pauli matrices σx, σy, and σz. These operators together constitute a complete set of n2−1 independent Hermitian operators, and we can write the n×n density matrix and the spin Hamiltonian of the system in terms of the Ii−jp operators. The commutation relations among the operators make it possible in many cases to solve the equation of motion of the density matrix analytically. Three examples of the use of the Ii−jp operators are presented. Firstly a system of noninteracting spins with I=1 is considered. The Ii−jp operators for this case are compared with the Iq,k operator defined earlier. The cw signal intensities of the single and double quantum transitions for the I=1 spin system are derived. Secondly a spin system with I=3/2 is described as a simple extension of the use of the Ii−jp operators. The excitation and the detection of the triple quantum coherence are discussed for noninteracting nuclei in solids. Finally the double quantum effects in a system of two interacting spins with I=1/2 are discussed.
A formalism is presented that describes the time behavior of the spin density matrix of a nuclear spin system with arbitrary spin in terms of fictitious spin −(1/2) operators. This formalism is an extension of that used earlier for nuclei with spin I=1. For a spin system with n eigenstates we define for every pair of eigenstates ‖i〉 and ‖j〉 three operators Ii−jp, with p=x, y, and z, according to the three 2×2 Pauli matrices σx, σy, and σz. These operators together constitute a complete set of n2−1 independent Hermitian operators, and we can write the n×n density matrix and the spin Hamiltonian of the system in terms of the Ii−jp operators. The commutation relations among the operators make it possible in many cases to solve the equation of motion of the density matrix analytically. Three examples of the use of the Ii−jp operators are presented. Firstly a system of noninteracting spins with I=1 is considered. The Ii−jp operators for this case are compared with the Iq,k operator defined earlier. The cw signal intensities of the single and double quantum transitions for the I=1 spin system are derived. Secondly a spin system with I=3/2 is described as a simple extension of the use of the Ii−jp operators. The excitation and the detection of the triple quantum coherence are discussed for noninteracting nuclei in solids. Finally the double quantum effects in a system of two interacting spins with I=1/2 are discussed.
An operator formalism is presented which conveniently treats the interaction of a spin-1 nucleus with a weak radio frequency field. The Hamiltonian in the rotating frame is ℋ=−Δω Iz−ω1Ix+(1/3) ωQ[3 I2z−I (I+1)], where Δω is the resonance offset (Δω=ω0−ω), ω1 is the intensity of the rf field, and ωQ is the quadrupolar splitting. Nine fictitious spin−1/2 operators, Ip,i where p=x,y,z and i=1,2,3, are defined where p refers to the transition between two of the levels and i the Cartesian component. The operators, which are the generators of the group SU (3), satisfy spin-1/2 commutation relations [Ip,j, Ip,k]=i Ip,l, where j,k,l=1,2,3 or cyclic permutation. Thus each p defines a three-dimensional space termed p space. For irradiation near one of the quadrupolar satellites, for example, Δω=ωQ+δω with δω, ω1≪ωQ, it is shown that the effective Hamiltonian can be written ℋ?−δωIx,3−√2 ω1Ix,1, i.e., a fictitious spin-1/2 Hamiltonian in x space with effective magnetogyric ratio γ along the 3 (resonance offset) axis and √2 γ along the 1 (rf field) axis. For irradiation near the center we can effect double quantum transitions between m=±1. The formalism allows us to write the effective operators for these transitions. For example, if we take Δω=δω again with δω, ω1≪ωQ we find the effective double quantum (DQ) Hamiltonian H?−2 δω Iz,1−(ω21/ωQ) Iz,3. Thus the z space is referred to as the double quantum frame with effective magnetogyric ratio 2γ along the 1 (resonance offset) axis and (ω1/ωQ) γ along the 3 (rf field) axis. The limiting expressions are compared with exact calculations for arbitrary ω1 done by high speed computer. The theory is applied to various cases of irradiation including our previously reported technique of Fourier transform double quantum NMR. Various pulse sequences for preparing, storing, and maintaining the evolution of double quantum coherence are analyzed for single crystal and polycrystalline samples. Finally, the effects of rf phase on the double quantum phase are presented briefly, and the possibility of double quantum spin locking is analyzed.
Multiple-quantum spin dynamics is studied using analytic and numerical methods for one-dimensional finite linear chains and rings of nuclear spins 1/2 coupled by dipole-dipole interactions. An approximation of dipole-dipole interaction between nearest neighbors having the same constants is used to obtain exact expressions for the intensities of the multiple-quantum coherences in the spin systems studied, which are initially in thermal equilibrium and whose evolution is described by a two-spin two-quantum Hamiltonian. An approximation of nearest neighbors with arbitrary dipole-dipole interaction constants is used to establish a simple relationship between the multiple-quantum dynamics and the dynamics of spin systems with an XY Hamiltonian. Numerical methods are developed to calculate the intensities of multiple-quantum coherences in multiple-quantum NMR spectroscopy. The integral of motion is obtained to expand the matrix of the two-spin two-quantum Hamiltonian into two independent blocks. Using the nearest-neighbor approximation the Hamiltonian is factorized according to different values of the projection operator of the total spin momentum on the direction of the external magnetic field. Results of calculations of the multiple-quantum dynamics in linear chains of seven and eight nuclear spins and a six-spin ring are presented. It is shown that the evolution of the intensities of the lowest-order multiple-quantum coherences in linear chains is accurately described allowing for dipole-dipole interaction of nearest and next-nearest neighbors only. Numerical calculations are used to compare the contributions of nearest and remote spins to the intensities of the multiple-quantum coherences.
Abstract Advances in quantum information processing can open a way for numerous applications of the processing in various fields of science and technology: communication, precision measurement, computing, nano-scale detectors, and sensors. Classical and various quantum correlations have been studied in real spin 1/2 systems. The nonlocality measures provide a novel classification scheme for bipartite states, highlighting that nonlocality is a quantum resource distinct from other types of quantum correlations. We first studied the temperature and field dependencies of nonlocality measure in the three fictitious spin 1/2 system, which represents a nuclear spin-7/2 placed in magnetic and inhomogeneous electric fields. The relationship between nonlocality and other quantum correlations (entanglement and geometric discord) was studied. The Hamiltonian and spin operators for a spin 7/2 are represented in the basis formed by the Kronecker products of the Pauli matrices. This transformation allows us to represent a spin 7/2 as a system of three coupled fictitious spins 1/2 and, from the quantum information point of view, as an equivalent system of three coupling qubits. Well-developed methods were used to calculate measures of quantum correlations. For example, we consider 59Co (spin 7/2) in the compounds [Co(NH3)5Cl]Cl2 and Ca3Co2O6. The interaction between the fictitious spins of 59Co nuclei depends on the magnitude and direction of the external magnetic field. Other potential cases of quantum correlations can be realized based on nuclear spins 7/2 in solid-state systems, for instance, such as 51V, 165Ho, or 123Sb.
We investigated dynamics of entangled states on the basis of multiple-quantum (MQ) NMR methods. A time evolution of MQ coherences of nuclear spins coupled by the dipole-dipole interactions (DDI) in solids is simply connected with dynamics of quantum entangled states. We studied analytically dynamics of the entangled states for two- and three-spin systems. In this case dynamics of the quantum entanglement is uniquely determined by the time evolution of MQ coherences of the second order. The real part of the density matrix describing MQ dynamics in solids is responsible for MQ coherences of the zeroth order while its imaginary part is responsible for the second order. Thus, one can conclude that dynamics of the entanglement is connected with transitions from the real part of the density matrix to the imaginary one and vice versa.
Abstract The spin-independent properties of an electronic system are completely determined by spinless density functions, P1(1; 1') and P 2( 1,2; 1',2 '), derived from the 1-and 2-electron density matrices, p1(1; 1') and p2(1,2 ; 1',2'). These functions, and their physical inter-pretation, have been dealt with in part I: the present paper contains the generalizations necessary when the Hamiltonian contains spin terms (as in discussions of electron and nuclear spin resonance). The density matrices, and more generally the transition density matrices p1(kλ|1; 1') and p2(kλ|l,2; 1',2') associated with states and Φkand Φλ are resolved into spinless components associated with different spin situations: p1 has four such components (one giving the density of a-spin electrons, a second the density of β-spin electrons, and two with less direct physical significance), while p2 has sixteen components. It is shown that all components, for states k=(S, M),λ= (S',M') of given S, S', are determined by three 2-electron functions.For k=λ these reduce to p2, the spinless pair function, from which the electron density p1 may be derived by integration; Q2a ‘conditional' spin density, from which the (1-electron) spin density Q1 may be derived (as in the case of p1 and P2); Q c. a., a ‘coupling anisotropy function', which describes the anisotropy of spin-spin coupling associated with quantization of the spin z-component. It is also useful to introduce (though it is not an independent function). Qc, a ‘coupling density function', which measures the coupling between the spins of two electrons at different points in space. All spin-dependent effects, including the usual spin-spin and spin-orbit couplings and also (indirect) nuclear and electron-nuclear spin-spin couplings, may be related to the many- electron wave function through the above density functions. All the densities have a physical interpretation, independent of the precise nature of the wave functions (which may, for example, be the exact eigenfunctions of a spinless Hamiltonian or merely approximations of orbital form). The derivation of the density functions from approximate wave functions is considered in some detail. For functions describing weakly coupled electron groups (e. g. inner-shell and valence electrons) the densities may be expressed in terms of those of the separate groups. This reduction may be followed by an orbital description of each group; and subsequently, by a linear-combination-of-atomic-orbitals (l. c. a. o.) approximation. In the simpler approximations, all the coupling effects discussed are determined by electron and spin ‘populations'. Preliminary calculations suggest that such approximations may in many cases be adequate.
The density matrix is a very convenient way to do calculations for a large number of spin systems and is developed from the fundamental ideas of quantum mechanics. The idea of pure and mixed states is introduced and used to develop an expression for the single-spin density matrix as it applies to NMR spectroscopy. Multiple-spin density matrices are produced by using the outer product of single-spin matrices and their commutation properties are examined. A very useful form of the scalar coupling density operator is developed and used, along with the chemical shift operator, to calculate the spectrum of a weakly coupled two-spin system. The density operator of spin-1 is explored briefly. Density matrix calculations in perturbed systems are investigated in preparation for relaxation calculations. Strong coupling is discussed and compared to the weak coupling approximation, using the full scalar coupling Hamiltonian and matrix diagonalization techniques.