The multiple quantum NMR dynamics in systems of equivalent spins with a dipolar ordered initial state

The multiple quantum (MQ) NMR dynamics in the system of equivalent spins with the dipolar ordered initial state is considered. The high symmetry of the Hamiltonian responsible for the MQ NMR dynamics (the MQ Hamiltonian) is used to develop analytic and numerical methods for the investigation of the MQ NMR dynamics in systems consisting of hundreds of spins from the “first principles.” We obtain the dependence of the intensities of the MQ NMR coherences on their orders (profiles of the MQ NMR coherences) for systems of 200–600 spins. It is shown that these profiles may be well approximated by exponential distribution functions. We also compare the MQ NMR dynamics in the systems of equivalent spins having two different initial states, the dipolar ordered state and the thermal equilibrium state in a strong external magnetic field.     

Multiple Quantum Coherences (MQ) NMR and Entanglement Dynamics in the Mixed-Three-Spin XXX Heisenberg Model with Single-Ion Anisotropy

We analytically investigate Multiple Quantum (MQ) NMR dynamics in a mixed-three-spin (1/2,1,1/2) system with XXX Heisenberg model at the front of an external homogeneous magnetic field B. A single-ion anisotropy property ζ is considered for the spin-1. The intensities dependence of MQ NMR coherences on their orders (zeroth and second orders) for two pairs of spins (1,1/2) and (1/2,1/2) of the favorite tripartite system are obtained. It is also investigated dynamics of the pairwise quantum entanglement for the bipartite (sub)systems (1,1/2) and (1/2,1/2) permanently coupled by, respectively, coupling constants J₁ and J₂, by means of concurrence and fidelity. Then, some straightforward comparisons are done between these quantities and the intensities of MQ NMR coherences and ultimately some interesting results are reported. We also show that the time evolution of MQ coherences based on the reduced density matrix of the pair spins (1,1/2) is closely connected with the dynamics of the pairwise entanglement. Finally, we prove that one can introduce MQ coherence of the zeroth order corresponds to the pair spins (1,1/2) as an entanglement witness at some special time intervals.     

Line shapes of multiple quantum NMR coherences in one-dimensional quantum spin chains in solids

General formulae for intensities of multiple quantum (MQ) NMR coherences in systems of nuclear spins coupled by the dipole-dipole interactions are derived. The second moments of the MQ coherences of zero- and second orders are calculated for infinite linear chains in the approximation of the nearest neighbor interactions. Supercomputer simulations of intensities of MQ coherences of linear chains are performed at different times of preparation and evolution periods of MQ NMR experiments. The second moments obtained from the developed theory are compared with the results of the supercomputer analysis of MQ NMR dynamics. The linewidth information in MQ NMR experiments is discussed.     

Dipolar temperature and multiple-quantum NMR dynamics in dipolar ordered-spin systems

We investigate analytically and numerically the multiple-quantum (MQ) NMR dynamics in systems of nuclear spins 1/2 coupled by dipole-dipole interactions in the case of the dipolar-ordered initial state. We suggest a new method of MQ NMR based on the measurement of the dipolar temperature in the quasi-equilibrium state, which establishes after the time of order ω _loc ⁻¹ (ω_loc is the dipolar local field) after the MQ NMR experiment. Manyspin clusters and correlations are created faster in such an experiment than in usual MQ NMR experiments and can be used for the investigation of the many-spin dynamics of nuclear spins in solids. The text was submitted by the authors in English.     

Low temperature MQ NMR dynamics in dipolar ordered state

We investigate analytically and numerically the Multiple Quantum (MQ) NMR dynamics in dipolar ordered spin systems of nuclear spins 1/2 at low temperatures. We consider two different methods of MQ NMR. One of them is based on the measurement of the dipolar energy. The other method uses an additional resonance (π/4)_y-pulse after the preparation period of the standard MQ NMR experiment in solids and allows one to measure the Zeeman energy. Both considered methods are sensitive to the contribution of remote spins in the interaction and to the spin system structure. The QS method is sensitive to the spin number in the molecule while the PS method gives very similar time dependencies of the intensities of MQ coherences for different spin numbers. It is shown that the use of the dipolar ordered initial state has the advantage of exciting the highest order MQ coherences in clusters of 4m identical spins, where m=1,2,3,…, that is impossible to do with the standard MQ method. MQ NMR methods based on the dipolar ordered initial states at low temperatures complement the standard NMR spectroscopy for better studying structures and dynamic processes in solids.     

Dipolar Relaxation of Multiple Quantum NMR Coherences as a Model of Decoherence of Many-Qubit Coherent Clusters

Dipolar relaxation of multiple quantum (MQ) nuclear magnetic resonance (NMR) coherence is investigated on the evolution period of the MQ NMR experiment in chains of ¹⁹F nuclei in a single crystal of calcium fluorapatite. The dependence of the relaxation time of the MQ coherence of the second order on the size of the coherent spin cluster formed on the preparation period is obtained. The dipolar relaxation of MQ NMR coherences is considered as a model for the investigation of decoherence of quantum states of many-qubit spin clusters.     

A simple approximation for Ising spin models

A simple method is introduced for Ising spin systems based on the correlated molecular-field theory. Here, we consider an interacting triple in the mean field of its surrounding lattice points taking into account the product of three spins in the cluster. The present results for Curie temperature are compared to the mean-field theory(MFT), Bethe–Peierls–Weiss(BPW) approach, and self-consistent correlated field(SCCF) approximation, respectively. A procedure of triangular clusters is investigated that yields very distinguishable improvement of the critical temperature, as well.     

Multiple-quantum NMR spin dynamics of inhomogeneous one-dimensional systems in solids

Multiple-quantum NMR spin dynamics of inhomogeneous one-dimensional systems in solids is investigated by analytical and numerical methods. A fermion approach for MQ spin dynamics of one-dimensional inhomogeneous systems is developed in the approximation of the dipole–dipole interactions (DDI) of nearest neighbors. It is shown that only MQ coherences of the zeroth and plus/minus second orders appear in the approximation of the DDI of the nearest neighbors even in inhomogeneous one-dimensional systems. We also investigate MQ dynamics of inhomogeneous chains numerically. Intensities of MQ NMR coherences for a linear chain consisting of 3000 spins are calculated.     

Variational cluster approach to correlated electron systems in low dimensions

A self-energy-functional approach is applied to construct cluster approximations for correlated lattice models. It turns out that the cluster-perturbation theory [Phys. Rev. Lett. 84, 522 (2000)]] and the cellular dynamical mean-field theory [Phys. Rev. Lett. 87, 186401 (2001)]] are limiting cases of a more general cluster method. The results for the one-dimensional Hubbard model are discussed with regard to boundary conditions, bath degrees of freedom, and cluster size.     

Scaling of decoherence in wide NMR quantum registers

Among the most important parameters for the usefulness of quantum computers are the size of the quantum register and the decoherence time for the quantum information. The decoherence time is expected to get shorter with the number of correlated qubits, but experimental data are only available for small numbers of qubits. Solid-state nuclear magnetic resonance allows one to correlate large numbers of qubits (several hundred) and measure their decoherence rates. We use a modified magnetic dipole-dipole interaction to correlate the proton spins in a solid sample and observe the decay of the resulting highly correlated states. By systematically varying the number of correlated spins, we measure the increase of the decoherence rate with the size of the quantum register.     

Influence of large magnetic fields on non-radiative transitions from the A state of thiophosgene

In the present investigation we have examined fluorescence excitation spectra and fluorescence decay profiles for various vibronic bands in the X → A transitions of thiophosgene (Cl₂CS) under 10 mTorr in magnetic fields of up to 10 T. These experimental results indicated that the observed magnetic quenching (MQ) of the fluorescence can no longer be explained by the ordinary theory of the direct mechanism (DM). In order to interpret such experimental results in larger magnetic fields than 1.2 T, we have applied a new theory that was developed by solving the equation of motion for the density matrix. According to this theory, MQ due to DM is saturated in sufficiently large fields. This theoretical prediction is in agreement with the experimental results for the 4⁴ ₁, 4¹ ₀, 3¹ ₀4¹ ₀, 4³ ₀, and 1¹ ₀4¹ ₀ bands. Thus, we may conclude that the saturation of MQ due to DM is a new phenomenon characteristic of MQ in magnetic fields larger than 1.2 T. Moreover, we have examined the pressure dependence of MQ of the fluorescence in several vibronic bands. These experimental results show that MQ of the fluorescence under 10 mTorr is due mainly to the acceleration of intramolecular radiationless processes induced by magnetic fields.     

On the second moment of the multiquantum NMR spectrum of a solid

New experimental data on the time dependence of an increase in the number of correlated spins under the conditions of the observation of the multiquantum NMR spectrum of a solid are processed on the basis of a microscopic theory for describing the growth of the second moment of multiquantum NMR developed by us earlier. As follows from the theory, the growth is an exponential function of time for crystals with quite diverse structures. The results are discussed on the basis of semiphenomenological models.     

利用Raman磁共振研究四极核对AX体系弛豫行为的影响

本文利用一维多量子Raman磁共振谱线的线宽测定了氯仿(CHCl₃)中碳氢体系的多量子的弛豫时间,由此得到第二类标量耦合弛豫起主导作用时的碳氢核自旋弛豫的交叉相关系数,氯核与碳和氢核的标量耦合常数,以及它们的相对符号。     

Theory of FID NMR signal dephasing induced by mesoscopic magnetic field inhomogeneities in biological systems.

A theory of the NMR signal dephasing due to the presence of tissue-specific magnetic field inhomogeneities is developed for a two-compartment model. Randomly distributed magnetized objects of finite size embedded in a given media are modeled by ellipsoids of revolution (prolate and oblate spheroids). The model can be applied for describing blood vessels in a tissue, red blood cells in the blood, marrow within trabecular bones, etc. The time dependence of the dephasing function connected with the spins inside of the objects, s(i), is shown to be expressed by Fresnel functions and creates a powder-type signal in the frequency domain. The short-time regime of the dephasing function for spins outside the objects, s(e), is always characterized by Gaussian time dependence, s(e) approximately exp[-zeta(k)(t/tc)2], with zeta being a volume fraction occupied by the objects, t(c) being a characteristic dephasing time, and the coefficient k depending on the ellipsoid's shape through the aspect ratio of its axes (a/c). The long-time asymptotic behavior of s(e) is always "quasispherical"-linear exponential in time, s(e) approximately exp(-zetaCt/tc), with the same "spherical" decay rate for any ellipsoidal shape. For long prolate spheroids (a/c)<1, there exists an intermediate characteristic regime with a linear exponential time behavior and an aspect-ratio-dependent decay rate smaller than (zetaC/tc).     

Concentration dependence of the wings of a dipole-broadened magnetic resonance line in magnetically diluted lattices

The singularities of the time autocorrelation functions (ACFs) of magnetically diluted spin systems with dipole–dipole interaction (DDI), which determine the high-frequency asymptotics of autocorrelation functions and the wings of a magnetic resonance line, are studied. Using the self-consistent fluctuating local field approximation, nonlinear equations are derived for autocorrelation functions averaged over the independent random arrangement of spins (magnetic atoms) in a diamagnetic lattice with different spin concentrations. The equations take into account the specificity of the dipole–dipole interaction. First, due to its axial symmetry in a strong static magnetic field, the autocorrelation functions of longitudinal and transverse spin components are described by different equations. Second, the long-range type of the dipole–dipole interaction is taken into account by separating contributions into the local field from distant and near spins. The recurrent equations are obtained for the expansion coefficients of autocorrelation functions in power series in time. From them, the numerical value of the coordinate of the nearest singularity of the autocorrelation function is found on the imaginary time axis, which is equal to the radius of convergence of these expansions. It is shown that in the strong dilution case, the logarithmic concentration dependence of the coordinate of the singularity is observed, which is caused by the presence of a cluster of near spins whose fraction is small but contribution to the modulation frequency is large. As an example a silicon crystal with different ²⁹Si concentrations in magnetic fields directed along three crystallographic axes is considered.     

Field-cycling NMR investigations of (13)C-(1)H cross-relaxation and cross-polarisation: the nuclear solid effect and dynamic nuclear polarisation

A field-cycling NMR investigation of (1)H-(13)C polarisation transfer using cross-relaxation and the nuclear solid effect (NSE) is described. Dynamic nuclear polarisation (DNP) of the (13)C spins is observed when forbidden transitions are driven by r.f. irradiation at the sum and difference Larmor frequencies of the two nuclei. When the (1)H spins are pre-polarised, a significant transfer of polarisation to the (13)C nuclei is achieved in a time short compared with the spin-lattice relaxation time of (13)C. The cross-polarisation arising from the NSE is studied as a function of B-field and time. These results are compared with the solutions of the differential equations that govern the coupled system of (1)H-(13)C spins. The effects of cross-relaxation are incorporated into the model for the first time and good agreement between theory and experiment is obtained. The experiments have been conducted at 20K on a (13)C-enriched sample of benzoic acid.     

Field-dependent nuclear relaxation of spins 1/2 induced by dipole-dipole couplings to quadrupole spins: LaF3 crystals as an example

A general theory of spin-lattice nuclear relaxation of spins I=1/2 caused by dipole-dipole couplings to quadrupole spins S1, characterized by a non-zero averaged (static) quadrupole coupling, is presented. In multispin systems containing quadrupolar and dipolar nuclei, transitions of spins 1/2 leading to their relaxation are associated through dipole-dipole couplings with certain transitions of quadrupole spins. The averaged quadrupole coupling attributes to the energy level structure of the quadrupole spin and influences in this manner relaxation processes of the spin 1/2. Typically, quadrupole spins exhibit also a complex multiexponential relaxation sensed by the dipolar spin as an additional modulation of the mutual dipole-dipole coupling. The proposed model includes both effects and is valid for an arbitrary magnetic field and an arbitrary quadrupole spin quantum number. The theory is applied to interpret fluorine relaxation profiles in LaF3 ionic crystals. The obtained results are compared with predictions of the 'classical' Solomon relaxation theory.     

Nucleation theorems applied to the Ising model

We use Monte Carlo simulations to study a single cluster of "up" spins in a sea of "down" spins in the three-dimensional Ising model. We evaluate the growth and decay rates for clusters of different sizes, identify the critical size for which these rates are equal, and obtain the internal energy of the critical size cluster. The results of the simulations at different temperatures and magnetic fields are used together with the first and second nucleation theorems to predict how the cluster nucleation rate changes when the external magnetic field and the temperature are changed. Our results are in agreement with literature values, but our method requires significantly less computational effort than the simulations reported earlier and avoids the difficult evaluation of free energies.     

Effects of nuclear spins on the quantum relaxation of the magnetization for the molecular nanomagnet Fe8

The strong influence of nuclear spins on resonant quantum tunneling in the molecular cluster Fe8 is demonstrated for the first time by comparing the relaxation rate of the standard Fe8 sample with two isotopic modified samples: (i) 56Fe is replaced by 57Fe, and (ii) a fraction of 1H is replaced by 2H. By using a recently developed "hole digging" method, we measured an intrinsic broadening which is driven by the hyperfine fields. Our measurements are in good agreement with numerical hyperfine calculations. For T>1.5 K, the influence of nuclear spins on the relaxation rate is less important, suggesting that spin-phonon coupling dominates the relaxation rate.