In this work, we overview time-reversal nuclear magnetic resonance (NMR) experiments in many-spin systems evolving under the dipolar Hamiltonian. The Loschmidt echo (LE) in NMR is the signal of excitations which, after evolving with a forward Hamiltonian, is recovered by means of a backward evolution. The presence of non-diagonal terms in the non-equilibrium density matrix of the many-body state is directly monitored experimentally by encoding the multiple quantum coherences. This enables a spin counting procedure, giving information on the spreading of an excitation through the Hilbert space and the formation of clusters of correlated spins. Two samples representing different spin systems with coupled networks were used in the experiments. Protons in polycrystalline ferrocene correspond to an 'infinite' network. By contrast, the liquid crystal N-(4-methoxybenzylidene)-4-butylaniline in the nematic mesophase represents a finite proton system with a hierarchical set of couplings. A close connection was established between the LE decay and the spin counting measurements, confirming the hypothesis that the complexity of the system is driven by the coherent dynamics.
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http://dx.doi.org/10.1098/rsta.2015.0155 | DOI Listing |
Phys Rev E
October 2023
Instituto de Física, Benemérita Universidad Autónoma de Puebla, Puebla, 72570, México.
We study the probability distribution function of the long-time values of observables being time-evolved by Hamiltonians modeling clean and disordered one-dimensional chains of many spin-1/2 particles. In particular, we analyze the return probability and its version for a completely extended initial state, the so-called spectral form factor. We complement our analysis with the spin autocorrelation and connected spin-spin correlation functions, both of interest in experiments with quantum simulators.
View Article and Find Full Text PDFbioRxiv
January 2023
Department of Biochemistry and Biophysics, Oregon State University, Corvallis, Oregon 97331, United States.
Studying protein structures and dynamics directly in the cellular environments in which they function is essential to fully understand the molecular mechanisms underlying cellular processes. Site-directed spin-labeling (SDSL)-in combination with double electron-electron resonance (DEER) spectroscopy-has emerged as a powerful technique for determining both the structural states and the conformational equilibria of biomacromolecules. In-cell DEER spectroscopy on proteins in mammalian cells has thus far not been possible due to the notable challenges of spin-labeling in live cells.
View Article and Find Full Text PDFPhys Rev Lett
July 2021
Interdisciplinary Center of Quantum Information, State Key Laboratory of Modern Optical Instrumentation, and Zhejiang Province Key Laboratory of Quantum Technology and Device, Department of Physics, Zhejiang University, Hangzhou 310027, China.
Statistical spin dynamics plays a key role in understanding the working principle for novel optical Ising machines. Here, we propose the gauge transformation for a spatial photonic Ising machine, where a single spatial phase modulator simultaneously encodes spin configurations and programs interaction strengths. Using gauge transformation, we experimentally evaluate the phase diagram of a high-dimensional spin-glass equilibrium system with 100 fully connected spins.
View Article and Find Full Text PDFPhys Rev E
April 2021
CAS Key Laboratory for Theoretical Physics, Institute of Theoretical Physics, Chinese Academy of Sciences, Beijing 100190, China.
The planted p-spin interaction model is a paradigm of random-graph systems possessing both a ferromagnetic phase and a disordered phase with the latter splitting into many spin-glass states at low temperatures. Conventional simulated annealing dynamics is easily blocked by these low-energy spin-glass states. Here we demonstrate that actually this planted system is exponentially dominated by a microcanonical polarized phase at intermediate energy densities.
View Article and Find Full Text PDFJ Chem Phys
July 2020
Donostia International Physics Center (DIPC), 20018 Donostia, Euskadi, Spain.
Analytic energy gradients with respect to nuclear motion are derived for non-singlet compounds in the natural orbital functional theory. We exploit the formulation for multiplets in order to obtain a simple formula valid for any many-electron system in its ground mixed state with a total spin S and all possible spin projection S values. We demonstrate that the analytic gradients can be obtained without resorting to linear response theory or involving iterative procedures.
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