Search arXiv⌕ Search

arXiv · cond-mat/0609151

$^{1}$H-NMR spin-echo measurements of the static and dynamic spin properties in $λ$-(BETS)$_{2}$FeCl$_{4}$

Abstract

$^{1}$H-NMR spin-echo measurements of the spin-echo decay $M(2τ)$ with a decay rate 1/$T_{2}$ and the frequency shift $Δν/ν_{0}$ under applied magnetic field $\mathbf{B}$$_{0}$ = 9 T along the a-axis over a temperature range 2.0$-$180 K are reported for a single crystal of the organic conductor $λ$-(BETS)$_{2}$FeCl$_{4}$. It provides the spin dynamic and static properties in the paramagnetic metal (PM) and antiferromagnetic insulator (AFI) states as well as across the PM$-$AFI phase transition. A large slow beat structure in the spin-echo decay is observed with a typical beat frequency of $f$ $\sim$ 7 kHz and it varies across the spectrum. Its origin is attributed to the $^{1}$H$-$$^{1}$H dipole interactions rather than to the much larger dipolar field contribution from the Fe$^{3+}$ electrons (spin $S$ = 5/2). A simple phenomenological model provides an excellent fit to the data. The dominant $^{1}$H-NMR frequency shift comes from the dipolar field from the 3d Fe$^{3+}$ ions, and the Fe$^{3+}$ $-$ Fe$^{3+}$ exchange interactions ($J_{0}$) ($J_{0} $ includes the d$-$d exchange interactions through the $π-$electrons) have a substantial effect to the local field at the proton sites expecially at low temperatures. A good fit is obtained with $J_{0}$ = - 1.7 K. The data of the spin-echo decay rate 1/$T_{2}$ indicates that there is a significant change in the slow fluctuations of the local magnetic field at the $^{1}$H-sites on traversing the PM to AFI phase. This evidence supports earlier reports that the PM$-$AFI phase transition in $λ$-(BETS)$_{2}% $FeCl$_{4} $ is driven magnetically and first order.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Guoqing Wu, P. Ranin, G. Gaidos, W. G. Clark, S. E. Brown, L. Balicas, L. K. Montgomery. 2007-03-23. $^{1}$H-NMR spin-echo measurements of the static and dynamic spin properties in $λ$-(BETS)$_{2}$FeCl$_{4}$. https://doi.org/10.1103/physrevb.75.174416

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Observable-Based Learning of Effective Entanglement Hamiltonians

Determining the entanglement Hamiltonian (EH) of an interacting quantum many-body system remains a fundamental challenge beyond special analytically tractable cases. Here we develop an observable-matching framework for learning effective EHs, which we demonstrate using response estimates from quantum Monte Carlo. As applications of this framework, we first calibrate the overall prefactor of the lattice Bisognano--Wichmann (LBW) construction using equal-time correlations and then learn spatially resolved couplings beyond its prescribed profile, without assuming a specific functional form for their spatial dependence. Trained solely on local correlations, the learned EHs reproduce benchmarked von Neumann and second Rényi entropies in $1$D and second Rényi entropies in $2$D. For a strong-bond cut associated with special surface criticality at the $(2+1)$D $O(3)$ Wilson--Fisher critical point, free-form learning outperforms the calibrated LBW ansatz in predicting the second Rényi entropy and reveals spatially nonuniform coupling renormalizations. Importantly, the learned EH also provides access to the von Neumann entropy in this setting, revealing a negative subleading correction and extending previous Rényi entropy findings to the von Neumann case. Directly evaluating the von Neumann entropy in such $(2+1)$D interacting quantum many-body systems remains challenging for conventional numerical methods. These results establish observable-based learning as a route to constructing effective entanglement Hamiltonians beyond prescribed spatial profiles in higher-dimensional interacting systems.

cond-mat.str-el↗

Extensions of the Haldane gap proof: higher dimensions, near degeneracy, fermions and tensor-network states

A recent remarkable paper by OpenAI showed that the spin-one Heisenberg chain with periodic boundary conditions has a spectral gap in the thermodynamic limit. The proof elegantly deduces this gap from the Hamiltonian's spectrum on a finite system. This basic idea is an inequality involving the purity of the original Gibbs state and a dual Gibbs state that is defined via space-time rotation. Here we consider a few generalizations of this purity bootstrap argument. We first extend it to arbitrary spatial dimensions. Our main result uses the space-time duality between symmetry generators and symmetry twists to obtain upper bounds on the splitting of nearly degenerate low-energy states, together with a nonzero gap above them, from finite-system information. As applications, we show that finite-system calculations for the 2+1-D toric code in a field and the 2+1-D transverse-field Ising model establish parameter regimes with four and two low-lying states whose splittings are bounded from above by $e^{-cL}$ and $e^{-cL^2}$ respectively for arbitrarily large system size $L$, while the gap above these states remains nonzero in the thermodynamic limit. Next, we extend it to fermionic systems and use a finite calculation to establish a symmetric mass generation phase in a $2+1$-D fermionic model. Finally, we apply the bootstrap to tensor-network states and establish exponential decay of connected correlations of all local operators in the symmetric square-lattice spin-one state introduced by Jian and Zaletel.

cond-mat.str-el↗

Interfacial polarity control of anomalous Hall effect in LaCoO3-SrIrO3 heterostructures

Interfacial polarity in oxide heterostructures can drive robust charge redistribution across the interface, yet its role in tailoring topological transport phenomena like the anomalous Hall effect (AHE) remains largely unexplored. Here, we control the sign of polarity-induced charge in SrIrO3-LaCoO3 interfaces by independently engineering the layer stacking sequence and the atomic termination. In-situ angle-resolved photoemission spectroscopy directly confirms the sign reversal of the induced charge in SrIrO3 through the contrasting electronic band shifts between different interfacial configurations. Magneto-transport measurements across a systematic matrix of four distinct heterostructures reveal that the AHE can be cleanly toggled on and off: it emerges exclusively under electron-doped conditions, while remaining suppressed for hole-doped SrIrO3. Our results establish that this response originates from an intrinsic, Berry-curvature-driven mechanism governed by polarity-controlled band filling of SrIrO3. These findings shift interfacial polarity from a passive structural consequence to an active design variable for engineering topological quantum states in oxide heterostructures.

cond-mat.str-el↗