Inelastic neutron scattering investigation of magnetostructural excitations in the spin-Peierls organic system (TMTTF)2PF6

Inelastic neutron scattering investigation of magnetostructural excitations in the spin-Peierls... One-dimensional (1D) conductors such as Bechgaard and Fabre salts are a prototypal example of correlated systems where the phase diagram is controlled by sizable electron-electron repulsions. In deuterated (TMTTF)2PF6, where this interaction achieves charge localization at ambient pressure on donor stacks, magnetostructural coupling plays a decisive role to stabilize a spin-Peierls (SPs) ground state at TSP=13K. In this paper, we present the first inelastic neutron scattering investigation of SP magnetic excitations in organics. Our paper reveals the presence above TSP of sizable critical fluctuations leading to the formation of a pseudogap in the 1D antiferromagnetic (AF) S=1/2 magnetic excitation spectrum of the donor stack, concomitant with the local formation of singlet of paired spins into dimers below TSPMF≈40K. In addition, the inelastic neutron scattering investigation allows us also to probe the SP critical lattice dynamics and to show that at ambient pressure these dynamics are of relaxation or order-disorder type. Below TSP, our paper reveals the emergence of a two gap SP magnetic excitation spectrum towards a well-defined S=1 magnon mode and a continuum of two excitations, as theoretically predicted. Our measurements allow us to locate the ambient pressure SP phase of (TMTTF)2PF6 in the classical (adiabatic) limit close to the classical/quantum crossover line. Then we provide arguments suggesting that pressurized (TMTTF)2PF6 shifts to the quantum (antiadiabatic) SP gapped phase, which ends in a quantum critical point allowing the stabilization of an AF phase that competes with superconductivity at higher pressure. Finally, we propose that the magnetostructural coupling mechanism in the Fabre salts is caused by dimer charge/spin fluctuations driven by the coupling of donors with anions. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Physical Review B American Physical Society (APS)

Inelastic neutron scattering investigation of magnetostructural excitations in the spin-Peierls organic system (TMTTF)2PF6

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Inelastic neutron scattering investigation of magnetostructural excitations in the spin-Peierls organic system (TMTTF)2PF6

Abstract

One-dimensional (1D) conductors such as Bechgaard and Fabre salts are a prototypal example of correlated systems where the phase diagram is controlled by sizable electron-electron repulsions. In deuterated (TMTTF)2PF6, where this interaction achieves charge localization at ambient pressure on donor stacks, magnetostructural coupling plays a decisive role to stabilize a spin-Peierls (SPs) ground state at TSP=13K. In this paper, we present the first inelastic neutron scattering investigation of SP magnetic excitations in organics. Our paper reveals the presence above TSP of sizable critical fluctuations leading to the formation of a pseudogap in the 1D antiferromagnetic (AF) S=1/2 magnetic excitation spectrum of the donor stack, concomitant with the local formation of singlet of paired spins into dimers below TSPMF≈40K. In addition, the inelastic neutron scattering investigation allows us also to probe the SP critical lattice dynamics and to show that at ambient pressure these dynamics are of relaxation or order-disorder type. Below TSP, our paper reveals the emergence of a two gap SP magnetic excitation spectrum towards a well-defined S=1 magnon mode and a continuum of two excitations, as theoretically predicted. Our measurements allow us to locate the ambient pressure SP phase of (TMTTF)2PF6 in the classical (adiabatic) limit close to the classical/quantum crossover line. Then we provide arguments suggesting that pressurized (TMTTF)2PF6 shifts to the quantum (antiadiabatic) SP gapped phase, which ends in a quantum critical point allowing the stabilization of an AF phase that competes with superconductivity at higher pressure. Finally, we propose that the magnetostructural coupling mechanism in the Fabre salts is caused by dimer charge/spin fluctuations driven by the coupling of donors with anions.
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Publisher
The American Physical Society
Copyright
Copyright © ©2017 American Physical Society
ISSN
1098-0121
eISSN
1550-235X
D.O.I.
10.1103/PhysRevB.96.035127
Publisher site
See Article on Publisher Site

Abstract

One-dimensional (1D) conductors such as Bechgaard and Fabre salts are a prototypal example of correlated systems where the phase diagram is controlled by sizable electron-electron repulsions. In deuterated (TMTTF)2PF6, where this interaction achieves charge localization at ambient pressure on donor stacks, magnetostructural coupling plays a decisive role to stabilize a spin-Peierls (SPs) ground state at TSP=13K. In this paper, we present the first inelastic neutron scattering investigation of SP magnetic excitations in organics. Our paper reveals the presence above TSP of sizable critical fluctuations leading to the formation of a pseudogap in the 1D antiferromagnetic (AF) S=1/2 magnetic excitation spectrum of the donor stack, concomitant with the local formation of singlet of paired spins into dimers below TSPMF≈40K. In addition, the inelastic neutron scattering investigation allows us also to probe the SP critical lattice dynamics and to show that at ambient pressure these dynamics are of relaxation or order-disorder type. Below TSP, our paper reveals the emergence of a two gap SP magnetic excitation spectrum towards a well-defined S=1 magnon mode and a continuum of two excitations, as theoretically predicted. Our measurements allow us to locate the ambient pressure SP phase of (TMTTF)2PF6 in the classical (adiabatic) limit close to the classical/quantum crossover line. Then we provide arguments suggesting that pressurized (TMTTF)2PF6 shifts to the quantum (antiadiabatic) SP gapped phase, which ends in a quantum critical point allowing the stabilization of an AF phase that competes with superconductivity at higher pressure. Finally, we propose that the magnetostructural coupling mechanism in the Fabre salts is caused by dimer charge/spin fluctuations driven by the coupling of donors with anions.

Journal

Physical Review BAmerican Physical Society (APS)

Published: Jul 17, 2017

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