59
Views
49
CrossRef citations to date
0
Altmetric
Low Dimensional Solids and Molecular Crystals

Overhauser Shift of the Conduction Electron Spin Resonance in (FA)2PF6 Single Crystals

&
Pages 335-360 | Received 17 Oct 1985, Published online: 20 Apr 2011
 

Abstract

The shift ΔB ov of the ESR line due to saturation of the NMR of the hyperfine coupled nuclei (Overhauser shift) was measured for single crystals of the organic conductor (FA)2PF6. ΔBov , is proportional to [Abar] tt , being the average hyperfine interaction between the conduction electrons and the protons in resonance, and the dynamic nuclear spin polarization (DNP), respectively. The DNP enhancement factor V was determined for the two orientations of the static magnetic field B o , perpendicular (V = 525 ± 40) and parallel (V = 280 ± 25) to the needle axis a, respectively. The absolute value of the average hyperfine coupling is [Abar]zz = –(1.16 ± 0.05) Gauss · ge μ B . Both, the temperature dependence and the anisotropy of the proton spin relaxation times T 1 p and T 1 p were measured from the time dependence of the Overhauser shift, ΔBov (t) after rf-pulses or after switching “on” and “off” the ESR saturation. Within the metallic phase of the crystal the proton relaxation is governed by a Korringa law. The experiments definitely show, that the electron spins, showing up in the ESR are those of the conduction electrons.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.