Electron spin coherence in metallofullerenes: Y, Sc, and La@C82

Endohedral fullerenes encapsulating a spin-active atom or ion within a carbon cage offer a route to self-assembled arrays such as spin chains. In the case of metallofullerenes the charge transfer between the atom and the fullerene cage has been thought to limit the electron spin phase coherence time...

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Main Authors: Brown, R, Ito, Y, Warner, J, Ardavan, A, Shinohara, H, Briggs, G, Morton, J
Format: Journal article
Language:English
Published: 2010
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author Brown, R
Ito, Y
Warner, J
Ardavan, A
Shinohara, H
Briggs, G
Morton, J
author_facet Brown, R
Ito, Y
Warner, J
Ardavan, A
Shinohara, H
Briggs, G
Morton, J
author_sort Brown, R
collection OXFORD
description Endohedral fullerenes encapsulating a spin-active atom or ion within a carbon cage offer a route to self-assembled arrays such as spin chains. In the case of metallofullerenes the charge transfer between the atom and the fullerene cage has been thought to limit the electron spin phase coherence time (T 2) to the order of a few microseconds. We study electron spin relaxation in several species of metallofullerene as a function of temperature and solvent environment, yielding a maximum T2 in deuterated o-terphenyl greater than 200 μs for Y, Sc, and La@C82. The mechanisms governing relaxation (T1, T2) arise from metal-cage vibrational modes, spin-orbit coupling and the nuclear spin environment. The T2 times are over 2 orders of magnitude longer than previously reported and consequently make metallofullerenes of interest in areas such as spin labeling, spintronics, and quantum computing. © 2010 The American Physical Society.
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spelling oxford-uuid:fe57b612-832c-424d-8cdf-a2ac5b681afc2022-03-27T13:35:47ZElectron spin coherence in metallofullerenes: Y, Sc, and La@C82 Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fe57b612-832c-424d-8cdf-a2ac5b681afcEnglishSymplectic Elements at Oxford2010Brown, RIto, YWarner, JArdavan, AShinohara, HBriggs, GMorton, JEndohedral fullerenes encapsulating a spin-active atom or ion within a carbon cage offer a route to self-assembled arrays such as spin chains. In the case of metallofullerenes the charge transfer between the atom and the fullerene cage has been thought to limit the electron spin phase coherence time (T 2) to the order of a few microseconds. We study electron spin relaxation in several species of metallofullerene as a function of temperature and solvent environment, yielding a maximum T2 in deuterated o-terphenyl greater than 200 μs for Y, Sc, and La@C82. The mechanisms governing relaxation (T1, T2) arise from metal-cage vibrational modes, spin-orbit coupling and the nuclear spin environment. The T2 times are over 2 orders of magnitude longer than previously reported and consequently make metallofullerenes of interest in areas such as spin labeling, spintronics, and quantum computing. © 2010 The American Physical Society.
spellingShingle Brown, R
Ito, Y
Warner, J
Ardavan, A
Shinohara, H
Briggs, G
Morton, J
Electron spin coherence in metallofullerenes: Y, Sc, and La@C82
title Electron spin coherence in metallofullerenes: Y, Sc, and La@C82
title_full Electron spin coherence in metallofullerenes: Y, Sc, and La@C82
title_fullStr Electron spin coherence in metallofullerenes: Y, Sc, and La@C82
title_full_unstemmed Electron spin coherence in metallofullerenes: Y, Sc, and La@C82
title_short Electron spin coherence in metallofullerenes: Y, Sc, and La@C82
title_sort electron spin coherence in metallofullerenes y sc and la c82
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