Transverse spin relaxation time in organic molecules

B. Kanchibotla, S. Pramanik, S. Bandyopadhyay, and M. Cahay
Phys. Rev. B 78, 193306 – Published 13 November 2008

Abstract

We report a measurement of the ensemble-averaged transverse spin relaxation time (T2) in bulk and few molecules of the organic semiconductor tris-(8-hydroxyquinolinolato aluminum) or Alq3. This system exhibits two characteristic T2 times: the longer of which is temperature independent and the shorter is temperature dependent, indicating that the latter is most likely limited by spin-phonon interaction. Based on the measured data, we infer that the single-particle T2 time is probably long enough to meet Knill’s criterion for fault-tolerant quantum computing even at room temperature. Alq3 is also an optically active organic, and we propose a simple optical scheme for spin qubit readout. Moreover, we found that the temperature-dependent T2 time is considerably shorter in bulk Alq3 powder than in few molecules confined in 1–2-nm-sized cavities. Because carriers in organic molecules are localized over individual molecules or atoms but the phonons are delocalized, we believe that this feature is caused by phonon bottleneck effect.

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  • Received 7 October 2008

DOI:https://doi.org/10.1103/PhysRevB.78.193306

©2008 American Physical Society

Authors & Affiliations

B. Kanchibotla, S. Pramanik, and S. Bandyopadhyay*

  • Department of Electrical and Computer Engineering, Virginia Commonwealth University, Richmond, Virginia 23284, USA

M. Cahay

  • Department of Electrical and Computer Engineering, University of Cincinnati, Ohio 45221, USA

  • *Corresponding author; sbandy@vcu.edu

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Issue

Vol. 78, Iss. 19 — 15 November 2008

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