2007 APS March Meeting
Volume 52, Number 1
Monday–Friday, March 5–9, 2007;
Denver, Colorado
Session W3: Magnetotransport in Organic Conductors and Semiconductors
2:30 PM–5:30 PM,
Thursday, March 8, 2007
Colorado Convention Center
Room: Korbel 2A-3A
Sponsoring
Unit:
DCMP
Chair: Zeev Vardeny, University of Utah
Abstract ID: BAPS.2007.MAR.W3.2
Abstract: W3.00002 : Spin correlations in organic semiconductors
3:06 PM–3:42 PM
Preview Abstract
Abstract
Author:
John Lupton
(Department of Physics, University of Utah)
Organic semiconductors differ from their inorganic counterparts
by large
exchange interactions and weak spin orbit coupling. As a result,
parallel
and anti-parallel spin configurations are highly non-degenerate and
spectroscopically well-defined. Whereas singlet excitons are highly
emissive, triplet excitons generally decay non-radiatively.
Addition of
heavy metal centres to the polymer backbone induces localized
spin-orbit
coupling, which can activate radiative triplet decay through
phosphorescence
[1]. By tuning the concentration of these triplet acceptors to
match the
diffusion length of the triplets (which exceeds that of the
singlets),
triplets can be harvested radiatively without significantly
affecting the
actual triplet formation pathway through intersystem crossing of
the singlet
[2]. Using this technique we can study the interconversion
between spin
states of exciton precursors (charge carrier pairs) as a function
of time,
temperature, and electric and magnetic fields [3]. We find that the
probability of a spin change occurring in the exciton precursor
state is
extremely small, which suggests that the primary recombination
pathway in
organic light-emitting diodes is governed by spin statistics [3].
Phosphorescence spectroscopy of organic semiconductors has a
number of
immediate applications. Stimulated emission competes with
intersystem
crossing required for triplet generation so that a phosphorescent
polymer
laser acts as a highly non-degenerate all-optical excitonic
switch [4].
Singlet-triplet mixing in metallorganics with strong spin-orbit
coupling
also provides a versatile method for ultrafast luminescence based
molecular
thermometry [5,6].
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[1] Lupton et al., \textit{Phys. Rev. Lett.} \textbf{89}, 167401
(2002).
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[2] Reufer et al., \textit{Phys. Rev. B Rapid} (in press 2006).
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[3] Reufer et al., \textit{Nature Mat.} \textbf{4}, 340 (2005).
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[4] Reufer et al., \textit{Appl. Phys. Lett.} \textbf{89}, 141111
(2006).
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[5] Stehr et al., \textit{Adv. Mater.} \textbf{16}, 2170 (2004).
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[6] Balouchev et al., \textit{US Patent} \textbf{7097354} (2006).
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2007.MAR.W3.2