TY - JOUR
T1 - Optically induced dynamic nuclear spin polarisation in diamond
AU - Scheuer, Jochen
AU - Schwartz, Ilai
AU - Chen, Qiong
AU - Schulze-Sünninghausen, David
AU - Carl, Patrick
AU - Höfer, Peter
AU - Retzker, Alexander
AU - Sumiya, Hitoshi
AU - Isoya, Junichi
AU - Luy, Burkhard
AU - Plenio, Martin B.
AU - Naydenov, Boris
AU - Jelezko, Fedor
N1 - Publisher Copyright:
© 2016 IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - The sensitivity of magnetic resonance imaging (MRI) depends strongly on nuclear spin polarisation and, motivated by this observation, dynamical nuclear spin polarisation has recently been applied to enhance MRI protocols (Kurhanewicz et al 2011 Neoplasia 13 81). Nuclear spins associated with the 13C carbon isotope (nuclear spin I = 1/2) in diamond possess uniquely long spin lattice relaxation times (Reynhardt and High 2011 Prog. Nucl. Magn. Reson. Spectrosc. 38 37). If they are present in diamond nanocrystals, especially when strongly polarised, they form a promising contrast agent for MRI. Current schemes for achieving nuclear polarisation, however, require cryogenic temperatures. Here we demonstrate an efficient scheme that realises optically induced 13C nuclear spin hyperpolarisation in diamond at room temperature and low ambient magnetic field. Optical pumping of a nitrogen-vacancy centre creates a continuously renewable electron spin polarisation which can be transferred to surrounding 13C nuclear spins. Importantly for future applications we also realise polarisation protocols that are robust against an unknown misalignment between magnetic field and crystal axis.
AB - The sensitivity of magnetic resonance imaging (MRI) depends strongly on nuclear spin polarisation and, motivated by this observation, dynamical nuclear spin polarisation has recently been applied to enhance MRI protocols (Kurhanewicz et al 2011 Neoplasia 13 81). Nuclear spins associated with the 13C carbon isotope (nuclear spin I = 1/2) in diamond possess uniquely long spin lattice relaxation times (Reynhardt and High 2011 Prog. Nucl. Magn. Reson. Spectrosc. 38 37). If they are present in diamond nanocrystals, especially when strongly polarised, they form a promising contrast agent for MRI. Current schemes for achieving nuclear polarisation, however, require cryogenic temperatures. Here we demonstrate an efficient scheme that realises optically induced 13C nuclear spin hyperpolarisation in diamond at room temperature and low ambient magnetic field. Optical pumping of a nitrogen-vacancy centre creates a continuously renewable electron spin polarisation which can be transferred to surrounding 13C nuclear spins. Importantly for future applications we also realise polarisation protocols that are robust against an unknown misalignment between magnetic field and crystal axis.
KW - diamond
KW - dynamical nuclear polarisation (DNP)
KW - nitrogen-vacancy (NV)
KW - nuclear magnetic resonance (NMR)
UR - http://www.scopus.com/inward/record.url?scp=84957584218&partnerID=8YFLogxK
U2 - 10.1088/1367-2630/18/1/013040
DO - 10.1088/1367-2630/18/1/013040
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AN - SCOPUS:84957584218
SN - 1367-2630
VL - 18
JO - New Journal of Physics
JF - New Journal of Physics
IS - 1
M1 - 013040
ER -