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Spin polarization in chiral molecules is a magnetic molecular response associated with electron transport and enantioselective bond polarization that occurs even in the absence of an external magnetic field. An unexpected finding by Santos and co-workers reported enantiospecific NMR responses in solid-state cross-polarization (CP) experiments, suggesting a possible additional contribution to the indirect nuclear spin-spin coupling in chiral molecules induced by bond polarization in the presence of spin-orbit coupling. Herein we provide a theoretical treatment for this phenomenon, presenting an effective spin-Hamiltonian for helical molecules like DNA and density functional theory (DFT) results on amino acids that confirm the dependence of J-couplings on the choice of enantiomer. The connection between nuclear spin dynamics and chirality could offer insights for molecular sensing and quantum information sciences. These results establish NMR as a potential tool for chiral discrimination without external agents.
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Time-dependent growth of nuclear spin polarization under periodic optical pumping
Consecutive circularly-polarized optical pulses generate and rotate electron spin polarization through optical orientation and the optical Stark effect. We perform time- and magnetic-field-dependent optical pump-probe measurements on gallium arsenide and observe a variable Overhauser field growth that depends on the external magnetic field and laser wavelength. We show that the time dependence of the nuclear spin polarization can be attributed to the time-averaged electron spin polarization produced along the external magnetic field direction.
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- Award ID(s):
- 2207162
- PAR ID:
- 10506877
- Publisher / Repository:
- NSF-PAR
- Date Published:
- Journal Name:
- Physical Review B
- Volume:
- 108
- Issue:
- 11
- ISSN:
- 2469-9950
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1103/PhysRevB.108.115203
