Chiral-induced spin selectivity: A polaron transport model

Weak hyperfine interactions and spin-orbit coupling (SOC) in organic materials result in long spin lifetimes, which is very promising for spintronics. On the other hand, they also make it challenging to achieve spin polarization, which is of crucial importance for spintronics devices. To overcome th...

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Veröffentlicht in:Physical review. B 2020-12, Vol.102 (21), p.1, Article 214303
Hauptverfasser: Zhang, Longlong, Hao, Yuying, Qin, Wei, Xie, Shijie, Qu, Fanyao
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Sprache:eng
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Zusammenfassung:Weak hyperfine interactions and spin-orbit coupling (SOC) in organic materials result in long spin lifetimes, which is very promising for spintronics. On the other hand, they also make it challenging to achieve spin polarization, which is of crucial importance for spintronics devices. To overcome this obstacle, we have proposed a physical model for spin-polarized electron transport through a chiral molecule based on the chiral-induced spin selectivity. Because the transport in the chiral molecule is not an isolated one, but rather an electron coupled to its surrounding lattice distortions, namely, a spatial localized polaron, an indispensable polaron effect is incorporated in our model. We show that the polaron transport through the chiral molecule exhibits a spin-momentum-locked feature. Interestingly, no matter what their initial spin state is, all of the polarons could transmit through the molecule with their spins being aligned to the same orientation due to the effective "inverse Faraday effect." The coexistence of the electron-lattice coupling and SOC results in the spin and lattice being coupled, which leads to a strongly enhanced spin coherence and then a very high spin polarization of 70%. In addition, the effects of the helix pitch, polaron size, and drift velocity on spin polarization are also discussed. Our results open the possibility of using chiral molecules in spintronics applications and offer a paradigm for information processing and transmission.
ISSN:2469-9950
2469-9969
DOI:10.1103/PhysRevB.102.214303