2015
DOI: 10.1103/physrevb.92.045431
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Spin vibronics in interacting nonmagnetic molecular nanojunctions

Abstract: We show that in the presence of ferromagnetic electronic reservoirs and spin-dependent tunnel couplings, molecular vibrations in nonmagnetic single molecular transistors induce an effective intramolecular exchange magnetic field. It generates a finite spin-accumulation and -precession for the electrons confined on the molecular bridge and occurs under (non)equilibrium conditions. The effective exchange magnetic field is calculated here to lowest order in the tunnel coupling for a nonequilibrium transport setup… Show more

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Cited by 11 publications
(15 citation statements)
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References 43 publications
(52 reference statements)
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“…where n + (ω) = [exp(ω/k B T ) − 1] denotes the Bose function and n − (ω) = n + (ω) + 1. Assuming that the two total spin values form a pseudospin-1/2, the oscillations can be seen as an electron spin precessing around an effective exchange field [47][48][49][51][52][53][54][55][56]. Such an analogy has also been observed in the context of quantum transport though spatially localized [50,57,58] and non-localized orbitals [59].…”
Section: Modelmentioning
confidence: 85%
“…where n + (ω) = [exp(ω/k B T ) − 1] denotes the Bose function and n − (ω) = n + (ω) + 1. Assuming that the two total spin values form a pseudospin-1/2, the oscillations can be seen as an electron spin precessing around an effective exchange field [47][48][49][51][52][53][54][55][56]. Such an analogy has also been observed in the context of quantum transport though spatially localized [50,57,58] and non-localized orbitals [59].…”
Section: Modelmentioning
confidence: 85%
“…In the presence of the counting field, time translation invariance is broken and there is no simple frequency representation of ∆ −1 [η] similar to Eq. (18). However, since we are only interested in calculating the current (and not higher-order correlation functions), we can expand ∆ −1 [η] to linear order in η α at a single Trotter index m (that corresponds to the time t m at which the current is measured) and drop the counting field anywhere else.…”
Section: B Keldysh Functional Integralmentioning
confidence: 99%
“…The resulting expression for ∆ −1 [η] is given by Eq. (18) with Γ ασ being replaced by Γ ασ [1− iδt 2 η α (νδ ml −ν δ ml )]. Furthermore, we observe that multiplying ∆ −1 [η] − Σ C (s) in Eq.…”
Section: B Keldysh Functional Integralmentioning
confidence: 99%
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“…} is the Fermi function of lead r. A spin opposite to σ is denoted by s . Moreover, we also account for spin relaxation by including the spin-flip rate G  in the master equation (6)- (9). Spin relaxation may originate from hyperfine interaction with a local nuclei bath [35][36][37][38].…”
Section: Negative-u Anderson Impuritymentioning
confidence: 99%