Research output: Contribution to journal › Article › peer-review
The role of Heisenberg spin exchange and the quantum Zeno effect in the spin-selective reaction between spin-1/2 and spin-1 particles. / Bagryansky, Victor A.; Melnikov, Anatoly R.; Molin, Yuri N. et al.
In: Journal of Chemical Physics, Vol. 157, No. 6, 064306, 14.08.2022.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - The role of Heisenberg spin exchange and the quantum Zeno effect in the spin-selective reaction between spin-1/2 and spin-1 particles
AU - Bagryansky, Victor A.
AU - Melnikov, Anatoly R.
AU - Molin, Yuri N.
AU - Borovkov, Vsevolod I.
N1 - Funding Information: The development of a program for numerical simulation of the spin dynamics in a pair of paramagnetic particles in the presence of an irreversible spin-dependent reaction was funded by the Russian Science Foundation (Project No. 21-13-00278). A.R.M. is grateful to have been awarded a personal scholarship for Support of Young Researchers (Project No. SP-272.2021.5). Publisher Copyright: © 2022 Author(s).
PY - 2022/8/14
Y1 - 2022/8/14
N2 - The kinetics of spin-selective reactions involving triplet molecules, such as triplet-triplet annihilation or electron transfer to dioxygen molecules in the ground triplet spin state, are strongly dependent on the dipole-dipole interaction (DDI) of electron spins in spin-1 particles. The effect of this interaction on the intersystem crossing in the reaction encounter complex of the paramagnetic particles was previously considered for some particular cases using oversimplified approaches. In this study, we consider a rigorous kinetic model of the irreversible reaction between the spin-1/2 and spin-1 particles in an encounter complex with the reactive doublet state. This model explicitly includes both isotropic exchange coupling of the reactants and spin dependence of the reaction rate in the form of the Haberkorn reaction term. For the time-independent DDI, an analytical expression for the reaction kinetics was derived. The effect of DDI fluctuations was analyzed using numerical simulations. It was found that increasing both the exchange coupling and the reaction rate constants can significantly slow down the quartet-doublet spin transitions and, as a consequence, the observed spin-selective reaction rate. Additionally, the presence of the irreversible reaction in the doublet states affects a coherent evolution in the non-reactive quartet subsystem.
AB - The kinetics of spin-selective reactions involving triplet molecules, such as triplet-triplet annihilation or electron transfer to dioxygen molecules in the ground triplet spin state, are strongly dependent on the dipole-dipole interaction (DDI) of electron spins in spin-1 particles. The effect of this interaction on the intersystem crossing in the reaction encounter complex of the paramagnetic particles was previously considered for some particular cases using oversimplified approaches. In this study, we consider a rigorous kinetic model of the irreversible reaction between the spin-1/2 and spin-1 particles in an encounter complex with the reactive doublet state. This model explicitly includes both isotropic exchange coupling of the reactants and spin dependence of the reaction rate in the form of the Haberkorn reaction term. For the time-independent DDI, an analytical expression for the reaction kinetics was derived. The effect of DDI fluctuations was analyzed using numerical simulations. It was found that increasing both the exchange coupling and the reaction rate constants can significantly slow down the quartet-doublet spin transitions and, as a consequence, the observed spin-selective reaction rate. Additionally, the presence of the irreversible reaction in the doublet states affects a coherent evolution in the non-reactive quartet subsystem.
UR - http://www.scopus.com/inward/record.url?scp=85136335314&partnerID=8YFLogxK
U2 - 10.1063/5.0101173
DO - 10.1063/5.0101173
M3 - Article
C2 - 35963733
AN - SCOPUS:85136335314
VL - 157
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
SN - 0021-9606
IS - 6
M1 - 064306
ER -
ID: 37081869