Generalized Holstein model for spin-dependent electron transfer reaction
arXiv:1110.1918 · doi:10.1103/PhysRevA.85.032707
Abstract
Some chemical reactions are described by electron transfer (ET) processes. The underlying mechanism could be modeled as a polaron motion in the molecular crystal-the Holstein model. By taking spin degrees of freedom into consideration, we generalize the Holstein model (molecular crystal model) to microscopically describe an ET chemical reaction. In our model, the electron spins in the radical pair simultaneously interact with a magnetic field and their nuclear-spin environments. By virtue of the perturbation approach, we obtain the chemical reaction rates for different initial states. It is discovered that the chemical reaction rate of the triplet state demonstrates its dependence on the direction of the magnetic field while the counterpart of the singlet state does not. This difference is attributed to the explicit dependence of the triplet state on the direction when the axis is rotated. Our model may provide a possible candidate for the microscopic origin of avian compass.
9 pages, 6 figures
References in corpus (4)
Cited by in corpus (7)
- Coherent and incoherent theories for photosynthetic energy transfer
- The radical-pair mechanism as a paradigm for the emerging science of quantum biology
- Quantum metrology with one auxiliary particle in a correlated bath and its quantum simulation
- Multi-Radical Lipkin-Meshkov-Glick Model for Avian Navigation
- Quantum Simulation of Bound-State-Enhanced Quantum Metrology
- A precise measure of avian magnetoreception based on quantum metrology
- Dark state population determines magnetic sensitivity in radical pair magnetoreception model