On optical spectroscopy of molecular junctions
arXiv:1503.03890 · doi:10.1063/1.4916523
Abstract
We compare theoretical techniques utilized for description of optical response in molecular junctions, and their application to simulate Raman spectroscopy in such systems. Strong and weak sides of the Hilbert vs. Liouville space, as well as quasiparticles vs. many-body states, formulations are discussed. Common origins of the methodologies and different approximations utilized in different formulations are identified.
arXiv comment17 pages, 4 figures
References in corpus (18)
- Nonequilibrium fluctuations, fluctuation theorems, and counting statistics in quantum systems
- Nonequilibrium dynamical mean-field theory and its applications
- Mesoscopic quantum transport: Resonant tunneling in the presence of strong Coulomb interaction
- Simultaneous measurements of electronic conduction and Raman response in molecular junctions
- Vibrational and electronic heating in nanoscale junctions
- Heat conduction in molecular transport junctions
- Kadanoff-Baym approach to quantum transport through interacting nanoscale systems: From the transient to the steady-state regime
- Kinetic Equations for Transport Through Single-Molecule Transistors
- Transport in molecular states language: Generalized quantum master equation approach
- Superoperator nonequilibrium Green's function theory of many-body systems; Applications to charge transfer and transport in open junctions
- Fermionic superoperators for zero-temperature non-linear transport: real-time perturbation theory and renormalization group for Anderson quantum dots
- Raman scattering in current carrying molecular junctions. A preliminary account
- Nonequilibrium dynamical mean-field theory based on weak-coupling perturbation expansions: Application to dynamical symmetry breaking in the Hubbard model
- Nonequilibrium isolated molecule limit
- Transport and optical response of molecular junctions driven by surface plasmon-polaritons
- Non-equilibrium theory for strongly coupled quantum dot with arbitrary on-site correlation strength
- Theory of strongly correlated f and d-electron systems. I. Exact Hamiltonian, Hubbard-Anderson models and perturbation theory near atomic limit within non-orthogonal basis set
- Transport theory of coupled quantum dots based on auxiliary operator method