Geva, Eitan - Department of Chemistry, University of Michigan

• Optimization of laser-driven intramolecular hydrogen transfer in the presence of dephasing
• Computational Study of the One and Two Dimensional Infrared Spectra of a Vibrational Mode Strongly Coupled to Its Environment: Beyond the Cumulant and Condon
• On the irreversible performance of a quantum heat engine Department of Chemistry, University of Michigan, 930 N. University,
• Israel Journal of Chemistry Vol. 42 2002 pp. 225236 *Authortowhomcorrespondenceshouldbeaddressed.E-mail
• Semiclassical Theory of Vibrational Energy Relaxation in the Condensed Phase Qiang Shi and Eitan Geva*
• Vibrational Energy Relaxation in Liquid Oxygen from a Semiclassical Molecular Dynamics Qiang Shi and Eitan Geva*
• Stimulated Raman adiabatic passage in the presence of dephasing Qiang Shi and Eitan Gevaa)
• A derivation of the mixed quantum-classical Liouville equation from the influence functional formalism
• Nonradiative Electronic Relaxation Rate Constants from Approximations Based on Linearizing the Path-Integral Forward-Backward Action
• A comparison between different semiclassical approximations for optical response functions in nonpolar liquid solutions
• The influence of nonbilinear system-bath coupling on quantum-mechanical activated rate processes
• Vibrational Energy Relaxation of Polyatomic Molecules in Liquid Solution via the Linearized Semiclassical Method
• Nonequilibrium quantum dynamics in the condensed phase via the generalized quantum master equation
• Vibrational Energy Relaxation Rates of H2 and D2 in Liquid Argon via the Linearized Semiclassical Method
• Subscriber access provided by UNIV OF MICHIGAN The Journal of Physical Chemistry B is published by the American Chemical
• Multidimensional Spectra via the Mixed Quantum-Classical Liouville Method: Signatures of Nonequilibrium Dynamics
• Signatures of Nonequilibrium Solvation Dynamics on Multidimensional
• Two-Dimensional Infrared Spectroscopy of Dimanganese Decacarbonyl and Its Photoproducts: An Ab Initio Study
• A Benchmark Study of Different Methods for Calculating One-And Two-Dimensional Optical Spectra
• Two-Dimensional Infrared Spectroscopy of Metal Carbonyls
• Extracting the Time Scales of Conformational Dynamics from Single-Molecule Single-Photon Fluorescence Statistics
• A nonperturbative calculation of nonlinear spectroscopic signals in liquid solution
• A comparison between different semiclassical approximations for optical response functions in nonpolar liquid solution. II. The signature
• Classical vs Quantum Vibrational Energy Relaxation Pathways in Solvated Polyatomic Being J. Ka and Eitan Geva*
• Vibrational Energy Relaxation of a Hydrogen-Bonded Complex Dissolved in a Polar Liquid via the Mixed Quantum-Classical Liouville Method
• Computational Study of a Single Surface-Immobilized Two-Stranded Coiled-Coil Polypeptide
• Vibrational Energy Relaxation Rates via the Linearized Semiclassical Approximation: Applications to Neat Diatomic Liquids and Atomic-Diatomic Liquid Mixtures
• Quantum-mechanical reaction rate constants from centroid molecular dynamics simulations
• Homogeneity and Markovity of electronic dephasing in liquid solutions Being J. Ka, Ming-Liang Zhang, and Eitan Gevaa
• A semiclassical generalized quantum master equation for an arbitrary system-bath coupling
• Comparison between the LandauTeller and flux-flux methods for computing vibrational energy relaxation rate constants
• A self-consistent treatment of electron transfer in the limit of strong friction via the mixed quantum classical Liouville method
• Protein Structure and Dynamics from Single-Molecule Fluorescence Resonance Energy Dong Wang and Eitan Geva*
• A Computational Study of the Correlations between Structure and Dynamics in Free and Surface-Immobilized Single Polymer Chains
• A new approach to calculating the memory kernel of the generalized quantum master equation for an arbitrary systembath coupling
• A relationship between semiclassical and centroid correlation functions Qiang Shi and Eitan Geva
• On the calculation of vibrational energy relaxation rate constants from centroid molecular dynamics simulations
• Centroid-based methods for calculating quantum reaction rate constants: Centroid sampling versus centroid dynamics