Related Experiment Video
Updated: Jun 23, 2026

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
Published on: April 12, 2019
Simulating the kinetics and thermodynamics of transitions via forward flux/umbrella sampling
Ernesto E Borrero1, Fernando A Escobedo
1School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, USA.
Abstract:
First, a technique is introduced for computing equilibrium probability distributions for transitional rare-event simulations by combining the ensemble of trajectories generated by forward flux sampling (FFS) and by umbrella sampling (US) in multiple windows along an order parameter of interest; this method is denoted FFS-US. Second, the FFS algorithm is extended to obtain rate constants of partial transitions involving intermediate states from a single simulation; this is denoted "multiple state" FFS. For the FFS-US method, a FFS algorithm (preoptimized for order parameter and staging) is used to take advantage of its zero potential bias of phase-space sampling to gather histogram data with which to jump start the US and get the equilibrium distributions. In this way, kinetic data (like the rate constants and the transition path ensemble) and the underlying free-energy landscape (or probability distribution) of the system are obtained efficiently and concurrently. The applicability of these techniques is illustrated by studying several test systems, including two that involve potential energy surfaces having multiple metastable states and transition pathways, representative of complex kinetic behavior.
Related Concept Videos
Path Between Thermodynamics States
Fast Reactions
Thermal Sigmatropic Reactions: Overview
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in 1,5-hexadiene, referred to as...
Reaction Mechanisms: The Steady-State Approximation
Transition State Theory
Reaction Mechanisms: Rate-limiting Step Approximation
