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Sampling the energy landscape: thermodynamics and rates

Wales, D (Cambridge)
Friday 03 November 2006, 14:00-15:15

Seminar Room 1, Newton Institute


Stationary points of the potential energy surface provide a natural way to coarse-grain calculations of thermodynamics and kinetics, as well as a framework for basin-hopping global optimisation. Thermodynamic properties can be obtained from samples of local minima using the basin-sampling approach, and kinetic information can be extracted if the samples are extended to include transition states. Using statistical rate theory a minimum-to-minimum rate constant can be associated with each transition state, and phenomenological rates between sets of local minima that define thermodynamic states of interest can be calculated using a new graph transformation approach. Since the number of stationary points grows exponentially with system size a sampling scheme is required to produce representative pathways. The discrete path sampling approach provides a systematic way to achieve this objective once a single connected path between products and reactants has been located. In large systems such paths may involve dozens of stationary points of the potential energy surface. New algorithms have been developed for both geometry optimisation and making connections between distant local minima, which have enabled rates to be calculated for a wide variety of systems.


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