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A '''transition state''' (TS) in chemistry refers to a high-energy, short-lived configuration that occurs during a chemical reaction as reactants transform into products{{Cite|tst:web}}. At this point, the reaction's progress is maximized. In other words, the transition state is a metastable structure that corresponds to a saddle point on the high-dimensional potential surface{{Cite|hratchian:schlegel:2005}}. Identifying the transition state is essential for understanding reaction mechanisms, energy barriers, and reaction rates. There are various methods available to pinpoint transition states in VASP. | [[File:Transition_state_pathway.png|400px|thumb|right|Reaction profile for the substitution reaction of chloromethane by chloride. This is a symmetric reaction, where the products and reactants are identical. The maximum of the reaction profile is the transition state (TS). The arrows indicate the direction of motion, showing the attack of the chloromethane by one chloride and then the ejection by the new chloride.]]A '''transition state''' (TS) in chemistry refers to a high-energy, short-lived configuration that occurs during a chemical reaction as reactants transform into products{{Cite|tst:web}}. At this point, the reaction's progress is maximized. In other words, the transition state is a metastable structure that corresponds to a saddle point on the high-dimensional potential surface{{Cite|hratchian:schlegel:2005}}. Identifying the transition state is essential for understanding reaction mechanisms, energy barriers, and reaction rates. There are various methods available to pinpoint transition states in VASP. | ||
= Static methods = | = Static methods = | ||
Revision as of 10:31, 15 October 2024
A transition state (TS) in chemistry refers to a high-energy, short-lived configuration that occurs during a chemical reaction as reactants transform into products[1]. At this point, the reaction's progress is maximized. In other words, the transition state is a metastable structure that corresponds to a saddle point on the high-dimensional potential surface[2]. Identifying the transition state is essential for understanding reaction mechanisms, energy barriers, and reaction rates. There are various methods available to pinpoint transition states in VASP.
Static methods
There are three methods implemented in VASP for finding transition states using the static, or harmonic, approach: the improved dimer method (IDM), nudged elastic band (NEB), and following the intrinsic reaction coordinate (IRC). The potential energy surface (PES) is modeled and the maximum point of this found, i.e. the TS.
Improved dimer method
The dimer method[3] is a technique for determining activated transitions without knowledge of the final state. Beginning with a trial transition state (TS) structure, a relaxed TS is obtained. In VASP, the improved dimer method (IDM) by Heyden et al. is implemented. The modification reduces the number of gradient calculations per cycle, improving algorithm performance. A detailed presentation of the method can be found in their paper[4]. The main tag is IBRION=44.
Follow the how-to in order to learn how to perform an IDM calculation.
Nudged elastic bands
The nudged elastic band (NEB) method[5][6] involves the creation of an initial path connecting the system's initial and final states, utilizing a set of intermediate configurations (IMAGES). Hence, as a prerequisite, the initial and final state (e.g., reactant and product) must be known. The images are interconnected by springs (SPRING), forming a flexible band. Through iterative adjustments (nudging), the positions of the images along the band are modified, minimizing energy until a minimum energy pathway, referred to as the nudged elastic band, is attained.
Learn how to perform an NEB calculation.
Intrinsic reaction coordinate
Following the intrinsic reaction coordinate (IRC) implies following the steepest descent path from the transition state to reactants and products. The IRC method employs a classical trajectory integration method with fixed velocity, i.e., the damped-velocity Verlet algorithm, incorporating an adaptive time step such that the dynamic reaction pathway resembles the IRC. Hence, as a prerequisite, the transition state must be known. The main tag is IBRION=40.
Learn how to perform an IRC calculation.
Dynamic methods
B
References
- ↑ Transition state theory, www.wikipedia.org (2024)
- ↑ H. Hratchian, H. Schlegel, Theory and Application of Computational Chemistry, Chapter 10 - Finding minima, transition states, and following reaction pathways on ab initio potential energy surfaces (2005), p. 195-249
- ↑ G. Henkelman and H. Jónsson, A dimer method for finding saddle points on high dimensional potential surfaces using only first derivatives, J. Chem. Phys. 111, 7010–7022 (1999).
- ↑ A. Heyden, A. T. Bell, and F. J. Keil, Efficient methods for finding transition states in chemical reactions: Comparison of improved dimer method and partitioned rational function optimization method, J. Chem. Phys. 123, 224101 (2005).
- ↑ G. Mills, H. Jonsson and G. K. Schenter, Reversible work transition state theory: application to dissociative adsorption of hydrogen, Surf. Sci., 324, 305 (1995).
- ↑ H. Jonsson, G. Mills and K. W. Jacobsen, Nudged Elastic Band Method for Finding Minimum Energy Paths of Transitions, in Classical and Quantum Dynamics in Condensed Phase Simulations, ed. B. J. Berne, G. Ciccotti and D. F. Coker (World Scientific, 1998).
Pages in category "Transition states"
The following 17 pages are in this category, out of 17 total.