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Variable charge many-body interatomic potentials

Published online by Cambridge University Press:  09 May 2012

Yun Kyung Shin
Affiliation:
Department of Mechanical and Nuclear Engineering, Pennsylvania State University; [email protected]
Tzu-Ray Shan
Affiliation:
Sandia National Laboratories, Albuquerque, NM; [email protected]
Tao Liang
Affiliation:
Department of Materials Science and Engineering, University of Florida; [email protected]
Mark J. Noordhoek
Affiliation:
Department of Materials Science and Engineering, University of Florida; [email protected]
Susan B. Sinnott
Affiliation:
Department of Materials Science and Engineering, University of Florida; [email protected]
Adri C.T. van Duin
Affiliation:
Department of Mechanical and Nuclear Engineering, Pennsylvania State University; [email protected]
Simon R. Phillpot
Affiliation:
Department of Materials Science and Engineering, University of Florida; [email protected]
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Abstract

Recent developments in reactive potentials for the simulation of complex bonding and complex chemistry are reviewed. In particular, the reactive force field and charged optimized many-body methods are two paradigms that enable atoms to autonomously determine their charge state and the nature of their local bonding environments. The capabilities of these methods are illustrated by examples involving ionic-covalent systems, a metal-covalent system, a high-k dielectric gate stack, and the interaction of water with an oxide. Prospects for future development and applications are also discussed.

Type
Research Article
Copyright
Copyright © Materials Research Society 2012

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