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Nonequilibrium electromagnetics: Local and macroscopic fields and constitutive relationships
James Baker-Jarvis1, Pavel Kabos, Christopher L Holloway
1NIST, Electromagnetics Divsion, MS 818-01, Boulder, Colorado 80305, USA. jjarvis@boulder.nist.gov
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|November 5, 2004
Summary
This study presents a new statistical-mechanical theory for material electrodynamics, focusing on microscopic and nonequilibrium systems. It enables self-consistent calculation of macroscopic fields from molecular properties without multipole expansions.
Area of Science:
- Statistical Mechanics
- Electrodynamics
- Materials Science
Background:
- Traditional electrodynamics often relies on macroscopic approximations or Taylor expansions.
- Microscopic and nonequilibrium systems present challenges for existing theoretical frameworks.
- Understanding material electrodynamics at molecular scales is crucial for advanced applications.
Purpose of the Study:
- To develop a Liouville-Hamiltonian-based statistical-mechanical theory for electrodynamics.
- To enable accurate modeling of microscopic and nonequilibrium systems.
- To provide a framework valid from molecular to submolecular scales.
Main Methods:
- Utilizes a Liouville-Hamiltonian-based statistical-mechanical approach.
- Employs an inverse problem to derive the statistical-density function from molecular multipoles.
- Avoids Taylor series expansion of charge density for multipole determination.
Main Results:
- Derives expressions for local and macroscopic electromagnetic fields.
- Develops evolution equations for constitutive parameters.
- Obtains equations for the local field based on various applied and material properties.
Conclusions:
- The developed theory offers a self-consistent method for constructing averaging functions.
- It allows for the treatment of molecules as point multipoles or with internal microstructure.
- Provides a robust framework for studying electrodynamics in complex materials and conditions.