4.6 Article

Renormalized site density functional theory

出版社

IOP Publishing Ltd
DOI: 10.1088/1742-5468/abdeb3

关键词

correlation functions; structural correlations; series expansions

资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences
  2. United States Department of Energy under DOE [DE-AC05-76RL1830]

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Site density functional theory provides a rigorous framework for the statistical mechanics analysis of inhomogeneous molecular liquids, with the use of dual space methodology to improve accuracy in calculations. This approach allows for the decoupling of analysis of intra- and inter-molecular interactions, demonstrating the transformation of the molecular liquid system behavior at the inter-molecular level to resemble that of an effective simple fluid mixture.
Site density functional theory (SDFT) provides a rigorous framework for statistical mechanics analysis of inhomogeneous molecular liquids. The key defining feature of these systems is the presence of two very distinct interactions scales (intra- and inter-molecular), and as such proper description of both effects is critical to the accuracy of the calculations. Current SDFT applications utilize the same approximation scheme for both interaction motifs, which negatively impacts the results. Dual space methodology, used in this work, alleviates this issue by providing the flexibility of evaluating part of the interactions in traditional field representation. For molecular liquid this translates into retaining density representation for inter-molecular interactions but describing stiff intra-molecular remainder by more appropriate conventional field based methods. This opens the way to decouple analysis of the two interactions scales-the idea which is developed further in this work for the case of homogeneous reference approximation of inter-molecular interactions. We demonstrate that by defining new collective variables, the behaviour of the original molecular liquid system at the inter-molecular level can be transformed to resemble that of an effective simple fluid mixture. The latter is linked to intra-molecular scale through renormalized interaction parameters. We illustrate this renormalization procedure for several types of diatomic liquids, showing that this approach cures many of the shortcomings of existing SDFT methods.

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