dc.contributorUniversidad Industrial de Santander
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:29:40Z
dc.date.available2018-12-11T17:29:40Z
dc.date.created2018-12-11T17:29:40Z
dc.date.issued2016-01-01
dc.identifierPhysical Chemistry Chemical Physics, v. 18, n. 37, p. 25984-25992, 2016.
dc.identifier1463-9076
dc.identifierhttp://hdl.handle.net/11449/178295
dc.identifier10.1039/c6cp01659f
dc.identifier2-s2.0-84988566307
dc.description.abstractWe herein demonstrate that capacitance spectroscopy (CS) experimentally allows access to the energy associated with the quantum mechanical ground state of many-electron systems. Priorly, electrochemical capacitance, C[ρ], was previously understood from conceptual and computational density functional theory (DFT) calculations. Thus, we herein propose a quantum mechanical experiment-based variational method for electron charging processes based on an experimentally-designed functional of the ground state electron density. In this methodology, the electron state density, ρ, and an energy functional of the electron density, E[ρ], can be obtained from CS data. CS allows the derivative of the electrochemical potential with respect to the electron density, (δ[ρ]/δρ), to be obtained as a unique functional of the energetically minimised system, i.e., β/C[ρ], where β is a constant (associated with the size of the system) and C[ρ] is an experimentally observable quantity. Thus the ground state energy (at a given fixed external potential) can be obtained simply as E[ρ], from the experimental measurement of C[ρ]. An experimental data-set was interpreted to demonstrate the potential of this quantum mechanical experiment-based variational principle.
dc.languageeng
dc.relationPhysical Chemistry Chemical Physics
dc.relation1,686
dc.rightsAcesso restrito
dc.sourceScopus
dc.titleDensity functional theory and an experimentally-designed energy functional of electron density
dc.typeArtículos de revistas


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