On the origin independence of the Verdet tensor†

The condition for invariance under a translation of the coordinate system of the Verdet tensor and the Verdet constant, calculated via quantum chemical methods using gaugeless basis sets, is expressed by a vanishing sum rule involving a third-rank polar tensor. The sum rule is, in principle, satisfi...

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Autor principal: Caputo, María Cristina
Publicado: 2013
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00268976_v111_n9-11_p1405_Caputo
http://hdl.handle.net/20.500.12110/paper_00268976_v111_n9-11_p1405_Caputo
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spelling paper:paper_00268976_v111_n9-11_p1405_Caputo2023-06-08T14:54:00Z On the origin independence of the Verdet tensor† Caputo, María Cristina Faraday effect sum rule for origin independence symmetry unique components Verdet constant Verdet tensor Algebraic approximation Electronic wave functions Gaussian functions Quantum-chemical methods Random phase approximations Sum rule Variational calculation Verdet constant Sum rule Verdet constant Faraday effect Molecules Quantum chemistry Variational techniques Tensors Faraday effect The condition for invariance under a translation of the coordinate system of the Verdet tensor and the Verdet constant, calculated via quantum chemical methods using gaugeless basis sets, is expressed by a vanishing sum rule involving a third-rank polar tensor. The sum rule is, in principle, satisfied only in the ideal case of optimal variational electronic wavefunctions. In general, it is not fulfilled in non-variational calculations and variational calculations allowing for the algebraic approximation, but it can be satisfied for reasons of molecular symmetry. Group-theoretical procedures have been used to determine (i) the total number of non-vanishing components and (ii) the unique components of both the polar tensor appearing in the sum rule and the axial Verdet tensor, for a series of symmetry groups. Test calculations at the random-phase approximation level of accuracy for water, hydrogen peroxide and ammonia molecules, using basis sets of increasing quality, show a smooth convergence to zero of the sum rule. Verdet tensor components calculated for the same molecules converge to limit values, estimated via large basis sets of gaugeless Gaussian functions and London orbitals. © 2013 Copyright Taylor and Francis Group, LLC. Fil:Caputo, M.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2013 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00268976_v111_n9-11_p1405_Caputo http://hdl.handle.net/20.500.12110/paper_00268976_v111_n9-11_p1405_Caputo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Faraday effect
sum rule for origin independence
symmetry unique components
Verdet constant
Verdet tensor
Algebraic approximation
Electronic wave functions
Gaussian functions
Quantum-chemical methods
Random phase approximations
Sum rule
Variational calculation
Verdet constant
Sum rule
Verdet constant
Faraday effect
Molecules
Quantum chemistry
Variational techniques
Tensors
Faraday effect
spellingShingle Faraday effect
sum rule for origin independence
symmetry unique components
Verdet constant
Verdet tensor
Algebraic approximation
Electronic wave functions
Gaussian functions
Quantum-chemical methods
Random phase approximations
Sum rule
Variational calculation
Verdet constant
Sum rule
Verdet constant
Faraday effect
Molecules
Quantum chemistry
Variational techniques
Tensors
Faraday effect
Caputo, María Cristina
On the origin independence of the Verdet tensor†
topic_facet Faraday effect
sum rule for origin independence
symmetry unique components
Verdet constant
Verdet tensor
Algebraic approximation
Electronic wave functions
Gaussian functions
Quantum-chemical methods
Random phase approximations
Sum rule
Variational calculation
Verdet constant
Sum rule
Verdet constant
Faraday effect
Molecules
Quantum chemistry
Variational techniques
Tensors
Faraday effect
description The condition for invariance under a translation of the coordinate system of the Verdet tensor and the Verdet constant, calculated via quantum chemical methods using gaugeless basis sets, is expressed by a vanishing sum rule involving a third-rank polar tensor. The sum rule is, in principle, satisfied only in the ideal case of optimal variational electronic wavefunctions. In general, it is not fulfilled in non-variational calculations and variational calculations allowing for the algebraic approximation, but it can be satisfied for reasons of molecular symmetry. Group-theoretical procedures have been used to determine (i) the total number of non-vanishing components and (ii) the unique components of both the polar tensor appearing in the sum rule and the axial Verdet tensor, for a series of symmetry groups. Test calculations at the random-phase approximation level of accuracy for water, hydrogen peroxide and ammonia molecules, using basis sets of increasing quality, show a smooth convergence to zero of the sum rule. Verdet tensor components calculated for the same molecules converge to limit values, estimated via large basis sets of gaugeless Gaussian functions and London orbitals. © 2013 Copyright Taylor and Francis Group, LLC.
author Caputo, María Cristina
author_facet Caputo, María Cristina
author_sort Caputo, María Cristina
title On the origin independence of the Verdet tensor†
title_short On the origin independence of the Verdet tensor†
title_full On the origin independence of the Verdet tensor†
title_fullStr On the origin independence of the Verdet tensor†
title_full_unstemmed On the origin independence of the Verdet tensor†
title_sort on the origin independence of the verdet tensor†
publishDate 2013
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00268976_v111_n9-11_p1405_Caputo
http://hdl.handle.net/20.500.12110/paper_00268976_v111_n9-11_p1405_Caputo
work_keys_str_mv AT caputomariacristina ontheoriginindependenceoftheverdettensor
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