Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE
- Autores
- Díaz, C.; Olsen, R. A.; Busnengo, Heriberto Fabio; Kroes, G. J.
- Año de publicación
- 2010
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- We have constructed first principle based six-dimensional (6D) potential energy surfaces (PESs) describing the interaction of H2 with Cu(111) obtained by interpolation of a set of density functional theory (DFT) total energy data. The DFT calculations have been performed within the generalized gradient approximation (GGA) framework. In applying the GGA we have tested the two exchange-correlation (XC) functionals most popular in surface science, i.e., the PW91 and RPBE functionals. The interpolation of the PW91 PES has been performed using two different methods, the corrugation reducing procedure (CRP), which has been proven to be one of the most successful interpolation methods to build 6D PESs, and the modified Shepard (MS) interpolation method, a very promising method to build high dimensional (nD) PESs, which is computationally cheaper than the CRP. We show that, in spite of the difference between the CRP-PES and the MS-PES and the inaccuracies found in the latter, quantum and classical reaction and scattering probabilities obtained for both PESs are very similar. We also show that PW91 predicts higher reactivity than RPBE, due to the presence of lower energy dissociation barriers in the PW91-PES. The differences between the PW91-PES and the RPBE-PES are also reflected in the vibrational excitation and rotational excitation probabilities, and the diffraction patterns.
Fil: Díaz, C.. Leiden University; Países Bajos
Fil: Olsen, R. A.. Akershus University College; Noruega
Fil: Busnengo, Heriberto Fabio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Física de Rosario. Universidad Nacional de Rosario. Instituto de Física de Rosario; Argentina
Fil: Kroes, G. J.. Leiden University; Países Bajos - Materia
-
Density Functional Theory
exchange-correlation - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/277641
Ver los metadatos del registro completo
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Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBEDíaz, C.Olsen, R. A.Busnengo, Heriberto FabioKroes, G. J.Density Functional Theoryexchange-correlationhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1We have constructed first principle based six-dimensional (6D) potential energy surfaces (PESs) describing the interaction of H2 with Cu(111) obtained by interpolation of a set of density functional theory (DFT) total energy data. The DFT calculations have been performed within the generalized gradient approximation (GGA) framework. In applying the GGA we have tested the two exchange-correlation (XC) functionals most popular in surface science, i.e., the PW91 and RPBE functionals. The interpolation of the PW91 PES has been performed using two different methods, the corrugation reducing procedure (CRP), which has been proven to be one of the most successful interpolation methods to build 6D PESs, and the modified Shepard (MS) interpolation method, a very promising method to build high dimensional (nD) PESs, which is computationally cheaper than the CRP. We show that, in spite of the difference between the CRP-PES and the MS-PES and the inaccuracies found in the latter, quantum and classical reaction and scattering probabilities obtained for both PESs are very similar. We also show that PW91 predicts higher reactivity than RPBE, due to the presence of lower energy dissociation barriers in the PW91-PES. The differences between the PW91-PES and the RPBE-PES are also reflected in the vibrational excitation and rotational excitation probabilities, and the diffraction patterns.Fil: Díaz, C.. Leiden University; Países BajosFil: Olsen, R. A.. Akershus University College; NoruegaFil: Busnengo, Heriberto Fabio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Física de Rosario. Universidad Nacional de Rosario. Instituto de Física de Rosario; ArgentinaFil: Kroes, G. J.. Leiden University; Países BajosAmerican Chemical Society2010-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/277641Díaz, C.; Olsen, R. A.; Busnengo, Heriberto Fabio; Kroes, G. J.; Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE; American Chemical Society; Journal of Physical Chemistry C; 114; 25; 5-2010; 11192-112011932-7447CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/jp1027096info:eu-repo/semantics/altIdentifier/doi/10.1021/jp1027096info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-12-23T14:07:59Zoai:ri.conicet.gov.ar:11336/277641instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-12-23 14:08:00.091CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| title |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| spellingShingle |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE Díaz, C. Density Functional Theory exchange-correlation |
| title_short |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| title_full |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| title_fullStr |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| title_full_unstemmed |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| title_sort |
Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE |
| dc.creator.none.fl_str_mv |
Díaz, C. Olsen, R. A. Busnengo, Heriberto Fabio Kroes, G. J. |
| author |
Díaz, C. |
| author_facet |
Díaz, C. Olsen, R. A. Busnengo, Heriberto Fabio Kroes, G. J. |
| author_role |
author |
| author2 |
Olsen, R. A. Busnengo, Heriberto Fabio Kroes, G. J. |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
Density Functional Theory exchange-correlation |
| topic |
Density Functional Theory exchange-correlation |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
We have constructed first principle based six-dimensional (6D) potential energy surfaces (PESs) describing the interaction of H2 with Cu(111) obtained by interpolation of a set of density functional theory (DFT) total energy data. The DFT calculations have been performed within the generalized gradient approximation (GGA) framework. In applying the GGA we have tested the two exchange-correlation (XC) functionals most popular in surface science, i.e., the PW91 and RPBE functionals. The interpolation of the PW91 PES has been performed using two different methods, the corrugation reducing procedure (CRP), which has been proven to be one of the most successful interpolation methods to build 6D PESs, and the modified Shepard (MS) interpolation method, a very promising method to build high dimensional (nD) PESs, which is computationally cheaper than the CRP. We show that, in spite of the difference between the CRP-PES and the MS-PES and the inaccuracies found in the latter, quantum and classical reaction and scattering probabilities obtained for both PESs are very similar. We also show that PW91 predicts higher reactivity than RPBE, due to the presence of lower energy dissociation barriers in the PW91-PES. The differences between the PW91-PES and the RPBE-PES are also reflected in the vibrational excitation and rotational excitation probabilities, and the diffraction patterns. Fil: Díaz, C.. Leiden University; Países Bajos Fil: Olsen, R. A.. Akershus University College; Noruega Fil: Busnengo, Heriberto Fabio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Física de Rosario. Universidad Nacional de Rosario. Instituto de Física de Rosario; Argentina Fil: Kroes, G. J.. Leiden University; Países Bajos |
| description |
We have constructed first principle based six-dimensional (6D) potential energy surfaces (PESs) describing the interaction of H2 with Cu(111) obtained by interpolation of a set of density functional theory (DFT) total energy data. The DFT calculations have been performed within the generalized gradient approximation (GGA) framework. In applying the GGA we have tested the two exchange-correlation (XC) functionals most popular in surface science, i.e., the PW91 and RPBE functionals. The interpolation of the PW91 PES has been performed using two different methods, the corrugation reducing procedure (CRP), which has been proven to be one of the most successful interpolation methods to build 6D PESs, and the modified Shepard (MS) interpolation method, a very promising method to build high dimensional (nD) PESs, which is computationally cheaper than the CRP. We show that, in spite of the difference between the CRP-PES and the MS-PES and the inaccuracies found in the latter, quantum and classical reaction and scattering probabilities obtained for both PESs are very similar. We also show that PW91 predicts higher reactivity than RPBE, due to the presence of lower energy dissociation barriers in the PW91-PES. The differences between the PW91-PES and the RPBE-PES are also reflected in the vibrational excitation and rotational excitation probabilities, and the diffraction patterns. |
| publishDate |
2010 |
| dc.date.none.fl_str_mv |
2010-05 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/277641 Díaz, C.; Olsen, R. A.; Busnengo, Heriberto Fabio; Kroes, G. J.; Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE; American Chemical Society; Journal of Physical Chemistry C; 114; 25; 5-2010; 11192-11201 1932-7447 CONICET Digital CONICET |
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http://hdl.handle.net/11336/277641 |
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Díaz, C.; Olsen, R. A.; Busnengo, Heriberto Fabio; Kroes, G. J.; Dynamics on Six-Dimensional Potential Energy Surfaces for H 2 /Cu(111): Corrugation Reducing Procedure versus Modified Shepard Interpolation Method and PW91 versus RPBE; American Chemical Society; Journal of Physical Chemistry C; 114; 25; 5-2010; 11192-11201 1932-7447 CONICET Digital CONICET |
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eng |
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eng |
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openAccess |
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application/pdf application/pdf |
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American Chemical Society |
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American Chemical Society |
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