Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling
- Autores
- Brito, Mariano Exequiel; Carignano, Marcelo A.; Marconi, Veronica Iris
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Nanocolloids having directional interactions are highly relevant for designing new self-assembled materials easy to control. In this article we report stochastic dynamics simulations of finite-size pseudo-dipolar colloids immersed in an implicit dielectric solvent using a realistic continuous description of the quasi-hard Coulombic interaction. We investigate structural and dynamical properties near the low-temperature and highly-diluted limits. This system self-assembles in a rich variety of string-like configurations, depicting three clearly distinguishable regimes with decreasing temperature: fluid, composed by isolated colloids; string-fluid, a gas of short string-like clusters; and string-gel, a percolated network. By structural characterization using radial distribution functions and cluster properties, we calculate the state diagram, verifying the presence of string-fluid regime. Regarding the string-gel regime, we show that the antiparallel alignment of the network chains arises as a novel self-assembly mechanism when the characteristic interaction energy exceeds the thermal energy in two orders of magnitude, ud/kBT ≈ 100. This is associated to relevant structural modifications in the network connectivity and porosity. Furthermore, our results give insights about the dynamically-arrested nature of the string-gel regime, where we show that the slow relaxation takes place in minuscule energy steps that reflect local rearrangements of the network.
Fil: Brito, Mariano Exequiel. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Carignano, Marcelo A.. Qatar Environment And Energy Research Institute; Qatar
Fil: Marconi, Veronica Iris. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina - Materia
-
GEL
COLLOID
DIPOLAR
SELF-ASSEMBLY - 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:11336/137098
Ver los metadatos del registro completo
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Self-assembly of pseudo-dipolar nanoparticles at low densities and strong couplingBrito, Mariano ExequielCarignano, Marcelo A.Marconi, Veronica IrisGELCOLLOIDDIPOLARSELF-ASSEMBLYhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Nanocolloids having directional interactions are highly relevant for designing new self-assembled materials easy to control. In this article we report stochastic dynamics simulations of finite-size pseudo-dipolar colloids immersed in an implicit dielectric solvent using a realistic continuous description of the quasi-hard Coulombic interaction. We investigate structural and dynamical properties near the low-temperature and highly-diluted limits. This system self-assembles in a rich variety of string-like configurations, depicting three clearly distinguishable regimes with decreasing temperature: fluid, composed by isolated colloids; string-fluid, a gas of short string-like clusters; and string-gel, a percolated network. By structural characterization using radial distribution functions and cluster properties, we calculate the state diagram, verifying the presence of string-fluid regime. Regarding the string-gel regime, we show that the antiparallel alignment of the network chains arises as a novel self-assembly mechanism when the characteristic interaction energy exceeds the thermal energy in two orders of magnitude, ud/kBT ≈ 100. This is associated to relevant structural modifications in the network connectivity and porosity. Furthermore, our results give insights about the dynamically-arrested nature of the string-gel regime, where we show that the slow relaxation takes place in minuscule energy steps that reflect local rearrangements of the network.Fil: Brito, Mariano Exequiel. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Carignano, Marcelo A.. Qatar Environment And Energy Research Institute; QatarFil: Marconi, Veronica Iris. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaNature Research2020-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/137098Brito, Mariano Exequiel; Carignano, Marcelo A.; Marconi, Veronica Iris; Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling; Nature Research; Scientific Reports; 10; 1; 3-2020; 1-132045-2322CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.nature.com/articles/s41598-020-60417-4info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-020-60417-4info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-12T09:46:42Zoai:ri.conicet.gov.ar:11336/137098instacron: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:34982025-11-12 09:46:43.111CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| title |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| spellingShingle |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling Brito, Mariano Exequiel GEL COLLOID DIPOLAR SELF-ASSEMBLY |
| title_short |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| title_full |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| title_fullStr |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| title_full_unstemmed |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| title_sort |
Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling |
| dc.creator.none.fl_str_mv |
Brito, Mariano Exequiel Carignano, Marcelo A. Marconi, Veronica Iris |
| author |
Brito, Mariano Exequiel |
| author_facet |
Brito, Mariano Exequiel Carignano, Marcelo A. Marconi, Veronica Iris |
| author_role |
author |
| author2 |
Carignano, Marcelo A. Marconi, Veronica Iris |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
GEL COLLOID DIPOLAR SELF-ASSEMBLY |
| topic |
GEL COLLOID DIPOLAR SELF-ASSEMBLY |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Nanocolloids having directional interactions are highly relevant for designing new self-assembled materials easy to control. In this article we report stochastic dynamics simulations of finite-size pseudo-dipolar colloids immersed in an implicit dielectric solvent using a realistic continuous description of the quasi-hard Coulombic interaction. We investigate structural and dynamical properties near the low-temperature and highly-diluted limits. This system self-assembles in a rich variety of string-like configurations, depicting three clearly distinguishable regimes with decreasing temperature: fluid, composed by isolated colloids; string-fluid, a gas of short string-like clusters; and string-gel, a percolated network. By structural characterization using radial distribution functions and cluster properties, we calculate the state diagram, verifying the presence of string-fluid regime. Regarding the string-gel regime, we show that the antiparallel alignment of the network chains arises as a novel self-assembly mechanism when the characteristic interaction energy exceeds the thermal energy in two orders of magnitude, ud/kBT ≈ 100. This is associated to relevant structural modifications in the network connectivity and porosity. Furthermore, our results give insights about the dynamically-arrested nature of the string-gel regime, where we show that the slow relaxation takes place in minuscule energy steps that reflect local rearrangements of the network. Fil: Brito, Mariano Exequiel. Helmholtz Gemeinschaft. Forschungszentrum Jülich; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina Fil: Carignano, Marcelo A.. Qatar Environment And Energy Research Institute; Qatar Fil: Marconi, Veronica Iris. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina |
| description |
Nanocolloids having directional interactions are highly relevant for designing new self-assembled materials easy to control. In this article we report stochastic dynamics simulations of finite-size pseudo-dipolar colloids immersed in an implicit dielectric solvent using a realistic continuous description of the quasi-hard Coulombic interaction. We investigate structural and dynamical properties near the low-temperature and highly-diluted limits. This system self-assembles in a rich variety of string-like configurations, depicting three clearly distinguishable regimes with decreasing temperature: fluid, composed by isolated colloids; string-fluid, a gas of short string-like clusters; and string-gel, a percolated network. By structural characterization using radial distribution functions and cluster properties, we calculate the state diagram, verifying the presence of string-fluid regime. Regarding the string-gel regime, we show that the antiparallel alignment of the network chains arises as a novel self-assembly mechanism when the characteristic interaction energy exceeds the thermal energy in two orders of magnitude, ud/kBT ≈ 100. This is associated to relevant structural modifications in the network connectivity and porosity. Furthermore, our results give insights about the dynamically-arrested nature of the string-gel regime, where we show that the slow relaxation takes place in minuscule energy steps that reflect local rearrangements of the network. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020-03 |
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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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publishedVersion |
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http://hdl.handle.net/11336/137098 Brito, Mariano Exequiel; Carignano, Marcelo A.; Marconi, Veronica Iris; Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling; Nature Research; Scientific Reports; 10; 1; 3-2020; 1-13 2045-2322 CONICET Digital CONICET |
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http://hdl.handle.net/11336/137098 |
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Brito, Mariano Exequiel; Carignano, Marcelo A.; Marconi, Veronica Iris; Self-assembly of pseudo-dipolar nanoparticles at low densities and strong coupling; Nature Research; Scientific Reports; 10; 1; 3-2020; 1-13 2045-2322 CONICET Digital CONICET |
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eng |
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eng |
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