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<dc:title>Uncovering the magnetic properties of the AgxNiy (x + y = 55) nanoalloys in the whole composition range</dc:title>
<dc:creator>Aguilera del Toro, Rodrigo Humberto</dc:creator>
<dc:creator>Alvarado Leyva, Pedro Gilberto</dc:creator>
<dc:creator>Vega Hierro, Andrés</dc:creator>
<dc:description>Producción Científica</dc:description>
<dc:description>Nickel and silver are metals with interesting properties of technological relevance: nickel is a&#xd;
well known ferromagnet and silver has antibacterial properties. Both exist in the face centered&#xd;
cubic phase but are immiscible. In the context of alloys at the nanoscale, one can play with the&#xd;
size to  ne tune a desired property, or to achieve new properties and functionalities that do not&#xd;
exist at the macroscopic regime. In this work, we explore how the subtle interaction between&#xd;
Ni and Ag triggers the chemical order, the electronic structure, and the magnetic properties of a&#xd;
AgNi nanoalloy of 55 atoms, a size that can accommodate core/shell con gurations with sizable&#xd;
parts. Calculations are conducted within the density functional theory at the generalized gradient&#xd;
approximation for exchange and correlation. We determine, in the whole composition range, the&#xd;
chemical order, absolute and relative stabilities by means of binding energy, excess energy and&#xd;
second energy di erence, as well as total and part-projected spin-polarized electronic densities of&#xd;
states and local charge and spin magnetic moments distribution. Ni-core/Ag-shell structures are&#xd;
particularly stable, but contrary to what one would expect by simply extrapolating the properties&#xd;
of the pure Ag and Ni clusters or of pure fcc bulks, we  nd unexpected behaviors along the&#xd;
composition range, such as quenched magnetic moments in Ni, total magnetic moments essentially&#xd;
contributed in some cases by Ag, or electronic charge transfer that changes its sign depending on&#xd;
the stoichiometry. These behaviors lead to magnetic transitions as a function of the composition,&#xd;
and di er, in some cases, from those of the smaller 13-atoms AgNi nanoalloys of the same symmetry&#xd;
with which we compare, a further demonstration of the complex nature of nanostructures. The&#xd;
above trends are robust against ionization and electron capture.</dc:description>
<dc:date>2019-07-05T11:51:36Z</dc:date>
<dc:date>2019-07-05T11:51:36Z</dc:date>
<dc:date>2019</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Journal of Magnetism and Magnetic Materials, 2019,  vol. 474. p. 551-562</dc:identifier>
<dc:identifier>0304-8853</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/36706</dc:identifier>
<dc:identifier>10.1016/j.jmmm.2018.11.056</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://www.sciencedirect.com/science/article/pii/S0304885318324922</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>© 2019 Elsevier</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>Elsevier</dc:publisher>
<dc:peerreviewed>SI</dc:peerreviewed>
</ow:Publication>
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