<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-27T20:23:22Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/36706" metadataPrefix="marc">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/36706</identifier><datestamp>2025-03-26T19:10:03Z</datestamp><setSpec>com_10324_1159</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1310</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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<subfield code="a">dc</subfield>
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<subfield code="a">Aguilera del Toro, Rodrigo Humberto</subfield>
<subfield code="e">author</subfield>
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<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Alvarado Leyva, Pedro Gilberto</subfield>
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<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Vega Hierro, Andrés</subfield>
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<datafield tag="260" ind1=" " ind2=" ">
<subfield code="c">2019</subfield>
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<subfield code="a">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.</subfield>
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<subfield code="a">Journal of Magnetism and Magnetic Materials, 2019,  vol. 474. p. 551-562</subfield>
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<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">0304-8853</subfield>
</datafield>
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<subfield code="a">http://uvadoc.uva.es/handle/10324/36706</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">10.1016/j.jmmm.2018.11.056</subfield>
</datafield>
<datafield tag="245" ind1="0" ind2="0">
<subfield code="a">Uncovering the magnetic properties of the AgxNiy (x + y = 55) nanoalloys in the whole composition range</subfield>
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