<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0035-001X</journal-id>
<journal-title><![CDATA[Revista mexicana de física]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. fis.]]></abbrev-journal-title>
<issn>0035-001X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Física]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0035-001X2008000800006</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Energy transfer in Sr0.6Ba0.4Nb2O6 through its ferroelectric phase transition]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Caldiño]]></surname>
<given-names><![CDATA[U]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martín-Rodríguez]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Jaque]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Garcia Solé]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bettinelli]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Autónoma Metropolitana-Iztapalapa Departamento de Física ]]></institution>
<addr-line><![CDATA[México DF]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad Autónoma de Madrid Departamento de Física de Materiales ]]></institution>
<addr-line><![CDATA[Madrid ]]></addr-line>
<country>Spain</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Universita di Verona Dipartimento Scientifico e Tecnológico ]]></institution>
<addr-line><![CDATA[Verona ]]></addr-line>
<country>Italy</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>11</month>
<year>2008</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>11</month>
<year>2008</year>
</pub-date>
<volume>54</volume>
<fpage>39</fpage>
<lpage>43</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0035-001X2008000800006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0035-001X2008000800006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0035-001X2008000800006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Resonant Nd3+ <img border=0 src="../../../../../img/revistas/rmf/v54s2/a6s1.jpg">Yb3+ energy-transfer in the Nd3+ and Yb3+ co-doped Sr0.6Ba0.4(NbO3)2 (SBN) crystal is investigated by using pulsed and steady state laser spectroscopy. Spectroscopic data revealed that the energy transfer occurs via a non-radiative process. The efficiency of this energy transfer was estimated from spectral data in around 35%. Back energy transfer is not observed at the 295-415 K temperature range. A marked reduction in the luminescence intensity of Yb3+ ions directly excited into their ²F7/2<img border=0 src="../../../../../img/revistas/rmf/v54s2/a6s1.jpg"> ²F5/2 transition, taking place at around 345 K, is due to the ferro to paraelectric phase transition in SBN. This thermal behavior, which is not clearly manifested when Yb3+ ions are excited via Nd3+ ions, has been explained in terms of structural changes taking place around the Yb3+ ions when the crystal becomes non-polar.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[La transferencia de energía resonante Nd3+ <img border=0 src="../../../../../img/revistas/rmf/v54s2/a6s1.jpg">Yb3+ en el cristal Sr0.6Ba0.4(NbO3)2 (SBN) codopado conYb3+ y Nd3+ es investigada mediante espectroscopia láser pulsado y estacionario. Datos espectroscópicos revelaron que la transferencia de energía ocurre vía un proceso no-radiativo. La eficiencia de esta transferencia de energía fue estimada de los datos espectrales en alrededor de 35%. La transferencia de energía a la inversa (Yb3+ <img border=0 src="../../../../../img/revistas/rmf/v54s2/a6s1.jpg">Nd3+) no es observada en el rango de temperaturas 295-415 K. Una marcada reduccion en la intensidad de luminiscencia de los iones Yb3+ directamente excitados dentro de su transición ²F7/2 <img border=0 src="../../../../../img/revistas/rmf/v54s2/a6s1.jpg">2F5/2, ocurriendo en alrededor de 345 K, es debida a la transicion de fase ferro a paraeléctrica de SBN. Esta conducta térmica, la cual no es claramente manifestada cuando los iones Yb3+ son excitados vía los iones Nd3+, ha sido explicada en terminos de cambios estructurales ocurriendo alrededor de los iones Yb3+ cuando el cristal se convierte en no-polar.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Energy transfer efficiency]]></kwd>
<kwd lng="en"><![CDATA[luminescence]]></kwd>
<kwd lng="en"><![CDATA[spectroscopy]]></kwd>
<kwd lng="en"><![CDATA[SBN]]></kwd>
<kwd lng="en"><![CDATA[Nd3+]]></kwd>
<kwd lng="en"><![CDATA[Yb3+]]></kwd>
<kwd lng="en"><![CDATA[phase transition]]></kwd>
<kwd lng="es"><![CDATA[Transferencia de energía]]></kwd>
<kwd lng="es"><![CDATA[luminiscencia]]></kwd>
<kwd lng="es"><![CDATA[transiciones de fase]]></kwd>
<kwd lng="es"><![CDATA[espectroscopia]]></kwd>
<kwd lng="es"><![CDATA[SBN]]></kwd>
<kwd lng="es"><![CDATA[Nd3+]]></kwd>
<kwd lng="es"><![CDATA[Yb3+]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center"><font face="verdana" size="4"><b>Energy transfer in Sr<sub>0.6</sub>Ba<b><sub>0.4</sub></b>Nb<sub>2</sub>O<sub>6</sub> through its ferroelectric phase transition</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>U. Caldi&ntilde;o&ordf;, E. Mart&iacute;n&#150;Rodr&iacute;guez<sup>b</sup>, D. Jaque<sup>b</sup> and J. Garcia Sol&eacute;<sup>b</sup> and M. Bettinelli</b><b><sup>c</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>&ordf; Departamento de F&iacute;sica, Universidad Aut&oacute;noma Metropolitana&#150;Iztapalapa, PO Box 55&#150;534, 09340 M&eacute;xico, DF, M&eacute;xico, </i>e&#150;mail: <a href="mailto:cald@xanum.uam.mx">cald@xanum.uam.mx</a></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>b</sup>Departamento de F&iacute;sica de Materiales, Universidad Aut&oacute;noma de Madrid, Cantoblanco, 28049, Madrid, Spain, </i>e&#150;mail: <a href="mailto:emma.martin@uam.es">emma.martin@uam.es</a>, <a href="mailto:jose.garciasole@uam.es">daniel.jaque@uam.es</a>, <a href="mailto:jose.garciasole@uam.es">jose.garciasole@uam.es</a></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>c</sup> Dipartimento Scientifico e Tecnol&oacute;gico, Universita di Verona, and INSTM, UdR Verona, StradaLe Grazie 15,I&#150;37314 Verona, Italy, </i>e&#150;mail: <a href="mailto:marco.bettinelli@univr.it">marco.bettinelli@univr.it</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Recibido el  9 de noviembre de 2007    <br>   Aceptado el 9 de agosto de 2008</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2">Resonant Nd<sup>3+</sup> <img src="/img/revistas/rmf/v54s2/a6s1.jpg"> Yb<sup>3+</sup> energy&#150;transfer in the Nd<sup>3+</sup> and Yb<sup>3+</sup> co&#150;doped Sr<sub>0.6</sub>Ba<sub>0.4</sub>(NbO<sub>3</sub>)<sub>2</sub> (SBN) crystal is investigated by using pulsed and steady state laser spectroscopy. Spectroscopic data revealed that the energy transfer occurs via a non&#150;radiative process. The efficiency of this energy transfer was estimated from spectral data in around 35%. Back energy transfer is not observed at the 295&#150;415 K temperature range. A marked reduction in the luminescence intensity of Yb<sup>3+</sup> ions directly excited into their <sup>2</sup>F<sub>7</sub>/<sub>2<img src="/img/revistas/rmf/v54s2/a6s1.jpg"></sub> <sup>2</sup>F<sub>5</sub>/<sub>2</sub> transition, taking place at around 345 K, is due to the ferro to paraelectric phase transition in SBN. This thermal behavior, which is not clearly manifested when Yb<sup>3+</sup> ions are excited via Nd<sup>3+</sup> ions, has been explained in terms of structural changes taking place around the Yb<sup>3+</sup> ions when the crystal becomes non&#150;polar.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>Energy transfer efficiency; luminescence; spectroscopy; SBN; Nd<sup>3+</sup>; Yb<sup>3+</sup>; phase transition.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">La transferencia de energ&iacute;a resonante Nd<sup>3+</sup> <img src="/img/revistas/rmf/v54s2/a6s1.jpg">Yb<sup>3+</sup> en el cristal Sr<sub>0.6</sub>Ba<sub>0.4</sub>(NbO<sub>3</sub>)<sub>2</sub> (SBN) codopado conYb<sup>3+</sup> y Nd<sup>3+</sup> es investigada mediante espectroscopia l&aacute;ser pulsado y estacionario. Datos espectrosc&oacute;picos revelaron que la transferencia de energ&iacute;a ocurre v&iacute;a un proceso no&#150;radiativo. La eficiencia de esta transferencia de energ&iacute;a fue estimada de los datos espectrales en alrededor de 35%. La transferencia de energ&iacute;a a la inversa (Yb<sup>3+</sup> <img src="/img/revistas/rmf/v54s2/a6s1.jpg"> Nd<sup>3+</sup>) no es observada en el rango de temperaturas 295&#150;415 K. Una marcada reduccion en la intensidad de luminiscencia de los iones Yb<sup>3+</sup> directamente excitados dentro de su transici&oacute;n <sup>2</sup>F<sub>7</sub>/<sub>2</sub> <sup><img src="/img/revistas/rmf/v54s2/a6s1.jpg"> 2</sup>F<sub>5</sub>/<sub>2</sub>, ocurriendo en alrededor de 345 K, es debida a la transicion de fase ferro a parael&eacute;ctrica de SBN. Esta conducta t&eacute;rmica, la cual no es claramente manifestada cuando los iones Yb<sup>3+ </sup>son excitados v&iacute;a los iones Nd<sup>3+</sup>, ha sido explicada en terminos de cambios estructurales ocurriendo alrededor de los iones Yb<sup>3+</sup> cuando el cristal se convierte en no&#150;polar.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Descriptores: </b>Transferencia de energ&iacute;a; luminiscencia; transiciones de fase; espectroscopia; SBN; Nd<sup>3+</sup>; Yb<sup>3+</sup>.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">PACS: 42.55.Rz; 42.62.Fi; 42.70.Hj; 42.70.Mp</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><a href="/pdf/rmf/v54s2/v54s2a6.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgments</b></font></p>     <p align="justify"><font face="verdana" size="2">This work has been supported by the Spanish Ministry of Science and Technology under project contract MAT2004&#150;03347 and by the CONACyT (M&eacute;xico) under project contract 43016&#150;F.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. E. Montoya, J. Capmany, L.E. Baus&aacute;, T. Kellner, A. Diening, and G. Huber, <i>Appl. Phys. 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