<?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>1665-3521</journal-id>
<journal-title><![CDATA[Superficies y vacío]]></journal-title>
<abbrev-journal-title><![CDATA[Superf. vacío]]></abbrev-journal-title>
<issn>1665-3521</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Ciencia y Tecnología de Superficies y Materiales A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1665-35212008000200005</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Análisis de reacciones en la transición de CdS (semiconductor) a CdCO3 (aislante) en formato de películas delgadas obtenidas mediante DBQ]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lima-Lima]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Portillo-Moreno]]></surname>
<given-names><![CDATA[O.]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Espinosa Montes de Oca]]></surname>
<given-names><![CDATA[L. M.]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lozada Morales]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zelaya-Ángel]]></surname>
<given-names><![CDATA[O.]]></given-names>
</name>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Benemérita Universidad Autónoma de Puebla Laboratorio de Materiales de la Facultad de Ciencias Químicas ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Benemérita Universidad Autónoma de Puebla Facultad de Ciencias Fisicomatemáticas Posgrado en Optoelectrónica]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Instituto Politécnico Nacional Departamento de Física Centro de Investigación y de Estudios Avanzados]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2008</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2008</year>
</pub-date>
<volume>21</volume>
<numero>2</numero>
<fpage>21</fpage>
<lpage>26</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1665-35212008000200005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1665-35212008000200005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1665-35212008000200005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Mediante la Técnica de Depósito por Baño Químico, se obtienen películas delgadas sobre sustratos de vidrio portaobjetos en el intervalo de temperatura de 80°C - 20°C. Las soluciones utilizadas: CdCl2 0.02 M, KOH 1.5 M, NH4NO3 0.5 M y SC(NH2)2 0.2 M, se preparan a temperatura ambiente utilizando agua desionizada. El volumen de los reactivos, la velocidad de agitación y la temperatura de reacción se mantuvieron constantes y el pH de la reacción fue de aproximadamente 8.3. El tiempo de depósito varía con la temperatura. De resultados previos de absorción óptica, se obtiene el ancho de banda prohibida: para CdS a 80°C, Eg = 2.42 eV y para CdCO3 a 20°C, Eg = 3.87 eV. Por Difracción de Rayos X (DXR) se identifica CdS en fase cúbica a 80°C, con un pico localizado en la posición angular: 2&#952; = [26.68] y a 20 °C se observan señales en 2&#952; = [23.36, 30.22, 36.30, 43.8, 49.9] que corresponden al CdCO3 en fase romboédrica. En el intervalo 40°C<T<60°C, se identifican señales de ambos compuestos. En fotografías obtenidas mediante Microscopia Óptica (MO) se observa la transición gradual de CdS&#8594;CdCO3 con crecimiento de los cristales identificados como CdCO3. Los precursores de los iones sulfuro (S2-) y carbonato (CO(-2)3), con base a las reacciones propuestas en este trabajo son, ácido sulfhídrico (H2S) y ácido carbónico (H2CO3), respectivamente. Ambos ácidos provienen de la descomposición hidrolítica de la tiourea. Se considera la solubilidad del CO2 y H2S en el intervalo de la temperatura de depósito y la influencia de esta en la reacción, así como del pH.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[By Chemical Bath was obtained thin films on glass-substrates with temperature interval of 80°C - 20°C. The used solution are: CdCl2 0.02 M, KOH 1.5 M, NH4OH 0.5 M and SC(NH2)2 0.2 M, they were prepared at room temperature using deionised water. Volume of reagents, velocity of agitation and reaction temperature stayed constant. The pH of reaction was approximately 8.3. The deposit time varies with temperature. From previous results on Optic Absorption, is obtained the prohibited bandwidth, for CdS at 80°C, Eg = 2.42 eV and CdCO3 at 20°C, Eg = 3.87 eV. By X-ray diffraction was identified the cubic phase of CdS at 80°C, with a peak located in the angular position: 2&#952; = [26.68] and at 20°C it observed signals at 2&#952; = [23.26, 30.22, 36.30, 43.8, 49.90] that correspond to CdCO3 in rombohedral phase. In interval 40°C<T<60°C, was identified signal from both compounds. By Optic Microscopy was obtained pictures that shown the gradual transition of CdS&#8594;CdCO3 with growth of crystal. The precursors of ions sulphur (S-2) and carbonate (CO(-2)3) are sulphydric acid (H2S) and carbonic acid (H2CO3), respectively, in according this work. Both acids come from of hydrolytic decomposition of thiourea. The influence of pH, solubility of (H2S) and CO2 are considered in the interval of temperature deposited, and the influence of last in the reaction.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Solubilidad]]></kwd>
<kwd lng="es"><![CDATA[Películas delgadas]]></kwd>
<kwd lng="es"><![CDATA[Ion carbonato]]></kwd>
<kwd lng="es"><![CDATA[Complejo de coordinación]]></kwd>
<kwd lng="en"><![CDATA[Solubility]]></kwd>
<kwd lng="en"><![CDATA[Thin films]]></kwd>
<kwd lng="en"><![CDATA[Carbonate ion]]></kwd>
<kwd lng="en"><![CDATA[Coordinate complex]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center"><font face="verdana" size="4"><b>An&aacute;lisis de reacciones en la transici&oacute;n de CdS (semiconductor) a CdCO<sub>3</sub> (aislante) en formato de pel&iacute;culas delgadas obtenidas mediante DBQ</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>H. Lima&#150;Lima<sup>1</sup>, O. Portillo&#150;Moreno<sup>1</sup>, L. M. Espinosa Montes de Oca<sup>1</sup>, R. Lozada Morales<sup>2</sup>, O. Zelaya&#150;&Aacute;ngel<sup>3</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>1</sup> Laboratorio de Materiales de la Facultad de Ciencias Qu&iacute;micas BUAP.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>2</sup> Posgrado en Optoelectr&oacute;nica. Facultad de Ciencias Fisicomatem&aacute;ticas BUAP.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>3</sup> Centro de Investigaci&oacute;n y de Estudios Avanzados del IPN, Departamento de F&iacute;sica Av. PN 2508 Col San Pedro Zacatenco P. O. Box 14&#150;740, M&eacute;xico 07360 D.F. </i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Recibido: 26 de febrero de 2008.    <br> Aceptado: 13 de mayo 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>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">Mediante la T&eacute;cnica de Dep&oacute;sito por Ba&ntilde;o Qu&iacute;mico, se obtienen pel&iacute;culas delgadas sobre sustratos de vidrio portaobjetos en el intervalo de temperatura de 80&deg;C &#150; 20&deg;C. Las soluciones utilizadas: CdCl<sub>2</sub> 0.02 M, KOH 1.5 M, NH<sub>4</sub>NO<sub>3</sub> 0.5 M y SC(NH<sub>2</sub>)<sub>2</sub> 0.2 M, se preparan a temperatura ambiente utilizando agua desionizada. El volumen de los reactivos, la velocidad de agitaci&oacute;n y la temperatura de reacci&oacute;n se mantuvieron constantes y el pH de la reacci&oacute;n fue de aproximadamente 8.3. El tiempo de dep&oacute;sito var&iacute;a con la temperatura. De resultados previos de absorci&oacute;n &oacute;ptica, se obtiene el ancho de banda prohibida: para CdS a 80&deg;C, E<sub>g</sub> = 2.42 eV y para CdCO<sub>3</sub> a 20&deg;C, E<sub>g</sub> = 3.87 eV. Por Difracci&oacute;n de Rayos X (DXR) se identifica CdS en fase c&uacute;bica a 80&deg;C, con un pico localizado en la posici&oacute;n angular: 2&#952; = &#91;26.68&#93; y a 20 &deg;C se observan se&ntilde;ales en 2&#952; = &#91;23.36, 30.22, 36.30, 43.8, 49.9&#93; que corresponden al CdCO<sub>3</sub> en fase rombo&eacute;drica. En el intervalo 40&deg;C<u>&lt;</u>T<u>&lt;</u>60&deg;C, se identifican se&ntilde;ales de ambos compuestos. En fotograf&iacute;as obtenidas mediante Microscopia &Oacute;ptica (MO) se observa la transici&oacute;n gradual de CdS&#8594;CdCO<sub>3</sub> con crecimiento de los cristales identificados como CdCO<sub>3</sub>. Los precursores de los iones sulfuro (S<sup>2&#150;</sup>) y carbonato (CO<sup>&#150;2</sup><sub>3</sub>), con base a las reacciones propuestas en este trabajo son, &aacute;cido sulfh&iacute;drico (H<sub>2</sub>S) y &aacute;cido carb&oacute;nico (H<sub>2</sub>CO<sub>3</sub>), respectivamente. Ambos &aacute;cidos provienen de la descomposici&oacute;n hidrol&iacute;tica de la tiourea. Se considera la solubilidad del CO<sub>2</sub> y H<sub>2</sub>S en el intervalo de la temperatura de dep&oacute;sito y la influencia de esta en la reacci&oacute;n, as&iacute; como del pH.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Solubilidad; Pel&iacute;culas delgadas; Ion carbonato; Complejo de coordinaci&oacute;n.</font></p>     <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">By Chemical Bath was obtained thin films on glass&#150;substrates with temperature interval of 80&deg;C &#150; 20&deg;C. The used solution are: CdCl<sub>2</sub> 0.02 M, KOH 1.5 M, NH4OH 0.5 M and SC(NH<sub>2</sub>)<sub>2</sub> 0.2 M, they were prepared at room temperature using deionised water. Volume of reagents, velocity of agitation and reaction temperature stayed constant. The pH of reaction was approximately 8.3. The deposit time varies with temperature. From previous results on Optic Absorption, is obtained the prohibited bandwidth, for CdS at 80&deg;C, Eg = 2.42 eV and CdCO<sub>3</sub> at 20&deg;C, Eg = 3.87 eV. By X&#150;ray diffraction was identified the cubic phase of CdS at 80&deg;C, with a peak located in the angular position: 2&#952; = &#91;26.68&#93; and at 20&deg;C it observed signals at 2&#952; = &#91;23.26, 30.22, 36.30, 43.8, 49.90&#93; that correspond to CdCO<sub>3</sub> in rombohedral phase. In interval 40&deg;C<u>&lt;</u>T<u>&lt;</u>60&deg;C, was identified signal from both compounds. By Optic Microscopy was obtained pictures that shown the gradual transition of CdS&#8594;CdCO<sub>3</sub> with growth of crystal. The precursors of ions sulphur (S<sup>&#150;2</sup>) and carbonate (CO<sup>&#150;2</sup><sub>3</sub>) are sulphydric acid (H<sub>2</sub>S) and carbonic acid (H<sub>2</sub>CO<sub>3</sub>), respectively, in according this work. Both acids come from of hydrolytic decomposition of thiourea. The influence of pH, solubility of (H<sub>2</sub>S) and CO<sub>2</sub> are considered in the interval of temperature deposited, and the influence of last in the reaction.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>Solubility; Thin films; Carbonate ion; Coordinate complex.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><a href="/pdf/sv/v21n2/v21n2a5.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></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>Referencias</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">&#91;1&#93; A. Luque. "Solar Cells and Optics for Photovoltaics Concentration". Espa&ntilde;a, Taylor and Francis, (1989).    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=9686242&pid=S1665-3521200800020000500001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">&#91;2&#93; J. Onofre Polvo, Tesis de. Licenciatura en Ciencias Qu&iacute;micas de la Benem&eacute;rita Universidad Aut&oacute;noma de Puebla, "Degradaci&oacute;n del CdS &#150; CdCO<sub>3</sub> por Influencia de la Temperatura de Deposici&oacute;n mediante la T&eacute;cnica DBQ" (2002).    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=9686244&pid=S1665-3521200800020000500002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">&#91;3&#93; Transition from CdS to CdCO<sub>3</sub> by deposition temperature influence. Superficies y Vac&iacute;o <b>15, </b>19 (2002).    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=9686246&pid=S1665-3521200800020000500003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">&#91;4&#93; O. Portillo Moreno, H. Lima Lima, R. Lozada Morales, R. Palomino Merino, O. Zelaya &Aacute;ngel Journal of Materials Science <b>40, </b>4489 (2005).    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=9686248&pid=S1665-3521200800020000500004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </font></p>     ]]></body>
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