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Photo-assisted electrodeposition of polypyrrole back contact to CdS/CdTe solar cell structures

Identifieur interne : 000741 ( Main/Repository ); précédent : 000740; suivant : 000742

Photo-assisted electrodeposition of polypyrrole back contact to CdS/CdTe solar cell structures

Auteurs : RBID : Pascal:13-0229225

Descripteurs français

English descriptors

Abstract

Glass/indium tin oxide/CdS/CdTe photovoltaic structures were prepared using the high vacuum evaporation method, followed by a typical activation procedure, which involves annealing of the structures at 415-430 °C in the presence of CdCl2 in air. The main purpose of this work was to prepare and evaluate the performance of complete CdS/CdTe solar cell structures with polypyrrole (PPy) back contact and compare it to the structures with standard, copper containing back contact. Back contact layers of PPy doped with β-naphthalene sulfonate were deposited onto activated CdTe layers by photo-assisted electrodeposition technique in a three-electrode electrochemical cell. It was found that intensive white light illumination from a xenon lamp facilitates PPy deposition at a lower applied potential range and improves quality of obtained polymer films. Applied technique gives the possibility to deposit the PPy layer strictly onto illuminated photoactive CdTe surface eliminating possible short-circuiting through pinholes and cracks in CdTe photoabsorber layer. Furthermore, relatively low deposition potential values give the possibility to reduce electrochemical degradation of CdS/CdTe photovoltaic structure in an electrochemical cell.

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Pascal:13-0229225

Le document en format XML

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<title xml:lang="en" level="a">Photo-assisted electrodeposition of polypyrrole back contact to CdS/CdTe solar cell structures</title>
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<name sortKey="Mellikov, E" uniqKey="Mellikov E">E. Mellikov</name>
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<s1>Tallinn University of Technology, Department of Materials Science, Ehitajate tee 5</s1>
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<idno type="ISSN">0040-6090</idno>
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<term>Annealing</term>
<term>Cadmium chloride</term>
<term>Cadmium sulfide</term>
<term>Cadmium tellurides</term>
<term>Cellular structure</term>
<term>Conducting polymers</term>
<term>Copper</term>
<term>Doping</term>
<term>Electrochemical electrodes</term>
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<term>Glass</term>
<term>High vacuum</term>
<term>II-VI semiconductors</term>
<term>Illumination</term>
<term>Indium oxide</term>
<term>Naphthalene</term>
<term>Photovoltaic cell</term>
<term>Pinholes</term>
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<term>Vacuum evaporation</term>
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<term>Dispositif photovoltaïque</term>
<term>Vide poussé</term>
<term>Evaporation sous vide</term>
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<term>Oxyde d'étain</term>
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<term>Eclairement</term>
<term>Xénon</term>
<term>Film polymère</term>
<term>Piqûre corrosion</term>
<term>Polymère conducteur</term>
<term>CdS</term>
<term>CdTe</term>
<term>CdCl2</term>
<term>Xe</term>
<term>8115P</term>
<term>8105D</term>
<term>8460J</term>
<term>8105H</term>
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<div type="abstract" xml:lang="en">Glass/indium tin oxide/CdS/CdTe photovoltaic structures were prepared using the high vacuum evaporation method, followed by a typical activation procedure, which involves annealing of the structures at 415-430 °C in the presence of CdCl
<sub>2</sub>
in air. The main purpose of this work was to prepare and evaluate the performance of complete CdS/CdTe solar cell structures with polypyrrole (PPy) back contact and compare it to the structures with standard, copper containing back contact. Back contact layers of PPy doped with β-naphthalene sulfonate were deposited onto activated CdTe layers by photo-assisted electrodeposition technique in a three-electrode electrochemical cell. It was found that intensive white light illumination from a xenon lamp facilitates PPy deposition at a lower applied potential range and improves quality of obtained polymer films. Applied technique gives the possibility to deposit the PPy layer strictly onto illuminated photoactive CdTe surface eliminating possible short-circuiting through pinholes and cracks in CdTe photoabsorber layer. Furthermore, relatively low deposition potential values give the possibility to reduce electrochemical degradation of CdS/CdTe photovoltaic structure in an electrochemical cell.</div>
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<s0>NLD</s0>
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<s0>Glass/indium tin oxide/CdS/CdTe photovoltaic structures were prepared using the high vacuum evaporation method, followed by a typical activation procedure, which involves annealing of the structures at 415-430 °C in the presence of CdCl
<sub>2</sub>
in air. The main purpose of this work was to prepare and evaluate the performance of complete CdS/CdTe solar cell structures with polypyrrole (PPy) back contact and compare it to the structures with standard, copper containing back contact. Back contact layers of PPy doped with β-naphthalene sulfonate were deposited onto activated CdTe layers by photo-assisted electrodeposition technique in a three-electrode electrochemical cell. It was found that intensive white light illumination from a xenon lamp facilitates PPy deposition at a lower applied potential range and improves quality of obtained polymer films. Applied technique gives the possibility to deposit the PPy layer strictly onto illuminated photoactive CdTe surface eliminating possible short-circuiting through pinholes and cracks in CdTe photoabsorber layer. Furthermore, relatively low deposition potential values give the possibility to reduce electrochemical degradation of CdS/CdTe photovoltaic structure in an electrochemical cell.</s0>
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<s0>230</s0>
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<s5>01</s5>
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<s5>01</s5>
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<s5>02</s5>
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<s5>02</s5>
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<s5>03</s5>
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<s5>03</s5>
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<s0>Structure cellulaire</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="3" l="ENG">
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<s5>04</s5>
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<s0>Verre</s0>
<s5>05</s5>
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<s0>Glass</s0>
<s5>05</s5>
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<s5>06</s5>
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<s5>06</s5>
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<s5>07</s5>
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<s5>08</s5>
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<s5>09</s5>
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<s5>09</s5>
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<s5>10</s5>
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<fC03 i1="10" i2="X" l="ENG">
<s0>Cadmium chloride</s0>
<s5>10</s5>
</fC03>
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<s0>Cadmio cloruro</s0>
<s5>10</s5>
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<fC03 i1="11" i2="3" l="FRE">
<s0>Cuivre</s0>
<s2>NC</s2>
<s5>11</s5>
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<fC03 i1="11" i2="3" l="ENG">
<s0>Copper</s0>
<s2>NC</s2>
<s5>11</s5>
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<fC03 i1="12" i2="X" l="FRE">
<s0>Dopage</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Doping</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Doping</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="3" l="FRE">
<s0>Naphtalène</s0>
<s2>NK</s2>
<s5>13</s5>
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<s0>Naphthalene</s0>
<s2>NK</s2>
<s5>13</s5>
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<fC03 i1="14" i2="3" l="FRE">
<s0>Sulfonate</s0>
<s5>14</s5>
</fC03>
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<s0>Sulfonates</s0>
<s5>14</s5>
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<s0>Pyrrole polymère</s0>
<s2>NK</s2>
<s5>15</s5>
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<s2>NK</s2>
<s5>15</s5>
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<fC03 i1="16" i2="X" l="FRE">
<s0>Sulfure de cadmium</s0>
<s5>16</s5>
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<s0>Cadmium sulfide</s0>
<s5>16</s5>
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<s0>Cadmio sulfuro</s0>
<s5>16</s5>
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<s5>17</s5>
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<s0>Cadmium tellurides</s0>
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<s5>17</s5>
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<fC03 i1="18" i2="X" l="FRE">
<s0>Oxyde d'indium</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="X" l="ENG">
<s0>Indium oxide</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="X" l="SPA">
<s0>Indio óxido</s0>
<s5>18</s5>
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<fC03 i1="19" i2="X" l="FRE">
<s0>Oxyde d'étain</s0>
<s5>19</s5>
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<fC03 i1="19" i2="X" l="ENG">
<s0>Tin oxide</s0>
<s5>19</s5>
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<fC03 i1="19" i2="X" l="SPA">
<s0>Estaño óxido</s0>
<s5>19</s5>
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<s5>29</s5>
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<s0>Electrochemical electrodes</s0>
<s5>29</s5>
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<fC03 i1="21" i2="3" l="FRE">
<s0>Eclairement</s0>
<s5>30</s5>
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<s0>Illumination</s0>
<s5>30</s5>
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<s0>Xénon</s0>
<s2>NC</s2>
<s5>31</s5>
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<s0>Xenon</s0>
<s2>NC</s2>
<s5>31</s5>
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<fC03 i1="23" i2="3" l="FRE">
<s0>Film polymère</s0>
<s5>32</s5>
</fC03>
<fC03 i1="23" i2="3" l="ENG">
<s0>Polymer films</s0>
<s5>32</s5>
</fC03>
<fC03 i1="24" i2="3" l="FRE">
<s0>Piqûre corrosion</s0>
<s5>33</s5>
</fC03>
<fC03 i1="24" i2="3" l="ENG">
<s0>Pinholes</s0>
<s5>33</s5>
</fC03>
<fC03 i1="25" i2="3" l="FRE">
<s0>Polymère conducteur</s0>
<s5>34</s5>
</fC03>
<fC03 i1="25" i2="3" l="ENG">
<s0>Conducting polymers</s0>
<s5>34</s5>
</fC03>
<fC03 i1="26" i2="3" l="FRE">
<s0>CdS</s0>
<s4>INC</s4>
<s5>46</s5>
</fC03>
<fC03 i1="27" i2="3" l="FRE">
<s0>CdTe</s0>
<s4>INC</s4>
<s5>47</s5>
</fC03>
<fC03 i1="28" i2="3" l="FRE">
<s0>CdCl2</s0>
<s4>INC</s4>
<s5>48</s5>
</fC03>
<fC03 i1="29" i2="3" l="FRE">
<s0>Xe</s0>
<s4>INC</s4>
<s5>49</s5>
</fC03>
<fC03 i1="30" i2="3" l="FRE">
<s0>8115P</s0>
<s4>INC</s4>
<s5>71</s5>
</fC03>
<fC03 i1="31" i2="3" l="FRE">
<s0>8105D</s0>
<s4>INC</s4>
<s5>72</s5>
</fC03>
<fC03 i1="32" i2="3" l="FRE">
<s0>8460J</s0>
<s4>INC</s4>
<s5>73</s5>
</fC03>
<fC03 i1="33" i2="3" l="FRE">
<s0>8105H</s0>
<s4>INC</s4>
<s5>74</s5>
</fC03>
<fN21>
<s1>210</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
<pR>
<fA30 i1="01" i2="1" l="ENG">
<s1>E-MRS Spring Meeting 2012. Symposium B "Thin Film Chalcogenide Photovoltaic Materials"</s1>
<s3>Strasbourg FRA</s3>
<s4>2012-05-14</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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