A new alcohol-soluble electron-transporting molecule for efficient inverted polymer solar cells
Identifieur interne : 001208 ( Main/Repository ); précédent : 001207; suivant : 001209A new alcohol-soluble electron-transporting molecule for efficient inverted polymer solar cells
Auteurs : RBID : Pascal:13-0254904Descripteurs français
- Pascal (Inist)
- Cellule solaire organique, Produit nouveau, Diacide carboxylique, Echelle grande, Méthode en solution, Procédé fabrication, Addition étain, Couche active, Orbitale moléculaire, Méthode MO, Conversion énergie, Taux conversion, Système tampon, Cathode, Phénanthroline, Semiconducteur type n, Molécule petite, Oxyde de zinc, Oxyde d'indium, Thiophène dérivé polymère, Acide butyrique, Ester, Composé du fullerène, Couche autoassemblée, Matériau dopé, 8105T, 8116D, ZnO, ITO, Bathocuproïne, Couche de transport d'électrons.
- Wicri :
- concept : Produit nouveau.
English descriptors
- KwdEn :
- Active layer, Bathocuproine, Buffer system, Butyric acid, Cathode, Conversion rate, Dicarboxylic acid, Doped materials, Electron transport layer, Energy conversion, Ester, Fullerene compounds, Growth from solution, Indium oxide, Large scale, MO method, Manufacturing process, Molecular orbital, New product, Organic solar cells, Phenanthrolines, Self-assembled layer, Small molecule, Thiophene derivative polymer, Tin addition, Zinc oxide, n type semiconductor.
Abstract
A new electron-transporting material 4,7-diphenyl-1,10-phenanthroline-2,9-dicarboxylic acid (DPPA) was synthesized by modifying a n-type small molecule bathocuproine (BCP). The introduced carboxyl groups make DPPA soluble in polar solvent and compatible with large-scale solution-processing techniques. The anchoring of carboxyl on ZnO (or ITO) substrates helps to form a DPPA electron transporting layer, building an improved interfacial contact between the substrate and active layer. Furthermore, the highest occupied molecular orbital level of DPPA shifts to -6.45 eV, which is 0.38 eV deeper than that of BCP, suggesting enhanced hole-blocking. Inverted polymer solar cells using P3HT:PCBM blend as the active layer and DPPA modified ZnO as the electron transporting layer were fabricated. A power conversion efficiency (PCE) of 3.55% was obtained, which is about 10% higher than that of the conventional ZnO buffered devices (3.25%). The DPPA was also used to replace ZnO as the sole electron-extracting layer, resulting in an improved PCE of 3.46%, which indicates that DPPA-ETL/ITO forms a better cathode than conventional ZnO/ITO.
Links toward previous steps (curation, corpus...)
- to stream Main, to step Corpus: 000969
Links to Exploration step
Pascal:13-0254904Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">A new alcohol-soluble electron-transporting molecule for efficient inverted polymer solar cells</title><author><name>JING LI</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-Ai Road, Suzhou Industrial Park</s1><s2>Suzhou, Jiangsu 215123</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Suzhou, Jiangsu 215123</wicri:noRegion></affiliation><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 57</s1><s2>9000 Aalborg</s2><s3>DNK</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>Danemark</country><wicri:noRegion>9000 Aalborg</wicri:noRegion></affiliation></author><author><name>XIAODONG HUANG</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-Ai Road, Suzhou Industrial Park</s1><s2>Suzhou, Jiangsu 215123</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Suzhou, Jiangsu 215123</wicri:noRegion></affiliation><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 57</s1><s2>9000 Aalborg</s2><s3>DNK</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>Danemark</country><wicri:noRegion>9000 Aalborg</wicri:noRegion></affiliation></author><author><name>JIANYU YUAN</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-Ai Road, Suzhou Industrial Park</s1><s2>Suzhou, Jiangsu 215123</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Suzhou, Jiangsu 215123</wicri:noRegion></affiliation><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 57</s1><s2>9000 Aalborg</s2><s3>DNK</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>Danemark</country><wicri:noRegion>9000 Aalborg</wicri:noRegion></affiliation></author><author><name>KUNYUAN LU</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-Ai Road, Suzhou Industrial Park</s1><s2>Suzhou, Jiangsu 215123</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Suzhou, Jiangsu 215123</wicri:noRegion></affiliation><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 57</s1><s2>9000 Aalborg</s2><s3>DNK</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>Danemark</country><wicri:noRegion>9000 Aalborg</wicri:noRegion></affiliation></author><author><name>WEI YUE</name><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 57</s1><s2>9000 Aalborg</s2><s3>DNK</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>Danemark</country><wicri:noRegion>9000 Aalborg</wicri:noRegion></affiliation></author><author><name>WANLI MA</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-Ai Road, Suzhou Industrial Park</s1><s2>Suzhou, Jiangsu 215123</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Suzhou, Jiangsu 215123</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><idno type="inist">13-0254904</idno><date when="2013">2013</date><idno type="stanalyst">PASCAL 13-0254904 INIST</idno><idno type="RBID">Pascal:13-0254904</idno><idno type="wicri:Area/Main/Corpus">000969</idno><idno type="wicri:Area/Main/Repository">001208</idno></publicationStmt><seriesStmt><idno type="ISSN">1566-1199</idno><title level="j" type="abbreviated">Org. electron. : (Print)</title><title level="j" type="main">Organic electronics : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Active layer</term><term>Bathocuproine</term><term>Buffer system</term><term>Butyric acid</term><term>Cathode</term><term>Conversion rate</term><term>Dicarboxylic acid</term><term>Doped materials</term><term>Electron transport layer</term><term>Energy conversion</term><term>Ester</term><term>Fullerene compounds</term><term>Growth from solution</term><term>Indium oxide</term><term>Large scale</term><term>MO method</term><term>Manufacturing process</term><term>Molecular orbital</term><term>New product</term><term>Organic solar cells</term><term>Phenanthrolines</term><term>Self-assembled layer</term><term>Small molecule</term><term>Thiophene derivative polymer</term><term>Tin addition</term><term>Zinc oxide</term><term>n type semiconductor</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Cellule solaire organique</term><term>Produit nouveau</term><term>Diacide carboxylique</term><term>Echelle grande</term><term>Méthode en solution</term><term>Procédé fabrication</term><term>Addition étain</term><term>Couche active</term><term>Orbitale moléculaire</term><term>Méthode MO</term><term>Conversion énergie</term><term>Taux conversion</term><term>Système tampon</term><term>Cathode</term><term>Phénanthroline</term><term>Semiconducteur type n</term><term>Molécule petite</term><term>Oxyde de zinc</term><term>Oxyde d'indium</term><term>Thiophène dérivé polymère</term><term>Acide butyrique</term><term>Ester</term><term>Composé du fullerène</term><term>Couche autoassemblée</term><term>Matériau dopé</term><term>8105T</term><term>8116D</term><term>ZnO</term><term>ITO</term><term>Bathocuproïne</term><term>Couche de transport d'électrons</term></keywords><keywords scheme="Wicri" type="concept" xml:lang="fr"><term>Produit nouveau</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A new electron-transporting material 4,7-diphenyl-1,10-phenanthroline-2,9-dicarboxylic acid (DPPA) was synthesized by modifying a n-type small molecule bathocuproine (BCP). The introduced carboxyl groups make DPPA soluble in polar solvent and compatible with large-scale solution-processing techniques. The anchoring of carboxyl on ZnO (or ITO) substrates helps to form a DPPA electron transporting layer, building an improved interfacial contact between the substrate and active layer. Furthermore, the highest occupied molecular orbital level of DPPA shifts to -6.45 eV, which is 0.38 eV deeper than that of BCP, suggesting enhanced hole-blocking. Inverted polymer solar cells using P3HT:PCBM blend as the active layer and DPPA modified ZnO as the electron transporting layer were fabricated. A power conversion efficiency (PCE) of 3.55% was obtained, which is about 10% higher than that of the conventional ZnO buffered devices (3.25%). The DPPA was also used to replace ZnO as the sole electron-extracting layer, resulting in an improved PCE of 3.46%, which indicates that DPPA-ETL/ITO forms a better cathode than conventional ZnO/ITO.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1566-1199</s0></fA01><fA03 i2="1"><s0>Org. electron. : (Print)</s0></fA03><fA05><s2>14</s2></fA05><fA06><s2>9</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>A new alcohol-soluble electron-transporting molecule for efficient inverted polymer solar cells</s1></fA08><fA11 i1="01" i2="1"><s1>JING LI</s1></fA11><fA11 i1="02" i2="1"><s1>XIAODONG HUANG</s1></fA11><fA11 i1="03" i2="1"><s1>JIANYU YUAN</s1></fA11><fA11 i1="04" i2="1"><s1>KUNYUAN LU</s1></fA11><fA11 i1="05" i2="1"><s1>WEI YUE</s1></fA11><fA11 i1="06" i2="1"><s1>WANLI MA</s1></fA11><fA14 i1="01"><s1>Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-Ai Road, Suzhou Industrial Park</s1><s2>Suzhou, Jiangsu 215123</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 57</s1><s2>9000 Aalborg</s2><s3>DNK</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA20><s1>2164-2171</s1></fA20><fA21><s1>2013</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27255</s2><s5>354000506504570100</s5></fA43><fA44><s0>0000</s0><s1>© 2013 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>23 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>13-0254904</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Organic electronics : (Print)</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>A new electron-transporting material 4,7-diphenyl-1,10-phenanthroline-2,9-dicarboxylic acid (DPPA) was synthesized by modifying a n-type small molecule bathocuproine (BCP). The introduced carboxyl groups make DPPA soluble in polar solvent and compatible with large-scale solution-processing techniques. The anchoring of carboxyl on ZnO (or ITO) substrates helps to form a DPPA electron transporting layer, building an improved interfacial contact between the substrate and active layer. Furthermore, the highest occupied molecular orbital level of DPPA shifts to -6.45 eV, which is 0.38 eV deeper than that of BCP, suggesting enhanced hole-blocking. Inverted polymer solar cells using P3HT:PCBM blend as the active layer and DPPA modified ZnO as the electron transporting layer were fabricated. A power conversion efficiency (PCE) of 3.55% was obtained, which is about 10% higher than that of the conventional ZnO buffered devices (3.25%). The DPPA was also used to replace ZnO as the sole electron-extracting layer, resulting in an improved PCE of 3.46%, which indicates that DPPA-ETL/ITO forms a better cathode than conventional ZnO/ITO.</s0></fC01><fC02 i1="01" i2="X"><s0>001D06C02D1</s0></fC02><fC02 i1="02" i2="3"><s0>001B80A05T</s0></fC02><fC02 i1="03" i2="3"><s0>001B80A16D</s0></fC02><fC02 i1="04" i2="X"><s0>230</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Cellule solaire organique</s0><s5>01</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Organic solar cells</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Produit nouveau</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>New product</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Producto nuevo</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Diacide carboxylique</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Dicarboxylic acid</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Diácido carboxílico</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Echelle grande</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Large scale</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Escala grande</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Méthode en solution</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Growth from solution</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Método en solución</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Procédé fabrication</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Manufacturing process</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Procedimiento fabricación</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Addition étain</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Tin addition</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Adición estaño</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Couche active</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Active layer</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Capa activa</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Orbitale moléculaire</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Molecular orbital</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Orbital molecular</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Méthode MO</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>MO method</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Método orbital molecular</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Conversion énergie</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Energy conversion</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Conversión energética</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Taux conversion</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Conversion rate</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Factor conversión</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Système tampon</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Buffer system</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Sistema amortiguador</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Cathode</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Cathode</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Cátodo</s0><s5>14</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>Phénanthroline</s0><s2>NK</s2><s5>22</s5></fC03><fC03 i1="15" i2="3" l="ENG"><s0>Phenanthrolines</s0><s2>NK</s2><s5>22</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Semiconducteur type n</s0><s5>23</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>n type semiconductor</s0><s5>23</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Semiconductor tipo n</s0><s5>23</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Molécule petite</s0><s5>24</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Small molecule</s0><s5>24</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Molécula pequeña</s0><s5>24</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Oxyde de zinc</s0><s5>25</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Zinc oxide</s0><s5>25</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Zinc óxido</s0><s5>25</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>Oxyde d'indium</s0><s5>26</s5></fC03><fC03 i1="19" i2="X" l="ENG"><s0>Indium oxide</s0><s5>26</s5></fC03><fC03 i1="19" i2="X" l="SPA"><s0>Indio óxido</s0><s5>26</s5></fC03><fC03 i1="20" i2="X" l="FRE"><s0>Thiophène dérivé polymère</s0><s2>NK</s2><s5>27</s5></fC03><fC03 i1="20" i2="X" l="ENG"><s0>Thiophene derivative polymer</s0><s2>NK</s2><s5>27</s5></fC03><fC03 i1="20" i2="X" l="SPA"><s0>Tiofeno derivado polímero</s0><s2>NK</s2><s5>27</s5></fC03><fC03 i1="21" i2="X" l="FRE"><s0>Acide butyrique</s0><s2>NK</s2><s5>28</s5></fC03><fC03 i1="21" i2="X" l="ENG"><s0>Butyric acid</s0><s2>NK</s2><s5>28</s5></fC03><fC03 i1="21" i2="X" l="SPA"><s0>Butírico ácido</s0><s2>NK</s2><s5>28</s5></fC03><fC03 i1="22" i2="X" l="FRE"><s0>Ester</s0><s5>29</s5></fC03><fC03 i1="22" i2="X" l="ENG"><s0>Ester</s0><s5>29</s5></fC03><fC03 i1="22" i2="X" l="SPA"><s0>Ester</s0><s5>29</s5></fC03><fC03 i1="23" i2="3" l="FRE"><s0>Composé du fullerène</s0><s5>30</s5></fC03><fC03 i1="23" i2="3" l="ENG"><s0>Fullerene compounds</s0><s5>30</s5></fC03><fC03 i1="24" i2="X" l="FRE"><s0>Couche autoassemblée</s0><s5>31</s5></fC03><fC03 i1="24" i2="X" l="ENG"><s0>Self-assembled layer</s0><s5>31</s5></fC03><fC03 i1="24" i2="X" l="SPA"><s0>Capa autoensamblada</s0><s5>31</s5></fC03><fC03 i1="25" i2="3" l="FRE"><s0>Matériau dopé</s0><s5>46</s5></fC03><fC03 i1="25" i2="3" l="ENG"><s0>Doped materials</s0><s5>46</s5></fC03><fC03 i1="26" i2="X" l="FRE"><s0>8105T</s0><s4>INC</s4><s5>56</s5></fC03><fC03 i1="27" i2="X" l="FRE"><s0>8116D</s0><s4>INC</s4><s5>57</s5></fC03><fC03 i1="28" i2="X" l="FRE"><s0>ZnO</s0><s4>INC</s4><s5>82</s5></fC03><fC03 i1="29" i2="X" l="FRE"><s0>ITO</s0><s4>INC</s4><s5>83</s5></fC03><fC03 i1="30" i2="X" l="FRE"><s0>Bathocuproïne</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="30" i2="X" l="ENG"><s0>Bathocuproine</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="31" i2="X" l="FRE"><s0>Couche de transport d'électrons</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="31" i2="X" l="ENG"><s0>Electron transport layer</s0><s4>CD</s4><s5>97</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Composé II-VI</s0><s5>15</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>II-VI compound</s0><s5>15</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Compuesto II-VI</s0><s5>15</s5></fC07><fN21><s1>245</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard></inist></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=IndiumV3/Data/Main/Repository
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001208 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Repository/biblio.hfd -nk 001208 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= *** parameter Area/wikiCode missing ***
|area= IndiumV3
|flux= Main
|étape= Repository
|type= RBID
|clé= Pascal:13-0254904
|texte= A new alcohol-soluble electron-transporting molecule for efficient inverted polymer solar cells
}}
| This area was generated with Dilib version V0.5.77. |  |