Design and synthesis of indole-substituted fullerene derivatives with different side groups for organic photovoltaic devices
Identifieur interne : 000295 ( Chine/Analysis ); précédent : 000294; suivant : 000296Design and synthesis of indole-substituted fullerene derivatives with different side groups for organic photovoltaic devices
Auteurs : RBID : Pascal:13-0112125Descripteurs français
- Pascal (Inist)
- Electronique organique, Cellule solaire organique, Dispositif photovoltaïque, Cellule solaire, Centre accepteur, Couche active, Substitut, Structure électronique, Microstructure, Morphologie, Evaluation performance, Absorption optique, Caractéristique optique, Spectre absorption, Propriété optique, Propriété électrochimique, Solubilité, Addition étain, Encapsulation, Recuit thermique, Cristallinité, Dérivé de l'indole, Composé du fullerène, Fullerènes, Oxyde d'indium, Oxyde de zinc, Thiophène dérivé polymère, Oxyde de molybdène, Acide butyrique, Ester, Couche mince, Matériau dopé, Packaging électronique, 8105T, 8535, 8460J, 7322, ITO, ZnO, MoO3, 6865, 7840R, 7867.
English descriptors
- KwdEn :
- Absorption spectrum, Acceptor center, Active layer, Butyric acid, Crystallinity, Doped materials, Electrochemical properties, Electronic packaging, Electronic structure, Encapsulation, Ester, Fullerene compounds, Fullerenes, Indium oxide, Indole derivatives, Microstructure, Molybdenum oxide, Morphology, Optical absorption, Optical characteristic, Optical properties, Organic electronics, Organic solar cells, Performance evaluation, Photovoltaic cell, Solar cell, Solubility, Substitute, Thermal annealing, Thin film, Thiophene derivative polymer, Tin addition, Zinc oxide.
Abstract
A series of indole-substituted fulleropyrrolidine derivatives with different side groups on a pyrrolidine rings, including methyl (OIMC60P), benzyl (OIBC60P), 2,5-difluoroinebenzyl (OIB2FC60P), and 2,3,4,5,6-pentafluoroinebenzyl (OIB5FC60P), have been synthesized and used as electron acceptor in the active layer of polymer-fullerene solar cells to investigate the effect of various substitute groups on the electronic structures, morphologies, and device performances. Optical absorption, electrochemical properties and solubility of the fullerene derivatives have been explored and compared. The inverted photovoltaic devices with the configuration ITO/ZnO/Poly(3-hexylthiophene)(P3HT):[60]fullerene derivatives/MoO3/Ag have been prepared including the reference cell based on the P3HT: methyl [6,6]-phenyl-C61-butylate (PCBM) blend films. All the devices properties were measured in air without encapsulation. We also investigated the effect of the thermal annealing on the crystallinity and morphology of the active layer and the device performance. The device based on the blend film of P3HT and OIBC60P showed a power conversion efficiency of 2.46% under illumination by AM1.5G (100 mW/cm2) after the annealing treatment at 120 °C for 10 min in air.
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Design and synthesis of indole-substituted fullerene derivatives with different side groups for organic photovoltaic devices</title><author><name>NING WANG</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author><author><name>XICHANG BAO</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author><author><name>CHUNPENG YANG</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author><author><name>JUN WANG</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author><author><name>HAN YOUNG WOO</name><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Nanofusion Technology, Department of Cogno-Mechatronics Engineering (WCU), Pusan National University</s1><s2>Miryang 627-706</s2><s3>KOR</s3><sZ>5 aut.</sZ></inist:fA14><country>Corée du Sud</country><wicri:noRegion>Miryang 627-706</wicri:noRegion></affiliation></author><author><name>ZHENGGANG LAN</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author><author><name>WEICHAO CHEN</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author><author><name>RENQIANG YANG</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14><country>République populaire de Chine</country><wicri:noRegion>Qingdao 266101</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><idno type="inist">13-0112125</idno><date when="2013">2013</date><idno type="stanalyst">PASCAL 13-0112125 INIST</idno><idno type="RBID">Pascal:13-0112125</idno><idno type="wicri:Area/Main/Corpus">001160</idno><idno type="wicri:Area/Main/Repository">000F46</idno><idno type="wicri:Area/Chine/Extraction">000295</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>Absorption spectrum</term><term>Acceptor center</term><term>Active layer</term><term>Butyric acid</term><term>Crystallinity</term><term>Doped materials</term><term>Electrochemical properties</term><term>Electronic packaging</term><term>Electronic structure</term><term>Encapsulation</term><term>Ester</term><term>Fullerene compounds</term><term>Fullerenes</term><term>Indium oxide</term><term>Indole derivatives</term><term>Microstructure</term><term>Molybdenum oxide</term><term>Morphology</term><term>Optical absorption</term><term>Optical characteristic</term><term>Optical properties</term><term>Organic electronics</term><term>Organic solar cells</term><term>Performance evaluation</term><term>Photovoltaic cell</term><term>Solar cell</term><term>Solubility</term><term>Substitute</term><term>Thermal annealing</term><term>Thin film</term><term>Thiophene derivative polymer</term><term>Tin addition</term><term>Zinc oxide</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Electronique organique</term><term>Cellule solaire organique</term><term>Dispositif photovoltaïque</term><term>Cellule solaire</term><term>Centre accepteur</term><term>Couche active</term><term>Substitut</term><term>Structure électronique</term><term>Microstructure</term><term>Morphologie</term><term>Evaluation performance</term><term>Absorption optique</term><term>Caractéristique optique</term><term>Spectre absorption</term><term>Propriété optique</term><term>Propriété électrochimique</term><term>Solubilité</term><term>Addition étain</term><term>Encapsulation</term><term>Recuit thermique</term><term>Cristallinité</term><term>Dérivé de l'indole</term><term>Composé du fullerène</term><term>Fullerènes</term><term>Oxyde d'indium</term><term>Oxyde de zinc</term><term>Thiophène dérivé polymère</term><term>Oxyde de molybdène</term><term>Acide butyrique</term><term>Ester</term><term>Couche mince</term><term>Matériau dopé</term><term>Packaging électronique</term><term>8105T</term><term>8535</term><term>8460J</term><term>7322</term><term>ITO</term><term>ZnO</term><term>MoO3</term><term>6865</term><term>7840R</term><term>7867</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A series of indole-substituted fulleropyrrolidine derivatives with different side groups on a pyrrolidine rings, including methyl (OIMC60P), benzyl (OIBC60P), 2,5-difluoroinebenzyl (OIB2FC60P), and 2,3,4,5,6-pentafluoroinebenzyl (OIB5FC60P), have been synthesized and used as electron acceptor in the active layer of polymer-fullerene solar cells to investigate the effect of various substitute groups on the electronic structures, morphologies, and device performances. Optical absorption, electrochemical properties and solubility of the fullerene derivatives have been explored and compared. The inverted photovoltaic devices with the configuration ITO/ZnO/Poly(3-hexylthiophene)(P3HT):[60]fullerene derivatives/MoO<sub>3</sub>/Ag have been prepared including the reference cell based on the P3HT: methyl [6,6]-phenyl-C61-butylate (PCBM) blend films. All the devices properties were measured in air without encapsulation. We also investigated the effect of the thermal annealing on the crystallinity and morphology of the active layer and the device performance. The device based on the blend film of P3HT and OIBC60P showed a power conversion efficiency of 2.46% under illumination by AM1.5G (100 mW/cm<sup>2</sup>) after the annealing treatment at 120 °C for 10 min in air.</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>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Design and synthesis of indole-substituted fullerene derivatives with different side groups for organic photovoltaic devices</s1></fA08><fA11 i1="01" i2="1"><s1>NING WANG</s1></fA11><fA11 i1="02" i2="1"><s1>XICHANG BAO</s1></fA11><fA11 i1="03" i2="1"><s1>CHUNPENG YANG</s1></fA11><fA11 i1="04" i2="1"><s1>JUN WANG</s1></fA11><fA11 i1="05" i2="1"><s1>HAN YOUNG WOO</s1></fA11><fA11 i1="06" i2="1"><s1>ZHENGGANG LAN</s1></fA11><fA11 i1="07" i2="1"><s1>WEICHAO CHEN</s1></fA11><fA11 i1="08" i2="1"><s1>RENQIANG YANG</s1></fA11><fA14 i1="01"><s1>Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Rd.</s1><s2>Qingdao 266101</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Nanofusion Technology, Department of Cogno-Mechatronics Engineering (WCU), Pusan National University</s1><s2>Miryang 627-706</s2><s3>KOR</s3><sZ>5 aut.</sZ></fA14><fA20><s1>682-692</s1></fA20><fA21><s1>2013</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27255</s2><s5>354000503710470340</s5></fA43><fA44><s0>0000</s0><s1>© 2013 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>53 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>13-0112125</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 series of indole-substituted fulleropyrrolidine derivatives with different side groups on a pyrrolidine rings, including methyl (OIMC60P), benzyl (OIBC60P), 2,5-difluoroinebenzyl (OIB2FC60P), and 2,3,4,5,6-pentafluoroinebenzyl (OIB5FC60P), have been synthesized and used as electron acceptor in the active layer of polymer-fullerene solar cells to investigate the effect of various substitute groups on the electronic structures, morphologies, and device performances. Optical absorption, electrochemical properties and solubility of the fullerene derivatives have been explored and compared. The inverted photovoltaic devices with the configuration ITO/ZnO/Poly(3-hexylthiophene)(P3HT):[60]fullerene derivatives/MoO<sub>3</sub>/Ag have been prepared including the reference cell based on the P3HT: methyl [6,6]-phenyl-C61-butylate (PCBM) blend films. All the devices properties were measured in air without encapsulation. We also investigated the effect of the thermal annealing on the crystallinity and morphology of the active layer and the device performance. The device based on the blend film of P3HT and OIBC60P showed a power conversion efficiency of 2.46% under illumination by AM1.5G (100 mW/cm<sup>2</sup>) after the annealing treatment at 120 °C for 10 min in air.</s0></fC01><fC02 i1="01" i2="X"><s0>001D06C02D1</s0></fC02><fC02 i1="02" i2="X"><s0>001D03F15</s0></fC02><fC02 i1="03" i2="3"><s0>001B70A15</s0></fC02><fC02 i1="04" i2="3"><s0>001B70H20C</s0></fC02><fC02 i1="05" i2="X"><s0>230</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Electronique organique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Organic electronics</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Electrónica orgánica</s0><s5>01</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Cellule solaire organique</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Organic solar cells</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Dispositif photovoltaïque</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Photovoltaic cell</s0><s5>03</s5></fC03><fC03 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óptica</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Caractéristique optique</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Optical characteristic</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Característica óptica</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Spectre absorption</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Absorption spectrum</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Espectro de absorción</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Propriété optique</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Optical properties</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Propiedad óptica</s0><s5>15</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Propriété électrochimique</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Electrochemical properties</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Propiedad electroquímica</s0><s5>16</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Solubilité</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Solubility</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Solubilidad</s0><s5>17</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Addition étain</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Tin addition</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Adición estaño</s0><s5>18</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>Encapsulation</s0><s5>19</s5></fC03><fC03 i1="19" i2="X" l="ENG"><s0>Encapsulation</s0><s5>19</s5></fC03><fC03 i1="19" i2="X" l="SPA"><s0>Encapsulación</s0><s5>19</s5></fC03><fC03 i1="20" i2="X" l="FRE"><s0>Recuit thermique</s0><s5>20</s5></fC03><fC03 i1="20" i2="X" l="ENG"><s0>Thermal annealing</s0><s5>20</s5></fC03><fC03 i1="20" i2="X" l="SPA"><s0>Recocido térmico</s0><s5>20</s5></fC03><fC03 i1="21" i2="X" l="FRE"><s0>Cristallinité</s0><s5>21</s5></fC03><fC03 i1="21" i2="X" l="ENG"><s0>Crystallinity</s0><s5>21</s5></fC03><fC03 i1="21" i2="X" l="SPA"><s0>Cristalinidad</s0><s5>21</s5></fC03><fC03 i1="22" i2="X" l="FRE"><s0>Dérivé de l'indole</s0><s5>22</s5></fC03><fC03 i1="22" i2="X" l="ENG"><s0>Indole derivatives</s0><s5>22</s5></fC03><fC03 i1="22" i2="X" l="SPA"><s0>Indol derivado</s0><s5>22</s5></fC03><fC03 i1="23" i2="3" l="FRE"><s0>Composé du fullerène</s0><s5>23</s5></fC03><fC03 i1="23" i2="3" l="ENG"><s0>Fullerene compounds</s0><s5>23</s5></fC03><fC03 i1="24" i2="X" l="FRE"><s0>Fullerènes</s0><s5>24</s5></fC03><fC03 i1="24" i2="X" l="ENG"><s0>Fullerenes</s0><s5>24</s5></fC03><fC03 i1="25" i2="X" l="FRE"><s0>Oxyde d'indium</s0><s5>25</s5></fC03><fC03 i1="25" i2="X" l="ENG"><s0>Indium oxide</s0><s5>25</s5></fC03><fC03 i1="25" i2="X" l="SPA"><s0>Indio óxido</s0><s5>25</s5></fC03><fC03 i1="26" i2="X" l="FRE"><s0>Oxyde de zinc</s0><s5>26</s5></fC03><fC03 i1="26" i2="X" l="ENG"><s0>Zinc oxide</s0><s5>26</s5></fC03><fC03 i1="26" i2="X" l="SPA"><s0>Zinc óxido</s0><s5>26</s5></fC03><fC03 i1="27" i2="X" l="FRE"><s0>Thiophène dérivé polymère</s0><s2>NK</s2><s5>27</s5></fC03><fC03 i1="27" i2="X" l="ENG"><s0>Thiophene derivative polymer</s0><s2>NK</s2><s5>27</s5></fC03><fC03 i1="27" i2="X" l="SPA"><s0>Tiofeno derivado polímero</s0><s2>NK</s2><s5>27</s5></fC03><fC03 i1="28" i2="X" l="FRE"><s0>Oxyde de molybdène</s0><s5>28</s5></fC03><fC03 i1="28" i2="X" l="ENG"><s0>Molybdenum oxide</s0><s5>28</s5></fC03><fC03 i1="28" i2="X" l="SPA"><s0>Molibdeno óxido</s0><s5>28</s5></fC03><fC03 i1="29" i2="X" l="FRE"><s0>Acide butyrique</s0><s2>NK</s2><s5>29</s5></fC03><fC03 i1="29" i2="X" l="ENG"><s0>Butyric acid</s0><s2>NK</s2><s5>29</s5></fC03><fC03 i1="29" i2="X" l="SPA"><s0>Butírico ácido</s0><s2>NK</s2><s5>29</s5></fC03><fC03 i1="30" i2="X" l="FRE"><s0>Ester</s0><s5>30</s5></fC03><fC03 i1="30" i2="X" l="ENG"><s0>Ester</s0><s5>30</s5></fC03><fC03 i1="30" i2="X" l="SPA"><s0>Ester</s0><s5>30</s5></fC03><fC03 i1="31" i2="X" l="FRE"><s0>Couche mince</s0><s5>31</s5></fC03><fC03 i1="31" i2="X" l="ENG"><s0>Thin film</s0><s5>31</s5></fC03><fC03 i1="31" i2="X" l="SPA"><s0>Capa fina</s0><s5>31</s5></fC03><fC03 i1="32" i2="3" l="FRE"><s0>Matériau dopé</s0><s5>46</s5></fC03><fC03 i1="32" i2="3" l="ENG"><s0>Doped materials</s0><s5>46</s5></fC03><fC03 i1="33" i2="X" l="FRE"><s0>Packaging électronique</s0><s5>47</s5></fC03><fC03 i1="33" i2="X" l="ENG"><s0>Electronic packaging</s0><s5>47</s5></fC03><fC03 i1="33" i2="X" l="SPA"><s0>Packaging electrónico</s0><s5>47</s5></fC03><fC03 i1="34" i2="X" l="FRE"><s0>8105T</s0><s4>INC</s4><s5>56</s5></fC03><fC03 i1="35" i2="X" l="FRE"><s0>8535</s0><s4>INC</s4><s5>57</s5></fC03><fC03 i1="36" i2="X" l="FRE"><s0>8460J</s0><s4>INC</s4><s5>58</s5></fC03><fC03 i1="37" i2="X" l="FRE"><s0>7322</s0><s4>INC</s4><s5>59</s5></fC03><fC03 i1="38" i2="X" l="FRE"><s0>ITO</s0><s4>INC</s4><s5>82</s5></fC03><fC03 i1="39" i2="X" l="FRE"><s0>ZnO</s0><s4>INC</s4><s5>83</s5></fC03><fC03 i1="40" i2="X" l="FRE"><s0>MoO3</s0><s4>INC</s4><s5>84</s5></fC03><fC03 i1="41" i2="X" l="FRE"><s0>6865</s0><s4>INC</s4><s5>85</s5></fC03><fC03 i1="42" i2="X" l="FRE"><s0>7840R</s0><s4>INC</s4><s5>86</s5></fC03><fC03 i1="43" i2="X" l="FRE"><s0>7867</s0><s4>INC</s4><s5>87</s5></fC03><fN21><s1>084</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)
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|wiki= *** parameter Area/wikiCode missing ***
|area= IndiumV3
|flux= Chine
|étape= Analysis
|type= RBID
|clé= Pascal:13-0112125
|texte= Design and synthesis of indole-substituted fullerene derivatives with different side groups for organic photovoltaic devices
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