Donor-acceptor copolymers incorporating polybenzo [1,2-b:4,5-b']dithiophene and tetrazine for high open circuit voltage polymer solar cells
Identifieur interne : 000293 ( Chine/Analysis ); précédent : 000292; suivant : 000294Donor-acceptor copolymers incorporating polybenzo [1,2-b:4,5-b']dithiophene and tetrazine for high open circuit voltage polymer solar cells
Auteurs : RBID : Pascal:13-0254898Descripteurs français
- Pascal (Inist)
- Centre donneur, Centre accepteur, Haute tension, Tension circuit ouvert, Cellule solaire organique, Bande interdite, Polymérisation, Comportement thermique, Propriété thermique, Résonance magnétique nucléaire, Perméation, Thermogravimétrie, Stabilité thermique, Décomposition thermique, Voltammétrie cyclique, Orbitale moléculaire, Méthode MO, Niveau énergie, Combinaison diversité, Hétérojonction, Addition étain, Copolymère, Dérivé du thiophène, Polymère conjugué, Hétérostructure, Acide butyrique, Ester, Oxyde d'indium, Verre, Matériau dopé, 6580, 8245R, 8105K, 6182R, ITO.
- Wicri :
- concept : Verre.
English descriptors
- KwdEn :
- Acceptor center, Butyric acid, Conjugated polymer, Copolymer, Cyclic voltammetry, Diversity combining, Donor center, Doped materials, Energy gap, Energy level, Ester, Glass, Heterojunction, Heterostructures, High voltage, Indium oxide, MO method, Molecular orbital, Nuclear magnetic resonance, Open circuit voltage, Organic solar cells, Permeation, Polymerization, Thermal behavior, Thermal decomposition, Thermal properties, Thermal stability, Thermogravimetry, Thiophene derivatives, Tin addition.
Abstract
Two new low band gap conjugated polymers containing a benzo[1,2-b:4,5-b']dithiophene donor unit and a tetrazine acceptor unit were synthesized by Stille cross-coupling polymerization. The structural and thermal properties of copolymers were characterized using nuclear magnetic resonance, gel permeation chromatography and thermogravimetric analysis. The results show that the donor-acceptor copolymers thus developed have good thermal stability with decomposition temperature of 294 °C and 305 °C. Cyclic voltammetric study revealed that the copolymers possess a deep-lying highest occupied molecular orbital energy level, which is desired for high open circuit voltage polymer solar cells (PSCs) and is also favorable for stable device operation in air. Bulk-heterojunction PSCs based on blend of low band gap copolymers: [6,6]-phenyl-C71-butyric acid methyl ester on indium tin oxide/glass substrates were fabricated. This work yielded a promising power conversion efficiency of >5.0%, with a high open circuit voltage of ∼1.0 V, measured under air mass 1.5 global irradiation of 100 mW/cm2.
Links toward previous steps (curation, corpus...)
- to stream Main, to step Corpus: 000971
- to stream Main, to step Repository: 000F29
- to stream Chine, to step Extraction: 000293
Links to Exploration step
Pascal:13-0254898Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Donor-acceptor copolymers incorporating polybenzo [1,2-b:4,5-b']dithiophene and tetrazine for high open circuit voltage polymer solar cells</title><author><name>WEIDONG CHENG</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>State Key Laboratory of Supramolecular Structure and Materials, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14><country>République populaire de Chine</country><placeName><settlement type="city">Changchun</settlement><region type="province">Jilin</region><region type="groupement">Dongbei</region></placeName></affiliation></author><author><name>ZHENGHUI WU</name><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Physics and Institute of Advanced Materials, Hong Kong Baptist University</s1><s2>Kowloon Tong</s2><s3>HKG</s3><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Hong Kong</country><wicri:noRegion>Kowloon Tong</wicri:noRegion></affiliation></author><author><name>SHANPENG WEN</name><affiliation wicri:level="1"><inist:fA14 i1="03"><s1>State Key Laboratory on Integrated Optoelectonics, College of Electronic Science and Engineering, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>3 aut.</sZ></inist:fA14><country>République populaire de Chine</country><placeName><settlement type="city">Changchun</settlement><region type="province">Jilin</region><region type="groupement">Dongbei</region></placeName></affiliation></author><author><name>BIN XU</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>State Key Laboratory of Supramolecular Structure and Materials, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14><country>République populaire de Chine</country><placeName><settlement type="city">Changchun</settlement><region type="province">Jilin</region><region type="groupement">Dongbei</region></placeName></affiliation></author><author><name>HUI LI</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>State Key Laboratory of Supramolecular Structure and Materials, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14><country>République populaire de Chine</country><placeName><settlement type="city">Changchun</settlement><region type="province">Jilin</region><region type="groupement">Dongbei</region></placeName></affiliation></author><author><name>FURONG ZHU</name><affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Physics and Institute of Advanced Materials, Hong Kong Baptist University</s1><s2>Kowloon Tong</s2><s3>HKG</s3><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14><country>Hong Kong</country><wicri:noRegion>Kowloon Tong</wicri:noRegion></affiliation></author><author><name>WENJING TIAN</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>State Key Laboratory of Supramolecular Structure and Materials, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14><country>République populaire de Chine</country><placeName><settlement type="city">Changchun</settlement><region type="province">Jilin</region><region type="groupement">Dongbei</region></placeName></affiliation></author></titleStmt><publicationStmt><idno type="inist">13-0254898</idno><date when="2013">2013</date><idno type="stanalyst">PASCAL 13-0254898 INIST</idno><idno type="RBID">Pascal:13-0254898</idno><idno type="wicri:Area/Main/Corpus">000971</idno><idno type="wicri:Area/Main/Repository">000F29</idno><idno type="wicri:Area/Chine/Extraction">000293</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>Acceptor center</term><term>Butyric acid</term><term>Conjugated polymer</term><term>Copolymer</term><term>Cyclic voltammetry</term><term>Diversity combining</term><term>Donor center</term><term>Doped materials</term><term>Energy gap</term><term>Energy level</term><term>Ester</term><term>Glass</term><term>Heterojunction</term><term>Heterostructures</term><term>High voltage</term><term>Indium oxide</term><term>MO method</term><term>Molecular orbital</term><term>Nuclear magnetic resonance</term><term>Open circuit voltage</term><term>Organic solar cells</term><term>Permeation</term><term>Polymerization</term><term>Thermal behavior</term><term>Thermal decomposition</term><term>Thermal properties</term><term>Thermal stability</term><term>Thermogravimetry</term><term>Thiophene derivatives</term><term>Tin addition</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Centre donneur</term><term>Centre accepteur</term><term>Haute tension</term><term>Tension circuit ouvert</term><term>Cellule solaire organique</term><term>Bande interdite</term><term>Polymérisation</term><term>Comportement thermique</term><term>Propriété thermique</term><term>Résonance magnétique nucléaire</term><term>Perméation</term><term>Thermogravimétrie</term><term>Stabilité thermique</term><term>Décomposition thermique</term><term>Voltammétrie cyclique</term><term>Orbitale moléculaire</term><term>Méthode MO</term><term>Niveau énergie</term><term>Combinaison diversité</term><term>Hétérojonction</term><term>Addition étain</term><term>Copolymère</term><term>Dérivé du thiophène</term><term>Polymère conjugué</term><term>Hétérostructure</term><term>Acide butyrique</term><term>Ester</term><term>Oxyde d'indium</term><term>Verre</term><term>Matériau dopé</term><term>6580</term><term>8245R</term><term>8105K</term><term>6182R</term><term>ITO</term></keywords><keywords scheme="Wicri" type="concept" xml:lang="fr"><term>Verre</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two new low band gap conjugated polymers containing a benzo[1,2-b:4,5-b']dithiophene donor unit and a tetrazine acceptor unit were synthesized by Stille cross-coupling polymerization. The structural and thermal properties of copolymers were characterized using nuclear magnetic resonance, gel permeation chromatography and thermogravimetric analysis. The results show that the donor-acceptor copolymers thus developed have good thermal stability with decomposition temperature of 294 °C and 305 °C. Cyclic voltammetric study revealed that the copolymers possess a deep-lying highest occupied molecular orbital energy level, which is desired for high open circuit voltage polymer solar cells (PSCs) and is also favorable for stable device operation in air. Bulk-heterojunction PSCs based on blend of low band gap copolymers: [6,6]-phenyl-C71-butyric acid methyl ester on indium tin oxide/glass substrates were fabricated. This work yielded a promising power conversion efficiency of >5.0%, with a high open circuit voltage of ∼1.0 V, measured under air mass 1.5 global irradiation of 100 mW/cm<sup>2</sup>.</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>Donor-acceptor copolymers incorporating polybenzo [1,2-b:4,5-b']dithiophene and tetrazine for high open circuit voltage polymer solar cells</s1></fA08><fA11 i1="01" i2="1"><s1>WEIDONG CHENG</s1></fA11><fA11 i1="02" i2="1"><s1>ZHENGHUI WU</s1></fA11><fA11 i1="03" i2="1"><s1>SHANPENG WEN</s1></fA11><fA11 i1="04" i2="1"><s1>BIN XU</s1></fA11><fA11 i1="05" i2="1"><s1>HUI LI</s1></fA11><fA11 i1="06" i2="1"><s1>FURONG ZHU</s1></fA11><fA11 i1="07" i2="1"><s1>WENJING TIAN</s1></fA11><fA14 i1="01"><s1>State Key Laboratory of Supramolecular Structure and Materials, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Physics and Institute of Advanced Materials, Hong Kong Baptist University</s1><s2>Kowloon Tong</s2><s3>HKG</s3><sZ>2 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="03"><s1>State Key Laboratory on Integrated Optoelectonics, College of Electronic Science and Engineering, Jilin University</s1><s2>Changchun 130012</s2><s3>CHN</s3><sZ>3 aut.</sZ></fA14><fA20><s1>2124-2131</s1></fA20><fA21><s1>2013</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27255</s2><s5>354000506504570040</s5></fA43><fA44><s0>0000</s0><s1>© 2013 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>26 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>13-0254898</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>Two new low band gap conjugated polymers containing a benzo[1,2-b:4,5-b']dithiophene donor unit and a tetrazine acceptor unit were synthesized by Stille cross-coupling polymerization. The structural and thermal properties of copolymers were characterized using nuclear magnetic resonance, gel permeation chromatography and thermogravimetric analysis. The results show that the donor-acceptor copolymers thus developed have good thermal stability with decomposition temperature of 294 °C and 305 °C. Cyclic voltammetric study revealed that the copolymers possess a deep-lying highest occupied molecular orbital energy level, which is desired for high open circuit voltage polymer solar cells (PSCs) and is also favorable for stable device operation in air. Bulk-heterojunction PSCs based on blend of low band gap copolymers: [6,6]-phenyl-C71-butyric acid methyl ester on indium tin oxide/glass substrates were fabricated. This work yielded a promising power conversion efficiency of >5.0%, with a high open circuit voltage of ∼1.0 V, measured under air mass 1.5 global irradiation of 100 mW/cm<sup>2</sup>.</s0></fC01><fC02 i1="01" i2="X"><s0>001D06C02D1</s0></fC02><fC02 i1="02" i2="3"><s0>001B70F60</s0></fC02><fC02 i1="03" i2="X"><s0>001D03F02</s0></fC02><fC02 i1="04" i2="3"><s0>001B60E80</s0></fC02><fC02 i1="05" i2="X"><s0>230</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Centre donneur</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Donor center</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Centro dador</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Centre accepteur</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Acceptor center</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Centro aceptor</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Haute tension</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>High voltage</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Alta tensión</s0><s5>03</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Tension circuit ouvert</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Open circuit voltage</s0><s5>04</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Cellule solaire organique</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Organic solar cells</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Bande interdite</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Energy gap</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Banda prohibida</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Polymérisation</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Polymerization</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Polimerización</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Comportement thermique</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Thermal behavior</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Comportamiento térmico</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Propriété thermique</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Thermal properties</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Propiedad térmica</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Résonance magnétique nucléaire</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Nuclear magnetic resonance</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Resonancia magnética nuclear</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Perméation</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Permeation</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Permeación</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Thermogravimétrie</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Thermogravimetry</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Termogravimetría</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Stabilité thermique</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Thermal stability</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Estabilidad térmica</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Décomposition thermique</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Thermal decomposition</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Descomposición térmica</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Voltammétrie cyclique</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Cyclic voltammetry</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Voltametría cíclica</s0><s5>15</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Orbitale moléculaire</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Molecular orbital</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Orbital molecular</s0><s5>16</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Méthode MO</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>MO method</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Método orbital molecular</s0><s5>17</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Niveau énergie</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Energy level</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Nivel energía</s0><s5>18</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>Combinaison diversité</s0><s5>19</s5></fC03><fC03 i1="19" i2="X" l="ENG"><s0>Diversity combining</s0><s5>19</s5></fC03><fC03 i1="19" i2="X" l="SPA"><s0>Combinación diversidad</s0><s5>19</s5></fC03><fC03 i1="20" i2="X" l="FRE"><s0>Hétérojonction</s0><s5>20</s5></fC03><fC03 i1="20" i2="X" l="ENG"><s0>Heterojunction</s0><s5>20</s5></fC03><fC03 i1="20" i2="X" l="SPA"><s0>Heterounión</s0><s5>20</s5></fC03><fC03 i1="21" i2="X" l="FRE"><s0>Addition étain</s0><s5>21</s5></fC03><fC03 i1="21" i2="X" l="ENG"><s0>Tin addition</s0><s5>21</s5></fC03><fC03 i1="21" i2="X" l="SPA"><s0>Adición estaño</s0><s5>21</s5></fC03><fC03 i1="22" i2="X" l="FRE"><s0>Copolymère</s0><s2>NK</s2><s5>22</s5></fC03><fC03 i1="22" i2="X" l="ENG"><s0>Copolymer</s0><s2>NK</s2><s5>22</s5></fC03><fC03 i1="22" i2="X" l="SPA"><s0>Copolímero</s0><s2>NK</s2><s5>22</s5></fC03><fC03 i1="23" i2="X" l="FRE"><s0>Dérivé du thiophène</s0><s5>23</s5></fC03><fC03 i1="23" i2="X" l="ENG"><s0>Thiophene derivatives</s0><s5>23</s5></fC03><fC03 i1="23" i2="X" l="SPA"><s0>Tiofeno derivado</s0><s5>23</s5></fC03><fC03 i1="24" i2="X" l="FRE"><s0>Polymère conjugué</s0><s5>24</s5></fC03><fC03 i1="24" i2="X" l="ENG"><s0>Conjugated polymer</s0><s5>24</s5></fC03><fC03 i1="24" i2="X" l="SPA"><s0>Polímero conjugado</s0><s5>24</s5></fC03><fC03 i1="25" i2="3" l="FRE"><s0>Hétérostructure</s0><s5>25</s5></fC03><fC03 i1="25" i2="3" l="ENG"><s0>Heterostructures</s0><s5>25</s5></fC03><fC03 i1="26" i2="X" l="FRE"><s0>Acide butyrique</s0><s2>NK</s2><s5>26</s5></fC03><fC03 i1="26" i2="X" l="ENG"><s0>Butyric acid</s0><s2>NK</s2><s5>26</s5></fC03><fC03 i1="26" i2="X" l="SPA"><s0>Butírico ácido</s0><s2>NK</s2><s5>26</s5></fC03><fC03 i1="27" i2="X" l="FRE"><s0>Ester</s0><s5>27</s5></fC03><fC03 i1="27" i2="X" l="ENG"><s0>Ester</s0><s5>27</s5></fC03><fC03 i1="27" i2="X" l="SPA"><s0>Ester</s0><s5>27</s5></fC03><fC03 i1="28" i2="X" l="FRE"><s0>Oxyde d'indium</s0><s5>28</s5></fC03><fC03 i1="28" i2="X" l="ENG"><s0>Indium oxide</s0><s5>28</s5></fC03><fC03 i1="28" i2="X" l="SPA"><s0>Indio óxido</s0><s5>28</s5></fC03><fC03 i1="29" i2="X" l="FRE"><s0>Verre</s0><s5>29</s5></fC03><fC03 i1="29" i2="X" l="ENG"><s0>Glass</s0><s5>29</s5></fC03><fC03 i1="29" i2="X" l="SPA"><s0>Vidrio</s0><s5>29</s5></fC03><fC03 i1="30" i2="3" l="FRE"><s0>Matériau dopé</s0><s5>46</s5></fC03><fC03 i1="30" i2="3" l="ENG"><s0>Doped materials</s0><s5>46</s5></fC03><fC03 i1="31" i2="X" l="FRE"><s0>6580</s0><s4>INC</s4><s5>56</s5></fC03><fC03 i1="32" i2="X" l="FRE"><s0>8245R</s0><s4>INC</s4><s5>57</s5></fC03><fC03 i1="33" i2="X" l="FRE"><s0>8105K</s0><s4>INC</s4><s5>58</s5></fC03><fC03 i1="34" i2="X" l="FRE"><s0>6182R</s0><s4>INC</s4><s5>59</s5></fC03><fC03 i1="35" i2="X" l="FRE"><s0>ITO</s0><s4>INC</s4><s5>82</s5></fC03><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/Chine/Analysis
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000293 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Chine/Analysis/biblio.hfd -nk 000293 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= *** parameter Area/wikiCode missing ***
|area= IndiumV3
|flux= Chine
|étape= Analysis
|type= RBID
|clé= Pascal:13-0254898
|texte= Donor-acceptor copolymers incorporating polybenzo [1,2-b:4,5-b']dithiophene and tetrazine for high open circuit voltage polymer solar cells
}}
| This area was generated with Dilib version V0.5.77. |  |