IndiumV3, Main, Repository, bibRecord, 000A37

Influence of the Bridging Atom in Fluorene Analogue Low-Bandgap Polymers on Photophysical and Morphological Properties of Copper Indium Sulfide/Polymer Nanocomposite Solar Cells

Identifieur interne : 000A37 ( Main/Repository ); précédent : 000A36; suivant : 000A38

Influence of the Bridging Atom in Fluorene Analogue Low-Bandgap Polymers on Photophysical and Morphological Properties of Copper Indium Sulfide/Polymer Nanocomposite Solar Cells

Auteurs : RBID : Pascal:13-0312685

Descripteurs français

Pascal (Inist)
- Nanocomposite, Carbazole dérivé copolymère, Thiophène copolymère, Copolymère hétérocyclique azote, Copolymère silicium, Copolymère conjugué, Copolymère aromatique, Terpolymère, Cuivre Indium Sulfure, Structure supramoléculaire, Topographie surface, Absorption optique, Photoluminescence, Transistor effet champ, Mobilité porteur charge, Cellule solaire organique, Tension circuit ouvert, Courant court circuit, Facteur remplissage, Effet concentration, Etude comparative, Etude expérimentale, Silafluorène dérivé copolymère, Carbazole(9-[1-octylnonyl]) copolymère, Benzothiadiazole copolymère.

English descriptors

KwdEn :
- Aromatic copolymer, Carbazole derivative copolymer, Charge carrier mobility, Comparative study, Concentration effect, Conjugated copolymer, Copper Indium Sulfides, Experimental study, Field effect transistor, Fill factor, Nanocomposite, Nitrogen heterocycle copolymer, Open circuit voltage, Optical absorption, Organic solar cells, Photoluminescence, Short circuit currents, Silicon copolymer, Supramolecular structure, Surface topography, Terpolymer, Thiophene copolymer.

Abstract

This contribution presents the correlation between structural, morphological, and fluorescence properties as well as device performance of nanocomposite solar cells comprising two low-band gap polymers, poly[[9-(1-octylnonyl)-9H-carbazole-2,7-diyl]-2,5-thiophenediyl-2,1,3-benzothiadiazole-4,7-diyl-2,5-thiophenediyl] (PCDTBT) and poly[2,1,3-benzothiadiazole-4, 7-diyl-2,5-thiophenediyl(9,9-dioctyl-9H-9-silafluorene-2,7-diyl)-2,5-thiophenediyl] (PSiF-DBT) and copper indium sulfide (CIS). It shows that, in analogy to organic solar cells, the device efficiency is strongly determined by different polymer structures leading to a different packing of the polymer chains and consequently to diverse morphologies. X-ray diffraction investigation indicates increased semicrystallinity in PSiF-DBT compared with the nitrogen analogue PCDTBT. The photoluminescence (PL) quenching of this polymer indicates that the higher photogeneration achieved in PSiF-DBT based films can be correlated to a favorable donor-acceptor phase separation. Transmission electron microscopy studies of PCDTBT:CIS blended films suggest the formation of polymer agglomerates in the layer resulting in a decreased PL quenching efficiency. For the considered polymer:CIS system, the combination of these effects leads to an enhanced overall device efficiency.

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Le document en format XML

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<title level="j" type="abbreviated">J. polym. sci., Part B, Polym. phys.</title>
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<term>Comparative study</term>
<term>Concentration effect</term>
<term>Conjugated copolymer</term>
<term>Copper Indium Sulfides</term>
<term>Experimental study</term>
<term>Field effect transistor</term>
<term>Fill factor</term>
<term>Nanocomposite</term>
<term>Nitrogen heterocycle copolymer</term>
<term>Open circuit voltage</term>
<term>Optical absorption</term>
<term>Organic solar cells</term>
<term>Photoluminescence</term>
<term>Short circuit currents</term>
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<term>Copolymère hétérocyclique azote</term>
<term>Copolymère silicium</term>
<term>Copolymère conjugué</term>
<term>Copolymère aromatique</term>
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<term>Cuivre Indium Sulfure</term>
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<term>Transistor effet champ</term>
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<front><div type="abstract" xml:lang="en">This contribution presents the correlation between structural, morphological, and fluorescence properties as well as device performance of nanocomposite solar cells comprising two low-band gap polymers, poly[[9-(1-octylnonyl)-9H-carbazole-2,7-diyl]-2,5-thiophenediyl-2,1,3-benzothiadiazole-4,7-diyl-2,5-thiophenediyl] (PCDTBT) and poly[2,1,3-benzothiadiazole-4, 7-diyl-2,5-thiophenediyl(9,9-dioctyl-9H-9-silafluorene-2,7-diyl)-2,5-thiophenediyl] (PSiF-DBT) and copper indium sulfide (CIS). It shows that, in analogy to organic solar cells, the device efficiency is strongly determined by different polymer structures leading to a different packing of the polymer chains and consequently to diverse morphologies. X-ray diffraction investigation indicates increased semicrystallinity in PSiF-DBT compared with the nitrogen analogue PCDTBT. The photoluminescence (PL) quenching of this polymer indicates that the higher photogeneration achieved in PSiF-DBT based films can be correlated to a favorable donor-acceptor phase separation. Transmission electron microscopy studies of PCDTBT:CIS blended films suggest the formation of polymer agglomerates in the layer resulting in a decreased PL quenching efficiency. For the considered polymer:CIS system, the combination of these effects leads to an enhanced overall device efficiency.</div>
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<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Conjugated copolymer</s0>
<s2>NK</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Copolímero conjugado</s0>
<s2>NK</s2>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Copolymère aromatique</s0>
<s2>NK</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Aromatic copolymer</s0>
<s2>NK</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Copolímero aromático</s0>
<s2>NK</s2>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Terpolymère</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Terpolymer</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Terpolímero</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Cuivre Indium Sulfure</s0>
<s1>SEC</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Copper Indium Sulfides</s0>
<s1>SEC</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Cobre Indio Sulfuro</s0>
<s1>SEC</s1>
<s2>NC</s2>
<s2>NA</s2>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Structure supramoléculaire</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Supramolecular structure</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Estructura supramolecular</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="3" l="FRE"><s0>Topographie surface</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="3" l="ENG"><s0>Surface topography</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>Absorption optique</s0>
<s5>17</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>Optical absorption</s0>
<s5>17</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>Absorción óptica</s0>
<s5>17</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Photoluminescence</s0>
<s5>18</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>Photoluminescence</s0>
<s5>18</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>Fotoluminiscencia</s0>
<s5>18</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE"><s0>Transistor effet champ</s0>
<s5>19</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG"><s0>Field effect transistor</s0>
<s5>19</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA"><s0>Transistor efecto campo</s0>
<s5>19</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Mobilité porteur charge</s0>
<s5>20</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG"><s0>Charge carrier mobility</s0>
<s5>20</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA"><s0>Movilidad portador carga</s0>
<s5>20</s5>
</fC03>
<fC03 i1="16" i2="3" l="FRE"><s0>Cellule solaire organique</s0>
<s5>21</s5>
</fC03>
<fC03 i1="16" i2="3" l="ENG"><s0>Organic solar cells</s0>
<s5>21</s5>
</fC03>
<fC03 i1="17" i2="3" l="FRE"><s0>Tension circuit ouvert</s0>
<s5>22</s5>
</fC03>
<fC03 i1="17" i2="3" l="ENG"><s0>Open circuit voltage</s0>
<s5>22</s5>
</fC03>
<fC03 i1="18" i2="3" l="FRE"><s0>Courant court circuit</s0>
<s5>23</s5>
</fC03>
<fC03 i1="18" i2="3" l="ENG"><s0>Short circuit currents</s0>
<s5>23</s5>
</fC03>
<fC03 i1="19" i2="3" l="FRE"><s0>Facteur remplissage</s0>
<s5>24</s5>
</fC03>
<fC03 i1="19" i2="3" l="ENG"><s0>Fill factor</s0>
<s5>24</s5>
</fC03>
<fC03 i1="20" i2="X" l="FRE"><s0>Effet concentration</s0>
<s5>25</s5>
</fC03>
<fC03 i1="20" i2="X" l="ENG"><s0>Concentration effect</s0>
<s5>25</s5>
</fC03>
<fC03 i1="20" i2="X" l="SPA"><s0>Efecto concentración</s0>
<s5>25</s5>
</fC03>
<fC03 i1="21" i2="X" l="FRE"><s0>Etude comparative</s0>
<s5>27</s5>
</fC03>
<fC03 i1="21" i2="X" l="ENG"><s0>Comparative study</s0>
<s5>27</s5>
</fC03>
<fC03 i1="21" i2="X" l="SPA"><s0>Estudio comparativo</s0>
<s5>27</s5>
</fC03>
<fC03 i1="22" i2="X" l="FRE"><s0>Etude expérimentale</s0>
<s5>28</s5>
</fC03>
<fC03 i1="22" i2="X" l="ENG"><s0>Experimental study</s0>
<s5>28</s5>
</fC03>
<fC03 i1="22" i2="X" l="SPA"><s0>Estudio experimental</s0>
<s5>28</s5>
</fC03>
<fC03 i1="23" i2="X" l="FRE"><s0>Silafluorène dérivé copolymère</s0>
<s2>NK</s2>
<s4>INC</s4>
<s5>32</s5>
</fC03>
<fC03 i1="24" i2="X" l="FRE"><s0>Carbazole(9-[1-octylnonyl]) copolymère</s0>
<s2>NK</s2>
<s4>INC</s4>
<s5>33</s5>
</fC03>
<fC03 i1="25" i2="X" l="FRE"><s0>Benzothiadiazole copolymère</s0>
<s2>NK</s2>
<s4>INC</s4>
<s5>34</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Propriété optique</s0>
<s5>16</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Optical properties</s0>
<s5>16</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Propiedad óptica</s0>
<s5>16</s5>
</fC07>
<fN21><s1>294</s1>
</fN21>
<fN44 i1="01"><s1>PSI</s1>
</fN44>
<fN82><s1>PSI</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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   |texte=   Influence of the Bridging Atom in Fluorene Analogue Low-Bandgap Polymers on Photophysical and Morphological Properties of Copper Indium Sulfide/Polymer Nanocomposite Solar Cells
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Influence of the Bridging Atom in Fluorene Analogue Low-Bandgap Polymers on Photophysical and Morphological Properties of Copper Indium Sulfide/Polymer Nanocomposite Solar Cells

Influence of the Bridging Atom in Fluorene Analogue Low-Bandgap Polymers on Photophysical and Morphological Properties of Copper Indium Sulfide/Polymer Nanocomposite Solar Cells

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