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Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells

Identifieur interne : 000415 ( Main/Repository ); précédent : 000414; suivant : 000416

Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells

Auteurs : RBID : Pascal:13-0098742

Descripteurs français

Pascal (Inist)
- Cellule solaire organique, Polymère conjugué, Donneur électron, Propriété optique, Propriété électrochimique, Mobilité trou, Microscopie force atomique, Morphologie, Solubilité, Formation film, Stabilité thermique, Spectre visible, Système photovoltaïque, Spectre absorption, Etude comparative, Transfert charge, Méthode en solution, Transistor effet champ, Semiconducteur type p, Transistor couche mince, Dispositif photovoltaïque, Copolymère, Acide butyrique, Ester, Composé du fullerène, Oxyde d'indium, Styrènesulfonate polymère, Thiophène dérivé polymère, ITO.

English descriptors

KwdEn :
- Absorption spectrum, Atomic force microscopy, Butyric acid, Charge transfer, Comparative study, Conjugated polymer, Copolymer, Electrochemical properties, Electron donor, Ester, Field effect transistor, Film formation, Fullerene compounds, Growth from solution, Hole mobility, Indium oxide, Morphology, Optical properties, Organic solar cells, Photovoltaic cell, Photovoltaic system, Solubility, Styrenesulfonate polymer, Thermal stability, Thin film transistor, Thiophene derivative polymer, Visible spectrum, p type semiconductor.

Abstract

A new conjugated polymer containing pentaselenophene (5Se) electron donor moieties was designed for use in polymer solar cells and synthesized via a Stille coupling reaction. The structure, optical properties, electrochemical properties, hole mobility, photovoltaic properties, and AFM morphology of the homopolymer (P5Se) and the donor-acceptor copolymer (P5SeDTDPP) with a diketopyrrolopyrrole (DPP) acceptor were investigated and are discussed. The polymers showed good solubility, film-forming properties, and thermal stabilities. P5Se exhibited a broad absorption across the visible range, 400-700 nm, which is a prerequisite for photovoltaic applications. P5SeDTDPP yielded a broader absorption spectrum, enhanced π-π interactions, and a lower band gap compared to P5Se, due to the enhanced intramolecular charge transfer interactions between the donating moiety (pentaselenophene) and the DPP accepting moiety. Solution-processed field effect transistors fabricated from these polymers displayed p-type organic thin film transistor characteristics. P5Se and P5SeDTDPP exhibited typical p-type organic semiconductor characteristics with hole mobilities of 2.3 × 10^-3 and 1.2 x 10-² cm² V^-1 s^-1, respectively. Photovoltaic devices were fabricated using polymer:PCBM blends in ITO/PEDOT:PSS/blend/Al structures. The P5SeDTDPP device exhibited an open circuit voltage (V_OC) of 0.44 V, a short circuit current (J_SC) of 10.67 mA/cm², a fill factor (FF) of 0.51, and a power conversion efficiency (PCE) of 2.40% under AM 1.5 G (100 mW/cm²) conditions.

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Pascal:13-0098742

Le document en format XML

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<author><name sortKey="Lee, Woo Hyung" uniqKey="Lee W">Woo-Hyung Lee</name>
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<country>Corée du Sud</country>
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<author><name sortKey="Lee, Sang Kyu" uniqKey="Lee S">Sang-Kyu Lee</name>
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<author><name sortKey="Shin, Won Suk" uniqKey="Shin W">Won-Suk Shin</name>
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<author><name sortKey="Moon, Sang Jin" uniqKey="Moon S">Sang-Jin Moon</name>
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<author><name sortKey="Lee, Soo Hyoung" uniqKey="Lee S">Soo-Hyoung Lee</name>
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<s2>Jeonju</s2>
<s3>KOR</s3>
<sZ>5 aut.</sZ>
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<country>Corée du Sud</country>
<wicri:noRegion>Jeonju</wicri:noRegion>
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</author>
<author><name sortKey="Kang, In Nam" uniqKey="Kang I">In-Nam Kang</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Chemistry, The Catholic University of Korea</s1>
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<s3>KOR</s3>
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<term>Comparative study</term>
<term>Conjugated polymer</term>
<term>Copolymer</term>
<term>Electrochemical properties</term>
<term>Electron donor</term>
<term>Ester</term>
<term>Field effect transistor</term>
<term>Film formation</term>
<term>Fullerene compounds</term>
<term>Growth from solution</term>
<term>Hole mobility</term>
<term>Indium oxide</term>
<term>Morphology</term>
<term>Optical properties</term>
<term>Organic solar cells</term>
<term>Photovoltaic cell</term>
<term>Photovoltaic system</term>
<term>Solubility</term>
<term>Styrenesulfonate polymer</term>
<term>Thermal stability</term>
<term>Thin film transistor</term>
<term>Thiophene derivative polymer</term>
<term>Visible spectrum</term>
<term>p type semiconductor</term>
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<term>Polymère conjugué</term>
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<term>Propriété optique</term>
<term>Propriété électrochimique</term>
<term>Mobilité trou</term>
<term>Microscopie force atomique</term>
<term>Morphologie</term>
<term>Solubilité</term>
<term>Formation film</term>
<term>Stabilité thermique</term>
<term>Spectre visible</term>
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<term>Spectre absorption</term>
<term>Etude comparative</term>
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<term>Méthode en solution</term>
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<term>Copolymère</term>
<term>Acide butyrique</term>
<term>Ester</term>
<term>Composé du fullerène</term>
<term>Oxyde d'indium</term>
<term>Styrènesulfonate polymère</term>
<term>Thiophène dérivé polymère</term>
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<front><div type="abstract" xml:lang="en">A new conjugated polymer containing pentaselenophene (5Se) electron donor moieties was designed for use in polymer solar cells and synthesized via a Stille coupling reaction. The structure, optical properties, electrochemical properties, hole mobility, photovoltaic properties, and AFM morphology of the homopolymer (P5Se) and the donor-acceptor copolymer (P5SeDTDPP) with a diketopyrrolopyrrole (DPP) acceptor were investigated and are discussed. The polymers showed good solubility, film-forming properties, and thermal stabilities. P5Se exhibited a broad absorption across the visible range, 400-700 nm, which is a prerequisite for photovoltaic applications. P5SeDTDPP yielded a broader absorption spectrum, enhanced π-π interactions, and a lower band gap compared to P5Se, due to the enhanced intramolecular charge transfer interactions between the donating moiety (pentaselenophene) and the DPP accepting moiety. Solution-processed field effect transistors fabricated from these polymers displayed p-type organic thin film transistor characteristics. P5Se and P5SeDTDPP exhibited typical p-type organic semiconductor characteristics with hole mobilities of 2.3 × 10<sup>-3</sup>
 and 1.2 x 10-<sup>2</sup>
 cm<sup>2</sup>
 V<sup>-1</sup>
 s<sup>-1</sup>
, respectively. Photovoltaic devices were fabricated using polymer:PCBM blends in ITO/PEDOT:PSS/blend/Al structures. The P5SeDTDPP device exhibited an open circuit voltage (V<sub>OC</sub>
) of 0.44 V, a short circuit current (J<sub>SC</sub>
) of 10.67 mA/cm<sup>2</sup>
, a fill factor (FF) of 0.51, and a power conversion efficiency (PCE) of 2.40% under AM 1.5 G (100 mW/cm<sup>2</sup>
) conditions.</div>
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<fA08 i1="01" i2="1" l="ENG"><s1>Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells</s1>
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<fA11 i1="01" i2="1"><s1>LEE (Woo-Hyung)</s1>
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<fA11 i1="02" i2="1"><s1>LEE (Sang-Kyu)</s1>
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<fA11 i1="03" i2="1"><s1>SHIN (Won-Suk)</s1>
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<fA11 i1="05" i2="1"><s1>LEE (Soo-Hyoung)</s1>
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<fA11 i1="06" i2="1"><s1>KANG (In-Nam)</s1>
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<fA14 i1="01"><s1>Department of Chemistry, The Catholic University of Korea</s1>
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<sZ>3 aut.</sZ>
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<fC01 i1="01" l="ENG"><s0>A new conjugated polymer containing pentaselenophene (5Se) electron donor moieties was designed for use in polymer solar cells and synthesized via a Stille coupling reaction. The structure, optical properties, electrochemical properties, hole mobility, photovoltaic properties, and AFM morphology of the homopolymer (P5Se) and the donor-acceptor copolymer (P5SeDTDPP) with a diketopyrrolopyrrole (DPP) acceptor were investigated and are discussed. The polymers showed good solubility, film-forming properties, and thermal stabilities. P5Se exhibited a broad absorption across the visible range, 400-700 nm, which is a prerequisite for photovoltaic applications. P5SeDTDPP yielded a broader absorption spectrum, enhanced π-π interactions, and a lower band gap compared to P5Se, due to the enhanced intramolecular charge transfer interactions between the donating moiety (pentaselenophene) and the DPP accepting moiety. Solution-processed field effect transistors fabricated from these polymers displayed p-type organic thin film transistor characteristics. P5Se and P5SeDTDPP exhibited typical p-type organic semiconductor characteristics with hole mobilities of 2.3 × 10<sup>-3</sup>
 and 1.2 x 10-<sup>2</sup>
 cm<sup>2</sup>
 V<sup>-1</sup>
 s<sup>-1</sup>
, respectively. Photovoltaic devices were fabricated using polymer:PCBM blends in ITO/PEDOT:PSS/blend/Al structures. The P5SeDTDPP device exhibited an open circuit voltage (V<sub>OC</sub>
) of 0.44 V, a short circuit current (J<sub>SC</sub>
) of 10.67 mA/cm<sup>2</sup>
, a fill factor (FF) of 0.51, and a power conversion efficiency (PCE) of 2.40% under AM 1.5 G (100 mW/cm<sup>2</sup>
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<fC02 i1="01" i2="X"><s0>001D06C02D1</s0>
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<fC02 i1="02" i2="X"><s0>001D06C02D2</s0>
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<fC02 i1="03" i2="X"><s0>001D05I03D</s0>
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<fC02 i1="04" i2="X"><s0>230</s0>
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<s5>01</s5>
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<s5>03</s5>
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<s5>05</s5>
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<s5>05</s5>
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<s5>06</s5>
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<s5>06</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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<s5>10</s5>
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<s5>10</s5>
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<s5>11</s5>
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<s5>11</s5>
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<s5>16</s5>
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<s5>16</s5>
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<s5>18</s5>
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<s5>18</s5>
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<s5>20</s5>
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<s5>20</s5>
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<fC03 i1="20" i2="X" l="SPA"><s0>Transistor capa delgada</s0>
<s5>20</s5>
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<s5>21</s5>
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<s5>21</s5>
</fC03>
<fC03 i1="21" i2="X" l="SPA"><s0>Dispositivo fotovoltaico</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>Acide butyrique</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="23" i2="X" l="ENG"><s0>Butyric acid</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="23" i2="X" l="SPA"><s0>Butírico ácido</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="24" i2="X" l="FRE"><s0>Ester</s0>
<s5>24</s5>
</fC03>
<fC03 i1="24" i2="X" l="ENG"><s0>Ester</s0>
<s5>24</s5>
</fC03>
<fC03 i1="24" i2="X" l="SPA"><s0>Ester</s0>
<s5>24</s5>
</fC03>
<fC03 i1="25" i2="3" l="FRE"><s0>Composé du fullerène</s0>
<s5>25</s5>
</fC03>
<fC03 i1="25" i2="3" l="ENG"><s0>Fullerene compounds</s0>
<s5>25</s5>
</fC03>
<fC03 i1="26" i2="X" l="FRE"><s0>Oxyde d'indium</s0>
<s5>26</s5>
</fC03>
<fC03 i1="26" i2="X" l="ENG"><s0>Indium oxide</s0>
<s5>26</s5>
</fC03>
<fC03 i1="26" i2="X" l="SPA"><s0>Indio óxido</s0>
<s5>26</s5>
</fC03>
<fC03 i1="27" i2="X" l="FRE"><s0>Styrènesulfonate polymère</s0>
<s2>NK</s2>
<s5>27</s5>
</fC03>
<fC03 i1="27" i2="X" l="ENG"><s0>Styrenesulfonate polymer</s0>
<s2>NK</s2>
<s5>27</s5>
</fC03>
<fC03 i1="27" i2="X" l="SPA"><s0>Estireno sulfonato polímero</s0>
<s2>NK</s2>
<s5>27</s5>
</fC03>
<fC03 i1="28" i2="X" l="FRE"><s0>Thiophène dérivé polymère</s0>
<s2>NK</s2>
<s5>28</s5>
</fC03>
<fC03 i1="28" i2="X" l="ENG"><s0>Thiophene derivative polymer</s0>
<s2>NK</s2>
<s5>28</s5>
</fC03>
<fC03 i1="28" i2="X" l="SPA"><s0>Tiofeno derivado polímero</s0>
<s2>NK</s2>
<s5>28</s5>
</fC03>
<fC03 i1="29" i2="X" l="FRE"><s0>ITO</s0>
<s4>INC</s4>
<s5>82</s5>
</fC03>
<fN21><s1>070</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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   |wiki=   *** parameter Area/wikiCode missing *** 
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   |texte=   Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells
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Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells

Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells

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