Monodispersed vs. polydispersed systems for bulk heterojunction solar cells: the case of dithienopyrrole/anthracene based materialsElectronic supplementary information (ESI) available: BHJ solar cell device tests at different blend compositions. See DOI: 10.1039/c2jm33795a
The article reports on the properties of a new class of arylene-ethynylene semiconductors incorporating anthracene and the bridged bithiophene dithienopyrrole. Two monodispersed structures were synthesised: the first with a dithienopyrrole core bound to two anthracenyl-ethynyl side groups namely the...
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container_end_page | 1976 |
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container_issue | 37 |
container_start_page | 19752 |
container_title | |
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creator | Grisorio, Roberto Allegretta, Giovanni Suranna, Gian Paolo Mastrorilli, Piero Loiudice, Anna Rizzo, Aurora Mazzeo, Marco Gigli, Giuseppe |
description | The article reports on the properties of a new class of arylene-ethynylene semiconductors incorporating anthracene and the bridged bithiophene dithienopyrrole. Two monodispersed structures were synthesised: the first with a dithienopyrrole core bound to two anthracenyl-ethynyl side groups namely the 2,6-bis(anthracen-9-ylethynyl)-4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole (
ADA
); in the second structure the anthracene core was functionalised with two dithienopyrrolylethynyl groups, obtaining 9,10-bis((4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrol-2-yl)ethynyl)anthracene (
DAD
). The properties of these materials were compared with those of the corresponding polymer: poly[4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole-2,6-diylethynylene-anthracen-9,10-diylethynylene] (
polyAD
). Devices employing PC
61
BM as an electron acceptor revealed that the monodispersed materials (
ADA
and
DAD
) were better performing than
polyAD
, seemingly due to the better homogeneity of the donor-acceptor blend, as revealed by AFM. The PCE value (1.3%) obtained with
DAD
ranks among the highest reported for non-polymeric small molecule-based BHJ solar cells constructed without the use of additives or annealing processes, thus demonstrating that ethynylene-containing electron-rich systems are promising donors for organic solar cell applications.
Monodispersed arylene-ethynylene semiconductors embodying anthracene and the bridged bithiophene dithienopyrrole perform unexpectedly better than the corresponding poly(arylene-ethynylene) in BHJ devices, reaching a PCE of 1.3%. |
doi_str_mv | 10.1039/c2jm33795a |
format | Article |
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H
-dithieno[3,2-
b
:2,3-
d
]pyrrole (
ADA
); in the second structure the anthracene core was functionalised with two dithienopyrrolylethynyl groups, obtaining 9,10-bis((4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrol-2-yl)ethynyl)anthracene (
DAD
). The properties of these materials were compared with those of the corresponding polymer: poly[4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole-2,6-diylethynylene-anthracen-9,10-diylethynylene] (
polyAD
). Devices employing PC
61
BM as an electron acceptor revealed that the monodispersed materials (
ADA
and
DAD
) were better performing than
polyAD
, seemingly due to the better homogeneity of the donor-acceptor blend, as revealed by AFM. The PCE value (1.3%) obtained with
DAD
ranks among the highest reported for non-polymeric small molecule-based BHJ solar cells constructed without the use of additives or annealing processes, thus demonstrating that ethynylene-containing electron-rich systems are promising donors for organic solar cell applications.
Monodispersed arylene-ethynylene semiconductors embodying anthracene and the bridged bithiophene dithienopyrrole perform unexpectedly better than the corresponding poly(arylene-ethynylene) in BHJ devices, reaching a PCE of 1.3%.</description><identifier>ISSN: 0959-9428</identifier><identifier>EISSN: 1364-5501</identifier><identifier>DOI: 10.1039/c2jm33795a</identifier><language>eng</language><creationdate>2012-08</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Grisorio, Roberto</creatorcontrib><creatorcontrib>Allegretta, Giovanni</creatorcontrib><creatorcontrib>Suranna, Gian Paolo</creatorcontrib><creatorcontrib>Mastrorilli, Piero</creatorcontrib><creatorcontrib>Loiudice, Anna</creatorcontrib><creatorcontrib>Rizzo, Aurora</creatorcontrib><creatorcontrib>Mazzeo, Marco</creatorcontrib><creatorcontrib>Gigli, Giuseppe</creatorcontrib><title>Monodispersed vs. polydispersed systems for bulk heterojunction solar cells: the case of dithienopyrrole/anthracene based materialsElectronic supplementary information (ESI) available: BHJ solar cell device tests at different blend compositions. See DOI: 10.1039/c2jm33795a</title><description>The article reports on the properties of a new class of arylene-ethynylene semiconductors incorporating anthracene and the bridged bithiophene dithienopyrrole. Two monodispersed structures were synthesised: the first with a dithienopyrrole core bound to two anthracenyl-ethynyl side groups namely the 2,6-bis(anthracen-9-ylethynyl)-4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole (
ADA
); in the second structure the anthracene core was functionalised with two dithienopyrrolylethynyl groups, obtaining 9,10-bis((4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrol-2-yl)ethynyl)anthracene (
DAD
). The properties of these materials were compared with those of the corresponding polymer: poly[4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole-2,6-diylethynylene-anthracen-9,10-diylethynylene] (
polyAD
). Devices employing PC
61
BM as an electron acceptor revealed that the monodispersed materials (
ADA
and
DAD
) were better performing than
polyAD
, seemingly due to the better homogeneity of the donor-acceptor blend, as revealed by AFM. The PCE value (1.3%) obtained with
DAD
ranks among the highest reported for non-polymeric small molecule-based BHJ solar cells constructed without the use of additives or annealing processes, thus demonstrating that ethynylene-containing electron-rich systems are promising donors for organic solar cell applications.
Monodispersed arylene-ethynylene semiconductors embodying anthracene and the bridged bithiophene dithienopyrrole perform unexpectedly better than the corresponding poly(arylene-ethynylene) in BHJ devices, reaching a PCE of 1.3%.</description><issn>0959-9428</issn><issn>1364-5501</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkM1Lw0AQxVdRsH4c9C6MNz20TZqmNT1WK60gHuq9bDcTsnWzs-xsC_nv3YJQQdDTwLzH770ZIW7SpJcmWdFXg02TZeMil8eik2ajYTfPk_REdJIiL7rFcPB4Js6ZN0mSpuNR3jm6fiNLpWaHnrGEHffAkWkPG245YMNQkYf11nxCjQE9bbZWBU0WmIz0oNAYnkCoEZRkBKqg1KHWaMm13pPBvrSh9lKhRVjLPbmREaSl4ZlBFTxZrYC3zhls0AbpW9A2pkbbPud-tlw8gNxJbeTa4ASm89cf4VDiTiuEgBwYZIjxVYU-giC6bQmKGkes96x44xIRnt8XE_j9uEtxWsVSePU9L8Tty-zjad71rFbO6yY2Wx3s2f_63V_6ypVV9gVCypGs</recordid><startdate>20120828</startdate><enddate>20120828</enddate><creator>Grisorio, Roberto</creator><creator>Allegretta, Giovanni</creator><creator>Suranna, Gian Paolo</creator><creator>Mastrorilli, Piero</creator><creator>Loiudice, Anna</creator><creator>Rizzo, Aurora</creator><creator>Mazzeo, Marco</creator><creator>Gigli, Giuseppe</creator><scope/></search><sort><creationdate>20120828</creationdate><title>Monodispersed vs. polydispersed systems for bulk heterojunction solar cells: the case of dithienopyrrole/anthracene based materialsElectronic supplementary information (ESI) available: BHJ solar cell device tests at different blend compositions. See DOI: 10.1039/c2jm33795a</title><author>Grisorio, Roberto ; Allegretta, Giovanni ; Suranna, Gian Paolo ; Mastrorilli, Piero ; Loiudice, Anna ; Rizzo, Aurora ; Mazzeo, Marco ; Gigli, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c2jm33795a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grisorio, Roberto</creatorcontrib><creatorcontrib>Allegretta, Giovanni</creatorcontrib><creatorcontrib>Suranna, Gian Paolo</creatorcontrib><creatorcontrib>Mastrorilli, Piero</creatorcontrib><creatorcontrib>Loiudice, Anna</creatorcontrib><creatorcontrib>Rizzo, Aurora</creatorcontrib><creatorcontrib>Mazzeo, Marco</creatorcontrib><creatorcontrib>Gigli, Giuseppe</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grisorio, Roberto</au><au>Allegretta, Giovanni</au><au>Suranna, Gian Paolo</au><au>Mastrorilli, Piero</au><au>Loiudice, Anna</au><au>Rizzo, Aurora</au><au>Mazzeo, Marco</au><au>Gigli, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monodispersed vs. polydispersed systems for bulk heterojunction solar cells: the case of dithienopyrrole/anthracene based materialsElectronic supplementary information (ESI) available: BHJ solar cell device tests at different blend compositions. See DOI: 10.1039/c2jm33795a</atitle><date>2012-08-28</date><risdate>2012</risdate><volume>22</volume><issue>37</issue><spage>19752</spage><epage>1976</epage><pages>19752-1976</pages><issn>0959-9428</issn><eissn>1364-5501</eissn><abstract>The article reports on the properties of a new class of arylene-ethynylene semiconductors incorporating anthracene and the bridged bithiophene dithienopyrrole. Two monodispersed structures were synthesised: the first with a dithienopyrrole core bound to two anthracenyl-ethynyl side groups namely the 2,6-bis(anthracen-9-ylethynyl)-4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole (
ADA
); in the second structure the anthracene core was functionalised with two dithienopyrrolylethynyl groups, obtaining 9,10-bis((4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrol-2-yl)ethynyl)anthracene (
DAD
). The properties of these materials were compared with those of the corresponding polymer: poly[4-(2-ethylhexyl)-4
H
-dithieno[3,2-
b
:2,3-
d
]pyrrole-2,6-diylethynylene-anthracen-9,10-diylethynylene] (
polyAD
). Devices employing PC
61
BM as an electron acceptor revealed that the monodispersed materials (
ADA
and
DAD
) were better performing than
polyAD
, seemingly due to the better homogeneity of the donor-acceptor blend, as revealed by AFM. The PCE value (1.3%) obtained with
DAD
ranks among the highest reported for non-polymeric small molecule-based BHJ solar cells constructed without the use of additives or annealing processes, thus demonstrating that ethynylene-containing electron-rich systems are promising donors for organic solar cell applications.
Monodispersed arylene-ethynylene semiconductors embodying anthracene and the bridged bithiophene dithienopyrrole perform unexpectedly better than the corresponding poly(arylene-ethynylene) in BHJ devices, reaching a PCE of 1.3%.</abstract><doi>10.1039/c2jm33795a</doi><tpages>9</tpages></addata></record> |
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title | Monodispersed vs. polydispersed systems for bulk heterojunction solar cells: the case of dithienopyrrole/anthracene based materialsElectronic supplementary information (ESI) available: BHJ solar cell device tests at different blend compositions. See DOI: 10.1039/c2jm33795a |
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