Acceptor-Substituted S,N-Heteropentacenes of Different Conjugation Length: Structure-Property Relationships and Solar Cell Performance
The synthesis, optoelectronic, and photovoltaic properties of novel acceptor–donor–acceptor (A–D–A) based π‐conjugated functional molecules 1–3, comprising a planar S,N‐heteropentacene as central donor substituted with various terminal acceptor units, such as 1,1‐dicyanovinylene (DCV) and 1‐(1,1‐dic...
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Published in | Advanced functional materials Vol. 25; no. 22; pp. 3414 - 3424 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Blackwell Publishing Ltd
01.06.2015
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Subjects | |
Online Access | Get full text |
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Abstract | The synthesis, optoelectronic, and photovoltaic properties of novel acceptor–donor–acceptor (A–D–A) based π‐conjugated functional molecules 1–3, comprising a planar S,N‐heteropentacene as central donor substituted with various terminal acceptor units, such as 1,1‐dicyanovinylene (DCV) and 1‐(1,1‐dicyanomethylene)‐cyclohex‐2‐ene (DCC), are reported. The structural variation of the end groups provides molecules 1–3 with gradually increased π‐conjugation due to a rising number of double bonds, which comes from the DCC unit(s). From optoelectronic investigation, structure–property relationships are deduced and the novel A–D–A heteropentacenes 1–3 are implemented as photoactive donor component in solution‐processed bulk heterojunction solar cells together with [6,6]‐phenyl‐C61‐butyric acid methyl ester as acceptor. The structural variation in the S,N‐heteropentacenes leads to clear trends in the photovoltaic performance and power conversion efficiencies of up to 4.9% are achieved. Furthermore, due to extension of the double bonds a clear trade‐off between the open circuit voltage (V
OC) and the short circuit current density (J
SC) values is observed. The role of additives on the optimization of the nanoscale morphology and device performance is investigated. The findings presented herein demonstrate that depending on the types of materials the additive may have significantly different effects on the active layer morphology and the device performance.
A new class of A–D–A‐type molecular donor materials based on S,N‐heteropentacene is developed for incorporation into solution‐processed bulk heterojunction solar cells providing promising power conversion efficiencies of 3.1–4.9%. The extension of the π‐system and increase in the highest occupied molecular orbital energy level provide direct correlation for the improved short circuit current (J
SC) and decreased open circuit voltage (V
OC) values. |
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AbstractList | The synthesis, optoelectronic, and photovoltaic properties of novel acceptor-donor-acceptor (A-D-A) based pi -conjugated functional molecules 1-3, comprising a planar S,N-heteropentacene as central donor substituted with various terminal acceptor units, such as 1,1-dicyanovinylene (DCV) and 1-(1,1-dicyanomethylene)-cyclohex-2-ene (DCC), are reported. The structural variation of the end groups provides molecules 1-3 with gradually increased pi -conjugation due to a rising number of double bonds, which comes from the DCC unit(s). From optoelectronic investigation, structure-property relationships are deduced and the novel A-D-A heteropentacenes 1-3 are implemented as photoactive donor component in solution-processed bulk heterojunction solar cells together with [6,6]-phenyl-C sub(61)-butyric acid methyl ester as acceptor. The structural variation in the S,N-heteropentacenes leads to clear trends in the photovoltaic performance and power conversion efficiencies of up to 4.9% are achieved. Furthermore, due to extension of the double bonds a clear trade-off between the open circuit voltage (V sub(OC)) and the short circuit current density (J sub(SC)) values is observed. The role of additives on the optimization of the nanoscale morphology and device performance is investigated. The findings presented herein demonstrate that depending on the types of materials the additive may have significantly different effects on the active layer morphology and the device performance. A new class of A-D-A-type molecular donor materials based on S,N-heteropentacene is developed for incorporation into solution-processed bulk heterojunction solar cells providing promising power conversion efficiencies of 3.1-4.9%. The extension of the pi -system and increase in the highest occupied molecular orbital energy level provide direct correlation for the improved short circuit current (J sub(SC)) and decreased open circuit voltage (V sub(OC)) values. The synthesis, optoelectronic, and photovoltaic properties of novel acceptor–donor–acceptor (A–D–A) based π‐conjugated functional molecules 1 – 3, comprising a planar S,N ‐heteropentacene as central donor substituted with various terminal acceptor units, such as 1,1‐dicyanovinylene (DCV) and 1‐(1,1‐dicyanomethylene)‐cyclohex‐2‐ene (DCC), are reported. The structural variation of the end groups provides molecules 1 – 3 with gradually increased π‐conjugation due to a rising number of double bonds, which comes from the DCC unit(s). From optoelectronic investigation, structure–property relationships are deduced and the novel A–D–A heteropentacenes 1 – 3 are implemented as photoactive donor component in solution‐processed bulk heterojunction solar cells together with [6,6]‐phenyl‐C 61 ‐butyric acid methyl ester as acceptor. The structural variation in the S,N ‐heteropentacenes leads to clear trends in the photovoltaic performance and power conversion efficiencies of up to 4.9% are achieved. Furthermore, due to extension of the double bonds a clear trade‐off between the open circuit voltage ( V OC ) and the short circuit current density ( J SC ) values is observed. The role of additives on the optimization of the nanoscale morphology and device performance is investigated. The findings presented herein demonstrate that depending on the types of materials the additive may have significantly different effects on the active layer morphology and the device performance. The synthesis, optoelectronic, and photovoltaic properties of novel acceptor–donor–acceptor (A–D–A) based π‐conjugated functional molecules 1–3, comprising a planar S,N‐heteropentacene as central donor substituted with various terminal acceptor units, such as 1,1‐dicyanovinylene (DCV) and 1‐(1,1‐dicyanomethylene)‐cyclohex‐2‐ene (DCC), are reported. The structural variation of the end groups provides molecules 1–3 with gradually increased π‐conjugation due to a rising number of double bonds, which comes from the DCC unit(s). From optoelectronic investigation, structure–property relationships are deduced and the novel A–D–A heteropentacenes 1–3 are implemented as photoactive donor component in solution‐processed bulk heterojunction solar cells together with [6,6]‐phenyl‐C61‐butyric acid methyl ester as acceptor. The structural variation in the S,N‐heteropentacenes leads to clear trends in the photovoltaic performance and power conversion efficiencies of up to 4.9% are achieved. Furthermore, due to extension of the double bonds a clear trade‐off between the open circuit voltage (V OC) and the short circuit current density (J SC) values is observed. The role of additives on the optimization of the nanoscale morphology and device performance is investigated. The findings presented herein demonstrate that depending on the types of materials the additive may have significantly different effects on the active layer morphology and the device performance. A new class of A–D–A‐type molecular donor materials based on S,N‐heteropentacene is developed for incorporation into solution‐processed bulk heterojunction solar cells providing promising power conversion efficiencies of 3.1–4.9%. The extension of the π‐system and increase in the highest occupied molecular orbital energy level provide direct correlation for the improved short circuit current (J SC) and decreased open circuit voltage (V OC) values. |
Author | Kast, Hannelore Schulz, Gisela L. Mishra, Amaresh Urdanpilleta, Marta Bäuerle, Peter Mena-Osteritz, Elena |
Author_xml | – sequence: 1 givenname: Hannelore surname: Kast fullname: Kast, Hannelore organization: Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany – sequence: 2 givenname: Amaresh surname: Mishra fullname: Mishra, Amaresh email: amaresh.mishra@uni-ulm.de organization: Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany – sequence: 3 givenname: Gisela L. surname: Schulz fullname: Schulz, Gisela L. organization: Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany – sequence: 4 givenname: Marta surname: Urdanpilleta fullname: Urdanpilleta, Marta organization: Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany – sequence: 5 givenname: Elena surname: Mena-Osteritz fullname: Mena-Osteritz, Elena organization: Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany – sequence: 6 givenname: Peter surname: Bäuerle fullname: Bäuerle, Peter email: amaresh.mishra@uni-ulm.de organization: Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany |
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Snippet | The synthesis, optoelectronic, and photovoltaic properties of novel acceptor–donor–acceptor (A–D–A) based π‐conjugated functional molecules 1–3, comprising a... The synthesis, optoelectronic, and photovoltaic properties of novel acceptor–donor–acceptor (A–D–A) based π‐conjugated functional molecules 1 – 3, comprising a... The synthesis, optoelectronic, and photovoltaic properties of novel acceptor-donor-acceptor (A-D-A) based pi -conjugated functional molecules 1-3, comprising a... |
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SubjectTerms | Additives bulk heterojunction solar cells Devices Energy conversion efficiency heteroacenes Heterojunctions Morphology Open circuit voltage Photovoltaic cells Solar cells solution processing structure-property relationship |
Title | Acceptor-Substituted S,N-Heteropentacenes of Different Conjugation Length: Structure-Property Relationships and Solar Cell Performance |
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