Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells. Issue 102 (19th October 2016)
- Record Type:
- Journal Article
- Title:
- Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells. Issue 102 (19th October 2016)
- Main Title:
- Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells
- Authors:
- Patil, Yuvraj
Misra, Rajneesh
Chen, F. C.
Keshtov, M. L.
Sharma, Ganesh D. - Abstract:
- Abstract : Two small moleculesDPP3 (D–π–A) andDPP4 (D–π–A–π–D) with triphenylamine (TPA) donors and diketopyrrolopyrrole (DPP) acceptors linked with ethyne linkers were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. Abstract : Two small moleculesDPP3 (D–π–A) andDPP4 (D–π–A–π–D) with triphenylamine (TPA) donors and diketopyrrolopyrrole (DPP) acceptors linked with ethyne linkers were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. Their photonic, electronic, thermal and computational properties were investigated. The red shift in the electronic absorption spectra ofDPP4 as compared toDPP3 is related to extended conjugation and increased donor–acceptor interaction. We have usedDPP3 andDPP4 as electron donors along with PC71 BM as an electron acceptor for solution processed bulk heterojunction organic solar cells. The solar cells prepared fromDPP3 :PC71 BM andDPP4 :PC71 BM (1 : 2) processed from chloroform (CF) exhibit a power conversion efficiency (PCE) of 2.23% ( J sc = 6.74 mA cm −2, V oc = 0.92 V and FF = 0.36) and 3.05% ( J sc = 8.26 mA cm −2, V oc = 0.88 V and FF = 0.42), respectively. The higher PCE of the device withDPP4 compared toDPP3 was demonstrated as to the higher hole mobility and broader IPCE spectra. The devices based onDPP3 :PC71 BM andDPP4 :PC71 BM processed with solvent additive (1 v% DIO, 1, 8-diiodooctane) showed PCE values of 4.06% and 5.31%, respectively. The device optimization resultsAbstract : Two small moleculesDPP3 (D–π–A) andDPP4 (D–π–A–π–D) with triphenylamine (TPA) donors and diketopyrrolopyrrole (DPP) acceptors linked with ethyne linkers were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. Abstract : Two small moleculesDPP3 (D–π–A) andDPP4 (D–π–A–π–D) with triphenylamine (TPA) donors and diketopyrrolopyrrole (DPP) acceptors linked with ethyne linkers were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. Their photonic, electronic, thermal and computational properties were investigated. The red shift in the electronic absorption spectra ofDPP4 as compared toDPP3 is related to extended conjugation and increased donor–acceptor interaction. We have usedDPP3 andDPP4 as electron donors along with PC71 BM as an electron acceptor for solution processed bulk heterojunction organic solar cells. The solar cells prepared fromDPP3 :PC71 BM andDPP4 :PC71 BM (1 : 2) processed from chloroform (CF) exhibit a power conversion efficiency (PCE) of 2.23% ( J sc = 6.74 mA cm −2, V oc = 0.92 V and FF = 0.36) and 3.05% ( J sc = 8.26 mA cm −2, V oc = 0.88 V and FF = 0.42), respectively. The higher PCE of the device withDPP4 compared toDPP3 was demonstrated as to the higher hole mobility and broader IPCE spectra. The devices based onDPP3 :PC71 BM andDPP4 :PC71 BM processed with solvent additive (1 v% DIO, 1, 8-diiodooctane) showed PCE values of 4.06% and 5.31%, respectively. The device optimization results from the improvement of the balanced charge transport and better nanoscale morphology induced by the solvent additive. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 102(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 102(2016)
- Issue Display:
- Volume 6, Issue 102 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 102
- Issue Sort Value:
- 2016-0006-0102-0000
- Page Start:
- 99685
- Page End:
- 99694
- Publication Date:
- 2016-10-19
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ra10442h ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10.xml