New 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI)-based small molecule semiconductors for organic solar cells. Issue 21 (18th May 2017)
- Record Type:
- Journal Article
- Title:
- New 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI)-based small molecule semiconductors for organic solar cells. Issue 21 (18th May 2017)
- Main Title:
- New 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI)-based small molecule semiconductors for organic solar cells
- Authors:
- Le Borgne, Mylène
Quinn, Jesse
Martin, Jaime
Stingelin, Natalie
Li, Yuning
Wantz, Guillaume - Abstract:
- Abstract : A series of donor–acceptor–donor (D–A–D) organic semiconductors, with 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI) as building block coupled with various end-capping moieties were synthesized and characterized for use in solar cells. Abstract : A series of new donor–acceptor–donor (D–A–D) small-molecule compounds, with 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI) as an electron acceptor building block coupled with various electron donor end-capping moieties (thiophene, bithiophene and benzofuran), were synthesized and characterized. When the fused-ring benzofuran is combined to EBI (EBI-BF ), the molecules displayed a perfectly planar conformation and afforded the best charge transport properties among these EBI compounds with a hole mobility of up to 0.02 cm 2 V −1 s −1 . All EBI-based small molecules were used as donor material along with a PC61 BM acceptor for the fabrication of solution-processed bulk-heterojunction (BHJ) solar cells. The best performing photovoltaic devices are based on the EBI derivative using the bithiophene end-capping moiety (EBI-2T ) with a maximum power conversion efficiency (PCE) of 1.92%, owing to the broad absorption spectra ofEBI-2T and the appropriate morphology of the BHJ. With the aim of establishing a correlation between the molecular structure and the thin film morphology, differential scanning calorimetry, atomic force microscopy and X-ray diffraction analysis were performed on neat and blend films of eachAbstract : A series of donor–acceptor–donor (D–A–D) organic semiconductors, with 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI) as building block coupled with various end-capping moieties were synthesized and characterized for use in solar cells. Abstract : A series of new donor–acceptor–donor (D–A–D) small-molecule compounds, with 3, 3′-(ethane-1, 2-diylidene)bis(indolin-2-one) (EBI) as an electron acceptor building block coupled with various electron donor end-capping moieties (thiophene, bithiophene and benzofuran), were synthesized and characterized. When the fused-ring benzofuran is combined to EBI (EBI-BF ), the molecules displayed a perfectly planar conformation and afforded the best charge transport properties among these EBI compounds with a hole mobility of up to 0.02 cm 2 V −1 s −1 . All EBI-based small molecules were used as donor material along with a PC61 BM acceptor for the fabrication of solution-processed bulk-heterojunction (BHJ) solar cells. The best performing photovoltaic devices are based on the EBI derivative using the bithiophene end-capping moiety (EBI-2T ) with a maximum power conversion efficiency (PCE) of 1.92%, owing to the broad absorption spectra ofEBI-2T and the appropriate morphology of the BHJ. With the aim of establishing a correlation between the molecular structure and the thin film morphology, differential scanning calorimetry, atomic force microscopy and X-ray diffraction analysis were performed on neat and blend films of each material. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 5:Issue 21(2017)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 5:Issue 21(2017)
- Issue Display:
- Volume 5, Issue 21 (2017)
- Year:
- 2017
- Volume:
- 5
- Issue:
- 21
- Issue Sort Value:
- 2017-0005-0021-0000
- Page Start:
- 5143
- Page End:
- 5153
- Publication Date:
- 2017-05-18
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7tc00711f ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4599.xml