Acene‐Modified Small‐Molecule Donors for Organic Photovoltaics. Issue 53 (20th August 2019)
- Record Type:
- Journal Article
- Title:
- Acene‐Modified Small‐Molecule Donors for Organic Photovoltaics. Issue 53 (20th August 2019)
- Main Title:
- Acene‐Modified Small‐Molecule Donors for Organic Photovoltaics
- Authors:
- Sung, Min Jae
Hong, Jisu
Cha, Hyojung
Jiang, Yifei
Park, Chan Eon
Durrant, James R.
An, Tae Kyu
Kwon, Soon‐Ki
Kim, Yun‐Hi - Abstract:
- Abstract: A series of acene‐modified small molecules have been designed and synthesized, and their photovoltaic characteristics were studied by using the small molecules in organic photovoltaics (OPVs). Different cores were introduced to modulate the conjugation lengths of the small molecules and the bulk heterojunction (BHJ) morphologies. Three small‐molecule donors were prepared, namely Ph‐TTR, Na‐TTR, and An‐TTR, which have phenyl, naphthalene, and anthracene moieties, respectively, as conjugated cores. These donors were synthesized in a few steps and exhibited favorable BHJ morphologies, thereby giving promising power conversion efficiencies (PCEs). The donors showed excellent miscibility with the acceptor PC71 BM, and the use of the additive 1, 8‐diiodooctane (DIO) led to a remarkable increase in crystallinity, thereby increasing the PCEs of their OPVs. Of the three donors, Na‐TTR showed the most efficient charge carrier generation and favorable molecular packing structures; hence, of the three types of devices tested, the Na‐TTR:PC71 BM devices exhibited the highest PCE, specifically 6.27 %, without pre‐ or post‐treatments. The promising PCEs achieved from these easily synthesized acene‐modified small molecules suggested that acene‐modified small molecules can be useful materials in OPVs. Abstract : Power conversion efficiencies : The morphologies and charge carrier dynamics of organic photovoltaics that incorporate new acene‐modified small molecules are studied (seeAbstract: A series of acene‐modified small molecules have been designed and synthesized, and their photovoltaic characteristics were studied by using the small molecules in organic photovoltaics (OPVs). Different cores were introduced to modulate the conjugation lengths of the small molecules and the bulk heterojunction (BHJ) morphologies. Three small‐molecule donors were prepared, namely Ph‐TTR, Na‐TTR, and An‐TTR, which have phenyl, naphthalene, and anthracene moieties, respectively, as conjugated cores. These donors were synthesized in a few steps and exhibited favorable BHJ morphologies, thereby giving promising power conversion efficiencies (PCEs). The donors showed excellent miscibility with the acceptor PC71 BM, and the use of the additive 1, 8‐diiodooctane (DIO) led to a remarkable increase in crystallinity, thereby increasing the PCEs of their OPVs. Of the three donors, Na‐TTR showed the most efficient charge carrier generation and favorable molecular packing structures; hence, of the three types of devices tested, the Na‐TTR:PC71 BM devices exhibited the highest PCE, specifically 6.27 %, without pre‐ or post‐treatments. The promising PCEs achieved from these easily synthesized acene‐modified small molecules suggested that acene‐modified small molecules can be useful materials in OPVs. Abstract : Power conversion efficiencies : The morphologies and charge carrier dynamics of organic photovoltaics that incorporate new acene‐modified small molecules are studied (see picture; PCBM=[6, 6]‐phenyl‐C61 ‐butyric acid methyl ester, PEDOT:PSS=poly(3, 4‐ethylenedioxythiophene)polystyrene sulfonate, ITO=indium tin oxide). … (more)
- Is Part Of:
- Chemistry. Volume 25:Issue 53(2019)
- Journal:
- Chemistry
- Issue:
- Volume 25:Issue 53(2019)
- Issue Display:
- Volume 25, Issue 53 (2019)
- Year:
- 2019
- Volume:
- 25
- Issue:
- 53
- Issue Sort Value:
- 2019-0025-0053-0000
- Page Start:
- 12316
- Page End:
- 12324
- Publication Date:
- 2019-08-20
- Subjects:
- acene-modified small molecules -- charge carriers -- conjugation -- crystallinity -- organic photovoltaic materials
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201902177 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11821.xml