Synthesis and Photovoltaic Properties of New Multifused Anthradithiophene‐Based Narrow‐Bandgap D–A Copolymers. Issue 13 (19th May 2014)
- Record Type:
- Journal Article
- Title:
- Synthesis and Photovoltaic Properties of New Multifused Anthradithiophene‐Based Narrow‐Bandgap D–A Copolymers. Issue 13 (19th May 2014)
- Main Title:
- Synthesis and Photovoltaic Properties of New Multifused Anthradithiophene‐Based Narrow‐Bandgap D–A Copolymers
- Authors:
- Liu, Qi‐Da
Peng, Rui‐Xiang
Chen, Shao‐Jie
Ai, Ling
Wang, She‐Yu
Liu, Zhi‐Yang
Ge, Zi‐Yi - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Three structurally novel donor–acceptor copolymers are synthesized and fully characterized using an anthradithiophene (ADT) derivative as the donor block. All of them exhibit broad absorption ranges and moderate hole and electron mobilities. The multifused ADT donor block makes them exhibit lower highest occupied molecular orbital (HOMO) energy levels than many reported benzodithiophene‐based polymers. Copolymer blends with [6, 6]‐phenyl C71 butyric acid methyl ester (PC<sub>71</sub>BM) as active layers are used to fabricate polymer solar cells (PSCs) and a variety of post‐treatment methods are employed to optimize the device performance. The conventional and inverted configuration devices are prepared to evaluate the photovoltaic properties. A maximum power conversion efficiency of 1.66% is achieved for the inverted‐configuration device. The improved efficiency is caused by the close energy alignment between the work function of MoO<sub>3</sub> and the HOMO energy levels of the copolymers, facilitating better charge transport and increased short‐circuit current density (<italic>J</italic><sub>sc</sub>) with the inverted devices. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pghnnq2214" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink"<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Three structurally novel donor–acceptor copolymers are synthesized and fully characterized using an anthradithiophene (ADT) derivative as the donor block. All of them exhibit broad absorption ranges and moderate hole and electron mobilities. The multifused ADT donor block makes them exhibit lower highest occupied molecular orbital (HOMO) energy levels than many reported benzodithiophene‐based polymers. Copolymer blends with [6, 6]‐phenyl C71 butyric acid methyl ester (PC<sub>71</sub>BM) as active layers are used to fabricate polymer solar cells (PSCs) and a variety of post‐treatment methods are employed to optimize the device performance. The conventional and inverted configuration devices are prepared to evaluate the photovoltaic properties. A maximum power conversion efficiency of 1.66% is achieved for the inverted‐configuration device. The improved efficiency is caused by the close energy alignment between the work function of MoO<sub>3</sub> and the HOMO energy levels of the copolymers, facilitating better charge transport and increased short‐circuit current density (<italic>J</italic><sub>sc</sub>) with the inverted devices. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pghnnq2214" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract> … (more)
- Is Part Of:
- Macromolecular chemistry and physics. Volume 215:Issue 13(2014:Jul.)
- Journal:
- Macromolecular chemistry and physics
- Issue:
- Volume 215:Issue 13(2014:Jul.)
- Issue Display:
- Volume 215, Issue 13 (2014)
- Year:
- 2014
- Volume:
- 215
- Issue:
- 13
- Issue Sort Value:
- 2014-0215-0013-0000
- Page Start:
- 1287
- Page End:
- 1296
- Publication Date:
- 2014-05-19
- Subjects:
- Polymers -- Periodicals
Polymerization -- Periodicals
Synthetic products -- Periodicals
Macromolecules -- Periodicals
547.7 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/macp.201400119 ↗
- Languages:
- English
- ISSNs:
- 1022-1352
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.398000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3264.xml