Benzodithiophene‐Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo[3, 4‐c]pyrrole Derivatives for Polymer Solar Cells. Issue 9 (16th March 2015)
- Record Type:
- Journal Article
- Title:
- Benzodithiophene‐Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo[3, 4‐c]pyrrole Derivatives for Polymer Solar Cells. Issue 9 (16th March 2015)
- Main Title:
- Benzodithiophene‐Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo[3, 4‐c]pyrrole Derivatives for Polymer Solar Cells
- Authors:
- Tamilavan, Vellaiappillai
Roh, Kyung Hwan
Agneeswari, Rajalingam
Lee, Dal Yong
Cho, Shinuk
Jin, Youngeup
Park, Sung Heum
Hyun, Myung Ho - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Two benzodithiophene (BDT)‐based broad absorbing low band gap random copolymers, <bold>P1</bold> and <bold>P2</bold>, incorporating electron accepting imide functionalized pyrrolo[3, 4‐c]pyrrole‐1, 3‐dione (TDPPDT) and lactam functionalized pyrrolo[3, 4‐c]pyrrole‐1, 4‐dione (DKPP) derivatives are prepared. The copolymerization of differently alkylated two TDPPDT derivatives with both of BDT and DKPP offers random copolymers <bold>P1</bold> and <bold>P2</bold>. The absorption bands of polymers <bold>P1</bold> and <bold>P2</bold> cover the region from 300 to 900 nm and the estimated band gaps of <bold>P1</bold> and <bold>P2</bold> are 1.43 and 1.39 eV, respectively. The highest occupied molecular orbital energy levels of <bold>P1</bold> and <bold>P2</bold> are identical, at –5.25 eV. The organic field effect transistors made from <bold>P1</bold> and <bold>P2</bold> provide a hole mobility <italic>μ</italic> of 3.0 × 10<sup>−4</sup> and 3.6 × 10<sup>−5</sup> cm<sup>2</sup> V<sup>−1</sup> s<sup>−1</sup>, respectively. Polymer solar cells (PSCs) prepared from <bold>P1</bold> and <bold>P2</bold> afford a maximum power conversion efficiency of 1.64% and 2.14%, respectively. <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgjkt4bxm2" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></p> </abstract>
- Is Part Of:
- Macromolecular chemistry and physics. Volume 216:Issue 9(2015:May)
- Journal:
- Macromolecular chemistry and physics
- Issue:
- Volume 216:Issue 9(2015:May)
- Issue Display:
- Volume 216, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 216
- Issue:
- 9
- Issue Sort Value:
- 2015-0216-0009-0000
- Page Start:
- 996
- Page End:
- 1007
- Publication Date:
- 2015-03-16
- 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.201400614 ↗
- 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:
- 3853.xml