A non-fullerene electron acceptor modified by thiophene-2-carbonitrile for solution-processed organic solar cells. Issue 10 (15th February 2016)
- Record Type:
- Journal Article
- Title:
- A non-fullerene electron acceptor modified by thiophene-2-carbonitrile for solution-processed organic solar cells. Issue 10 (15th February 2016)
- Main Title:
- A non-fullerene electron acceptor modified by thiophene-2-carbonitrile for solution-processed organic solar cells
- Authors:
- Li, Shuixing
Yan, Jielin
Li, Chang-Zhi
Liu, Feng
Shi, Minmin
Chen, Hongzheng
Russell, Thomas P. - Abstract:
- Abstract : An effective strategy to obtain a non-fullerene acceptor with good absorption and high electron mobility by introducing thiophene-2-carbonitrile groups. Abstract : Effective electron acceptor materials usually have a deep lowest unoccupied molecular orbital (LUMO) energy level that can split excitons and generate current. A non-fullerene electron acceptor (F8-DPPTCN) was developed, using fluorene as the core with arms of diketopyrrolopyrrole (DPP) having thiophene-2-carbonitrile as the terminal units. The new molecule had a LUMO of −3.65 eV and a narrow bandgap (Eg ) of 1.66 eV, owing to the electronegativity of the thiophene-2-carbonitrile group and its conjugation with DPP units. Organic solar cells (OSCs) with F8-DPPTCN as the acceptor and poly(3-hexylthiophene) (P3HT) as the donor were fabricated. A power conversion efficiency (PCE) of 2.37% was obtained with an open-circuit voltage ( V oc ) of 0.97 V, a short-circuit current ( J sc ) of 6.25 mA cm −2, and a fill factor (FF) of 0.39. Structural characterization showed that P3HT and F8-DPPTCN were kinetically trapped in a weakly separated state whereas thermal annealing led to the crystallization of P3HT and the formation of a network structure with a mesh-size of several hundred nanometers. When a solvent additive, diiodooctane, was used and the mixture was thermally annealed, both P3HT and F8-DPPTCN crystallized and a multi-length scale network was formed. Though the PCEs were low, the changes in the PCEAbstract : An effective strategy to obtain a non-fullerene acceptor with good absorption and high electron mobility by introducing thiophene-2-carbonitrile groups. Abstract : Effective electron acceptor materials usually have a deep lowest unoccupied molecular orbital (LUMO) energy level that can split excitons and generate current. A non-fullerene electron acceptor (F8-DPPTCN) was developed, using fluorene as the core with arms of diketopyrrolopyrrole (DPP) having thiophene-2-carbonitrile as the terminal units. The new molecule had a LUMO of −3.65 eV and a narrow bandgap (Eg ) of 1.66 eV, owing to the electronegativity of the thiophene-2-carbonitrile group and its conjugation with DPP units. Organic solar cells (OSCs) with F8-DPPTCN as the acceptor and poly(3-hexylthiophene) (P3HT) as the donor were fabricated. A power conversion efficiency (PCE) of 2.37% was obtained with an open-circuit voltage ( V oc ) of 0.97 V, a short-circuit current ( J sc ) of 6.25 mA cm −2, and a fill factor (FF) of 0.39. Structural characterization showed that P3HT and F8-DPPTCN were kinetically trapped in a weakly separated state whereas thermal annealing led to the crystallization of P3HT and the formation of a network structure with a mesh-size of several hundred nanometers. When a solvent additive, diiodooctane, was used and the mixture was thermally annealed, both P3HT and F8-DPPTCN crystallized and a multi-length scale network was formed. Though the PCEs were low, the changes in the PCE could be correlated with the morphological changes, opening pathways to increase performance further. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 10(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 10(2016)
- Issue Display:
- Volume 4, Issue 10 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 10
- Issue Sort Value:
- 2016-0004-0010-0000
- Page Start:
- 3777
- Page End:
- 3783
- Publication Date:
- 2016-02-15
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ta00056h ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2588.xml