Impact of strength and size of donors on the optoelectronic properties of D–π–A sensitizers. Issue 44 (15th April 2016)
- Record Type:
- Journal Article
- Title:
- Impact of strength and size of donors on the optoelectronic properties of D–π–A sensitizers. Issue 44 (15th April 2016)
- Main Title:
- Impact of strength and size of donors on the optoelectronic properties of D–π–A sensitizers
- Authors:
- Sivanadanam, J.
Ganesan, P.
Gao, Peng
Nazeeruddin, Md. K.
Emeline, Alexei
Bahnemann, Detlef
Rajalingam, R. - Abstract:
- Abstract : A series of carbazole based sensitizers have been synthesized to understand the influence of the strength of the donor moiety on the optical, electrochemical and photovoltaic properties. Abstract : A series of carbazole based sensitizers with either phenyl based donors (TBC, TMC, OMC, PC, TBR, TMR, OMR andPR ) or aryl amine based donors (OMNC, CNC andHNC ) as well as one without a donor group (CC ) have been synthesized to understand the influence of the strength of the donor moiety on the optical, electrochemical and photovoltaic properties. Two different acceptor moieties such as cyano acrylic acid and rhodanine acetic acid were introduced and evaluated. Different substituents on the phenyl group have a significant impact on the light harvesting ability of the sensitizers. Among phenyl based donors, anisole based carbazole (OMC ) shows the highest short circuit current ( J SC ) of 4.96 mA cm −2 with overall power conversion efficiency (PCE) of 2.69%. In the case of the sensitizers with aryl amine based donors, the increasing bulkiness of the donor group lead to increasing open circuit potential. Transient photocurrent and photovoltage measurements signify the importance of a bulky donor fragment in determining the open circuit potential of the dyes. Sensitizers with hexyloxy substituted phenyl amine as the donor group shows a J SC of 6.84 mA cm −2 with PCE of 3.33%. The overall investigation provides vital information about the influence of donor groups on theAbstract : A series of carbazole based sensitizers have been synthesized to understand the influence of the strength of the donor moiety on the optical, electrochemical and photovoltaic properties. Abstract : A series of carbazole based sensitizers with either phenyl based donors (TBC, TMC, OMC, PC, TBR, TMR, OMR andPR ) or aryl amine based donors (OMNC, CNC andHNC ) as well as one without a donor group (CC ) have been synthesized to understand the influence of the strength of the donor moiety on the optical, electrochemical and photovoltaic properties. Two different acceptor moieties such as cyano acrylic acid and rhodanine acetic acid were introduced and evaluated. Different substituents on the phenyl group have a significant impact on the light harvesting ability of the sensitizers. Among phenyl based donors, anisole based carbazole (OMC ) shows the highest short circuit current ( J SC ) of 4.96 mA cm −2 with overall power conversion efficiency (PCE) of 2.69%. In the case of the sensitizers with aryl amine based donors, the increasing bulkiness of the donor group lead to increasing open circuit potential. Transient photocurrent and photovoltage measurements signify the importance of a bulky donor fragment in determining the open circuit potential of the dyes. Sensitizers with hexyloxy substituted phenyl amine as the donor group shows a J SC of 6.84 mA cm −2 with PCE of 3.33%. The overall investigation provides vital information about the influence of donor groups on the optoelectronic properties of the sensitizers for its photovoltaic applications. … (more)
- Is Part Of:
- RSC advances. Volume 6:Issue 44(2016)
- Journal:
- RSC advances
- Issue:
- Volume 6:Issue 44(2016)
- Issue Display:
- Volume 6, Issue 44 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 44
- Issue Sort Value:
- 2016-0006-0044-0000
- Page Start:
- 37347
- Page End:
- 37361
- Publication Date:
- 2016-04-15
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ra01185c ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
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- 1244.xml