Asymmetric double donor-π-acceptor dyes based on phenothiazine and carbazole donors for dye-sensitized solar cells. Issue 44 (2nd November 2017)
- Record Type:
- Journal Article
- Title:
- Asymmetric double donor-π-acceptor dyes based on phenothiazine and carbazole donors for dye-sensitized solar cells. Issue 44 (2nd November 2017)
- Main Title:
- Asymmetric double donor-π-acceptor dyes based on phenothiazine and carbazole donors for dye-sensitized solar cells
- Authors:
- Zhu, Bo-ye
Wu, Liang
Ye, Qin
Gao, Jian-rong
Han, Liang - Abstract:
- Abstract: Four organic dyes with asymmetric double donor-π-acceptor system were designed, synthesized and utilized in dye-sensitized solar cells (DSSCs), where phenothiazine and carbazole were introduced as double donors, butyl or octyl chain as the linker and cyanoacetic acid or rhodanine acetic acid as the electron acceptor. The design of double donor-π-acceptor system contributes to a distinctive increase of the molar extinction coefficient and benefits light-harvesting capability of these dyes. Due to superior electron injection efficiency, CPC-series dyes with cyanoacetic acid acceptor exhibit broader IPCE spectra and high IPCE responsive value compared with rhodanine-3-acetic acid acceptor, leading to higher J SC . Long alkyl chain favors antiaggregation effect and low charge recombination rate is observed for dyes with octyl chain which display higher V OC than those with butyl chain. Among four dyes, dye with octyl chain and cyanoacetic acid acceptor exhibits the highest short-circuit photocurrent density (9.64 mA cm −2 ) and open-circuit photovoltage (720 mV), leading to the best overall power conversion efficiency of 4.76%. Graphical abstract: Four organic dyes with asymmetric double donor-π-acceptors system based on phenothiazine and carbazole donors were designed, synthesized and utilized in dye-sensitized solar cells (DSSCs). Among four dyes, dye with octyl chain and cyanoacetic acid acceptor exhibits the highest short-circuit photocurrent density (9.64 mA cm −2Abstract: Four organic dyes with asymmetric double donor-π-acceptor system were designed, synthesized and utilized in dye-sensitized solar cells (DSSCs), where phenothiazine and carbazole were introduced as double donors, butyl or octyl chain as the linker and cyanoacetic acid or rhodanine acetic acid as the electron acceptor. The design of double donor-π-acceptor system contributes to a distinctive increase of the molar extinction coefficient and benefits light-harvesting capability of these dyes. Due to superior electron injection efficiency, CPC-series dyes with cyanoacetic acid acceptor exhibit broader IPCE spectra and high IPCE responsive value compared with rhodanine-3-acetic acid acceptor, leading to higher J SC . Long alkyl chain favors antiaggregation effect and low charge recombination rate is observed for dyes with octyl chain which display higher V OC than those with butyl chain. Among four dyes, dye with octyl chain and cyanoacetic acid acceptor exhibits the highest short-circuit photocurrent density (9.64 mA cm −2 ) and open-circuit photovoltage (720 mV), leading to the best overall power conversion efficiency of 4.76%. Graphical abstract: Four organic dyes with asymmetric double donor-π-acceptors system based on phenothiazine and carbazole donors were designed, synthesized and utilized in dye-sensitized solar cells (DSSCs). Among four dyes, dye with octyl chain and cyanoacetic acid acceptor exhibits the highest short-circuit photocurrent density (9.64 mA cm −2 ) and open-circuit photovoltage (720 mV), leading to the best overall power conversion efficiency of 4.76%. … (more)
- Is Part Of:
- Tetrahedron. Volume 73:Issue 44(2017)
- Journal:
- Tetrahedron
- Issue:
- Volume 73:Issue 44(2017)
- Issue Display:
- Volume 73, Issue 44 (2017)
- Year:
- 2017
- Volume:
- 73
- Issue:
- 44
- Issue Sort Value:
- 2017-0073-0044-0000
- Page Start:
- 6307
- Page End:
- 6315
- Publication Date:
- 2017-11-02
- Subjects:
- DSSC -- Asymmetric organic dyes -- Phenothiazine -- Carbazole -- Double donor-π-acceptor
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tet.2017.09.018 ↗
- Languages:
- English
- ISSNs:
- 0040-4020
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4767.xml