Interaction of pyridine π-bridge-based poly(methacrylate) dyes for the fabrication of dye-sensitized solar cells with the influence of different strength phenothiazine, fluorene and anthracene sensitizers as donor units with new anchoring mode. (11th October 2018)
- Record Type:
- Journal Article
- Title:
- Interaction of pyridine π-bridge-based poly(methacrylate) dyes for the fabrication of dye-sensitized solar cells with the influence of different strength phenothiazine, fluorene and anthracene sensitizers as donor units with new anchoring mode. (11th October 2018)
- Main Title:
- Interaction of pyridine π-bridge-based poly(methacrylate) dyes for the fabrication of dye-sensitized solar cells with the influence of different strength phenothiazine, fluorene and anthracene sensitizers as donor units with new anchoring mode
- Authors:
- Prakash, Gopi
Subramanian, Kathavarayan - Abstract:
- Abstract : A simple and low-cost approach for the synthesis of three novel propeller-shaped (D2 )–π–A type organic polymer dyes has been developed; a new acceptor and π-bridge (PYN) were used to tune the photoelectric properties: DFT studies. Abstract : Herein, we report three new metal-free organic polymer sensitizers with the pyridine (PYN) π-bridge, having the structure (donor)2 –π–acceptor ((D2 )–π–A). They were labelled asPPNPP, FPNPP, andAPNPP due to the presence of a molecular framework, and used as photosensitizers for dye-sensitized solar cell (DSSC). Phenothiazine, fluorene and anthracene serve as the electron donor groups, nitrobenzene serves as the electron acceptor group, and pyridine serves as the π-bridge group. The detailed investigation of the relationship between the structure, thermal properties, electrochemical properties, and performance of DSSC is described herein. Furthermore, DFT studies were performed using the Gaussian 09 program with the B3LYP functional and 6-31G* basis set to evaluate their optimized geometry and HOMO–LUMO levels. The introduction of these three different donor units can drastically improve the sunlight-harvesting ability of DSSCs and the electron recombination, thus improving their performance. The polymerPPNPP shows a maximum power conversion efficiency (PCE, h) of 2.1%, which was achieved for the photovoltaic devices under AM 1.5 solar radiation (100 mW cm −2 ). With the addition of 10 mM CDCA as a co-adsorbent, the bestAbstract : A simple and low-cost approach for the synthesis of three novel propeller-shaped (D2 )–π–A type organic polymer dyes has been developed; a new acceptor and π-bridge (PYN) were used to tune the photoelectric properties: DFT studies. Abstract : Herein, we report three new metal-free organic polymer sensitizers with the pyridine (PYN) π-bridge, having the structure (donor)2 –π–acceptor ((D2 )–π–A). They were labelled asPPNPP, FPNPP, andAPNPP due to the presence of a molecular framework, and used as photosensitizers for dye-sensitized solar cell (DSSC). Phenothiazine, fluorene and anthracene serve as the electron donor groups, nitrobenzene serves as the electron acceptor group, and pyridine serves as the π-bridge group. The detailed investigation of the relationship between the structure, thermal properties, electrochemical properties, and performance of DSSC is described herein. Furthermore, DFT studies were performed using the Gaussian 09 program with the B3LYP functional and 6-31G* basis set to evaluate their optimized geometry and HOMO–LUMO levels. The introduction of these three different donor units can drastically improve the sunlight-harvesting ability of DSSCs and the electron recombination, thus improving their performance. The polymerPPNPP shows a maximum power conversion efficiency (PCE, h) of 2.1%, which was achieved for the photovoltaic devices under AM 1.5 solar radiation (100 mW cm −2 ). With the addition of 10 mM CDCA as a co-adsorbent, the best performing cells based on the polymer dyePPNPP exhibit an impressive conversion efficiency of 4.12% ( J sc = 7.23 mA cm 2, V oc = 0.76 V, FF = 69%). … (more)
- Is Part Of:
- New journal of chemistry. Volume 42:Number 22(2018)
- Journal:
- New journal of chemistry
- Issue:
- Volume 42:Number 22(2018)
- Issue Display:
- Volume 42, Issue 22 (2018)
- Year:
- 2018
- Volume:
- 42
- Issue:
- 22
- Issue Sort Value:
- 2018-0042-0022-0000
- Page Start:
- 17939
- Page End:
- 17949
- Publication Date:
- 2018-10-11
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c8nj04068k ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8443.xml