Pyrrolo[3, 2, 1-kl]phenothiazine-based D-π-A type organic dyes for efficient dye-sensitized solar cells. (April 2017)

• Record Type: Journal Article
• Authors: Li, Feng; Zhu, Yi-Zhou; Zhang, Shao-Chun; Gao, Huan-Huan; Pan, Bin; Zheng, Jian-Yu
• Is Part Of: Dyes and pigments. Volume 139(2017)
• Page Start: 292
• Page End: 299
• Publication Date: 2017-04
• Subjects: Dye-sensitized solar cells -- Organic dyes -- Pyrrolo[3, 2, 1-kl]phenothiazine -- Conjugated linker; Dyes and dyeing -- Periodicals; Pigments -- Periodicals; 667.2
• DOI: 10.1016/j.dyepig.2016.12.025
• Languages: English
• ISSNs: 0143-7208

Abstract

Abstract: Novel metal-free organic dyes based on polycyclic aromatic donor, pyrrolo[3, 2, 1-kl]phenothiazine, have been synthesized and applied in dye-sensitized solar cells. Combined with cyanoacrylic acid as the acceptor/anchoring group and simple π-spacers such as thiophene (JY40 ), furan (JY41 ), and terthiophene (JY42 ) as the conjugated linker, these dyes show good power conversion efficiency (PCE). The photophysical, electrochemical and photovoltaic properties, as well as theoretical calculations of these dyes were fully investigated. An attractive PCE up to 7.54%, with a short-circuit photocurrent density ( J sc ) of 17.76 mA cm −2, an open-circuit photovoltage ( V oc ) of 726 mV, and a fill factor (FF) of 0.58 has been achieved by theJY42 -based cell under standard AM 1.5 G irradiation in conjunction with an iodine electrolyte. Graphical abstract: Highlights: Three novel organic dyes with fused tetracyclic donor were designed for DSSCs. The nonplanar conformation of the dyes can impede dye aggregation. The effect of π-linkers on the photovoltaic properties of the dyes was evaluated. An attractive PCE up to 7.54% has been achieved.