Molecular Design of Coumarin Dyes for Efficient Dye-Sensitized Solar Cells

Citations Over TimeTop 1% of 2002 papers

Abstract

We have developed novel coumarin dyes for use in dye-sensitized nanocrystalline TiO2 solar cells (DSSCs). The absorption spectra of these novel coumarin dyes are red-shifted remarkably in the visible region relative to the spectrum of C343, a conventional coumarin dye. Introduction of a methine unit (−CHCH−) connecting both the cyano (−CN) and carboxyl (−COOH) groups into the coumarin framework expanded the π conjugation in the dye and thus resulted in a wide absorption in the visible region. These novel dyes performed as efficient photosensitizers for DSSCs. The monochromatic incident photon-to-current conversion efficiency (IPCE) from 420 to 600 nm for a DSSC based on NKX-2311 was over 70% with the maximum of 80% at 470 nm, which is almost equal to the efficiency obtained with the N3 dye system. The IPCE performance of DSSCs based on coumarin dyes depended remarkably on the LUMO levels of the dyes, which are estimated from the oxidation potential and 0−0 energy of the dye. The slow charge recombination, on the order of micro to milliseconds, between NKX-2311 cations and injected electrons in the conduction band of TiO2 (observed by transient absorption spectroscopy) resulted in efficient charge separation in this system. A HOMO−LUMO calculation indicated that the electron moves from the coumarin framework to the −CHCH− unit by photoexcitation of the dye (a π−π* transition). Our results strongly suggest that molecular design of the sensitizer is essential for the construction of highly efficient DSSCs. The structure of NKX-2311, whose carboxyl group is directly connected to the −CHCH− unit, is advantageous for effective electron injection from the dye into the conduction band of TiO2. In addition, the cyano group, owing to its strong electron-withdrawing ability, might play an important role in electron injection in addition to a red shift in the absorption region.

Related Papers

• → S1 and T1 species of .beta.-carotene generated by direct photoexcitation from the all-trans, 9-cis, 13-cis, and 15-cis isomers as revealed by picosecond transient absorption and transient Raman spectroscopies(1991)88 cited
• → Deep-Level Defect Effects on the Low-Temperature Photoexcitation Process in CdZnTe Crystals(2019)4 cited
• → Carrier photoexcitation from levels in quantum dots to states of the continuum in lasing(2001)6 cited
• → Potential Modulation of Semiconductor Dot Array System due to Photoexcitation(1999)3 cited
• → Potential modulation of a dot array system induced by pulsed photoexcitation(1999)