Indexed by:期刊论文

Date of Publication:2013-05-28

Journal:CHEMISTRY OF MATERIALS

Included Journals:SCIE、EI、ESI高被引论文、Scopus

Volume:25

Issue:10

Page Number:2146-2153

ISSN No.:0897-4756

Key Words:phenothiazine; dye-sensitized solar cells; pi-conjugation; aggregation; charge recombination

Abstract:A series of simple phenothiazine-based dyes have been synthesized, in which a cyanoacrylate acceptor directly attached to the C(3) position of phenothiazine, and an additional linear electron-rich (4-hexyloxy)phenyl group at C(7) on the opposite side of the acceptor, and an alkyl chain with different length at N(10) of the phenothiazine periphery are presented. The dye molecules have a linear shape which is favorable for the formation of a compact dye layer on the TiO2 surface, while their butterfly conformations can sufficiently inhibit molecular aggregation. Moreover, the structural features of (4-hexyloxy)phenyl donor moiety at the C(7) position of phenothiazine extends the pi-conjugation of the chromophore, thus enhancing the performance of dye-sensitized solar cells (DSSCs). Moreover, the alkyl substituents with different chain length at the N(10) atom of phenothiazine could further optimize the performance through completely shielding the surface of TiO2 from the I-/I3- electrolyte and subsequently reducing the leakage of dark current. Under simulated AM 1.5G irradiation, the PT-C6 based DSSC produces a short-circuit photocurrent of 15.32 mA cm(-2), an open-circuit photovoltage of 0.78 V, a fill factor of 0.69, corresponding to a power conversion efficiency (PCE) of 8.18%, which exceeds the reference N719 (7.73%) under identical fabrication conditions. Notably, the designed molecular structure represents the highest photovoltaic conversion efficiency value when compared with other reported phenothiazine-derived dyes.