摘要

Two donor-pi-spacer-acceptor porphyrin dyes were synthesized for use in dye-sensitized solar cells. The dyes comprised the same donor (porphyrin derivative) consisting of 3,4,5-trimethoxybenzaldehyde and acceptor/anchoring group (carboxyl group) but varying pi-spacer consisting of a Schiff base structure. Each of the dyes displayed different adsorption behavior and coverage on the TiO2 surface. The porphyrin dyes P-Zn-BIA-COOH studied in this work exhibit red-shifted and broadened electronic spectra respect to the reference P-Zn-COOH as expected. By the introduction of Schiff base unit at the meso positions, the energy level of E-ox (excited-state oxidation potentials) is significantly shifted to the positive compared with the reference P-Zn-COOH, indicating a decreased HOMO-LUMO gap. The highest power conversion efficiency of the two dyes based on DSSCs reached 1.75% under AM 1.5 G irradiation.