D–π–A type boron dipyrromethene (BODIPY) dye YH-1, which has two pyridyl groups as electron-withdrawing-anchoring groups at the end of the 3- and 5-positions and a carbazole-diphenylamine moiety as an electron donor at the 8-position on the BODIPY core, was designed and developed as a photosensitizer for dye-sensitized solar cells (DSSCs). It was found that the dye YH-1 possesses a good light-harvesting efficiency (LHE) in the red/near-IR (NIR) region and good adsorption ability on TiO₂ film. We demonstrate that the expansion of the π-conjugated system by the introduction of not only the carbazole-diphenylamine moiety and the thiophene unit at the 8-position but also two thienylpyridines at the 3- and 5-positions on the BODIPY core can lead to red-shift and broadening of the absorption band in the red/NIR region. DSSCs based on YH-1 exhibit incident photon-to-current conversion efficiency of ca. 10% over a range of 500 to 700 nm, with an onset at 800 nm.