Alkoxyphenyl-substituted carbazole-based metal-free organic dyes were synthesized and effectively used for dye-sensitized, visible-light-driven, photocatalytic hydrogen production. Photocatalytic hydrogen production was investigated using a TiO₂/dye/Pt structure with triethanolamine as the sacrificial reagent. The dye-loaded TiO₂ photocatalyst exhibited a high yield of hydrogen production when the length of the alkoxy chain was long enough to sufficiently improve the hydrophobicity at the interface between the dye-loaded TiO₂ and the water medium. In the alkoxyphenyl-substituted carbazole dyes, the dye with the longest alkoxy chain (C22) exhibited the best hydrogen production performance, but it had a yield only slightly better than that of the dye with the second longest chain length (C16). The dye C22 displayed a turnover number (TON) of 3094 after 24 h of visible light irradiation (>420 nm). However, the compound with no hydrophobic substituent (C1), exhibited the lowest hydrogen production performance with a TON of 1497. Thus, a 207% increase in the hydrogen production yield was observed when hydrophobic substituents were present. Analysis of time-resolved absorption spectra, impedance spectra and incident photon conversion efficiency spectra revealed that the alkoxy chain has a hydrophobic effect at the interface between the dye-loaded TiO₂ and the water. Specifically, the hydrophobicity of the dye improved the charge-recombination lifetime for electron injection from the dye into the TiO₂ surface in the water for hydrogen production.