摘要： The rational design of porphyrin sensitizers is always crucial for dye-sensitized solar cells (DSSCs), since the change of only a single atom can have a signi?cant in?uence on the photovoltaic performance. We incorporated the pyridothiadiazole group, as a stronger electron-withdrawing group, into the commonly well-established skeleton of D-porphyrin-triple bond-acceptor sensitizers by a single atom change for a well-known strong electron-withdrawing benzothiadiazole (BTD) unit as an auxiliary acceptor. The impact of the pyridothiadiazole group on the optical; electrochemical; and photovoltaic properties of D–π–A porphyrin sensitizers was investigated with comparison for a benzothiadiazole-substituted SGT-020 porphyrin. The pyridothiadiazole-substituted SGT-024 porphyrin dye was red-shifted so that the absorption range might be expected to achieve higher light harvest ef?ciency (LHE) than the SGT-020 porphyrin. However, all the devices were fabricated by utilizing SGT-020 and SGT-024, evaluated and found to achieve a cell ef?ciency of 10.3% for SGT-020-based DSSC but 4.2% for SGT-024-based DSSC under standard global AM 1.5G solar light conditions. The main reason is the lower charge collection ef?ciency of SGT-024-based DSSC than SGT-020-based DSSC, which can be attributed to the tilted dye adsorption mode on the TiO2 photoanode. This may allow for faster charge recombination, which eventually leads to lower Jsc, Voc and power conversion ef?ciency (PCE).