Interfacial electron transfer (IET) dynamics in dyesensitized Sn x Ti 1−x O 2 (x = 0, 0.25, 0.50, 0.75, and 1) were investigated using ultrafast transient absorption spectroscopy, linear absorption spectroscopy, and DFT calculations. We found that altering the composition of Sn x Ti 1−x O 2 allows for monotonic tunability of the conduction band, altering both the driving force for forward IET and the electronic states of the conduction band involved in IET. IET from a prototypical ruthenium(II) polypyridyl dye sensitizer can be tuned by Sn x Ti 1−x O 2 by both modulating the absorption spectrum of the adsorbed dye and altering the electron acceptor states in the conduction band. Periodic DFT calculations show that incorporation of Ti d-character in the conduction band plays a crucial role in promoting ultrafast electron injection.