Tuning the functional properties of nanocrystals is an important issue in nanoscience. Here, we are able to tune the photocatalytic properties of SnO<SUB>2</SUB> nanocrystals by controlling their size and shape. A structural analysis was carried out by using X-ray diffraction (XRD)/Rietveld and transmission electron microscopy (TEM). The results reveal that the number of oxygen-related defects varies upon changing the size and shape of the nanocrystals, which eventually influences their photocatalytic properties. Time-resolved spectroscopic studies of the carrier relaxation dynamics of the SnO<SUB>2</SUB> nanocrystals further confirm that the electron–hole recombination process is controlled by oxygen/defect states, which can be tuned by changing the shape and size of the materials. The degradation of dyes (90 %) in the presence of SnO<SUB>2</SUB> nanoparticles under UV light is comparable to that (88 %) in the presence of standard TiO<SUB>2</SUB> Degussa P-25 (P25) powders. The photocatalytic activity of the nanoparticles is significantly higher than those of nanorods and nanospheres because the effective charge separation in the SnO2 nanoparticles is controlled by defect states leading to enhanced photocatalytic properties. The size- and shape-dependent photocatalytic properties of SnO<SUB>2</SUB> nanocrystals make these materials interesting candidates for photocatalytic applications