On the formation of superoxide radicals on colloidal ATiO(3) (A = Sr and Ba) nanocrystal surfaces

Controlling the surface chemistry of colloidal semiconductor nanocrystals is critical to exploiting their rich electronic structures for various technologies. We recently demonstrated that the hydrothermal synthesis of colloidal nanocrystals of SrTiO(3), a technologically-relevant electronic material, provided a strong negative correlation between the presence of an O(2)-related surface defect and hydrazine hydrate [W. L. Harrigan, S. E. Michaud, K. A. Lehuta, and K. R. Kittilstved, Chem. Mater., 2016, 28(2), 430]. When hydrazine hydrate is omitted during the aerobic hydrothermal synthesis, the surface defect is observed. However, it can be removed by either the addition of hydrazine hydrate or by purging the reaction solution with argon gas before the hydrothermal synthesis. We also propose that the formation of the O(2)-related defect is mediated by the reduction of dissolved O(2) by lactate anions that are present from the titanium precursor. This work helps elucidate the nature of the O(2)-related defect as a superoxide anion [Image: see text] and presents a mechanism to explain its formation during the hydrothermal synthesis of SrTiO(3) and related BaTiO(3) nanocrystals.