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Cerium oxide has attracted attention recently for its photocatalytic properties, but there are gaps in understanding its performance, especially at low and high pH. UV irradiation of ceria nanoparticles causes electrons from photogenerated electron-hole pairs to localize as small polarons, yielding Ce3+ ions. In pH 10 solution, ceria nanoparticles capped with polyacrylic acid ligands can accumulate large numbers of Ce3+ defects as revealed by strong bleaching of the absorption onset. In contrast, we show that UV irradiation of several-nanometer diameter ceria nanoparticles in acidic (pH < 3) aqueous solution releases Ce3+ ions into solution with a quantum yield that approaches 70% and that varies with excitation wavelength, particle size, and the presence of a hole scavenger (glycerol) on the nanoparticle surface. The instability of Ce3+ at the nanoparticle surface and the ability of electron small polarons to migrate to the surface by hopping strongly suggest that nanoceria is fully oxidized and essentially free of Ce3+ centers at pH < 3. Efficient photoreduction and the excellent stability of unirradiated nanoparticles make it easy to shrink the nanoparticles using only light, while maintaining them in a fully oxidized state. This enables study of the size-dependent absorption properties of ceria nanoparticles that are free of Ce3+ defects. No evidence of quantum confinement is observed, consistent with highly localized excited states. The observed quantum yields of photoreduction are higher than reported for other metal oxides, revealing that a significant fraction of electron-hole pairs are available for driving surface redox reactions, even in fully oxidized particles.

A stable sol of cerium oxide nanoparticles forms spontaneously when cerium(iv) ammonium nitrate (CAN) is dissolved in room-temperature water at mM concentrations. Electron microscopy experiments reveal the formation of highly crystalline cerium oxide particles several nm in diameter and suggest that they are formed from amorphous particles that are similar in size. Under the low pH conditions of the experiments, the nanoparticles form a stable dispersion and show no evidence of aggregation, even many months after synthesis. The absence of particles large enough to scatter light significantly makes it possible to observe the crystallization kinetics through dramatic changes in the UV-visible absorption spectra that occur during solution aging. Measurements show that the cerium oxide nanocrystals are formed roughly an order of magnitude more slowly in D2O than in H2O solution. This large solvent kinetic isotope effect (kH/kD ∼ 10), which is reported here for the first time for the crystallization of a solid metal oxide phase, indicates a rate-determining proton transfer reaction, which is assigned to the conversion of hydroxy to oxo bridges. In D2O solution, the absorption per mole of cerium ions increases by over 400% at 290 nm as the weakly absorbing precursor phase is transformed into nanocrystalline cerium oxide. An isosbestic point is detected at 368 nm, and the absorption spectra can be modeled throughout aging by the sum of spectra of just two interconverting species. Preliminary ultrafast transient absorption experiments confirm that the optical properties of the amorphous precursors differ greatly from those of the final, nanocrystalline phase. Crystallization of CeO2 from CAN in water has much in common with the crystallization of iron oxides from iron(iii) salts, including the importance of non-classical nucleation and growth pathways. It is an outstanding system for studying the poorly understood events that cause molecularly solvated ions to self-assemble into nanocrystals, following hydrolysis. At the same time, the strong susceptibility of CAN to spontaneously form CeO2 nanocrystals under the mildest of reaction conditions indicates that caution is needed when working with this common sacrificial oxidant.