Monodispersed cubic platinum (Pt) nanocrystals with an average size of approximately 10 nm were prepared by a reduction method with cetyltrimethylammonium bromide (CTAB) serving as steric stabilizer. The resulting Pt nanocrystals exhibit a peroxidase-like activity and catalyze the H2O2-mediated oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) to produce two colored products with high catalytic activity. The color-generating activity of this system may be influenced by several factors, and we examined several factors to optimize this colorimetric system including buffer types, pH, and concentrations of both H2O2 and Pt nanocrystals. The effect of agglomeration of Pt nanocrystals was also investigated, and we find that agglomeration of Pt nanocrystals in aqueous solution distinctly affects Pt nanocrystals catalytic activity. We attribute the catalytic activity of Pt nanocrystals to their acceleration of the electron-transfer process and the consequent facilitation of radical generation.

The second-order optical nonlinearity of CdS nanoparticles with different mean diameters of 28.0, 30.0, 31.5, 50.0, and 91.0 Å was studied by the incoherent hyper-Rayleigh scattering technique. Results show that the first-order hyperpolarizability β value per CdS particle decreases with decreasing size from 91.0 to 31.5 Å; however, as CdS particle size further decreases, this trend is reversed and the β value increases. Substantially, the normalized value of the first-order hyperpolarizability per CdS formula unit, β0, exhibits systematic enhancement with decreasing size. This is interpreted in terms of a so-called surface contribution mechanism. The two aspects of quantum size effects, the size dependence of optical band-gap and oscillator strength, cannot be adopted to explain the size dependence of the second-order optical nonlinearity of CdS nanoparticles.

Hyper-Rayleigh scattering technique was used to measure for the first time the first-order hyperpolarizability (β) of ZnS nanocrystals with 2.5 nm mean diameter. Results show that the ‘per ZnS particle’ β value is 2.34×10−27 esu and the ‘per ZnS formula unit’ β value is 1.63×10−28 esu. An increase by at least two orders of magnitude in the β value per ZnS formula unit is found when compared with bulk ZnS. Two possible contributions originating from nanocrystal surface electric field and solvent field were experimentally excluded. Other two contributions, bulk-like contribution and surface contribution, are considered. Especially, the latter is emphasized due to the special surface structure of nanocrystals.