We have developed an aqueous synthesis for glutathione capped ZnSe nanocrystals. The structure and optical properties of the obtained ZnSe nanocrystals were characterised by X-ray diffraction, dynamic light scattering analysis, TEM, ultraviolet–visible, photoluminescence spectroscopy and Fourier transform infrared spectroscopy. The ZnSe shows a cubic zincblende crystal phase and has a narrow size distribution. Experimental results indicate that the pH value and reaction time play crucial roles in determining optical features. With the pH increasing from 10 to 12, and reaction time from 0 to 2 h, the fluorescence emissions of ZnSe nanocrystals are tuneable between 360 and 405 nm. The high quantum yields are calculated to be in the range of 0·3–22%. Furthermore, the luminescence intensity can be enhanced significantly when the nanocrystal sample is illuminated by room light. The mechanism for the resulting high quality optical properties is also elucidated.
Zinc selenide (ZnSe) nanocrystals were synthesized via a phosphine-free route using the highly reactive alkylamine-H 2 Se complex as selenium precursor and zinc precursors with different reactivity. The reactivity of zinc precursor was tuned by using three kinds of zinc carboxylates with different alkyl chain lengths, including zinc acetate, zinc nonanoate, and zinc stearate. The effect of the reactivity and the amount of zinc precursor on nucleation and growth of ZnSe nanocrystals were investigated by ultraviolet-visible absorption and photoluminescence spectra. Result indicates that the growth and optical property of the resulting ZnSe nanocrystals are strongly dependent on the alkyl chain length and the amount of the zinc carboxylates and both shorter alkyl chain length, and more amount of zinc carboxylate will lead to faster growth of ZnSe nanocrystals. This allows that the controlled growth and excellent optical property of high-quality ZnSe nanocrystals can be achieved by combining the different reactivity and the used amount of zinc precursor, such as by using stoichiometric and reactive Zn precursor and Se precursor or by using larger amount of more unreactive Zn precursor relative to the highly reactive alkylamine-H 2 Se complex precursor.