A strain-induced exciton transition energy shift in CdSe nanoplatelets: the impact of an organic ligand shell.

We study the influence of surface passivating ligands on the optical and structural properties of zinc blende CdSe nanoplatelets. Ligand exchange of native oleic acid with aliphatic thiol or phosphonic acid on the surface of nanoplatelets results in a large shift of exciton transition energy for up to 240 meV. Ligand exchange also leads to structural changes (strain) in the nanoplatelet's core analysed by wide-angle X-ray diffraction. By correlating the experimental data with theoretical calculations we demonstrate that the exciton energy shift is mainly caused by the ligand-induced anisotropic transformation of the crystalline structure altering the well width of the CdSe core. Further the exciton reduced mass in these CdSe quantum wells is determined by a new method and this agrees well with the expected values substantiating that ligand-strain induced changes in the colloidal quantum well thickness are responsible for the observed spectral shifts. Our findings are important for theoretical modeling of other anisotropically strained systems and demonstrate an approach to tune the optical properties of 2D semiconductor nanocrystals over a broad region thus widening the range of possible applications of AIIBVI nanoplatelets in optics and optoelectronics.

Nanoplasmonic Raman detection of bromate in water.

The possibility of using surface enhanced Raman scattering (SERS) detection method for bromate-anion determination and quantitative evaluation in water has been demonstrated for the first time. The decreasing of Rhodamine 6G (R6G) Raman peaks intensity has been used as the analytical signal corresponding to the catalytic oxidation by bromate. Electrostatically immobilized silver nanoparticles have been proven as efficient SERS-active substrate. A linear relationship between the Raman intensity of Rh6G as a function of BrO(3)(-) was observed in the range of 0 - 10(-7) М and the detect limit was as low as 10(-10) M (nearly 0.01 µg/L). The results prove the potential of the proposed method for further application in the development of new portable SERS-based sensors for drinking water monitoring with high sensitivity, simplicity and the low cost.