Abstract

Highly emissive core−multi-shell (CdSe/CdS/ZnS) quantum dots (QDs) within size range of ∼ 2 nm–5 nm were prepared via hot injection method. Capping agent (polymers) were used to increase the lifetime of QDs, without a protective atmosphere. Red shift was observed in an absorption spectrum of QDs peaks at 362 nm, 365 nm, 558 nm, and 556 nm for CdSe/CdS and CdSe/CdS/ZnS with respect to CdSe core. Voltammetry measurements (Eg ∼ 2. 09 eV) for band gaps were in good agreement with the UV–visible spectroscopic data (Eg ∼ 2.65 eV). QDs exhibited three distinguished peaks comparing to (111), (220), and (311) planes of cubic structures of CdSe, CdSe/CdS and CdSe/CdS/ZnS within crystallite size of 20–27 nm as observed by XRD spectra. A larger active surface area 0.06 cm−2, computed by CV increased the catalytic activity of sensors by exposing the electroactive sites. Linear, nonlinear optical susceptibility and absorption coefficients were computed by an effective mass model. Quantum confinement was confirmed by taking electron probability density as function of radial distance of quantum dots.

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