A. S. Selyukov

Organic light-emitting diode with an emitter based on a planar layer of CdSe semiconductor nanoplatelets

Colloidal CdSe semiconductor nanoplatelets with characteristic longitudinal sizes of 20–70 nm and thicknesses of several atomic layers are synthesized. The spectra and kinetics of the photoluminescence of these quasi-two-dimensional nanostructures (quantum wells) at room and cryogenic temperatures are investigated. A hybrid light-emitting diode with the electron and hole transport layers based on TAZ and TPD organic compounds, respectively, and the active “emissive” element based on a layer of such single-component nanoplatelets is designed. The spectral and electrical characteristics of the fabricated device, emitting at a wavelength of λ = 515 nm, are determined. The use of quasi-two-dimensional nanostructures of this kind (nanoplatelets) is promising for the fabrication of hybrid light-emitting diodes with pure colors.

Electroluminescence of colloidal quasi-two-dimensional semiconducting CdSe nanostructures in a hybrid light-emitting diode

We report on the results of studying quasi-two-dimensional nanostructures synthesized here in the form of semiconducting CdSe nanoplatelets with a characteristic longitudinal size of 20–70 nm and a thick-ness of a few atomic layers. Their morphology is studied using TEM and AFM and X-ray diffraction analysis; the crystal structure and sizes are determined. At room and cryogenic temperatures, the spectra and kinetics of the photoluminescence of such structures (quantum wells) are investigated. A hybrid light-emitting diode operating on the basis of CdSe nanoplatelets as a plane active element (emitter) is developed using the organic materials TAZ and TPD to form electron and hole transport layers, respectively. The spectral and current-voltage characteristics of the constructed device with a radiation wavelength λ = 515 nm are obtained. The device triggering voltage is 5.5 V (visible glow). The use of quasi-two-dimensional structures of this type is promising for hybrid light-emitting diodes with pure color and low operating voltages.

Characterization of defects in colloidal CdSe nanocrystals by the modified thermostimulated luminescence technique

The temperature dependencies of the luminescence spectra of 5-nm-diameter CdSe semiconductor nanocrystals synthesized by colloidal-chemistry methods are investigated. The two bands observed in these spectra around 2.01 and 1.37 eV correspond to band-to-band transitions and luminescence of defect states, respectively. A model explaining the temperature behavior of the luminescence band intensities both upon cooling and heating is put forward. A new modification of spectrally resolved thermostimulated luminescence technique making it possible to determine the activation energies and the character of traps responsible for the temperature dependence of the luminescence intensities is suggested. This technique is used to obtain the activation energies of the emission and capture of electrons at traps (190 and 205 meV, respectively) and to determine the depth of the electron level (57 meV) responsible for luminescence in the 1.37-eV region.

Nonlinear optical response of planar and spherical CdSe nanocrystals

The nonlinear optical response of a colloidal solution of planar CdSe semiconductor nanocrystals (nanoplatelets) is studied for the first time. The nonlinear optical response of these nanoparticles is compared to that of spherical CdSe nanocrystals (quantum dots). The photoinduced nonlinearity is attributed to the optical generation of long-lived charge carriers in the nanoobjects under study. It is shown that, upon the exposure of a cell with the solution of nanoparticles to focused continuous-wave (cw) laser radiation with a wavelength of 473 nm, the nonlinear optical responses of CdSe nanoplatelets and quantum dots are somewhat different at identical optical densities at the above-indicated wavelength. The differences are supposedly associated with a higher diffusion rate of spherical nanoparticles in the solution because of their smaller size compared to that of nanoplatelets.