We fabricated and characterized quantum-dot light emitting devices (QLEDs) that consisted of a CdSe/ZnS quantum-dot (QD) emitting layer, a hole-transporting nickel oxide (NiO) layer and/or an electron-transporting zinc oxide (ZnO) layer. Both the p-type NiO and n-type ZnO layers were formed by using sol-gel processes. All the fabricated CdSe/ZnS QLEDs showed similar electroluminescence spectra that originated from the green CdSe/ZnS QDs. However, different combinations of hole- and electron-transporting layers resulted in efficiency variations. In addition to the control of the respective concentrations of holes and electrons within a multilayer device structure, which determines the luminance and efficiency of QLEDs, the use of metal oxide layers is advantageous for long-term stability of QLEDs because they are air stable and can block the permeation of water vapor and oxygen in ambient air to a QD emitting layer. Moreover, the wet chemistry processing for their formation makes metal oxide layers attractive for low cost and/or large area manufacture of QLEDs.

We fabricated hybrid light emitting devices based on colloidal CdSe/ZnS core/shell quantum dots and a solution-processed NiO layer. The use of a sol-gel NiO layer as a hole injection layer (HIL) resulted in overall improvement in device operation compared to a control device with a more conventional poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) HIL. In particular, luminous efficiency increased substantially because of the suppression of excessive currents and became as large as 2.45 cd/A. To manifest the origin of current reduction, temperature- and electric field-dependent variations of currents with respect to bias voltages were investigated. In a low bias voltage range below the threshold for luminance turn-on, the Poole-Frenkel (PF) emission mechanism was responsible for the current-density variation. However, the space-charge-limited current modified with PF-type mobility ruled the current-density variation in high bias voltage range above the threshold.

A series of inorganic-organic hybrid light-emitting devices (HLEDs) based on orange CdSe/ZnS quantum dots were fabricated and their operation characteristics were investigated. Other than replacing an organic light-emitting layer (EML) with a CdSe/ZnS-QD EML spin-coated from a colloidal QD solution, the structure of HLEDs was kept identical to that of conventional organic light-emitting devices. Comparison of the operation characteristics of two types of CdSe/ZnS-QD HLEDs with a either Bebq 2 or Alq 3 electron transport layer (ETL) showed that the control of the injection and transport of electrons is the key step for the improvement of the luminance yield, power efficiency, and color purity of our HLEDs. The most common ETL material Alq 3 turned out to be sufficient to make HLEDs with promising device performance.

We report systematic efficiency improvement of green-emitting CdSe@ZnS quantum-dot LEDs with respect to the concentration of a 1,2-ethanedithiol solution used for in situ treatment.

We report a five-fold luminance increase of green-light-emitting CdSe@ZnS quantum-dot LEDs (QLEDs) in response to treatment with a 2-ethoxyethanol solution of cesium carbonate (Cs2CO3). The maximum luminous yield of Cs2CO3-treated QLED is as high as 3.41 cd A−1 at 6.4 V. To elucidate device-performance improvement, we model measured currents as the sum of radiative and non-radiative recombination components, which are respectively represented by modified Shockley equations. Variations in model parameters show that a shift in Fermi level, reduction of barrier heights, and passivation of mid-gap defect states are the main results of Cs2CO3 treatment. In spite of a large luminance difference, light-extraction efficiency remains the same at 9% regardless of Cs2CO3 treatment because of the similarity in optical structures.