Quantum dots (QDs) are promising candidates for producing bright, color-pure, cost-efficient, and long-lasting QD-based light-emitting diodes (QDLEDs). However, one of the significant problems in achieving high efficiency of QDLEDs is the imbalance between the rates of charge-carrier injection into the emissive QD layer and their transport through the device components. Here we investigated the effect of the parameters of the deposition of a poly (methyl methacrylate) (PMMA) electron-blocking layer (EBL), such as PMMA solution concentration, on the characteristics of EBL-enhanced QDLEDs. A series of devices was fabricated with the PMMA layer formed from acetone solutions with concentrations ranging from 0.05 to 1.2 mg/mL. The addition of the PMMA layer allowed for an increase of the maximum luminance of QDLED by a factor of four compared to the control device without EBL, that is, to 18,671 cd/m², with the current efficiency increased by an order of magnitude and the turn-on voltage decreased by ~1 V. At the same time, we have demonstrated that each particular QDLED characteristic has a maximum at a specific PMMA layer thickness; therefore, variation of the EBL deposition conditions could serve as an additional parameter space when other QDLED optimization approaches are being developed or implied in future solid-state lighting and display devices.

Colloidal quantum dots (QDs) are a promising luminescent material for the development of next generation hybrid light-emitting diodes (QDLEDs). In particular, QDs are of great interest in terms of the development of solid-state light sources with an emission spectrum that mimics daylight. In this study, we used CdSe(core)/ZnS/CdS/ZnS(shell) QDs with organic ligands mimicking polyfluorene and its modified derivatives to obtain QD–polymer composites emitting white light. We found that the emission of the composites obtained by spin-coating, being strongly dependent on the chemical structure of the polymer matrix and the QD-to-polymer mass ratio, can be accurately controlled and adjusted to bring its emission spectrum close to the spectrum of daylight (CIE coordinates: 1931 0.307; 0.376). Moreover, the light emission of these composites has been found to be temporally stable, which is due to the minimal structural instability and volume-uniform charge and energy transfer properties. Thus, the use of the synthesized polyfluorene-based organic ligands with controllable chemical structures adaptable to the structure of the polymer matrix can significantly increase the stability of white light emission from QD composites, which can be considered promising electroluminescent materials for fabrication of white QDLEDs.