Two exciplexes were detected for the first time for the known exciplex-forming system consisting of electron donating 1,3-bis(N-carbazolyl)benzene and electron accepting 2,4,6-tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine. Exploiting thermal treatment, sky-blue (high-energy) and orange (low-energy) exciplexes were observed for a solid-state mixture of the compounds under electrical excitation. Similarly, stable high-energy and low-energy exciplexes were observed for new exciplex-forming systems consisting of 2,4,6-tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine and one of four selected carbazole and fluorene hybrid trimers as donors. The high-energy exciplexes were observed when there was a small energy barrier between the locally excited state and the high-energy exciplex state. A large energy barrier between the locally excited state and the low-energy exciplex state was the reason that the dual nature of exciplexes was not discovered yet. Emission of both exciplexes was observed in electroluminescence spectra of exciplex-interface based devices using developed exiplex-forming systems as emitters. Observed under optical and electrical excitations, the low-energy exciplexes were separated using thermal treatment of the studied exciplex-forming systems. The exciplex-forming system consisting of 2,4,6-tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine and 3,6-di(9-carbazolyl)-9-(2-ethylhexyl)carbazole, which exhibits thermally activated delayed fluorescence, showed the best performance in organic light-emitting diodes (OLEDs) based on interface and volume exciplex emitters. The best device showed maximum external quantum and maximum current efficiencies of 18% and 54 cd A−1 respectively. Additionally, white OLEDs were fabricated exploiting sky-blue and orange emissions from a single exciplex-forming system. Our findings provide evidence of the dual nature of exciplexes and pave the way towards design of new exciplex-forming systems with high photoluminescence quantum yields and efficient exciplex-based devices.

We report on the complex GaSe-based hierarchical structures GaSe(CS(NH₂)₂), GaSe(SmCl₃) and GaSe(CS(NH₂)₂(SmCl₃)) synthesized by an intercalation method. The conductive properties of synthesized clathrates and their relation to hierarchical structural complexity were explored by an impedance spectroscopy technique. The impedance response, thermostimulated discharge spectra, and photo- and magnetoresistive effects are reported. Based on the obtained results, the impurity energy spectra were calculated. A strong low-frequency inductive response, observable in the GaSe(SmCl₃) clathrate, makes this material promising for the development of gyrator-free nanodelay lines potentially applicable in nanoelectronics. Hierarchical GaSe(CS(NH₂)₂(SmCl₃)) clathrate, on the other hand, reveals hysteresis of the current–voltage characteristics, apparently confirming an accumulation of electric energy at interphase boundaries. A relevant spin battery effect, observable experimentally in stationary magnetic fields, demonstrates a principal possibility of the electric energy accumulation at a quantum level.

In the present paper hybrid core–shell InP/ZnS quantum dots were prepared by the one pot synthesis method which does not require additional component injections and which complies more with cost requirements. The synthesized quantum dots were characterized by X-ray diffraction and optical spectroscopy methods. The applicability of the synthesized InP/ZnS core–shell particles in inverted solar cells fabricated with a step-by-step procedure which combines thermal vacuum deposition and spin-coating techniques was investigated. The resulting efficiency of the fabricated inverted solar cell is comparable to that of quantum-dot sensitized TiO₂ based solar cells. Therefore, hybrid core–shell InP/ZnS particles can be considered as multifunctional light-harvesting materials useful for implementation in different types of photovoltaic devices, such as quantum dot sensitized solar cells and inverted solar cells.