A self-host thermally activated delayed fluorescence (TADF) dendrimer POCz-DPS for solution-processed nondoped blue organic light-emitting diodes (OLEDs) was designed and synthesized, in which the bipolar phosphine oxide carbazole moiety was introduced by alkyl chain to ensure balanced charge transfer. The investigation of physical properties showed that the bipolar dendrons not only improve the morphological stability but also restrain the concentration quenching effect of the TADF emissive core. The spin-coated OLEDs featuring POCz-DPS as the host-free blue emitter achieved the highest external quantum efficiency (7.3%) and color purity compared with those of doped or nondoped devices based on the parent molecule DMOC-DPS, which indicates that incorporating the merits of encapsulation and bipolar dendron is an effective way to improve the electroluminescent performance of the TADF emitter used for a solution-processed nondoped device.

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Two soluble bipolar host materials (mCP-BPBI and CP-QPBI), comprising different proportions of hole-transporting carbazole and electron-transporting benzimidazole, were synthesized. Their thermal, physical, and electrochemical properties were characterized. The designated bulky star-shaped structures efficiently suppress the direct intramolecular interaction between the donor and acceptor subunits to give high triplet energies. Through computational studies, varying the ratio of hole- and electron-transporting moieties could significantly change the carrier injection/transporting abilities and charge balance properties of the host materials. Indeed, CP-QPBI with more benzimidazole units shows extremely enhanced current density at the same voltage when compared to mCP-BPBI. The operating voltage of solution-processed phosphorescent light-emitting diodes with CP-QPBI as host were dramatically reduced by ∼3 V compared with the similar devices of mCP-BPBI. At the same time, the power efficiencies were improved for 2-2.5 times at the corresponding voltage. Importantly, both blue and green devices maintain their high efficiencies even at brightness up to 1000 cd m(-2), which clearly demonstrates that the new strategy applied to improve electron-transporting ability and charge-balance property of the solution-processable host material by tuning the ratio of donor and acceptor unit is profitable.

Due to the encapsulation of the emissive core, the concentration quenching effect of the TADF material can be effectively restrained.

A liquid/liquid interfacial reaction system was designed to fabricate α-Fe2O3 cubes. The reaction system uses a hydrophobic ionic liquid containing iron ions ([(C8H17)2(CH3)2N]FeCl4) for manufacturing α-Fe2O3 cubes by a novel and environmentally friendly hydrothermal method under low-temperature conditions (140 °C). The iron-containing ionic liquid is hydrophobic and can form a liquid/liquid interface with water, which is vital for fabrication of the α-Fe2O3 cubes. Nanomaterials synthesized from hydrophobic iron-containing ionic liquids show good crystallinity, well-developed morphology, and uniform size. The effect of different ionic liquids on the morphology of α-Fe2 O3 was investigated in detail. [(C8H17)2(CH3)2N]FeCl4 is assumed to perform the triple role of forming a liquid/liquid interface with water and acting as reactant and template at the same time. The effect of the reaction temperature on the formation of the α-Fe2O3 cubes was also studied. Temperatures lower or higher than 140 °C are not conducive to formation of the α-Fe2O3 cubes. Their photoelectrochemical properties were tested by means of the transient photocurrent response of electrodes modified with as-prepared α-Fe2O3 cubes. The photocurrent response of an α-Fe2O3 cubes/indium tin oxide electrode is high and stable, and it shows great promise as a photoelectrochemical glucose sensor with high sensitivity and fast response, which are beneficial to practical applications of nanosensors.