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.

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.

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Three solution-processable exciplex-type host materials were successfully designed and characterized by equal molar blending hole transporting molecules with a newly synthesized electron transporting material, which possesses high thermal stability and good film-forming ability through a spin-coating technique. The excited-state dynamics and the structure-property relationships were systematically investigated. By gradually deepening the highest occupied molecular orbital (HOMO) level of electron-donating components, the triplet energy of exciplex hosts were increased from 2.64 to 3.10 eV. Low temperature phosphorescence spectra demonstrated that the excessively high triplet energy of exciplex would induce a serious energy leakage from the complex state to the constituting molecule. Furthermore, the low energy electromer state, which only exists under the electroexcitation, was found as another possible channel for energy loss in exciplex-based phosphorescent organic light-emitting diodes (OLEDs). In particular, as quenching of the exciplex-state and the triplet exciton were largely eliminated, solution-processed blue phosphorescence OLEDs using the exciplex-type host achieved an extremely low turn-on voltage of 2.7 eV and record-high power efficiency of 22.5 lm W(-1), which were among the highest values in the devices with identical structure.

Abstract. Highly selective molecularly imprinted nanocomposites MIP RhB -PPy/TiO 2 were successfully prepared by surface molecular imprinting technique with rhodamine B (RhB) as template molecule. The prepared MIP RhB -PPy/TiO 2 coated with a thin imprinted layer could respond to visible light. The static and dynamic binding experiments revealed that MIP RhB -PPy/TiO 2 possessed strong affinity, high adsorption capacity and fast adsorption rate for RhB. The selectivity experiments indicated that MIP RhB -PPy/TiO 2 had excellent recognition selectivity for RhB. Selective photocatalytic degradation experiments indicated that the apparent rate constant (k) for the photodegradation of RhB over MIP RhB -PPy/TiO 2 is 0.0158 min -1 , being 3.6 times of that over non-imprinted nanocomposites NIP-PPy/TiO 2 (0.0044 min -1 ). Compared with the NIP-PPy/TiO 2 , MIP RhB -PPy/TiO 2 showed higher photocatalytic selectivity toward RhB under visible light, which was attributed the introduction of the imprinted cavities on the surface of MIP RhB -PPy/TiO 2 . Moreover, MIP RhB -PPy/TiO 2 exhibited high reusability and stability. The results indicate that molecularly imprinted nanocomposites MIP RhB -PPy/TiO 2 have a promising perspective in industrial wastewater treatment.