Phenothiazinen-Dimesitylarylborane-Based Thermally Activated Delayed Fluorescence: High-Performance Non-doped OLEDs With Reduced Efficiency Roll-Off at High Luminescence.

We report a phenothiazinen-dimesitylarylborane thermally activated delayed fluorescence (TADF) molecule that exhibits high external quantum efficiency (EQE) in non-doped organic light-emitting diodes (OLEDs) at high luminescence. The non-doped device shows green electroluminescence with an emission peak of 540 nm and a maximum EQE of 19.66% obtained at a luminescence of ~170 cd m-2. The EQE is still as high as 17.31% at a high luminescence of 1,500 cd m-2 with small efficiency roll-off.

Efficient Non-doped Blue Fluorescent Organic Light-Emitting Diodes Based on Anthracene-Triphenylethylene Derivatives.

The development of efficient blue materials has been a continuous research topic in the field of organic light-emitting diodes (OLEDs). In this paper, three aggregation-induced emission enhancement active blue emitters, PIAnTPE, TPAAnTPE and CzAnTPE, are successfully synthesized by attaching a triphenylethylene unit and phenanthroimidazole/triphenylamine/carbazole moieties to the 9,10-positions of anthracene, respectively. The three compounds exhibit good thermal stabilities, appropriate for the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energy levels and display high photoluminescence quantum yields (PLQYs) of 65, 70 and 46 % in the solid state. Non-doped blue devices using PIAnTPE, TPAAnTPE and CzAnTPE as the emitting layers show good electroluminescent performances, with the maximum external quantum efficiencies (EQEs) of 4.46, 4.13 and 4.04 %, respectively. More importantly, EQEs of all the three devices can be still retained when the luminescence reaches 1000 cd m-2 , exhibiting quite small efficiency roll-offs in the non-doped OLEDs.

Supramolecular interaction-induced assemblies of polyanions and 2-aminopyridinium in two polyoxometalate-based hybrids.

Organic-inorganic hybrids consisting of organic cations and polyanions are promising functional materials due to their various compositions and structures. An important aspect of these materials is the interactions between the organic and inorganic components, which not only produce the final structures, but also influence the properties. Here, we investigated the interactions between organic cations and polyanions using protonated 2-aminopyridinium (Hap) as the cation, and successfully obtained two polyoxometalate-based hybrids, namely (C5H7N2)4[Mo8O26], (I), and (C5H7N2)2[NiMo6O16(OH)2{CH3C(CH2O)3}2]·4H2O, (II). In the crystal structure of (I), every Hap cation links with two polyanions by donating one or two N-H...O hydrogen bonds, and every polyanion is surrounded by eight Hap cations via terminal or bridging O atoms. Conversely, in compound (II), every Hap cation only links with one polyanion decorated by a triol ligand; this organic-inorganic component further assembles via uncoordinated water molecules. In the extended structures, Hap plays a key role, not only providing a counter charge, but also acting as `glue' linking polyanions in the role of hydrogen-bond donors. In both compounds, as the nodes of the supramolecular network, the polyanions exhibit an ordered two-dimensional arrangement due to strong hydrogen bonds and electrostatic interactions between the organic and inorganic parts. The electrochemistry of compound (I) shows that redox sourcing from polyanions is a surface-controlled process. Conversely, the magnetic behaviour of compound (II) indicates dominant antiferromagnetic properties.

Effect of External Electric Field on the Ordered Structure of Molecular Chains and Hole Mobility in Regioregular Poly(3-hexylthiophene) with Different Molecular Weights.

This research investigated the effect of a high-voltage external electric field on the ordered structure of molecular chains and hole mobility in regioregular poly(3-hexylthiophene) (P3HT) with different molecular weights through X-ray diffraction, atomic force microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, micro-Raman spectroscopy, UV-vis spectroscopy, photoluminescence spectroscopy, and organic field-effect transistors. The optimal magnitude of the external electric field was 5000 V/cm. With the optimized electric field applied to a series of P3HT films, the carrier mobility of all P3HT films increased, and the increase rate changed from 105% to 56%, closely depending on the increase in molecular weight from 33 kg/mol to 100 kg/mol. The results indicated that the increase in carrier mobility was attributed to the P3HT conformation order, which was controlled by the external electric field. Molecular weight was a critical factor in determining the P3HT conformation response to the external electric field. The external electric field orientated lower-molecular-weight (33 kg/mol) P3HT into ordered structures more obviously than higher-molecular-weight (100 kg/mol) P3HT. This research contributes to the understanding of the effect of an external electric field on the ordered structure of the chains and carrier mobility in P3HT with different molecular weights. This research also reveals the regularity and mechanism of the formation of ordered structures and essentially enhances the carrier mobility of P3HT films with different molecular weights, to fabricate photovoltaic devices with high efficiency, based on polymer physics.

Advancements of two dimensional correlation spectroscopy in protein researches.

The developments of two-dimensional correlation spectroscopy (2DCOS) applications in protein studies are discussed, especially for the past two decades. The powerful utilities of 2DCOS combined with various analytical techniques in protein studies are summarized. The emphasis is on the vibration spectroscopic techniques including IR, NIR, Raman and optical activity (ROA), as well as vibration circular dichroism (VCD) and fluorescence spectroscopy. In addition, some new developments, such as hetero-spectral 2DCOS, moving-window correlation, and model based correlation, are also reviewed for their utility in the investigation of the secondary structure, denaturation, folding and unfolding changes of protein. Finally, the new possibility and challenges of 2DCOS in protein research are highlighted as well.

Preparation of Cyano-Substituted Tetraphenylethylene Derivatives and Their Applications in Solution-Processable OLEDs.

Creation of organic luminescent materials with high solid-state efficiency is of vital importance for their applications in optoelectronic fields. Here, a series of AIE luminogens (AIE gens), (Z)-2,3-bis(4-(9,9-bis(6-(9H-carbazol-9-yl)hexyl)-9H-fluoren-2-yl)phenyl)-3-phenylacrylonitrile (SFC), and 2,3-bis(4-(9,9-bis(6-(9H-carbazol-9-yl)hexyl)-9H-fluoren-2-yl)phenyl)fumaronitrile (DFC), utilizing 2,3,3-triphenylacrylonitrile and 2,3-diphenylfumaronitrile as respective centers, are designed and synthesized by Suzuki coupling reactions with high yields. The cis- and trans-isomers of DFC are also successfully obtained. All of them are thermally stable and show good solubility in common organic solvents. They all emit weakly in solution, but become strong emitters when fabricated into solid films. It is found introduction of one additional cyano group in DFC induced a big red-shift in solid-state emission, owing to its high electron-withdrawing ability. The cis- and trans-DFC show similar photophysical and Cyclic voltammogram (CV) behaviors. Non-doped solution-processed organic light-emitting diodes (OLEDs) using the three compounds as light-emitting layers are fabricated. SFC gives the best device performance with a maximum luminance of 5201 cd m-2, a maximum current efficiency of 3.67 cd A-1 and a maximum external quantum efficiencies (EQE) of 1.37%. Red-shifted EL spectra are observed for cis- and trans-DFC-based device, and the OLED using trans-DFC as active layer exhibits better performance, which might derive from their different conformation in film state.

Immobilization of Lactobacillus rhamnosus in mesoporous silica-based material: An efficiency continuous cell-recycle fermentation system for lactic acid production.

Lactic acid bacteria immobilization methods have been widely used for lactic acid production. Until now, the most common immobilization matrix used is calcium alginate. However, Ca-alginate gel disintegrated during lactic acid fermentation. To overcome this deficiency, we developed an immobilization method in which Lactobacillus rhamnosus cells were successfully encapsulated into an ordered mesoporous silica-based material under mild conditions with a high immobilization efficiency of 78.77% by using elemental analysis. We also optimized the cultivation conditions of the immobilized L. rhamnosus and obtained a high glucose conversion yield of 92.4%. Furthermore, L. rhamnosus encapsulated in mesoporous silica-based material exhibited operational stability during repeated fermentation processes and no decrease in lactic acid production up to 8 repeated batches.

Pillar[5]arene-based supramolecular organic frameworks for highly selective CO2-capture at ambient conditions.

Low-density, solid-state, porous supramolecular organic frameworks are constructed using pillarenes. The frameworks have a honeycomb-like structure, permanent porosity, high thermal stability, and selective and reversible sorption properties toward CO2. The exceptionally selective CO2-sorption properties (375/1, 339/1) of one framework over N2 and CH4 indicate potential applications in CO2-capture for post-combustion power plants and natural gas sweetening.

Acetylcholine-triggered cargo release from supramolecular nanovalves based on different macrocyclic receptors.

Acetylcholine (ACh), a neurotransmitter located in cholinergic synapses, can trigger cargo release from mesoporous silica nanoparticles equipped with calixarene- or pillarene-based nanovalves by removing macrocycles from the stalk components. The amount and speed of cargo release can be controlled by varying the concentration of ACh in solution or changing the type of gating macrocycle. Although this proof-of-concept study is far from a real-life application, it provides a possible route to treat diseases related to the central nervous system.

[Spectroscopic ellipsometry investigations of amorphous diamond films deposited with filtered arc].

In order to investigate thoroughly the optical properties of amorphous diamond (alpha-D) films deposited by the filtered vacuum arc technology, the optical constants of the films were measured by spectroscopic ellipsometry. Moreover, the dispersion relations of the optical constants, and the correlations among refractive index, extinction coefficient, optical gap and the substrate bias were also analyzed. It has been shown that the refractive index of alpha-D films is higher than that of diamond crystal, and the absorption edge corresponding to the interband transformation can be described with the parabolic line shape. With increasing the wavelength, the extinction coefficient gradually declines and approaches nearly to zero in the infrared band. In addition, the adjustable amplitudes of the optical constants owing to the changing bias also reduce strikingly with the extension of the wavelength. With raising the bias, the refractive index and the optical gap firstly augment, then minish, and there is a maximal value when the substrate bias is -80 V. However, the extinction coefficient firstly minishes, then augments, and there is a minimal value when the bias is -80 V.