Step-scheme perylenediimide supramolecular nanosheet and TiO2 nanoparticle composites for boosted water splitting performance

Adjusting the band gap of organic-inorganic composites by chemical bonding can effectively construct Step-scheme (S-scheme) heterojunctions, featuring properties of fast photogenerated charge migration and excellent photocatalytic performance. In this work, a novel perylene-3, 4, 9, 10-tetracarboxylicdiimide (PDI)-titanium dioxide (TiO₂) heterojunction is elaborately synthesized through simple solvent compounding method. The monodispersed spherical TiO₂ nanoparticles was prepared with the capping agents of oleylamine and oleic acid, and suffered by a ligand exchange process with nitrosonium tetrafluoroborate (NOBF₄) to remove oleylamine and oleic acid. The NOBF₄ ligands were further replaced by PDI super molecular nanosheets to obtain two dimensional (2D)-zero dimensional (0D) PDI-TiO₂ composites. TiO₂ nanoparticles are evenly anchored on the surface of PDI nanosheets with intimate contact. The PDI-TiO₂ composites has emerged considerably superior activity in hydrogen evolution. The highest hydrogen evolution rate for PDI-TiO₂composites with the PDI weight percentage of 2.4% was 9766 μmol h^?1 g^?1 under solar light irradiation, which is 2.56 times of TiO₂-NOBF₄ catalyst. Moreover, PDI-TiO₂ composites possess stoichiometric overall water splitting performance with H₂ and O₂ release rates of 238.20 and 114.18 μmol h^?1 g^?1. The superior photocatalytic performance of PDI-TiO₂ composites can be attributed to the dramatic increase in visible and NIR light absorption caused by π-π stacking structure of PDI, the prevented charge recombination by the S-scheme heterojunction, and the enhanced oxygen evolution by the stronger oxidation capability of PDI. PDI supramolecular nanosheets may work as a novel functional support for many types of semiconductor nanomaterials as graphene, which will display a wide range of application prospects in the energy and environmental fields.     

Ferulic acid and EGCG alter the structural characteristics of ovalbumin and its application in mineral loading

This study aims to fabricate mineral-loading nanocarriers using natural materials. The interaction patterns between ovalbumin (OVA) and four water-soluble polyphenols, namely ferulic acid (FA), (-)-Epigallo-catechin 3-gallate (EGCG), gallic acid (GA) and epicatechin (EC), were investigated. Results showed that the optimised conditions for preparing stable OVA–polyphenol complexes are at the OVA–polyphenol ratio of 4:1 at pH 6, under which OVA–FA and OVA–EGCG showed the highest stability and mineral-loading capacity among four OVA–polyphenol complexes. The fluorescence results indicated that the addition of EGCG and FA induced a significant fluorescence quenching to OVA. The interaction between OVA and polyphenols involved hydrogen bonding, hydrophobic interaction and electrostatic interaction. Fourier transform infrared spectroscopy (FTIR) analysis suggested that both FA and EGCG enhanced the stability and orderliness of the structure of OVA. The transmission electron microscopy images also exhibited the spherical structure of OVA after the addition of FA and EGCG. Furthermore, scanning electron microscope–energy dispersive X-ray spectrum results suggested that OVA–FA and OVA–EGCG complexes were better mineral carriers than OVA–GA and OVA–EC. This study may serve as the theoretical support for the promising application of OVA in the fabrication of mineral-loading nanocarriers in functional food and pharmaceutic.     

Deep-blue thermally activated delayed fluorescence emitter with a very high fluorescence rate

Conventional thermally activated delayed fluorescence (TADF) molecules achieve small energy differences between the lowest singlet and triplet excited states (ΔE_ST) by enhancing the intramolecular charge transfer, which inevitably leads to a wide emission spectrum and low fluorescence rate. Here, we prepared a deep blue TADF molecule via a small ΔE_ST pyridine-phenol fluoroboron complex as the acceptor. The small ΔE_ST is maintained when carbazole donors are attached to the 4-position of the phenyl rings in the fluoroboron complex. Benefiting from the strong electron coupling between the donor (D) and acceptor (A) moieties, the compound Cz-4-BF exhibits a high fluorescence rate of 4.8 × 10⁸ s⁻¹ and a small D-A dihedral angle change in the excited state. Consequently, a photoluminescence (PL) quantum yield of nearly 100% and a PL spectrum with full-width at half-maximum (FWHM) < 60 nm were obtained in solution and low-concentration doped films. A TADF-sensitized fluorescence (TSF) device containing Cz-4-BF achieves an external quantum efficiency of 21%, which is higher than the devices employing classical fluorescent emitters and multiple resonance-type TADF emitters. The Cz-4-BF-based TSF device shows significantly improved color coordinates of (0.14, 0.10) versus a control device without Cz-4-BF.     

Effects of methyl cellulose-based coating on physiochemical properties and chemical hazards of Chinese fried dough cake during storage

Coating has been used as a practical method to ensure the physiochemical properties and reduce the chemical hazard of fried foods. Methyl cellulose (MC) was used as a coating material to pretreat Chinese fried dough cake (CFDC) before frying. The results showed that the water content, hardness and L* value of the 1% MC coated sample were 31.67%, 848.54 g and 51.62, respectively, at the seventh day at 25 °C. Coating contents 1% MC could reduce the oil content, hardness, and extent of browning and improve the physiochemical properties of CFDC on 7 days of storage. Coating contents 1% MC also reduced the acid value, peroxide value, p-anisidine value, malondialdehyde content, 4-hydroxy-2-(E)-hexenal content, 4-hydroxy-2-(E)-nonenal content, acrylamide content and glycidyl ester content in CFDC on 7 days of storage. Our work contributes to the control of the oil content and chemical hazards for fried food during storage by applying an edible coating.     

酶解-挤出复合工艺对高直链淀粉材料制备和性质的影响

以高直链淀粉为原料制备的淀粉基材料力学性质优良。但其熔融流变性差,挤出加工能耗高。本论文采用酶解-挤出复合工艺,考察了耐高温α淀粉酶对挤出环境的耐受性,以及酶加入量、挤出时间等参数对材料制备和性质的影响。结果表明,耐高温α淀粉酶在密炼机的挤出环境中依然有酶活力,能够促进淀粉颗粒的结构相变,从而降低单位机械能耗,缩短加工时间。具体而言,在0.25%的酶加入量下(淀粉干基重量),G50淀粉挤出加工的单位能耗下降了21%。但酶解也会造成分子链的降解,削弱材料性质。与空白材料相比,经酶解-挤出工艺的淀粉基材料,其拉伸强度降低了33%,断裂伸长率减少了83%。另一方面,耐高温α淀粉酶对G80淀粉挤出加工的影响不显著。上述结果表明,可以利用酶解-挤出复合工艺降低生产能耗,缩短加工时间,且酶解会提高淀粉的活性位点和反应效率,有利于淀粉的反应挤出。     

Comparison of microwave and high-pressure processing on bound phenolic composition and antioxidant activities of sorghum hull

The influence of microwave boiling (MB treated 5, 10 and 15 s was abbreviated as MB5, MB10 and MB15, respectively) and high-pressure boiling (HB processed 10, 20 and 30 min was denoted as HB10, HB20 and HB30, respectively) processing on the composition and content of bound phenolic substances of sorghum hull and their antioxidant capacity were evaluated. Nine bound phenolic profiles were identified by HPLC-ESI-MS/MS, including syringic acid, veratric acid, p-hydroxybenzonic acid, caffeic acid, sinapic alcohol, ascorbic acid, prenylnaringenin and luteolin. Compared with traditional hot water processing (HP treated 10, 30 and 50 min was abbreviated as HP10, HP30 and HP50, respectively), the content of free procyanidins and total phenolics of sorghum hull treated with HB increased by 35.92–58.87% and 6.20–18.70%, respectively. Sorghum hull treated with HB20 possessed the highest ABTS (ABTS radical scavenging capacity) and FRAP (ferric ion reducing antioxidant power) among all treatment groups.     

Thermogravimetric kinetics on catalytic combustion of bituminous coal

The catalytic combustion and non-isothermal kinetics of bituminous coal by CeO₂, Fe₂O₃, and NiO were investigated. The exothermic characteristics during catalytic combustion of bituminous coal were determined. Based on the Coats-Redfern method by introducing the function of kinetics mechanisms, the activation energies and pre-exponential factors of catalytic combustion of bituminous coal were estimated iteratively by regression. It is found that the catalysts promoted the transport of oxygen to the coal or char surface and effectively improved the combustion characteristics of bituminous coal. Under the same experimental conditions, the exothermic values were significantly increased and the catalysts of composite oxides exhibited higher exothermic values than pure metal oxide catalysts. The metal oxides significantly reduced the activation energies of bituminous coal combustion. SEM analysis presented that combustion residues became more porous with the addition of the catalyst.     

Layered NiFe-LDH/MXene nanocomposite electrode for high-performance supercapacitor

Layered double hydroxide (LDH) is potentially excellent supercapacitor (SC) materials, but the low conductivity and easy agglomeration limit the further improvement of their electrochemical properties. Therefore, LDHs are requisite to grow on some conductive substrates to produce high-performance SC. In this paper, the conductive two-dimensional (2D) transition metal carbides, nitrides and carbonitrides (called MXene) were explored as the substrate to directly deposit NiFe-LDH nanosheets by a one-step hydrothermal method, then a three-dimensional (3D) porous NiFe-LDH/MXene electrode was obtained. The morphology and electrochemical performance of the composite electrodes were analyzed and investigated. The results show that the NiFe-LDH/MXene electrode has larger specific capacitance (720.2 F/g) than NiFe-LDH (465 F/g), and the capacitance of the composite electrode retained 86% after 1000 cycles (only 24% for NiFe-LDH), showing excellent cycle stability. The improved electrochemical performance of the composites is caused by the stable sheet-like structure of NiFe-LDH during charge-discharge time and the conductive network formed by the MXene, which can accelerates electron transport. In addition, the asymmetric SC based on NiFe-LDH/MXene positive electrode display a power density of 758.27 W/kg at an energy density of 42.4 Wh/Kg. These results indicate the NiFe-LDH/MXene composites can be applied as the novel candidate of high-performance SC electrodes.     

Liquid-phase flash sintering 8YSZ with alkali halide sintering aids

The properties of ZrO₂: 8 mol% Y₂O₃ (8YSZ) ceramics with LiF and KCl sintering aids for liquid phase formation during electric field-assisted sintering were studied. Sintering experiments were carried out at 650 °C under 200 V cm⁻¹ AC electric field by varying current density, current application time, as well as LiF and KCl contents. Pellets sintered with KCl addition had cavities, cracks and fractures. Pellets sintered with 15 wt.% LiF, on the other hand, were homogeneous after thermal removal of LiF upon Joule heating. Low electric current densities coupled with longer application times produced homogeneous specimens. Three different stages were identified during sintering experiments: (i) LiF melting with the electric field applied at furnace temperatures lower than its melting point, (ii) shrinkage due to liquid phase formation and LiF removal, (iii) final densification due to grain growth and pore elimination. The electrical behavior and an estimate of the porosity were carried out by electrochemical impedance spectroscopy measurements.