Hydrogen reduced graphene oxide/metal grid hybrid film: towards high performance transparent conductive electrode for flexible electrochromic devices

The metal grid and reduced graphene oxide (RGO) are both promising transparent conductive materials for replacing the indium tin oxide (ITO) in flexible optoelectronics. However, the large empty area that exists in the grid together with the relatively high sheet resistance of RGO hinder both the materials for practical applications. In this work, we report for the first time a novel strategy for efficient combination of the metal grid and RGO by using a newly developed room-temperature reduction technique. The obtained RGO/metal grid hybrid films not only overcome the shortcomings of individual components but exhibit enhanced optical and electrical performances (R_s = 18 Ω sq⁻¹ and T = 80%) and excellent flexural endurance. With this hybrid film as the window electrode, a highly flexible electrochromic device with excellent stability and ultra-fast response shorter than 60 ms has been successfully fabricated. Considering its high efficiency, high quality, low cost and large area, the strategy would be particularly useful for economically fabricating various metal grid/RGO films which are quite promising high performance transparent and conductive materials for next generation optoelectronic devices.     

Mechanical properties of graphene films enhanced by homo-telechelic functionalized polymer fillers via π–π stacking interactions

Most researches on graphene/polymer composites are focusing on improving the mechanical and electrical properties of polymers at low graphene content instead of paying attention to constructing graphene’s macroscopic structures. In current study the homo-telechelic functionalized polyethylene glycols (FPEGs) were tailored with π-orbital-rich groups (namely phenyl, pyrene and di-pyrene) via esterification reactions, which enhanced the interaction between polyethylene glycol (PEG) molecules and chemical reduced graphene oxide (RGO) sheets. The π–π stacking interactions between graphene sheets and π-orbital-rich groups endowed the composite films with enhanced tensile strength and tunable electrical conductivity. The formation of graphene network structure mediated by the FPEGs fillers via π–π stacking non-covalent interactions should account for the experimental results. The experimental investigations were also complemented with theoretical calculation using a density functional theory. Atomic force microscope (AFM), scanning electron microscope (SEM), X-ray diffraction (XRD), nuclear magnetic resonance (NMR), thermal gravimetric analysis (TGA), UV–vis and fluorescence spectroscopy were used to monitor the step-wise preparation of graphene composite films.     

Self-terminated electrodeposition of platinum on titanium nitride for methanol oxidation reaction in acidic electrolyte

The development of high-performance electrocatalysts for methanol oxidation is an urgent task to enhance the efficiency of direct methanol fuel cells. We report a simple and controllable method to fabricate Pt-decorated TiN electrocatalysts using self-terminated electrodeposition at room temperature and ambient pressure. Under optimized deposition parameters such as electrolyte pH, TiN substrate pretreatment, and pulsed deposition potential, quenching of the Pt electrodeposition facilitates obtaining an extremely low Pt mass loading (0.93 μg/cm²) on the TiN substrate. Repeated deposition potential pulses enable a gradual increase in Pt loading, with a precise control of the loaded Pt mass. Maximum intrinsic and mass activities for the methanol oxidation reaction are achieved for the catalyst with a Pt loading mass of 55.0 μg/cm², prepared by 20 deposition pulses. The maximum intrinsic activity achieved with the Pt-decorated TiN electrocatalyst is five times higher than that obtained with bulk Pt. The present results thus provide a facile method for the fabrication of cost-effective electrocatalysts.     

The current detour effect observed on materials with random microstucture: experimental evidence from Li3xLa2/3−xTiO3 studied by impedance spectroscopy

Impedance spectroscopy (IS) has been used to study the influence on the low frequency part of the impedance diagrams of the microstructure of a fast ionic conductor, Li_3xLa_2/3−xTiO₃ with x = 0.10 (named hereafter LLTO). This oxide has been synthesised by sol–gel method. After synthesis, the powder of LLTO displays a large distribution of grain size and agglomerates. The grain size distribution and the porosity of the ceramic have been changed by heat-treatment from 600 °C to 1200 °C in air. The impedance spectra of these ceramics, recorded at different temperatures from room temperature (RT) to 400 °C, show a low-frequency depressed arc, which is characteristic of the grain boundary response of the ceramic. Its shape depends strongly on the heat-treatment of the ceramic, and therefore, on its microstructure. It is a simple arc when the pellet is well sintered but becomes very complex for non-sintered ceramics with high resistive grain boundary and pores. The observed “fish” shape indicates the presence of current “detours effect” in the material. This effect means that current detours around blocking grain boundary and/or pores occur to lower the impedance. Consequently, the brick layer model (BLM), which assumes an ideal microstructure, and then no current “detours effect”, can not be used to analyse these impedance data.     

Evaluation of amines for the selective catalytic reduction (SCR) of NOx from diesel engine exhaust

With a view to developing onboard generation of selective reductants for NO_x removal from diesel engine exhaust we compared the performance of a primary, secondary and tertiary amine to NH₃ using a typical mini core NH₃-SCR catalyst. Primary amines with short hydrocarbon chains, e.g. CH₃NH₂ (maximum NO_x conversion, 50%) approached the NO_x conversion obtained using NH₃ (maximum NO_x conversion, 70%). Increasing the amine to NO_x ratio greater than 1 results in NO_x conversions closer to those of NH₃ (maximum NO_x conversion increased to 60%). Secondary and tertiary amines had smaller NO_x conversions as a function of temperature and the drop in NO and NO_x conversion decreased with increasing amine hydrogen substitution. Also, the maximum NO_x conversion for each reductant tends to move to a lower temperature as the degree of substitution increases.Unlike NH₃, the amines can react in the gas phase at temperatures within the range of diesel engine exhaust. Due to this gas phase reactivity the NO_x conversions measured using the mini core SCR catalyst also contain a gas phase conversion component. Gas phase conversions were investigated by replacing the mini core SCR catalyst with an equivalent length of quartz beads. Subtraction of the two results highlighted the differences between the mini core catalytic and gas phase conversions measured in this manner over the temperature range investigated. These differential NO_x conversions for the three amines had maxima at about 375 °C.     

硅基表面无形貌改变的硫酸／过氧化氢氧化清洗

提出了一种利用硫酸／过氧化氢溶液氧化清洗硅基的方法．硅片经超声预清洗后,放入硫酸／过氧化氢溶液中,80℃下氧化清洗其表面的污染物．通过接触角检测,表征了清洗前后硅基表面的亲水性变化．通过原子力显微镜（AFM）表征了经硫酸／过氧化氢溶液清洗后硅基的表面形貌．结果显示,经硫酸／过氧化氢溶液亲水化清洗30min后的硅基表面的接触角为7．3°,显示出很强的亲水性,其表面均方根粗糙度（RMS）仅为0．03nm．因此,硫酸／过氧化氢氧化清洗法是一种硅基表面无形貌改变的亲水化清洗方法．     

硅基上金粒子诱导的聚氧硅烷纳米线的合成

采用液相法以硅基上原位合成的金纳米粒子作为催化剂和模板,在不同的反应条件下,用十八烷基硅烷（Octadecylsilane）作为前驱体合成了纳米线状化合物．研究了不同反应条件对该线状化合物形貌的影响,能量散射光谱实验结果表明该线状化合物为聚氧硅烷,扫描电镜结果显示当反应温度控制在110℃和反应时间90min的条件下,可得到均匀的纳米线状化合物．最后提出了聚氧硅烷化合物可能的形成机理,同时也为制备硅基上的硅氧纳米线状化合物提供了一种方便而简单的方法．     

Formation of CuS pineal microspheres via a pyridine-solvothermal process

CuS pineal microspheres congregated from interleaving nanoflakes with thickness of 40 to 200 nm were synthesized by a pyridine-solvothermal process via the reaction between cupric chloride(CuCl2·2H2O) and thioacetamide(TAA,CH3CSNH2).The products were characterized by X-ray diffraction and scanning electron microscopy.UV-Vis absorption spectrum,excitation and photoluminescence spectra of CuS pineal microspheres were obtained at room temperature to investigate their optical properties.A possible growth mechanism on the formation of CuS pineal microspheres is proposed.The factors influencing the evolution of morphologies of CuS crystals including the dosage of the reactants,surfactant,and sulphur-source were also analyzed.     

Phase-Separated Polyzwitterionic Hydrogels with Tunable Sponge-Like Structures for Stable Solar Steam Generation

Solar steam generation (SSG) through hydrogel-based evaporators has shown great promise for freshwater production. However, developing hydrogel-based evaporators with stable SSG performance in high-salinity brines remains challenging. Herein, phase-separated polyzwitterionic hydrogel-based evaporators are presented with sponge-like structures comprising interconnected pores for stable SSG performance, which are fabricated by photopolymerization of sulfobetaine methacrylate (SBMA) in water-dimethyl sulfoxide (DMSO) mixed solvents. It is shown that driven by competitive adsorption, the structures of the resulting poly(sulfobetaine methacrylate) (PSBMA) hydrogels can be readily tuned by the volume ratio of DMSO to achieve phase separation. The optimized phase-separated PSBMA hydrogels, combining the unique anti-polyelectrolyte effects of polyzwitterionic hydrogels, demonstrate a rapid water transport capability in brines. After introducing photothermal polypyrrole particles on the surface of the phase-separated PSBMA hydrogel evaporators, a stable water evaporation rate of ≈2.024 kg m⁻² h⁻¹ and high solar-to-vapor efficiency of ≈97.5% in a 3.5 wt.% brine are obtained under simulated solar light irradiation (1.0 kW m⁻²). Surprisingly, the evaporation rates remain stable even under high-intensity solar irradiation (2.0 kW m⁻²). It is anticipated that the polyzwitterionic hydrogel evaporators with sponge-like porous structures will contribute to developing SSG technology for high-salinity seawater applications.     

A Boronate Ester Driven Rechargeable Antibacterial Membrane for Fast Molecular Sieving

Membrane decorated with biocides is an effective way to suppress biofilm growth. However, their immediate biocidal effect usually suffers from a significant decline due to the irreversible consumption of the biocides. Here, a smart nanofiltration membrane is reported with rechargeable antibacterial capability that is fabricated by a facile interfacial polymerization via 3-aminophenylboronic acid and trimesoyl chloride on a polysulfone substrate. Biocides bearing diol groups can be grafted onto the membrane surface under neutral/alkaline condition and then released from the surface under acidic environment, due to the pH-responsive feature of boronate ester complexes. The resultant membrane exhibits integrated properties of fast bacterial inactivating efficiency, rechargeable antibacterial capability, and impressive stability. In addition, the achieved membrane shows remarkable separation efficiency to dye/monovalent salt system. The successful fabrication of the membrane with rechargeable anti-bacterial property provides new insights into the development of pH-responsive and sustainable antibacterial membranes.