Design of functionalized α-Fe2O3 (III) films with long-term anti-wetting properties

The design of functional anti-wetting ceramic coatings is always a bottleneck restricting the development of ceramic techniques. This study proposes a liquid phase synthesis method to fabricate α-Fe₂O₃ (III) ceramic powders with promising applications and introduces a facile electrophoretic deposition (EPD) technique to construct the corresponding functionalized hydrophobic films – superhydrophobic functionalized α-Fe₂O₃ ceramic films (SFOFS) with roughly even distribution and a high water contact angle (CA) of 169°±1° – followed by heat posttreatments. The microtopography and crystalline structures of the product were investigated by FESEM, EDX, and XRD techniques. The EPD controllability of SFOFS was studied by adjusting the EPD time and the applied field strengths. In addition, the SFOFS show excellent long-term anti-wetting properties for twenty-four months after undergoing a series of tests, including soaking, water droplet impacting, immersion by droplets with different surface tensions and exposure to different gases and relative humidity conditions, etc. This study substantially helps the design of other kinds of functional anti-wetting films through the proposed convenient method beyond the oxide limit.     

Tough salami-inspired Cf/ZrB2 UHTCMCs produced by electrophoretic deposition

One of the biggest challenges of the materials science is the mutual exclusion of strength and toughness. This issue was minimized by mimicking the natural structural materials. To date, few efforts were done regarding materials that should be used in harsh environments. In this work we present novel continuous carbon fiber reinforced ultra-high-temperature ceramic matrix composites (UHTCMCs) for aerospace featuring optimized fiber/matrix interfaces and fibers distribution. The microstructures – produced by electrophoretic deposition of ZrB₂ on unidirectional carbon fibers followed by ZrB₂ infiltration and hot pressing – show a maximum flexural strength and fracture toughness of 330 MPa and 14 MPa m^1/2, respectively. Fracture surfaces are investigated to understand the mechanisms that affect strength and toughness. The EPD technique allows the achievement of a peculiar salami-inspired architecture alternating strong and weak interfaces.     

微杯电子纸及其后加工制程

SiPix利用独特的微杯(Microcup)结构和顶部灌注封装技术，通过连续整卷高速涂布的制程成功地制造出高性能的双稳性、装填电泳微粒的电子纸。SiPix可提供下列两种规格形式任意的EPD卷式成品：(A)用于有源矩阵EPD和直接驱动产品的可剥离保护膜／已灌装及密封的Microcup／无图案导体膜夹层卷；及（P）用于无源矩阵的行导体膜／已灌装及密封的Microcup／列导体膜夹层卷。已经开发出将EPD卷制成不同的显示模块或产品的简单的后续加工制程。     

An adaptive generation method for electrophoretic display driving waveform design

Electrophoretic display (EPD) technology is attractive when used for reading devices such as e‐paper because of its paper‐like appearance. EPD driving is more complex than other display technologies such as liquid crystal display or organic light emission diode because the driving result of a pixel strongly depends on the initial display state. The particle size and distribution in the EPD film may vary, even if the initial state is the same. Therefore, the display devices vary between different manufacturing batches. Furthermore, different display modes such as videos, pictures or documents need different driving waveforms to achieve an optimal result. EPD manufacturers need to build a customized driving waveform for every manufacturing batch. This is very inconvenient if new applications on EPD are to be developed. And the workload is huge. In this work, an adaptive method is described for automatically creating EPD driving waveforms to fit different conditions. The central idea of this method is generally adjusting the driving time and the voltage state after getting the feedback from a measurement model. In this method, a new driving waveform is used to reduce refresh time and visual flicker. The experimental results show that the proposed approach can automatically and adaptively generate an EPD driving waveform with reasonable quality.     

Electrophoretic deposition of hydroxyapatite nanostructured coatings with controlled porosity

Hydroxyapatite (HA) coatings with controlled porosity were prepared by electrophoretic deposition (EPD) method. Carbon black (CB) particles were used as the sacrificial template (porogen agent). Two component suspensions containing different concentrations of HA and CB particles were prepared in isopropanol. It was found that the finer and positively charged HA nanoparticles are heterocoagulated on the coarser and negatively charged CB particles to form CB–HA composite particles with net positive charge. The deposition rate from the suspensions with WR (C_CB/C_HA ratio) of 0.25 was faster than that of those with WR: 0.5 at initial times of EPD. However the situation was reversed at longer EPD times. It was also found that the amount of porosity in the coatings increases as the CB concentration in the suspension increases (15%, 24%, 31%, 43% for the coatings deposited from the suspensions with 20 g/L HA nanoparticles and 0, 5, 10 and 20 g/L CB particles, respectively).     

On a transistor-type hydrogen gas sensor prepared by an electrophoretic deposition (EPD) approach

A Pd/GaN/AlGaN heterostructure field-effect transistor (HFET)-type hydrogen gas sensor, based on an electrophoretic deposition (EPD) approach, is fabricated and studied. Due to the formation of good Schottky gate contact by an EPD approach, the studied HFET shows improved DC performance including the suppressed gate current and better thermal stabilities on current–voltage (I–V) characteristics. This is mainly attributed to the reduction of interface trap density and improved Pd morphology. The EPD-based Pd morphologies are examined by X-ray diffraction, energy dispersive spectroscopy, Auger electron spectroscopy, scanning electron microscopy, and atomic force microscopy. For the used gate-dimension of 1 μm × 100 μm, an EPD-based HFET shows low gate current of 2.9 nA, maximum drain saturation current of 490 mA/mm, and maximum extrinsic transconductance of 78.9 mS/mm at room temperature. Also, solid thermal stabilities on maximum drain saturation current (−0.46 mA/mm K) and maximum extrinsic transconductance (−0.08 mS/mm K) are found as the temperature is increased from 300 to 600 K. For hydrogen gas sensing application, at 370 K, the maximum hydrogen sensitivity of 600.1 μA/mm ppm H₂/air under a 5 ppm H₂/air ambiance and fast response time (30 s) and recovery time (47 s) under a 10,000 ppm H₂/air ambiance are obtained. The EPD approach also demonstrates advantages of low cost, simple apparatus, easy process, little restriction on the shaped substrate, composited deposition, and adjustable alloy grain size. Therefore, the proposed EPD approach gives the promise for fabricating high-performance HFET devices and hydrogen gas sensors.     

Hydrogen production by aqueous-phase biomass reforming over carbon textile supported Pt-Ru bimetallic catalysts

The objective of this study is to develop highly efficient and low cost Pt-Ru bimetallic catalyst to convert biomass to bio-hydrogen fuel and chemicals by utilizing an aqueous-phase reforming (APR) reactor. The Pt-Ru bimetallic nanocatalysts on activated carbon supports were uniformly coated on the carbon textile as functionalized mesoporous media by electrophoretic deposition (EPD) method or dip-coating process. The carbon textile containing Pt-Ru nanoparticles was then rolled up and fastened to form pillar-like catalysts, which were placed in the reactor for the APR process. New catalytic processing techniques, which allow the design of catalyst at the atomistic level with controlled adsorption properties, are used to develop highly active catalysts for aqueous-phase process. The microstructure of the catalysts and activity/selectivity were optimized. This study provided a viable option for bio-hydrogen generation and reduced sugar production at the same time via a one-pot process to deal with low-cost energy crops or agriculture wastes as the substrate.     

碳纳米管场发射阴极电泳法制备及场发射特性研究

采用电泳沉积法在玻璃基板上成功制备出碳纳米管场发射阴极,采用扫描电子显微镜观察薄膜表面形貌,并对制备的碳纳米管阴极进行场发射测试.实验结果表明电泳2 min沉积的碳纳米管薄膜均匀连续且具有较好的场发射特性,其开启电场为3.1 V/μm,当外加电场强度为11.5 V/μm时场发射电流密度达到11.33 mA/cm2,经过10 V/μm的电场激活处理后样品具有较好的场发射稳定性.     

Growth of large-diameter ZnTe single crystals by liquid-encapsulated melt growth methods

The 80-mm-diameter ZnTe single crystals were successfully obtained by the liquid-encapsulated Kyropoulos (LEK) method. Both 〈100〉- and 〈110〉-oriented single crystals were reproducibly grown by using ZnTe seed crystals. Furthermore, 80-mm-diameter, 〈100〉 and 〈110〉 ZnTe single crystals were obtained by the pulling method. The etch pit densities (EPDs) of the grown crystals by the LEK and pulling methods were lower than 10,000 cm⁻². The strain in the grown crystals by the pulling method was lower than that of LEK crystals.     

ZnSe heteroepitaxy on GaAs (110) substrate

ZnSe heteroepitaxial layers have been grown on GaAs (100), (110) on axis, and (110) 6° miscut substrates by molecular beam epitaxy. ZnSe on GaAs (110) shows smooth and featureless spectra from Rutherford backscattering channeling measurements taken along major crystalline directions, whereas ZnSe on GaAs (100) without pre-growth treatments exhibit large interface disorder in channeling spectra. ZnSe films grown on GaAs (110) on axis show facet formation over a wide range of growth conditions. The use of (110) 6° miscut substrates is shown to suppress facet formation; and under the correct growth conditions, facet-free surfaces are achieved. Etch pit density measurements give dislocation densities for ZnSe epitaxial layers grown on GaAs (100), (110) on axis, and (110) 6° miscut substrates of 10⁷/cm², 3 × 10⁵/cm² and 5 × 10⁴/cm², respectively. These results suggest that with further improvements to ZnSe growth on GaAs (110)-off substrates it may be possible to fabricate defect free ZnSe based laser devices.