Ultrasonic-vibration-assisted laser annealing of fluorine-doped tin oxide thin films for improving optical and electrical properties: Overlapping rate optimization

An ultrasonic-vibration-assisted laser annealing method was developed to enhance the performance of fluorine-doped tin oxide (FTO) thin films. The influences of ultrasonic vibration, laser scan line overlapping rate (L_OR) and laser spot overlapping rate (S_OR) on surface morphology, FTO layer thickness, RMS roughness, crystal structure and photoelectric properties of the FTO films were investigated. The results indicated that the presence of ultrasonic vibration during laser annealing could significantly enhance the film compactness, and using moderate L_OR and S_OR values resulted in significantly decreased FTO layer thicknesses and RMS roughnesses as well as slightly increased crystallite sizes, thus yielding significantly improved optical transmittance values and slightly enhanced electrical conductivity values. It was found that the optimal L_OR and S_OR values for ultrasonic-vibration-assisted laser annealing of the FTO films were 80% and 90%, respectively. The as-obtained film possessed the best overall photoelectric property with an average transmittance (400–800?nm) of 85.9%, a sheet resistance of 8.7?Ω/sq and a figure of merit of 2.51?×?10^–2 Ω^–1. This work may be of great significance in terms of performance optimization of transparent conducting oxide (TCO) thin films.     

Tailoring the electron-blocking layer by addition of YSZ to Ba-containing anode for improvement of ceria-based solid oxide fuel cell

The in-situ fabrication of an electron-blocking layer between the Ba-containing anode and the ceria-based electrolyte is an effective approach in suppressing the internal electronic leakage in ceria-based solid oxide fuel cell (SOFC). To improve the thickness of the electron-blocking layer and to research the effect of the layer thickness on the improvement of SOFC, a Ba-containing compound (0.6NiO-0.4BaZr_0.1Ce_0.7Y_0.2O_3-δ) modified by Y stabilized zirconia (YSZ) was employed as a composite anode in this research. SEM analyses demonstrated that the thickness of the interlayer can be simply controlled by regulating the proportion of YSZ at anode. The in-situ formed interlayer in the cell with the anode modified by 20?mol% YSZ possesses a thickness of 0.9?µm which is more suitable for the cell achieving an enhanced performance.     

Study of tribological properties of polymer derived ZrB2-SiC ceramics

ZrB₂–SiC composite ceramics with different compositions (20 and 60?vol% ZrB₂–SiC, 20ZS and 60 ZS, respectively) were prepared. Wear tests were conducted on the obtained ceramics in multiple distances using ball-on-flat tribotester. Volume loss and cross-sectional profiles of samples were measured by three–dimensional (3D) profilometer to study the onset of track wear damages. Pressure–depth curves and hardness were measured by indentation to investigate defects produced in the tribo-film by the debris. The debris of 20ZS was found to be joined to the tribo-film and accumulated with distance, shifting from microcrack (＜10,000 cycles) to abrasive wear (50,000 cycles). Compared to 20ZS, lower debris accumulation of 60ZS resulted in better wear resistance, leading to thinner and more stable non-substrate regions for this sample. These differences between both samples basically resulted from different particle sizes. Fine grains were easily pulled out in the experiment, resulting in abrasive wear of the specimen. While transgranular fracture of grains and the pinning led to larger grains with less debris, the damage mode remained transgranular fracture.     

Garnet-like Li7-xLa3Zr2-xNbxO12 (x = 0−0.7) solid state electrolytes enhanced by self-consolidation strategy

Garnet-like Li₇La₃Zr₂O₁₂ electrolytes with Nb doping are synthesized by self-consolidation method. Different from conventional methods such as cold or hot isostatic pressing, not any pressing assistance is employed throughout the preparation process. Although the preparation process is dramatically simplified, both density and ionic conductivity of the obtained samples are enhanced. Nb-doped content plays a key role in the sintering of the packed precursor powders and in the structure stabilization of the obtained bulk samples. The optimized 0.60?mol Nb-doped sample with relative density of 94%, fine particle boundaries, and solitary cubic structure possesses the maximum total ionic conductivity of 5.22?×?10^?4?S?cm^?1 at 30?°C, which is comparable to the highest reported value of the samples prepared by conventional pressing methods. This work verifies that self-consolidation strategy is effective, reliable, and productive for the preparation of cubic Li₇La₃Zr₂O₁₂ electrolyte, which would significantly facilitate the development of ceramic electrolyte membrane technology.     

Phase stability and thermo-physical properties of ZrO2-CeO2-TiO2 ceramics for thermal barrier coatings

The properties of ZrO₂ co-stabilized by CeO₂ and TiO₂ ceramic bulks were investigated for potential thermal barrier coating (TBC) applications. Results showed that the (Ce_0.15Ti_x)Zr_0.85-xO7 (x?=?0.05, 0.10, 0.15) compositions with single tetragonal phase were more stable than the traditional 8YSZ at 1573?K. These compositions also showed a large thermal expansion coefficient (TEC) and a high fracture toughness, which were comparable to those of YSZ. However, the phase stability, fracture toughness and sintering resistance of the CeO₂-TiO₂-ZrO₂ system showed a decline tendency with the increase of TiO₂ content. The TEC of the ceramic bulks decreased with increase of TiO₂ content as well because the crystal energy was enhanced with increasing substitution of Zr⁴⁺ by smaller Ti⁴⁺. The (Ce_0.15Ti_0.05)Zr_0.8O₂ had the best comprehensive properties among the (Ce_0.15Ti_x)Zr_0.85-xO₂ compositions as well as a low thermal conductivity. Therefore, it can be explored as a TBC candidate material for high-temperature applications.     

Isothermal crystallization kinetics and subsequent melting behavior of β‐nucleated isotactic polypropylene/graphene oxide composites with different ordered structure

The effects of ordered structure on isothermal crystallization kinetics and subsequent melting behavior of β‐nucleated isotactic polypropylene/graphene oxide (iPP/GO) composites were studied using differential scanning calorimetry. The ordered structure status was controlled by tuning the fusion temperature (T_f). The results showed that depending on the variation of crystallization rate, the whole T_f range could be divided into three regions: Region I (T_f > 179 °C), Region II (170 °C ≤ T_f ≤ 179 °C) and Region III (T_f < 170 °C). As T_f decreased from Region I to Region III, the crystallization rate would increase substantially at two transition points, due to the variation of the ordered structure status. Calculation of Avrami exponent n indicated that the ordered structure induced the formation of two‐dimensional growing crystallites rather than three‐dimensional growing crystallites. Moreover, in the case of isothermal crystallization, the ordered structure effect (OSE) can also greatly increase the relative content of β‐phase (β_c). In Region II, OSE took place, resulting in evident increase of β_c, achieving 92.4% at maximum. The variation of the isothermal crystallization temperature (T_iso) had little influence on the T_f range (Region II) of the OSE. The higher T_f in Region II was more favorable for the formation of higher β_c. The ordered structure was favorable for the improvement of the nucleating efficiency of β‐nucleating agent (β‐NE), and was more effective for the improvement of lower β‐NE. © 2018 Society of Chemical Industry