Molecular design for thermally stable SiZrBOC structure from single source precursor with high ceramic yield

A new type of high-temperature-resistant SiZrBOC ceramics was prepared by sol-gel method using polymethyl-hydro siloxane (PMHS), boric acid (B(OH)₃), and n-propyl zirconate (Zr(OPr)₄) as raw materials. After high-temperature pyrolysis, the SiZrBOC precursor was transformed into a crystalline ceramic material with a yield of 89.5 wt%. Fourier infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) were applied to characterize the polymer-ceramic conversion process and thermal behavior of ceramic precursors. According to the results, the addition of boron elements led to the formation of Si-O-B links in the system. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were used to study the phase composition and microstructure of SiZrBOC ceramics. Finally, the oxidation test at 1200 °C revealed that SiZrBOC ceramics with a boron/zirconium molar ratio of 2.5:1 exhibited the best oxidation resistance at a weight gain of 0.4 wt% only.     

A kinetic model involving oxidation and volatilization in SiC-B4C-xAl2O3 ceramics system

In this paper, a new kinetic model considering both oxidation and volatilization kinetics is established and applied to analyze the oxidation of SiC-B₄C-xAl₂O₃ ceramics and other systems in various oxidation conditions. The effects of diffusion area and volume changes during the oxidation process are considered in this model. The physical meaning of each parameter in this model is explicit and simple. According to this model, the diffusion coefficient of species and the corresponding diffusion activation energy are easily available. The practicability of this model is well verified by the experimental data of SiC-B₄C-xAl₂O₃ and other systems oxidized under different conditions. In addition, the practice shows that the model is applicable not only to the systems where oxidation and volatilization coexist, but also to the system where only oxidation plays a major role. We hope the model proposed in this work can be used in other materials with more complex environments.     

Evolution of core–rim structures and phase transformations in infra-red transmitting Y-α-SiAlON ceramics

Core–rim structures were observed as common features in Y-α-SiAlON ceramics hot-pressed between 1550?1950 °C. We found most dopants were taken into α’-rims, and a transition layer grown first on α-cores from liquid-phase over-saturated with metal solutes. Elongated β’-grain were formed as minor phase with α’- or AlN-cores thus only after the α’ matrix had consumed up all Y solutes, revealing that the α’ → β’ transformation is controlled by the transient liquid-phase and similar defects and dangling bonds could be detected in both SiAlON phases by cathodoluminescence. Quantitative assessment of Y_m/3Si_12?(m+n)Al_m+nO_nN_16?n demonstrates the multiphase evolution, initiated by over-saturation of Y solutes at low temperatures thus retaining α-phase as cores to lower the infra-red transmittance, dictated by homogenization of Al solutes at higher temperature. The elimination of those phase boundaries leads to better dopant and sintering design for achieving transparent and high-performance SiAlON ceramics.     

火星表面散射光对太阳电池发电影响研究

火星表面存在大气,太阳光经过大气后,部分被大气吸收,部分光到达火星表面,形成直射光,还有一部分光被空气尘埃阻挡发生漫反射,形成散射光,地面反射的光也是散射光光源的一部分。直射光和散射光均会对火星车太阳电池发电产生影响。分析了火星探测漫游者(MER)任务中火星车太阳翼实际发电情况,调研了火星表面直/散光辐照数据,进行了地面直/散光辐照试验,并对上述三类数据进行比对,给出火星表面散射光对太阳电池发电影响的定量结果。     

Microstructure evolution and cooperative reinforcement mechanisms of Al2O3/Al2O3 joints brazed by low-melting borosilicate glass

The Al₂O₃/SiO₂–B₂O₃–Al₂O₃–Na₂O glass/Al₂O₃ joints reinforced cooperatively by glass matrix and in-situ Al₄B₂O₉ whiskers were obtained via a low-melting borosilicate glass braze. The composition of glass seam transformed from SiO₂–B₂O₃–Na₂O to SiO₂–B₂O₃–Al₂O₃–Na₂O due to continuous diffusion and dissolution of Al₂O₃. An appropriate amount of [AlO₄] units introduced into the glass braze played a vital role in strengthening the glass network structure resulting to considerably improved mechanical strength of the glass seam. Meanwhile, plenty of in-situ Al₄B₂O₉ whiskers growing from the Al₂O₃/glass braze interface to the center of glass seam in various directions generated. Three-dimensional crisscross structures were fabricated at the Al₂O₃/glass braze interface domains, where were enhanced by crack-bridging and pull-out effect of the whiskers. Generally, ascribed to the cooperative reinforcement of the glass matrix in the seam and in-situ Al₄B₂O₉ whiskers at Al₂O₃/glass braze interface domains through reactions of Al₂O₃ and borosilicate glass braze, strength of the as-brazed joints was promoted prominently. The shear strength of the joints reached a maximum of 61 MPa brazed at 1050 °C for 60 min.     

Ammonia borane assisted solid exfoliation of graphite fluoride for facile preparation of fluorinated graphene nanosheets

Fluorinated graphene, which combines the unique properties of graphite fluoride and graphene, has attracted considerable attention in recent years. Here, we developed a facile, efficient, and scalable method for high-yield exfoliation of graphite fluoride into fluorinated graphene (fluorographene) nanosheets. The exfoliation approach consists of solid ball milling of graphite fluoride with ammonia borane and followed washing with ethanol to get rid of ammonia borane from the products. The majority of the as-synthesized fluorographene nanosheets consist of 1–6 atomic layers with grain sizes in the range of 0.3–1 μm. X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy demonstrated that fluorographene has the same structure as pristine graphite fluoride.     

国外某高磷鲕状铁矿石工艺矿物学研究

为查明国外某高磷鲕状铁矿石的性质，采用化学分析、X射线衍射以及扫描电子显微镜等方法，研究了其化学组成、矿物组成、嵌布特征以及磷元素的赋存状态。结果表明，矿石中主要含铁矿物为赤铁矿和磁铁矿，还有少量菱铁矿以及针铁矿，主要脉石矿物为鲕绿泥石和方解石。矿石中48.61%的磷存在于磷灰石中，47.22%的磷分布于铁矿物中。铁矿物主要分布于鲕粒中，并与脉石矿物紧密共生，难以分离。大部分磷灰石存在于鲕粒中并被铁矿物包裹，粒度细且与铁矿物关系密切；存在于铁矿物中的磷均匀分布且无法用物理方法分离；少量的磷以纤磷钙铝石形式出现并被铁矿物包裹。鉴于矿石复杂的工艺矿物学尤其是磷的存在形式复杂，推荐采用直接还原—磁选工艺处理该铁矿石。     

Time-independent charge carrier mobility in a model polymer:fullerene organic solar cell

The technique of photo-CELIV (charge extraction by linearly increasing voltage) is one of the more straightforward and popular approaches to measure the faster carrier mobility in measurement geometries that are relevant for operational solar cells and other optoelectronic devices. It has been used to demonstrate a time-dependent photocarrier mobility in pristine polymers, attributed to energetic relaxation within the density of states. Conversely, in solar cell blends, the presence or absence of such energetic relaxation on transport timescales remains under debate. We developed a complete numerical model and performed photo-CELIV experiments on the model high efficiency organic solar cell blend poly[3,6-dithiophene-2-yl-2,5-di(2-octyldodecyl)-pyrrolo[3,4-c]pyrrole-1,4-dione-alt-naphthalene] (PDPP-TNT):[6,6]-phenyl-C₇₁-butyric-acid-methyl-ester (PC70BM). In the studied solar cells a constant, time-independent mobility on the scale relevant to charge extraction was observed, where thermalisation of photocarriers occurs on time scales much shorter than the transit time. Therefore, photocarrier relaxation effects are insignificant for charge transport in these efficient photovoltaic devices.