石榴石固体电解质Li3BO3界面改性研究

石榴石固体电解质由于其高的离子电导率,对锂金属稳定等优点成为了下一代高性能锂电池的重要研究方向之一。但锂金属负极界面浸润性与锂枝晶问题限制了其应用。本文通过简单的液相沉积结合高温烧结的方法,在石榴石固体电解质片表面构建了一层稳定的硼酸三锂(Li₃BO₃)修饰层。研究表明,Li₃BO₃修饰层可以有效改善石榴石固体电解质与锂金属负极界面接触,促进锂的均匀沉积/溶出,从而抑制锂枝晶生长,提高界面稳定性。Li₃BO₃修饰后石榴石电解质片与锂金属之间紧密结合,Li/石榴石界面阻抗由修饰前的1780 Ω·cm²降低至58 Ω·cm²。得益于界面接触的改善,Li₃BO₃修饰后的LLZTO电解质组装的对称电池可以在0.1 m·cm^-2的电流密度下稳定工作超过700 h。而未修饰的对称电池在0.05 mA·cm^-2的电流密度下短时间工作即出现微短路现象。     

新型聚合物多孔涂层毛细管开管柱的制备及电色谱研究

以甲基丙烯酸缩水甘油酯(GMA)和乙二醇二甲基丙烯酸酯(EDMA)为前驱体制备了新型聚合物多孔涂层毛细管开管(PLOT)柱固定相。通过优化聚合反应时间、致孔剂比例及交联剂比例获得了色谱性能良好的PLOT柱,扫描电镜结果显示毛细管柱内的多孔涂层厚度适中且均匀。在毛细管电色谱模式下,PLOT柱以反相色谱分离机理有效分离了中性、酸性和碱性小分子。人血清白蛋白(HSA)共价结合的蛋白亲和PLOT柱对5对手性对映体实现了较好的分离,且其分离度远高于HSA修饰的单层聚合物毛细管开管柱。PLOT柱分离烷基苯的日内、日间和柱间的相对标准偏差分别小于1.7%、4.8%和7.8%。     

Dynamic Docking and Undocking Processes Addressing Selectively the Outside and Inside of Polymersomes

Increasing complexity and diversity of polymersomes and their compartments is a key issue for mimicking cellular functions and protocells. Thus, new challenges arise in terms of achieving tunable membrane permeability and combining it with control over the membrane diffusion process, and thus enabling a localized and dynamic control of functionality and docking possibilities within or on the surface of polymeric compartments. This study reports the concept of polymersomes with pH‐tunable membrane permeability for controlling sequential docking and undocking processes of small molecules and nanometer‐sized protein mimics selectively on the inside and outside of the polymersome membrane as a further step toward the design of intelligent multifunctional compartments for use in synthetic biology and as protocells. Host–guest interactions between adamantane and β‐cyclodextrin as well as noncovalent interactions between poly(ethylene glycol) tails and β‐cyclodextrin are used to achieve selective and dynamic functionalization of the inner and outer spheres of the polymersome membrane.     

窄内径多孔层开管柱的制备及在液相色谱中的应用

近年来,微纳分离技术由于其内在的优势而受到越来越多的关注.多孔层开管柱是一种重要的微分离柱形式,与粗内径的多孔层开管柱(>25μm)相比,窄内径的多孔层开管柱具有更高的分离效率和更低的试剂消耗量.本文综述了内径≤25μm的窄内径多孔层开管毛细管柱的制备方法、与质谱检测联用技术以及在液相色谱中的应用研究进展,对其发展前景进行了展望.     

Optimisation of alignment materials for minimising residual retardation in in-plane switching liquid crystal display

The light leakage in a black state of in-plane switching (IPS) liquid crystal display (LCD) associated with rubbing process has been investigated. The mechanical rubbing process with a cloth caused orientation disorders in the liquid crystal directors and these partial orientation disorders result in residual retardations of the IPS LCD, causing the light leakages at the black state. In this study, we theoretically estimated how the light leakage is associated with the rubbing uniformity using 2 × 2 Jones matrix equation and also experimentally confirmed how it is associated with structural properties of the alignment layer. The light leakage was clearly reduced in the alignment layer with reduced crystallinity and flexibility.     

高残炭硼酚醛树脂的制备

酚醛树脂(PF)因其具有良好的耐热性能和机械性能而被广泛应用。但其耐热性能已经满足不了现代航空航天技术的需求,研究发现,采用硼酸对酚醛树脂进行改性,可以制得具有优良耐高温性能的硼酚醛树脂(BPF)。采用硼酸酯法合成硼酚醛树脂,n(苯酚)∶n(甲醛)=1∶1.5时耐热性最佳。热分析结果表明,合成的BPF在1000℃条件下的残炭率为78%,其耐热性能明显优于传统的酚醛树脂。同时讨论了不同硼酸含量对BPF耐热性能的影响,当n(硼酸)∶n(苯酚)0.33∶1时,残炭率趋于稳定。此外,利用差示扫描量热仪(DSC)方法确定BPF预固化温度为160℃,后固化温度为220℃。     

自由来流湍流与三维壁面局部粗糙诱导平板边界层不稳定T-S波的数值研究

采用直接数值模拟（DNS）方法,研究了在自由来流湍流与三维壁面局部粗糙作用下平板边界层内诱导产生不稳定T-S波的物理问题.数值结果可知,在平板边界层内发现了二维和三维T-S波组成的波包空间序列以及求得了波包向前传播的群速度大小,从而证明了自由来流湍流与三维壁面局部粗糙作用是激励平板边界层内诱导产生不稳定T-S波的一种机制.随后,建立了平板边界层内被激发的二维和三维T S波的初始幅值与自由来流湍流度,三维壁面局部粗糙的流向长度、展向宽度及法向高度之间的关系.这一问题的深入研究,进一步完善了流动稳定性与湍流理论.     

Influence of hybridization on in-plane shear properties of 2D & 3D thermoplastic composites reinforced with Kevlar/basalt fabrics

This paper investigates the characterization of in-plane shear properties of thermoplastic composites reinforced with Kevlar/basalt fabrics. Different fabrics had architectures of two dimensional plain woven (2D-P) and three dimensional angle-interlock (3D-A). Intralayer hybridization was performed during the weaving of the fabrics with the combination of Kevlar and basalt yarns. Five 2D-P and three 3D-A composite laminates were manufactured with polypropylene (PP) as a matrix, using compression molding. Iosipescu shear tests were carried out to evaluate the in-plane shear properties. The experimental results revealed that the shear properties including shear modulus, shear strength and shear failure strain of homogeneous composites were improved by 6.5–14.9%, 4.3–19.7%, and 3.2–46.7%, respectively. Similarly, change in the fabric architecture from 2D-P to 3D-A also enhanced the shear strength and shear failure strain by 32.0–41.6% and 7.2–22.5%, respectively. Intralayer hybrid composites had better in-plane shear properties than the interlayer hybrid composites. The fracture morphologies of the specimens were examined by scanning electron microscopy (SEM).     

Reliable and efficient reaction path and transition state finding for surface reactions with the growing string method

The computational challenge of fast and reliable transition state and reaction path optimization requires new methodological strategies to maintain low cost, high accuracy, and systematic searching capabilities. The growing string method using internal coordinates has proven to be highly effective for the study of molecular, gas phase reactions, but difficulties in choosing a suitable coordinate system for periodic systems has prevented its use for surface chemistry. New developments are therefore needed, and presented herein, to handle surface reactions which include atoms with large coordination numbers that cannot be treated using standard internal coordinates. The double‐ended and single‐ended growing string methods are implemented using a hybrid coordinate system, then benchmarked for a test set of 43 elementary reactions occurring on surfaces. These results show that the growing string method is at least 45% faster than the widely used climbing image‐nudged elastic band method, which also fails to converge in several of the test cases. Additionally, the surface growing string method has a unique single‐ended search method which can move outward from an initial structure to find the intermediates, transition states, and reaction paths simultaneously. This powerful explorative feature of single ended‐growing string method is demonstrated to uncover, for the first time, the mechanism for atomic layer deposition of TiN on Cu(111) surface. This reaction is found to proceed through multiple hydrogen‐transfer and ligand‐exchange events, while formation of H‐bonds stabilizes intermediates of the reaction. Purging gaseous products out of the reaction environment is the driving force for these reactions. © 2017 Wiley Periodicals, Inc.     

Adsorbing behavior of polycarboxylate superplasticizer in the presence of the ester group in side chain

The effect of the ester group in side chain on adsorbing behavior and dispersion of polycarboxylate superplasticizer (PC) was studied by comparing the performance of two types of PC. The fluidity of cement paste was tested to discuss the dispersing ability and dispersing retention ability of PC. The total organic carbon analyzer was used to measure the adsorption amount, and the adsorption layer was obtained by x-ray photoelectron spectroscopy. Fourier-transform infrared spectroscopy, nuclear magnetic resonance, and pH value were used to verify the stability of the ester group, and the electrokinetic properties of cement particle were confirmed using the zeta potential measurement. The results show that the ester group in side chain reduces the initial dispersing ability while it increases the dispersing retention ability. The dispersing retention ability depends on the increase of adsorption amount and adsorption layer in 5–60 minutes, and the greater increase leads to the better dispersing retention ability. The ester group can be decomposed to release carboxyl group to enhance the adsorbing ability of PC under the condition of cement hydration, which is the main reason for the greater increase of adsorption amount and adsorption layer and the improvement in dispersing retention ability. It suggests that grafting the ester group is a good way to enhance the dispersing retention ability.