人工界面层在金属锂负极中的应用

金属锂具有极高的比容量(3860 mAh·g^?1)和最低的电化学反应电位(相对标准氢电位为?3.040 V),被认为是高能量密度二次电池最具潜力的负极材料。然而金属锂负极界面稳定性差、不可控的枝晶生长、沉积/剥离过程中巨大的体积变化等严重阻碍了金属锂负极的商业化应用。在金属锂表面构建一层物理化学性质稳定的人工界面保护层被认为是解决金属锂负极界面不稳定和枝晶生长,缓解体积膨胀带来的界面波动等一系列问题的有效手段。本综述依据界面传导性质,从离子导通而电子绝缘的人工固态电解质界面(SEI)层、离子/电子混合传导界面、纳米界面钝化层三个部分对人工界面保护层进行了归纳总结。分析了人工界面保护层的物质结构与性能之间的构效关系,探讨了如何提高人工界面保护层的物理化学稳定性、界面离子输运、界面强度与柔韧性、界面兼容性等。最后,指出用于金属锂负极的人工界面保护层目前面临的主要挑战,并对其未来的发展进行了展望。     

Change in microstructure and surface properties of electrospray-synthesized silica layers

Silica layers with different microstructures were prepared by electrospraying. The microstructure of the layers was changed by controlling the viscosity of the precursor solutions in the electrospray deposition. Precursor solutions of low viscosity produced particulated silica layers, exhibiting superhydrophobicity. In contrast, fibrous silica layers exhibiting superhydrophilicity were attained with viscous precursor solutions. In particular, the particulated silica layers showed a good durability and resistance to ultraviolet illumination. The dramatic change in the wettability of silica layers without any chemical treatment is promising in speeding up their use in many fields.     

Adsorption-entanglement layers in flowing high molecular weight polymer solutions III: Solution concentration and solvent power

Adsorption entanglement layers are thick, i. e. multimolecular layers formed at solid surfaces during the flow of high molecular weight polymer solutions. The present publication is concerned with the influence of solution concentration and solvent power on the formation of these layers. Three polymers have been used, polyethylene, polymethylmethacrylate and atactic polystyrene in various solvents. The formation and thickness of layers were monitored from their effect on flow behaviour. Two flow geometries were used: Couette flow — where the layers cause peaks in the shear stress during continuous shearing, and capillary flow where the layers reduce the flow rate. The results indicate that there is a critical concentration below which no layers form, and that this critical concentration is an order of magnitude less than the conventionally defined overlap concentration. It is also deduced that the layers form more quickly, and grow to be thicker when better solvents are used.     

Alternate deposition of oriented calcite and amino acid layer on calcite substrates

Material synthesis inspired by novel nacre architecture and mechanism is popular and has attracted more and more attention. In this paper, iso-oriented calcite tablets/layers and amino acid layers were formed alternately on calcite wafers. It is interesting that the neonatal calcite tablets/layers have the same crystal orientation with their inorganic substrates through amino acid layers. It is quite possible that the amino acid layers in this study could transfer crystal orientation from formed inorganic layers to neighboring neonatal layers due to their fixed and appropriate structures, which may imply the process of nacre formation, and the role of aligned organic matrix sheets in nacre. Moreover, it could provide a new way to produce oriented calcite tablets/layers.     

Patterned and controlled polyelectrolyte fractal growth and aggregations

Two-dimensional patterned and controlled polyelectrolyte aggregations (e.g., tree-like ramified structures) created by microcontact printing have been demonstrated and discussed. Polyelectrolyte-micropatterned aggregations on surfaces were controlled by the micropattern size and shape of PDMS stamps. The formation of aggregates was dependent on the ink and surface conditions, and the aggregates consisted of two distinct layers; strongly adsorbed, primary uniform layers and weakly adsorbed, secondary aggregation layers positioned on top of the primary layers. The adsorption of the primary layers was strong enough not to be washed away, while the aggregated secondary layers were easily removed by washing. The aggregation of secondary layers showed typical tree-like ramified structures of fractal growth and aggregation. Directional and confined stamping led to directing and confining the growth of the fractal polyelectrolyte clusters, respectively. The micropatterned primary uniform layers were not removed by extensive washing, and they were identified by selective nickel plating and charged particle selective adsorption in which the surface formed positive and negative micropatterns. These functional and patterned surfaces have great potentials for advanced devices and sensors.     

Interface analysis of Ti/Al/Ti/Au ohmic contacts with regrown n+‐GaN layers using molecular beam epitaxy

The regrowth technique of highly doped n‐type GaN layers is reliable and effective for lowering the ohmic contact resistance. The interface between metal contacts with Ti/Al/Ti/Au and regrown n⁺‐GaN/GaN layers were analyzed in detail with transmission electron microscopy. During the annealing process, Ti metals and N atoms diffusing from GaN layers formed TiN epitaxial layers between metal alloys and n⁺‐GaN layers. The orientational relationship between GaN and TiN was [1 0 0]_GaN//[?1 1 0]_TiN verified by nano‐beam diffraction. Al atoms diffused through the GaN layers and formed thin AlGaN phase. Al content was confirmed as 60% by high‐resolution transmission electron microscopy images. Electron energy loss spectroscopy showed that Si dopants were confined within n⁺‐GaN layers. These results show that in regrowth technique both TiN layers and Si dopants affect the contact properties because the formation of TiN layers can induce nitrogen vacancies from GaN, while Si‐doped GaN layers can enhance the tunneling effect through the metal contacts resulting in reduced contact resistance. Copyright © 2011 John Wiley & Sons, Ltd.     

Langmuir-Blodgett assembly of graphite oxide single layers

Single-layer graphite oxide can be viewed as an unconventional type of soft material and has recently been recognized as a promising material for composite and electronics applications. It is of both scientific curiosity and technical importance to know how these atomically thin sheets assemble. There are two fundamental geometries of interacting single layers: edge-to-edge and face-to-face. Such interactions were studied at the air-water interface by Langmuir-Blodgett assembly. Stable monolayers of graphite oxide single layers were obtained without the need for any surfactant or stabilizing agent, due to the strong electrostatic repulsion between the 2D confined layers. Such repulsion also prevented the single layers from overlapping during compression, leading to excellent reversibility of the monolayers. In contrast to molecular and hard colloidal particle monolayers, the single layers tend to fold and wrinkle at edges to resist collapsing into multilayers. The monolayers can be transferred to a substrate, readily creating a large area of flat graphite oxide single layers. The density of such films can be continuously tuned from dilute, close-packed to overpacked monolayers of interlocking single layers. For size-mismatched single layers, face-to-face interaction caused irreversible stacking, leading to double layers. The graphite oxide monolayers can be chemically reduced to graphene for electronic applications such as transparent conducting thin films.     

Quantitative Analyse von Schichtsystemen mit der Methode der Rutherford-Weitwinkelstreuung

The use of Rutherford backscattering for the investigation of monocrystals overlaid with thin amorphous layers is briefly described. Using silicon crystals covered with silicon nitride and aluminium layers, methods are exhibited, which provide special informations about surface layers (mass and area concentration of the layer atoms, composition of the layers and density and thickness, respectively).      

Synthetic zeolites A and X as stationary phases in thin-layer chromatography

Summary The possibility of using synthetic zeolites A and X as stationary phases in thin-layer chromatography has been investigated and the method of preparing layers from crystalline zeolites and their gels determined, as was the possibility of separating certain mixtures on the layers obtained. Experiments were performed simultaneously on layers from zeolites A and X dried at room temperature and on layers activated at 120°C, and also on layers from amorphous forms but in this case only on those dried at room temperature. Dyes and inorganic cations were used as test substances. On the basis of the results obtained it has been established that only the crystalline compounds can be successfully used as thin layers for the separation of organic compounds.     

Super fast switching and low operating of liquid crystals sandwiched between ion beam-spurted ITO thin layers

Ion beam (IB)-spurted indium tin oxide (ITO) thin layers are used to align liquid crystals (LC) with a lower driving voltage. During IB spurting process, the microcrystals transforming to large crystals of ITO is intimated by the change of In (3d), Sn (3d) and O (1s) core level in XPS spectra and the surface topology modifications in SEM and AFM images, and IB-spurted ITO thin layers are comparably transparent and conductive compared with ITO thin layers. The increased interactions between LC and IB-spurted ITO thin layers together with the roughed surface topology of ITO thin layers are the main causes for LC alignment. The fast response and distribution of electrical dipoles to external voltage in LC causes LC’s extremely low threshold voltage drive; in addition, LC directly aligned on ITO thin layers free from alignment layers shield effect further decreases LC’s threshold voltage. 1.8-keV IB-spurted ITO thin layers are more appropriate to align LC with the threshold voltage of 0.4853 V and the rising time of 0.237 ms.     

Electrochemical interfacial capacitance in multilayer graphene sheets: Dependence on number of stacking layers

We engineered the number of stacking layers of multilayer graphene sheets by selective post-treatments. The most probable number of layers of graphene was determined according to specific surface area. The interfacial capacitance of multilayer graphene sheets relates to the number of layers. This result is attributed to the dependence of space charge layer capacitance on the number of layers.     

有序卤化银照相层的颗粒度的计算机模拟测量——方形采样孔效应

在本工作中,设计了几种照相层中卤化银颗粒有序排列的图案,并采用计算机模拟测量颗粒度的方法分析了颗粒按各种图案排列的照相层在曝光和显影之后的影象层的颗粒度随密度的变化,从而确定较佳的颗粒排列的图案。在对颗粒有序排列的照相层进行颗粒度模拟测量的时候发现:与颗粒随机排列照相层的颗粒度测量不同,方形采样孔尺寸的微小变化会引起颗粒度测量值颇大的波动。可以预料,方形采样孔在试样上的取向对测量结果也会有影响。因此,圆形采样孔可能比较适合于用来测量有序卤化银照相层的颗粒度。     

Adsorption and Exchange Dynamics in Aging Hydroxyethylcellulose Layers on Silica

The adsorption kinetics of hydroxyethylcellulose (HEC) on silica and relaxations in adsorbed HEC layers were probed using total internal reflectance fluorescence and near-Brewster reflectivity. Like many random-coil polymers, HEC was found to adsorb at the transport-limited rate. Relaxations occurred at nearly constant interfacial mass when HEC layers were exposed to aqueous solvent, causing the subsequent exchange of chains between the layer and the free solution to become increasingly hindered. Eventually, on the time scale of a day, layers became immobilized and unable to accommodate chains from free solution. A continued fluorescence decay, beyond time scales that could be probed with self exchange, suggested further relaxations of the adsorbed HEC. The polydisperse HEC system (with an average molecular weight near 450,000) behaved qualitatively similar to molecular weight standard polyethylene oxide (PEO) layers on silica. For instance, relaxations in PEO layers occurred on a time scale of 10-20 h, like the HEC layers. Young layers of the latter, however, exhibited self-exchange kinetics that were an order of magnitude slower than PEO layers of similar age. This difference in adsorbed layer dynamics was attributed to HEC's stiffer backbone, compared with flexible PEO. Copyright 2000 Academic Press.     

Formation and plasmonic response of self-assembled layers of colloidal gold nanorods and branched gold nanoparticles

The plasmonic properties of self-assembled layers of rod- and branched-shaped gold nanoparticles were investigated using optical techniques. Nanoparticles were synthesized by a surfactant-guided, seed-mediated growth method. The layers were obtained by gradual assembly of nanoparticles at the interface between a polar and a nonpolar solvent and were transferred to a glass slide. Polarization and angle-dependent extinction measurements showed that the layers made of gold nanorods were governed by an effective medium response. The response of the layers made by branched gold particles was characterized by random light scattering. Microscopic mapping of the spatial mode structure demonstrates a uniform optical response of the nanoparticle layers down to a submicrometer length scale.     

聚酯低聚物和聚乙二醇醚对蒙脱土的插层与剥离作用

高分子基 /层状硅酸盐钠米复合材料的制备得益于自然界存在的一类层状硅酸盐 .它具有阳离子可交换性和在一些介质中的可膨润性 .在层状硅酸盐中蒙脱土是使用较普遍的一种 .它的晶胞系由两层Ｓｉ—Ｏ四面体中间夹一层Ａｌ—Ｏ(ＯＨ)八面体组成 .晶胞呈平行迭置 .层内有剩余电子而使其带负电荷 ,它与层间的自由阳离子Ｎａ+、Ｋ+、Ｃａ2 +、Ｍｇ2 +等达到电荷平衡 ,保持其整体的电中性 .利用蒙脱土的阳离子可交换特性 ,将有机离子插层剂或反应单体插入ＭＭＴ层间 ,使其层间距撑大 ,并增加其在反应体系中的膨润性 ,使ＭＭＴ在反应体系中剥离 ,…     

Incorporation of Pigments in TEOS Derived Matrices

Small organic pigments were incorporated in TEOS derived sol-gel layers on glass. The layers were characterised on transparency, lightfastness and pencil hardness. It was found that transparent layers can be made. Pigment loaded layers have a better lightfastness than layers into which dyes are incorporated. As only moderate curing temperatures (160°C) were applied, the organic fraction originating from the organic stabilizer present in the pigment dispersion remains to a large extent in the layer. Therefore the pencil hardness decreases with the amount of stabilizer used to disperse the pigment particles. The type of pigment has no influence on the pencil hardness.     

TCNQ Interlayers for Colloidal Quantum Dot Light‐Emitting Diodes

CdSe/CdS/ZnS quantum dot light‐emitting diodes (QD‐LEDs) show increased brightness (from ca. 18 000 to 27 000 cd m^?2) with 7,7,8,8‐tetracyanoquinodimethane (TCNQ) between the QD and electron‐transfer layers of ZnO nanoparticles. As QD/ZnO layers are known to have interface defects, our finding leads to the importance of interface engineering for QD‐LEDs. Although the photoluminescent intensity and decay lifetime of ZnO/TCNQ/QD layers are similar to those of ZnO/QD layers, cyclic voltammetry suggests improved charge transfer of TCNQ/ZnO layers compared to that of pure ZnO layers. This helps us to understand the mechanism of electrically driven QD‐LED behavior, which differs from that of conventional solid‐state LEDs, and enables the rational design of QD‐based optoelectronic devices.     

Influence of Neighboring Layers on Interfacial Energy of Adjacent Layers

The binding energy and generalized stacking-fault energy (GSFE) are two critical interface properties of two dimensional layered materials, and it is still unclear how neighboring layers affect the interface energy of adjacent layers. Here, we investigate the effect of neighboring layers by comparing the differences of binding energy and GSFE between trilayer heterostructures (graphene/graphene/graphene, graphene/graphene/boron nitride, boron nitride/graphene/boron nitride) and bilayer heterostructures (graphene/graphene, graphene/boron nitride) using density functional theory. The binding energy of the adjacent layers changes from -2.3% to 22.55% due to the effect of neighboring layer, with a very small change of the interlayer distance. Neighboring layers also make a change from -2% to 10% change the GSFE, depending on the property of the interface between adjacent layers. In addition, a new simple expression is proven to describe the GSFE landscape of graphene-like structure with high accuracy.     

Characterization of metallic layer composites by means of AES/depth profile analysis

The adherence mechanism of arc sprayed Ni layers on structure steel St37 is investigated. AES depth profiles are obtained on single Ni particles still adhering to the substrate after the Ni layer has been separated from it. A comparison of interface shapes and results of adherence measurements reveals Fe-Ni layered structures for the best adhering layers, whereas less adhering layers are characterized by narrower interfaces caused by diffusion. Areas with no adherence are covered with oxidic layers.     

Enhancing photoinduced hydrophilicity of micro arc oxidized TiO2 nanostructured porous layers by V-doping

This study sheds light on the effect of vanadium doping on hydrophilicity properties of micro arc oxidized TiO₂ porous layers. Pure and V-doped titania layers, with a pore size of 50–400 nm, were grown by micro arc oxidation method. Morphology and topography of the layers were studied by SEM and AFM techniques where formation of a porous structure with a rough surface was confirmed. Moreover, phase structure and chemical composition of the samples were investigated employing XRD and XPS techniques. The pure TiO₂ layers consisted of anatase and rutile phase. Vanadia phase was also detected in V-doped layers. It was also revealed that V₂O₅ not only dispersed in the TiO₂ matrix, but also doped into the crystalline lattice. Optical properties and band gap energy of the synthesized layers were evaluated by a UV-Vis spectrophotometer. Our results showed that the band gap energy decreased when vanadium was introduced into the titania lattice. Finally, hydrophilicity of the pure and the doped layers was studied under ultraviolet and visible illuminations by measuring the water contact angle on their surface. The V-doped layers, especially those which were grown under intermediate voltages, revealed an enhanced hydrophilicity when compared to the pure TiO₂ layers.