PVDF静电纺纤维毡表面电性能

研究静电纺丝过程中纺丝液的质量浓度和性质、施加电压的极性和施加方式对所得聚偏二氟乙烯(PVDF)超细纤维微观形貌、纤维直径和纤维毡表面电性能的影响,并考察采用静电纺丝方法制备PVDF驻极体的可行性。结果表明:静电纺丝所得PVDF纤维毡表面有一定量的电荷残留,其电荷残留量与纺丝原液质量浓度成正比,但残留电荷很快耗散,不能直接用来制备驻极体;对比发现不同介电常数的接收介质(如:锡箔、非织造布、塑料薄膜等)对静电纺丝纤维毡表面电势残留有直接的影响。

纳米ZrO_2前驱物表面电性能的研究

利用3000HS型ζ-电位分析仪研究了ZrOCl2浓度、pH值、分散剂等因素对纳米氧化锆前驱物表面ζ-电位的影响。结果表明:低浓度ZrOCl2溶液生成的ZrO2前驱物的ζ-电位对pH值变化更加敏感;添加2%(质量分数,下同)的PEG6000和PEG20000使ZrO2前驱物的表面ζ-电位有所降低,添加2%的PEG100对前驱物ζ-电位的影响更为显著。

Ni离子注入多晶ZrO_2的表面电性能和结构

对氧化钇(Y_2O_3)部分稳定氧化锆(ZrO_2)样品在室温下进行了Ni离子注入(140kev,5×10^(15)-2×10^(17)ios/cm^2)和热退火处理.应用电学测量,Rutherford背散射技术(RBS),X射线光电子能谱(XPS)和喇曼光谱方法研究了Ni离子注入多晶ZrO_2的表面电性能,注入层结构及其热退火的影响。

Laser processing effects on Ti−45Nb alloy surface,corrosive and biocompatible properties

The Ti−45Nb(wt.%)alloy properties were investigated in relation to its potential biomedical use.Laser surface modification was utilized to improve its performance in biological systems.As a result of the laser treatment,(Ti,Nb)O scale was formed and various morphological features appeared on the alloy surface.The electrochemical behavior of Ti−45Nb alloy in simulated body conditions was evaluated and showed that the alloy was highly resistant to corrosion deterioration regardless of additional laser surface modification treatment.Nevertheless,the improved corrosion resistance after laser treatment was evident(the corrosion current density of the alloy before laser irradiation was 2.84×10^(−8)A/cm^(2),while that after laser treatment with 5 mJ was 0.65×10^(−8)A/cm^(2))and ascribed to the rapid formation of a complex and passivating bi-modal surface oxide layer.Alloy cytotoxicity and effects of the Ti−45Nb alloy laser surface modification on the MRC-5 cell viability,morphology,and proliferation were also investigated.The Ti−45Nb alloy showed no cytotoxic effect.Moreover,cells showed improved viability and adherence to the alloy surface after the laser irradiation treatment.The highest average cell viability of 115.37%was attained for the alloy laser-irradiated with 15 mJ.Results showed that the laser surface modification can be successfully utilized to significantly improve alloy performance in a biological environment.

Fe离子注入ZrO_2的研究(英文)

陶瓷材料的表面性能在很大程度上取决于其表面条件.例如:陶瓷的表面微裂纹影响着机械强度,而磁学及电学性能则对其表面结构及化学成份非常敏感.近年来离子注入法已经开辟了研制现代材料的新途径,并被广泛应用于金属、半导体及部分聚合物材料中.对于陶瓷材料,目前大多数有关这方面的研究集中于改善陶瓷表面的机械性能,很少有论文涉及其表面电性能的改善.本文介绍了一种改善ZrO2陶瓷表面导电性能的新方法.ZrO2陶瓷是绝缘体,常温下其电阻率大于1012Ωcm.通过不同剂量的离子注入可以使得样品表层产生不同程度的电性能变化.试验表明,当采用2×1017Fe/cm2注入,并在950℃下真空退火30分钟,ZrO2的表面电阻率将下降十余个数量级,从而大幅度提高了样品的导电性.文中还通过应 用X射线衍射及光电子能谱技术,分别对注入元素的化学结合状态及表面注入层的结晶相进行了较为详细的讨论.从XPS测试发现,注入离子在ZrO2表层中以Fe2+、Fe3+及Fe0三种形式的状态存在;X射线衍射数据表明,注入层中除ZrO2主晶相外,还存在少量的FeZrO3等晶相.文章的最后部分讨论了离子注入样品的导电机制.

分散剂对氧化铝悬浮液分散稳定性的影响

本文采用TURBISCAN浆体稳定性分析仪和Nano ZS-90纳米粒度及表面电位测试仪研究了柠檬酸、聚乙烯醇、聚丙烯酸钠和六偏磷酸钠等对Al2O3超细粉体的表面电性能和浆体分散稳定性的影响。研究结果表明,浆料体系的表面电性能及其分散性与体系的pH值、分散剂的种类和加入量等密切相关,浆体中加入适量的六偏磷酸钠、聚乙烯醇和聚丙烯酸钠可有效提高浆体的分散稳定性,六偏磷酸钠、聚乙烯醇和聚丙烯酸钠分别静电、空间位阻和静电位阻机制使浆体稳定。氧化铝浆体中加入柠檬酸和聚丙烯酸钠后,氧化铝表面因特征吸附阴离子而使表面电位变负,绝对值增大,等电点降低;而聚乙烯醇的加入,由于高分子链向体相中伸展,使剪切面向外移动更大的距离,从而使Zeta降低,并使等电点发生微小偏移。

Effects of surface nanocrystallization on corrosion resistance of β-type titanium alloy

Surface mechanical attrition treatment (SMAT) was performed on biomedicalβ-type TiNbZrFe alloy for 60 min at room temperature to study the effect of surface nanocrystallization on the corrosion resistance of TiNbZrFe alloy in physiological environment. The surface nanostructure was characterized by TEM, and the electrochemical behaviors of the samples with nanocrystalline layer and coarse grain were comparatively investigated in 0.9% NaCl and 0.2% NaF solutions, respectively. The results indicate that nanocrystallines with the size of 10-30 nm are formed within the surface layer of 30 μm in depth. The nanocrystallized surface behaves higher impedance, more positive corrosion potential and lower corrosion current density in 0.9%NaCl and 0.2%NaF solutions as compared with the coarse grain surface. The improvement of the corrosion resistance is attributed to the rapid formation of stable and dense passive film on the nanocrystallized surface of TiNbZrFe alloy.

Effect of surface treatment for aluminum foils on discharge properties of lithium-ion battery

Aluminum foils having thicknesses of 10-20 μm are commonly employed as current collectors for cathode electrodes in Li-ion batteries. The effects of the surface morphology of the foil on battery performance were investigated by using a foil with roughened surface by chemical etching and a plain foil with smooth surface on both sides. For high-conductivity LiCoO2 active materials with large particle size, there are no significant differences in battery performance between the two types of foils. But for low-conductivity LiFePO4 active materials with small particle size, high-rate discharge properties are significantly different. The possibility shows that optimizing both the surface morphology of the aluminum foil and particle size of active material leads to improvement of the battery performance.

Restructuring of well-defined Pt-based electrode surfaces under mild electrochemical conditions

Since the 1980s,single-crystal Pt electrodes with well-defined surface structures have been deemed stable under mild electrochemical conditions(e.g.,in the potential region of electric double layers,underpotential deposition of hydrogen,or mild hydrogen evolution/OH adsorption)and have served as model electrodes for unraveling the structure-performance relation in electrocatalysis.With the advancement of in situ electrochemical microscopy/spectroscopy techniques,subtle surface restructuring under mild electrochemical conditions has been achieved in the last decade.Surface restructuring can considerably modify electrocatalytic properties by generating/destroying highly active sites,thereby interfering with the deduction of the structure-performance relation.In this review,we summarize recent progress in the restructuring of well-defined Pt(-based)electrode surfaces under mild electrochemical conditions.The importance of the meticulous structural characterization of Pt electrodes before,during,and after electrochemical measurements is demonstrated using CO adsorption/oxidation,hydrogen adsorption/evolution,and oxygen reduction as examples.The implications of present findings for correctly identifying the reaction mechanisms and kinetics of other electrocatalytic systems are also briefly discussed.

Effects of Sintering Atmosphere on the Microstructure and Surface Properties of Symmetric TiO2 Membranes

The effects of sintering atmosphere on the properties of symmetric TiO2 membranes are studied with regard to sintering behavior, porosity, mean pore size, surface comPosition. and surface charge properties. The exerimental results show that the symmetric TiO2 membranes display better sintering activity in the air than in argon, and the mean pore diameters and porosities of the membrane sintered in argon are higher than those of the membrane sintered in the air at the same temperature. The surface compositions of the symmetric TiO2 membrane sintered in the air and in argon at different temperatures, as studied by X-ray photoelectron spectroscopy, are discussed in terms of their chemical composition, with particular emphasis on the valence state of the titanium ions. The correlation between the valence state of the titanium ions at the surface and the surface charge properties is examined.It is found that the presence of Ti^3＋, introduced at the surface of the symmetric TiO2 membranes by sintering in a lower partial pressure of oxygen, is related to a significant decrease in the isoelectric point. TiO2 with Ti^4＋ at the interface has an isoelectric point of 5.1, but the non-stoichiometric TiO2-x with Ti^3＋ at the interface has a lower isoelectric point of 3.6.

HIGH EMISSION PERFORMANCE IMPREGNATED DISPENSER CATHODE

In order to obtain higher emission performance than that of a traditional M-type cathode, we have developed a new type impregnated dispenser cathode. The new cathode is impregnated with a new active substance with molar ratio of 26BaO·29SrO·8Sc2O3 ·7CaO·Al2O3 . This paper introduces the emission performance, surface active material, and work function of the new cathode. At 1100℃B , the DC current density and pulse current density are 30.6±1.0 A/cm2 and 171.6±2.8 A/cm2 , respectively, 2.1 and 5.4 times of that of an M-type cathode. The work function of the new cathode is 1.668± 0.002 eV. High concentration O-Al-Sc-Sr-Ba and O-Al-Sc-Ba are found in the pores and at pore edges, respectively. By comparing the emission performances and surface characteristics of as-polished and as-cleaned cathodes, it is proposed that, the emission around pore ends forms the major part of the total emission for the new cathodes.

Calculation of Surface Excitation Parameters by a Monte Carlo Method

Electron inelastic mean free path （IMFP） is an important parameter for surface chemical quantification by surface electron spectroscopy techniques. It can be obtained from analysis of elastic peak electron spectroscopy （EPES） spectra measured on samples and a Monte Carlo simulation method. To obtain IMFP parameters with high accuracy, the surface excitation effect on the measured EPES spectra has to be quantified as a surface excitation parameter （SEP）, which can be calculated via a dielectric response theory. However, such calculated SEP does not include influence of elastic scattering of electrons inside samples during their incidence and emission processes, which should not be neglected simply in determining IMFP by an EPES method. In this work a Monte Carlo simulation method is employed to determine surface excitation parameter by taking account of the elastic scattering effect. The simulated SEPs for different primary energies are found to be in good agreement with the experiments particularly for larger incident or emission angles above 60° where the elastic scattering effect plays a more important role than those in smaller incident or emission angles. Based on these new SEPs, the IMFP measurement by EPES technique can provide more accurate data.

Li_(1.4)Al_(0.4)Ti_(1.6)(PO_(4))_(3) coated Li_(1.2)Ni_(0.13)Co_(0.13)Mn_(0.54)O_(2) for enhancing electrochemical performance of lithium-ion batteries

Lithium(Li)-rich manganese(Mn)-based cathode Li_(1.2)Ni_(0.13)Co_(0.13)Mn_(0.54)O_(2)(LRNCM)has attracted considerable attention owing to its high specific discharge capacity and low cost.However,unsatisfactory cycle performance and poor rate property hinder its large-scale application.The fast ionic conductor has been widely used as the cathode coating material because of its superior stability and excellent lithium-ion conductivity rate.In this study,Li_(1.2)Ni_(0.13)Co_(0.13)Mn_(0.54)O_(2) is modified by using Li_(1.4)Al_(0.4)Ti_(1.6)(PO_(4))_(3)(LATP)ionic conductor.The electrochemical test results show that the discharge capacity of the resulting LRNCM@LATP1 sample is 198 mA·h/g after 100 cycles at 0.2C,with a capacity retention of 81%.Compared with the uncoated pristine LRNCM(188.4 m A·h/g and 76%),LRNCM after the LATP modification shows superior cycle performance.Moreover,the lithium-ion diffusion coefficient D_(Li+)is a crucial factor affecting the rate performance,and the D_(Li+)of the LRNCM material is improved from 4.94×10^(-13) to 5.68×10^(-12)cm^(2)/s after modification.The specific capacity of LRNCM@LATP1 reaches 102.5 mA·h/g at 5C,with an improved rate performance.Thus,the modification layer can considerably enhance the electrochemical performance of LRNCM.

Effect of Properties of Carbon Materials on Performance of VRLA Batteries

In the present study, the relationship between properties of different carbon materials and their impact on performance of VRLA （valve regulated lead acid） battery was studied. The material properties undertaken for the study are： surface area, conductivity and water absorption of the carbon. The electrode morphology revealed the uniform distribution of active material when high surface area carbon was added to NAM （negative active material）. The porosity of the plate also exhibited changes with respect to type of carbon materials added. The study further revealed that, the addition of high surface area carbon （-1,400 m^2/g） improves the charge acceptance of the battery with higher loading. Further improvement in charge acceptance was observed with addition of graphite to higher surface area carbon. Nevertheless, the float current of the battery got affected due to graphite loading and found there was no impact on shelf life of the battery in all the cases. The study demonstrates the need for customized ＂carbon formulation＂ to obtain the maximum performance out of the battery.

锆盐文摘

水热法制备纳米氧化锆晶体，纳米ZrO2前驱物表面电性能的研究，低比表面积高烧结活性氧化锆粉体的制作方法，表面修饰纳米氧化锆的制备与表征，i—P包覆纳米氧化锆复合粉体的制备及性能研究。

Activated pyrolysed bacterial cellulose as electrodes for supercapacitors

In this paper, the bacterial celluloses(BCs) were pyrolysed in nitrogen and then activated by KOH to form a porous three- dimension-network electrode material for supercapacitor applications. Activated pyrolysed bacterial cellulose(APBC) samples with enlarged specific surface area and enhanced specific capacitances were obtained. In order to optimize electrochemical properties, APBC samples with different alkali-to-carbon ratios of 1, 2 and 3 were tested in two electrodes symmetrical capacitors. The optimized APBC sample holds the highest specific capacitance of 241.8 F/g, and the energy density of which is 5 times higher than that of PBC even at a current density of 5 A/g. This work presents a successful practice of preparing electrode material from environment-friendly biomass, bacterial cellulose.

Synthesis and High Electrocatalytic Performance of Hexagram Shaped Gold Particles Having an Open Surface Structure with Kinks

Hexagram shaped gold particles and their analogues enclosed by high index facets with kinks have been successfully synthesized by reducing HAuCl4 with ascorbic acid （AA） in the presence of poly（diallyldimethylammonium chloride） at room temperature. By using electron microscopy, the surfaces of the hexagram shaped Au particle were found to be {541} planes, which contain high-density steps and kinks. In addition, it was found that hexagonal shield-like and other kind of particles present in the product were analogues of the hexagram shaped Au particles structure, in that they had the same surface structure. In order to confirm the surface structure of all the prepared particles, surface structure sensitive underpotential deposition of Pb was carried out, and the cyclic voltammetric profile was in accordance with the proposed {541} surface. Finally, structure-property relationships of the Au hexagrams were experimentally analyzed by employing the electrocatalytic oxidation of AA as a probe reaction. The electrocatalytic reactions of gold cubes with low-index {100} facets and gold trioctahedra with {221} facets were studied as references. The experimental results showed that the hexagram shaped Au particles and their analogues with exposed {541} facets have the highest catalytic activity among the three kinds of gold particles, owing to the high density of kink atoms. This study should motivate us to further explore methods for the preparation of other well-defined polyhedral metal nanocrystals enclosed by high index surfaces.

Ultrathin Ni(OH)2 layer coupling with graphene for fast electron/ion transport in supercapacitor

Integration of fast electrochemical double-layer capacitance and large pseudocapacitance is a practical way to improve the overall capability of supercapacitor,yet remains challenging.Herein,an effective cyanogel synthetic strategy was demonstrated to prepare ultrathin Ni(OH)2 nanosheets coupling with conductive reduced graphene oxide(rGO)(rGO-Ni(OH)2)at ambient condition.Ultrathin Ni(OH)2 nanosheet with 3–4 layers of edge-sharing octahedral MO6 maximally exposes the active surface of Faradic reaction and promotes the ion diffusion,while the conductive rGO sheet boosts the electron transport during the reaction.Even at 30 A g−1,the optimal sample can deliver a specific capacitance of 1119.52 F g−1,and maintain 82.3%after 2000 cycles,demonstrating much higher electrochemical capability than bare Ni(OH)2 nanosheets.A maximum specific energy of 44.3 W h kg^−1(148.5 W kg^−1)is obtained,when assembled in a two-electrode system rGO-Ni(OH)2//rGO.This study provides an insight into efficient construction of two dimensional hybrid electrodes with high performance for the new-generation energy storage system.

The sorption mechanisms of Th(Ⅳ) on attapulgite

The surface properties of intrinsic and activated attapulgite were studied using potentiometric titration. The sorption mechanisms of Th（IV） on intrinsic and activated attapulgite were investigated by employing surface complexation model and FITEQL 3.2 code. The results indicated that the sorption sites of intrinsic attapulgite involved in the sorption process were main ion exchange site （ ≡ XNa/K）, strong site （≡ SsOH） and weak site （ ≡ SwOH）, while only strong site （ ≡SSOH） and weak site （≡SwOH） were predominant for activated attapulgite. At pH 〈 2.5, the species of Th（IV） was main Th4＋ in aqueous solution; then the hydrolysis species of Th（IV） （i.e., Th（OH）22＋, Th（OH）3＋ and Yh（OH）40） gradually formed as pH increasing. For the sorption of Th（IV） on intrinsic attapulgite, both ion exchange species （ ≡ X2Th） and inner-sphere surface complexes （ ≡ SsOTh） were dominant, while only inner-sphere surface complexes （i.e., ≡SSOThOH and ≡ SWOTh） were observed for Th（IV） sorption to activated attapulgite. In the presence of humic acid （HA）, the sorption of Th（IV） on activated attapulgite was obviously enhanced; and both ≡ SsOH-HA-Th and≡ SSOTh were the predominant speciation. It was also interesting to find that the addition of HA obviously provoked the desorption behavior of Th（IV）.

What are the practical limits for the specific surface area and capacitance of bulk sp^2 carbon materials?

The possible practical limits for the specific surface area and capacitance performance of bulk sp^2 carbon materials were investigated experimentally and theoretically using a variety of carbon materials. We find the limit for the specific surface area to be 3500–3700 m^2 g^(-1), and based on this, the corresponding best capacitance was predicted for various electrolyte systems. A model using an effective ionic diameter for the electrolyte ions was proposed and used to calculate the theoretical capacitance. A linear dependence of experimental capacitance versus effective specific surface area of various sp^2 carbon materials was obtained for all studied ionic liquid, organic and aqueous electrolyte systems. Furthermore, excellent agreement between the theoretical and experimental capacitance was observed for all the tested sp^2 carbon materials in these electrolyte systems, indicating that this model can be applied widely in the evaluation of various carbon materials for supercapacitors.