聚丙烯酸钠吸水树脂/聚乙烯醇/高氯酸锂聚电解质的制备与性能

制备了SPA/PVA/LiClO4凝胶电解质和固体导电膜。结果表明,LiClO4和SPA的质量分数分别为0.9%和3.5%的水凝胶电导率可达8.30×10-3S/cm;SPA、PVA、LiClO4的浓度分别为3.75g/100mL、3.75g/100mL和0.9g/100mL的水凝胶电解质电导率可达8.42×10-3S/cm,经过流延法制备的固体薄膜表面电导率为3.00×10-10S/cm,体积电导率9.8×10-8S/cm,证明固体膜具有固体电解质性能。固体膜的红外光谱分析表明PVA中的-OH基与SPA中的-COO-有氢键作用,使树脂对Li+,Na+的作用减弱,加速了Li+,Na+在弱交联网络中的络合-解离过程,提高了离子的迁移速率,从而实现了离子导电。

电解质的导电性实验的改进及探究

现行九年级化学教材中电解质的导电性实验教材和教参中的实验方案不适合课堂教学,若按教材、教参进行实验,很有可能导致实验失败。笔者经过反复实验,找出最佳试剂浓度,最佳实验装置。在保证最佳实验效果的前提下,使药品消耗大大降低了。

大型预焙阳极电解槽启动期间技术参数的控制

电解槽启动期间技术参数的控制十分关键,通过控制好槽工作电压、极距、电解质温度、电解质成分、电解质数量等技术参数,能使电解槽顺利启动,并且为电解槽以后高效平稳生产和延长槽寿命打下坚实基础.

两种新型化学仪器的构造与使用

介绍了新研制的两种化学实验仪器--电解质导电显示仪器和沉浮式气体发生器的构造、使用方法及其主要性能.

Oxygen ionic conductivity of a composite electrolyte SDC-LSGM prepared via glycine-nitrate process

Ce0.8Sm0.2O1.9-δ-La0.9Sr0.1Ga0.8Mg0.2O3-δ（SDC-LSGM）is prepared by the glycine-nitrate process（GNP）.SDC-LSGM composite electrolyte samples with different weight ratios are prepared by the co-combustion method so as to obtain homogeneous nano-sized precursor powders. The X-ray diffraction （XRD） and the scan electron microscope （SEM） are used to investigate the phases and microstructures. The measurements and analyses of oxygen ionic conductivity of SDC-LSGM are carried out through the four-terminal direct current （DC） method and the electrochemical impendence spectroscopy, respectively. The optimum weight ratio of SDC-LSGM is 8∶2, of which the ionic conductivity is 0.113 S/cm at 800℃ and the conductivity activation energy is 0.620 eV. The impendence spectra shows that the grain boundary resistance becomes the main barrier for the ionic conductivity of electrolyte at lower temperatures. The appropriate introduction of LSGM to the electrolyte SDC can not only decrease the electronic conductivity but also improve the conditions of the grain and grain boundary, which is advantageous to cause an increase in oxygen ionic conductivity.

Preparation and characterization of poly(lithium acrylate-arcylonitrile)/LiClO_4-LiNO_3-LiBr solid polymer electrolytes

Through orthogonal experiment, a new type of LiClO4-LiNO3-LiBr eutectic salt with optimum mole ratio of n（LiClO4）∶n（LiNO3）∶n（LiBr）=1.6∶3.8∶1.0 was prepared. The poly（lithium acrylate-acrylonitrile）/LiClO4-LiNO3-LiBr solid polymer electrolytes were prepared with poly（lithium acrylate-acrylonitrile） and （LiClO4-LiNO3-LiBr） eutectic salts. The effect of LiClO4-LiNO3-LiBr eutectic salts content on the conductivity of solid polymer electrolytes was studied by alternating current impedance method, and the structures of eutectic salts and solid polymer electrolytes were characterized by differential thermal analysis, infrared spectroscopy and X-ray diffractometry. The results show that the room temperature conductivity of LiClO4-LiNO3-LiBr eutectic salts reaches (3.11×10-4 S·cm-1.) The poly（lithium acrylate-acrylonitrile）/LiClO4-LiNO3-LiBr solid polymer electrolytes possess the highest room temperature conductivity at 70% LiClO4-LiNO3-LiBr eutectic salts content, and exhibit lower glass transition temperature of 75 ℃ compared with that of poly（lithium acrylate-acrylonitrile） of 105 ℃. A complex may be formed in the solid polymer electrolytes from the differential thermal analysis and infrared spectroscopy analysis. X-ray diffraction results show that the poly（lithium acrylate-acrylonitrile） can suppress the crystallization of eutectic salts in this system.

Theoretical Aspects on Doped-Zirconia for Solid Oxide Fuel Cells:from Structure to Conductivity

Solid oxide fuel cells(SOFCs)are regarded to be a key clean energy system to convert chemical energy(e.g.H_(2) and O_(2))into electrical energy with high efficiency,low carbon footprint,and fuel flexibility.The electrolyte,typically doped zirconia,is the"state of the heart"of the fuel cell technologies,determining the performance and the operating temperature of the overall cells.Yttria stabilized zirconia(YSZ)have been widely used in SOFC due to its excellent oxide ion conductivity at high temperature.The composition and temperature dependence of the conductivity has been hotly studied in experiment and,more recently,by theoretical simulations.The characterization of the atomic structure for the mixed oxide system with different compositions is the key for elucidating the conductivity behavior,which,however,is of great challenge to both experiment and theory.This review presents recent theoretical progress on the structure and conductivity of YSZ electrolyte.We compare different theoretical methods and their results,outlining the merits and deficiencies of the methods.We highlight the recent results achieved by using stochastic surface walking global optimization with global neural network potential(SSW-NN)method,which appear to agree with available experimental data.The advent of machine-learning atomic simulation provides an affordable,efficient and accurate way to understand the complex material phenomena as encountered in solid electrolyte.The future research directions for design better electrolytes are also discussed.

New pretreatment method for high-tension electrical separation of zircon from quartz

Electrostatic separation is one of the mineral processing methods based on mineral conductivity.This method has some significant problems such as being sensitive to humidity,high middling product,and impurity of non-conductive minerals.In this study,a new pretreatment method was proposed for the separation of zircon from quartz before electrostatic separation to solve these disadvantages.In this regard,two stages of pretreatment were applied which involved using collector of sodium dodecyl sulfate(SDS)for adjusting wettability of the zircon surface and spraying electrolyte aqueous solution to increase conductivity of the quartz surface.The effects of important parameters including pH,collector concentration,conditioning time,and concentration and type of electrolyte on the process efficiency were evaluated.The results showed that the optimal conditions of high-tension electrical separation were pH of 4,SDS concentration of 1×10-4 mol/L,conditioning time of 4 min and NaCl as an electrolyte with concentration of 4.27 mol/L.Separation efficiency of 95.12% was achieved in optimum conditions.This pretreatment method can be successfully used before high-tension electrical separation to separate the conductive or non-conductive minerals with various compositions.

Preparation and properties of PEO/LiClO_4/KH560-SiO_2 composite polymer electrolyte by sol-gel composite-in-situ method

Composite polymer electrolytes based on polyethylene oxide(PEO) were prepared by using LiClO4 as doping salt and silane-modified SiO2 as filler. SiO2 was formed in-situ in (PEO)8LiClO4 matrix by the hydrolysis and condensation reaction of Si(OC4H9)4. The crystallinity,morphology and ionic conductivity of composite polymer electrolyte films were examined by differential scanning calorimetry,scanning electron microscopy,atom force microscopy and alternating current impedance spectroscopy,respectively. Compared with the crystallinity of the unmodified SiO2 as inert filler,that of composite polymer electrolytes is decreased. The results show that silane-modified SiO2 particles are uniformly dispersed in (PEO)8LiClO4 composite polymer electrolyte film and the addition of silane-modified SiO2 increases the ionic conductivity of the (PEO)8LiClO4 more noticeably. When the mass fraction of SiO2 is about 10%,the conductivity of (PEO)8LiClO4-modified SiO2 attains a maximum value of 4.8×10-5 S·cm-1.

Influence of Li_3PO_4 addition on properties of lithium ion-conductive electrolyte Li_(1.3)Al_(0.3)Ti_(1.7)(PO_4)_3

The sintered Li1.3Al0.3Ti1.7（PO4）3 pellets with different mole fractions of Li3PO4 were prepared by sol-gel method.The structure,surface morphology,electrochemical window,ionic conductivity and activation energy of the sintered pellets were studied by X-ray diffraction,scan electron microscopy,cyclic voltammetry,and electrochemical impedance spectroscopy.The results show that all the sintered Li1.3Al0.3Ti1.7（PO4）3 pellets with different mole fractions of Li3PO4 have similar X-ray diffraction patterns.The sintered Li1.3Al0.3Ti1.7（PO4）3 pellet with Li3PO4 shows a lower porosity and is denser than the one without Li3PO4.The addition of Li3PO4 has a large effect on the porosity and density of the sintered Li1.3Al0.3Ti1.7（PO3）4 pellet,and little effect on its electrochemical window.Among the sintered Li1.3Al0.3Ti1.7（PO3）4 pellets with different mole fractions of Li3PO4,the one with 1% Li3PO4 shows the activation energy of 0.314 2 eV and the highest ionic conductivity of 6.15-10-4 S/cm.

Properties of Al_2O_3-Sm_2O_3-CeO_2 electrolyte

Cel-xSmxO2 （x=0, 0.1, 0.2 and 0.3） and Sm-doped ceria＋（2%-8%）Al2O3 were synthesized through sol-gel process followed by low temperature combustion. The synthesis, structure, densification, conductivity and thermal expansion were studied, and the structure and phase were confirmed by XRD. Dense ceramics were obtained through sintering the pellets at 1300 ℃. 2% and 4% Al2O3 were added into Ce0.8Sm0.2O2 to promote the densification at 1250 ℃. The surface morphology of the sintered pellets was analyzed using SEM. A two-probe AC impedance spectroscopy was used to study the total ionic conductivity.

Factors Affecting Diffusion of Ions in Soils

In this work the diffusion coefficients of Na+, K+, Ca2+, NO3- and Cl- ions were estimated in terms of measuring apparent direct current (DC) conductivities of latosol, red soil and yellow-brown earth containing, respectively, NaNO3, KCI, and CaCl2 of different concentrations (0.005, 0.05, 0.10, and 0.15 mol / L) in the case of moisture contents ranging from wet to water saturation. The results showed that when bulk density, moisture content, and electrolyte concentration were constant, the diffusion coefficients of cations were in the order Na+> K+> Ca2+ except for Na+ and K+ in latosol, while the order for anions was NO3- > Cl-. The diffusion coefficients (Di) of cations and anions were linearly proportional to volumetric moisture content (θ) as electrolyte concentration and bulk density were unchanged. When moisture content and bulk density were constant, the diffusion coefficients of cations decreased, to varying extents, with the increase of electrolyte concentration, and the decrement in different soils followed the order yellow-brown earth > red soil > latosol, but the decrement order of different cations was Na+> K+ > Ca2+.

Measurements of Conductivity for Low Concentration Strong-electrolytes in Organic Solvents (Ⅰ) LiBr, LiCl, and LiNO_3 in Alcohols

The conductivities of LiBr, LiCl, and LiNO 3 in methanol, ethanol, 1-propanol, and 2-propanol (with electrolyte concentrations <0.08 mol·L-1 ) were determined at 298.15 K, 313.15 K, and 323.15 K at atmosphere pressure separately by using a conductivity meter. The conductivity data were correlated with Foss-Chen-Justice (FCJ) equation and the limiting molar conductivities were obtained. The mean ionic activity coefficients of the salts in the organic solvents were calculated according to the Debye-Hückel limiting law and Onsager-Falkenhangen equations. The calculated results were compared with those activity coefficients in literature.

Fast-ionic conductor Li_(2.64)(Sc_(0.9)Ti_(0.1))_(2)(PO_(4))_(3) doped PVDF-HFP hybrid gel-electrolyte for lithium ion batteries

With increasing demand on energy density of lithium-ion battery,wide electrochemical window and safety performance are the crucial request for next generation electrolyte.Gel-electrolyte as a pioneer for electrolyte solidization development aims to solve the safety and electrochemical window problems.However,low ionic conductivity and poor physical performance prohibit its further application.Herein,a fast-ionic conductor(Li_(2.64)(Sc_(0.9)Ti_(0.1))_(2)(PO_(4))_(3))(LSTP)was added into poly(vinylidene fluoride-co-hexafluoropropylene)(PVDF-HFP)base gel-electrolyte to enhance mechanical properties and ionic conductivity.Evidences reveal that LSTP was able to weaken interforce between polymer chains,which increased the ionic conductibility and decreased interface resistance during the cycling significantly.The obtained LiFePO_(4)/hybrid gel-electrolyte/Li-metal coin cell exhibited excellent rate capacity(145 mA·h/g at 1C,95 mA·h/g at 3C,28℃)which presented a potential that can be comparable with commercialized liquid electrolyte system.

Empirical decay relationship between ionic conductivity and porosity of garnet type inorganic solid-state electrolytes

Ionic conductivity is one of the crucial parameters for inorganic solid-state electrolytes.To explore the relationship between porosity and ionic conductivity,a series of Li_(6.4)Ga_(0.2)La_(3)Zr_(2)O_(12) garnet type solid-state electrolytes with different porosities were prepared via solid-state reaction.Based on the quantified data,an empirical decay relationship was summarized and discussed by means of mathematical model and dimensional analysis method.It suggests that open porosity causes ionic conductivity to decrease exponentially.The pre-exponential factor obeys the Arrhenius Law quite well with the activation energy of 0.23 eV,and the decay constant is averaged to be 2.62%.While the closed porosity causes ionic conductivity to decrease linearly.The slope and intercept of this linear pattern also obey the Arrhenius Law and the activation energies are 0.24 and 0.27 eV,respectively.Moreover,the total porosity is linearly dependent on the open porosity,and different sintering conditions will lead to different linear patterns with different slopes and intercepts.

Mg2＋-ion Conducting Polymer Electrolytes： Materials Characterization and All-Solid-State Battery Performance Studies

For All-Solid-State battery applications, Mg2＋-ion conducting polymer electrolytes and Mg-metal electrode are currently considered as alternate choices in place of Li＋-ion conducting polymer electrolytes/Li-metal electrode. Present paper reports fabrication of All-Solid-State battery based on the following Mg2＋-ion conducting nano composite polymer electrolyte （NCPE） films： [85PEO： 15Mg（C104）2] ＋ 5% TiO2 （〈 100 nm）, [85PEO： 15Mg（CIO4）2] ＋ 3% SiO2（-8 nm）. [85PEO： 15Mg（CIO4）2] ＋ 3% MgO （〈 100 nm）, [85PEO：15Mg（C1O4）2] ＋ 3% MgO （-44 μm）. NCPE films were prepared by hot-press technique. Solid Polymer Electrolyte （SPE） composition： [85PEO： 15Mg（CIO4）2], identified as high conducting film at room temperature, has been used as ISt--phase host and nano/micro particles of active （MgO）/passive （SiO2, TiO2） fillers as IInd-phase dispersoid. Filler particle dependent conductivity studies identified above mentioned NCPE films as optimum conducting composition （OCC） at room temperature. Ion transport behavior of SPE/NCPE film materials was investigated previously. Present paper reports materials characterization and cell performance studies on All-Solid-State batteries： Mg （Anode） Ⅱ SPE or NCPE films tt C＋MnO2＋Electrolyte （Cathode）. Open circuit voltage （OCV） obtained was in the range： 1.79-1.92 V. The batteries were discharged at room temperature under different load conditions and some important battery parameters have been evaluated from plateau region of cell-potential discharge profiles. All the batteries performed quite satisfactorily specially under low current drain states.

Electrical conductivities for four ternary electrolyte aqueous solutions with one or two ionic liquid components at ambient temperatures and pressure

This work provides a method to explore the transport property of the electrolyte aqueous solutions with one or two ionic liquids, especially focus on their electrical conductivity. The conductivities were measured for the ternary systems Na Cl–[C6mim][Cl](1-hexyl-3-methylimidazolium chloride)–H2O, [C6mim][BF4]–[C6mim][Cl]–H2O,Na NO3–[C6mim][BF4](1-hexyl-3-methylimidazolium tetrafluoroborate)–H2O, and [C4mim][BF4](1-butyl-3-methylimidazolium tetrafluoroborate)–[C6mim][BF4]–H2O, and their binary subsystems NaN O3–H2O, NaC l–H2O,[C6mim][BF4]–H2O, [C6mim][Cl]–H2O, and [C4mim][BF4]–H2O, respectively. The conductivities of the ternary systems were also determined using generalized Young's rule and semi-ideal solution theory in terms of the data of their binary solutions. The comparison showed that the two simple equations provide good predictions for conductivity of mixed electrolyte solutions and the mixed ionic liquid solutions based on the conductivity of their binary subsystems.

Mircostructural and electrical properties of Ce_(0.8)Sm_(0.2)O_(2-δ)-BaZr_(0.9)Y_(0.1)O_(3-δ) composite electrolyte

The (1-x)BaZr0.9Y0.1O3-δ(BZY)-xCe0.8Sm0.2O2-δ(SDC, x =0.1,0.3,0.5 and 0.7) composite electrolytes were prepared by combining a gel polymerization method with a ball milling. X-ray diffraction (XRD) patterns show the mixture of BZY and SDC is only crystalline phase as the composite electrolyte. The relative density,grain size and total conductivity of composite electrolytes increase significantly with the increase of SDC content. The maximum conductivity of 0.1 BZY-0.9 SDC reaches 2×10^2 S·cm^-1 at 600 ℃ in wet air,which is close to the conductivity of SDC.

化学电源的发展

化学电源在二十世纪九十年代得到了雨后春笋似地发展,例如锌锰电池、镍氢电池、锂离子电池、第一代……第四代锂电池、锌镍电池、锌空气电池、燃料电池等等.市场和科学的发展极大地缩短了化学电源从常规研究成果转变成产品的周期.在21世纪直流电源将比交流电源更有价值.