聚丙烯纤维驻极体滤材的储电性能

采用电晕充电法制备了聚丙烯纤维驻极体滤材。考察了充电电压、充电时间、充电距离、环境湿度等因素对驻极体滤材储电性能的影响,通过正交试验设计,分析了各因素的影响程度。结果表明,用电晕充电法使聚丙烯纤维滤材形成驻极体是切实可行的,表面电位随充电电压、充电时间的增加而增加,而随充电距离和环境湿度的增加而减小,表面电位的保留率随环境湿度的增加而减小。充电电压对表面电位的影响非常显著,环境湿度的影响次之,充电时间和充电距离的影响最小。最佳工艺条件为:充电时间30 min,充电距离8 mm,充电电压10 kV,环境湿度35%。

孔洞结构聚合物驻极体的储电性和压电性

电极化的孔洞结构聚合物薄膜同时具有铁电材料(极化弛豫以及与极化相耦合的其它物理量的弛豫)和驻极体(存在过剩电荷)的特点,被命名为铁电驻极体(ferroelectret),是一类新型的机电传感器材料.这种材料的压电活性源于沉积在内部孔洞上下两壁极性相反的空间电荷和材料的孔洞结构.它除具有与压电陶瓷相当,甚至更高的压电d33系数(准静态d33高达1400pC/N,比铁电聚合物PVDF及其共聚物P(VDF/TrFE)的d33高出近二个量级)以外,还拥有聚合物的柔顺性、可大面积成膜、低成本、低电容率以及与空气和水相匹配的低声阻抗等突出特性.可以说,这种新型压电材料组合了压电陶瓷和铁电聚合物的各自优势,必将在通讯、保安、控制、医疗及军事等领域有广阔的应用前景.作者综述电极化孔洞结构聚合物薄膜的制备方法,电极化工艺,压电性,理论模型,应用前景,发展现状及其展望.

涤纶针刺非织造过滤材料储电性能研究

为提高涤纶针刺非织造过滤材料的储电性能,先分别对试样进行水洗和异丙酮处理,再对处理后的涤纶针刺非织造材料进行驻极处理,测试材料表面静电势的衰减时间,发现:水洗法及异丙醇法处理的涤纶针刺非织造材料的储电性能均显著提高,且异丙醇法的效果更好。此外,为进一步提高材料的储电性能,将涤纶针刺非织造材料与聚丙烯熔喷非织造材料进行不同方式的复合,并进行异丙醇处理,测试表明复合能进一步提高材料的储电性能,其中采用中间夹层方式得到的复合试样的储电性能最优。

PMMA/P(VDF-TrFE)共混体系的介电储电性能研究

制备了不同PMMA含量的PMMA/P(VDF-Tr FE)共混试样,研究了PMMA含量对共混试样介电和储能性能的影响。结果表明,非晶、低极性PMMA的稀释作用使共混物的结晶度降低、结晶尺寸减小,热焓、介电常数、极化值及储能密度均随之减小。此外,PMMA有效降低了P(VDF-Tr FE)的介电损耗,改善了材料释放电能的能力。含PMMA10%的淬火态试样具有相对高的储能密度和较低的能耗。

一步法与分步法活化对氮掺杂煤沥青基多孔碳电储能性能的对比

分析了一步法与分步法在制备氮掺杂煤沥青基多孔碳材料的结构和储电效能对比。研究表明,一步法因其简便的操作步骤和低能耗而适用于成本敏感的应用,且在使用三聚氰胺作为氮源时,该方法制备的材料展现出优异的电化学性能;分步法制备过程更为复杂和耗能,但其优势在于能够精确控制材料的微观结构和化学性质,尤其是在使用硫酸铵作为氮源时,显示出更佳的电容特性。

FEP和多孔PTFE复合膜铁电驻极体的压电性及电荷动态特性

报道了将致密的FEP和多孔PTFE交互层叠在一起，采用热粘合的方法制备出具有孔洞结构的聚合物复合膜，然后经电晕极化处理使该复合膜成为铁电驻极体。最后用准静态方法测量该铁电复合膜的压电系数d33，并通过热刺激电流放电（TSD）电流谱和等温衰减研究了FEP和多孔PTFE复合膜铁电驻极体的电荷动态特性。结果表明：该复合膜的压电系数d33可达200～500pC/N，在0～12kPa的压强范围内呈现出良好的线性，并且在90℃下老化160min后仍保持在原来的43％且趋于稳定；FEP和多孔PTFE复合膜铁电驻极体电荷在热激发脱阱后复合途径主要有2种：一种是沿着固体介质的表面迁移与异性电荷复合，另一种是穿过固体介质层与异性电荷复合。在低温区（7512附近）前者占优，高温区（120℃附近）后者占优。

蒙脱土增强聚乙烯醇复合膜的摩擦起电性

目的通过片层蒙脱土(MMT)插层聚乙烯醇(PVA)来增强PVA复合膜的摩擦起电性能和电荷保持能力,进而增强PVA基摩擦纳米发电机(TENG)的电输出性能。方法在3000 r/min的高速机械搅拌下将蒙脱土进行剥离,然后与PVA粉末混合,在80℃、机械搅拌下溶解并流延成膜。以空白PVA膜为对照,测试MMT@PVA复合膜的介电常数和静止状态下的摩擦电荷耗散曲线,以表征掺杂蒙脱土的PVA复合膜的介电性和储电性。以PVA-PTFE基TENG为对照,测试MMT@PVA-PTFE基TENG的电输出性能,以表征MMT的掺杂对PVA复合膜摩擦起电性能的影响。结果MMT的掺杂对PVA膜的介电性、摩擦起电性和电荷耗散性都有显著的影响。当的掺杂1%(相对于PVA的质量)的MMT后,PVA复合膜的介电常数增加了35%,电荷耗散率降低了46%,PVA基TENG的电输出增加了373%。MMT@PVA基TENG可以点亮868个LED灯,且具有稳定的电输出。结论MMT的掺杂可以显著提升PVA膜的摩擦起电性和储电性,并且有助于提升PVA基TENG的电输出,这对于拓宽PVA基TENG在能量收集、可穿戴电子器件和生物传感领域具有现实意义。

Pore structure effect on reservoir electrical properties and well logging evaluation

The reservoir pore structure controls the reservoir quality and resistivity response of hydrocarbon-bearing zones and thus, critically affects logging interpretation. We use petrophysical data in three types of reservoir with different pore structure characteristics to show that the complexity of pore structure had a significant effect on the effective porosity and permeability regardless of geological factors responsible for the formation of pore structure. Moreover,, the distribution and content of conductive fluids in the reservoir varies dramatically owing to pore structure differences, which also induces resistivity variations in reservoir rocks. Hence, the origin of low-resistivity hydrocarbon-bearing zones, except for those with conductive matrix and mud filtrate invasion, is attributed to the complexity of the pore structures. Consequently, reservoir-specific evaluation models, parameters, and criteria should be chosen for resistivity log interpretation to make a reliable evaluation of reservoir quality and fluids.

Phase structure and electrochemical properties of La_(0.7)Ce_(0.3)Ni_(3.75)Mn_(0.35)Al_(0.15)Cu_(0.75-x)Fe_x hydrogen storage alloys

La0.7Ce0.3Ni3.75Mn0.35Al0.15Cu0.75-xFex （x=0-0.20） hydrogen storage alloys were synthesized by induction melting and subsequent annealing treatment, and phase structure and electrochemical characteristics were investigated. All alloys consist of a single LaNi5 phase with CaCu5 structure, and the lattice constant a and the cell volume （V） of the LaNi5 phase increase with increasing x value. The maximum discharge capacity gradually decreases from 319.0 mA？h/g （x=0） to 291.9 mA？h/g （x=0.20） with the increase in x value. The high-rate dischargeability at the discharge current density of 1200 mA/g decreases monotonically from 53.1% （x=0） to 44.2% （x=0.20）. The cycling stability increases with increasing x from 0 to 0.20, which is mainly ascribed to the improvement of the pulverization resistance.

Preparation of LaMgNi_(4-x)Co_x alloys and hydrogen storage properties

The LaMgNi4xCox （x=0, 0.3, 0.5） compounds were prepared by the method of levitation melting and a subsequent heat treatment at 1073 K for 10 h. XRD analysis shows that the obtained LaMgNia-xCox alloys consist of a single phase with the structure of cubic SnMgCu4 （AuBe5 type）. The hydrogen absorption/desorption properties of LaMgNi4 were investigated by PCI measurement at various temperatures （T=373, 398, 423 K） and the results show that the maximum absorbed hydrogen capacity reaches 1.45% （5.79H/M） under a hydrogen pressure of 4.3 MPa at 373 K. The XRD patterns during absorbing procedure at 373 K indicate the phase structure changing from cubic （a-LaMgNi4） to orthorhombic （fl-LaMgNiaH3.41） and after hydrogenation finally back to cubic （y-LaMgNiaH4.87）, and a partial desorption was also observed under this condition. With increasing temperature, a slight decrease of the absorbed hydrogen content was observed and the number of plateaus reduces from two to one, but the hydrogen absorption kinetics improves. The electrochemical properties of the LaMgNiaxCox were measured by simulated battery test, which shows that the discharge capacity of the alloys significantly improves with the increase of Co content.

Electrochemical hydrogen storage characteristics of Ti_(0.10)Zr_(0.15)V_(0.35)Cr_(0.10)Ni_(0.30)-10% LaNi_3 composite and its synergetic effect

Hydrogen storage composite alloy Ti0.10Zr0.15V0.35Cr0.10Ni0.30–10% LaNi3 was prepared by two-step arc-melting to improve the electro-catalytic activity and the kinetic performance of Ti-V-based solid solution alloy. The electrochemical properties and synergetic effect of the composite alloy electrode were systematically investigated by using X-ray diffractometry, field emission scanning electron microscopy, energy-dispersive spectrometry, electrochemical impedance spectroscopy and galvanostatic charge/discharge test. It is found that the main phase of the composite alloy is composed of V-based solid solution phase with a BCC structure and C14 Laves phase with hexagonal structure, while the secondary phase is formed in the composite alloy. The comprehensive electrochemical properties of the composite alloy electrode are significantly improved. The activation cycle number, the maximum discharge capacity and the low temperature dischargeability of the composite alloy are 5 cycles, 362.5 mA-h/g and 65.84% at 233 K, respectively. It is suggested that distinct synergetic effect occurs in the activation process, composite process, cyclic process and discharge process at a low or high temperature under different current densities, in the charge–transfer resistance and exchange current density.

Electrochemical performances of AB_5-type hydrogen storage alloy modified with Co_3O_4

Anodic electrodes with the mixture of hydrogen storage alloys and different contents of Co3O4（2%,4%,6% and 8%,mass fraction） powders were made.The effects of Co3O4 on the electrochemical performance of the alloy electrodes were studied.The constant charge-discharge tests show that the discharge capacity of alloy electrodes with Co3O4 significantly increases,and the maximum discharge capacities of electrodes with 2%,4%,6% and 8% Co3O4 are higher than the electrode with no Co3O4 by 0.83%,4.86%,7.18% and 9.21%,accordingly.Linear polarization（LP） and electrochemical impedance spectroscopy（EIS） tests suggest that charge-transfer resistance decreases by the addition of Co3O4.Cyclic voltammogram（CV）,scanning electron microscopy（SEM） and energy dispersive spectrum（EDS） tests indicate that Co3O4 can partly dissolve and experience a reversible oxidation-reduction process of Co to Co（OH）2,leading to the improvement in the electrochemical performance of hydrogen storage alloy.

Washing effect on properties of Li Ni_(0.8)Co_(0.15)Al_(0.05)O_2 cathode material by ethanol solvent

Different LiNi0.8Co0.15Al0.05O2 cathode materials were washed by ethanol solvent. Inductively coupled plasma atomic emission spectroscopy（ICP-AES）, Fourier transformed infrared（FTIR） spectrum, X-ray diffraction（XRD）, scanning electron microscopy（SEM）, charge-discharge test and electrochemical impedance spectroscopy（EIS） were used to evaluate the elemental contents, structures, morphologies and electrochemical properties of samples. The results show that ethanol washing can remove effectively the synthetic residues LiOH/Li2 O on the freshly-prepared LiNi0.8Co0.15Al0.05O2 and make the sample much more resistant to H2O and CO2, without destroying its bulk structure, surface morphology and electrochemical performances. Moreover, the discharge specific capacity and cycle performance of LiNi0.8Co0.15Al0.05O2 after storage in air with a relative humidity of 80% for three months are improved by immediate ethanol washing.

Electrochemical lithium storage performance of three-dimensional foam-like biocarbon/MoS2 composites

Molybdenum disulfide(MoS2)was loaded on biocarbon using waste camellia dregs(CDs)as the carbon source,which was further coated with dopamine hydrochloride to construct biocarbon/MoS2 electrode composites.The electrochemical lithium storage performance of the composites with different MoS2 contents was investigated.SEM results demonstrated that the composite had a three-dimensional foam-like structure with MoS2 as the interlayer.XRD and HRTEM tests revealed that MoS2 interlayer spacing in the composite was expanded.XPS analysis showed that new Mo—N bonds were formed in the active material.The electrochemical tests showed that the composite with a MoS2 content of 63%had a high initial specific capacity of 1434 mA·h/g at a current density of 100 mA/g.After a long cycle at a high current,it also showed good cycling stability and the capacity retention was nearly 100%.In addition,it had good lithium ion deintercalation ability in the electrochemical kinetics test.

Structure and electrochemical hydrogen storage characteristics of La_(0.8-x)Pr_xMg_(0.2)Ni_(3.15)Co_(0.2)Al_(0.1)Si_(0.05) (x=0-0.4) electrode alloys

For the purpose of improving the electrochemical cycle stability of the La-Mg-Ni based A2BT-type electrode alloys, both reducing Mg content and substituting La with Pr were adopted. The Lao.8-xPrxMg0.2Ni3.15Co0.2A10.1Si0.05 （x=0, 0.1, 0.2, 0.3, 0.4） electrode alloys were fabricated by casting and annealing. The investigation on the structures and electrochemical performances of the alloys was performed. The obtained results reveal that the as-cast and annealed alloys comprise two major phases, （La, Mg）2Ni7 phase with the hexagonal Ce2NiT-type structure and LaNi5 phase with the hexagonal CaCus-type structure, as well as a little residual LaNi3 phase. It is also found that the addition of Pr element observably affects the electrochemical hydrogen storage characteristics of the alloys, just as the discharge capacity and high rate discharge ability （HRD） first rise then fall with the growing of Pr content, and among all the alloys, the as-cast and annealed （x=0.3） alloys generate the largest discharge capacities of 360.8 and 386.5 mA.h/g, respectively. Additionally, the electrochemical cycle stability of all the alloys markedly grows with the increase of Pr content. The capacity retaining rate （S100） at the 100th charging and discharging cycle is enhanced from 64.98% to 77.55% for the as-cast alloy, and from 76.60% to 95.72% for the as-annealed alloy by rising Pr content from 0 to 0.4. Furthermore, the substitution of Pr for La results in first increase and then decrease in the hydrogen diffusion coefficient （D）, the limiting current density （IL） as well as the electrochemical impedance.

Inter- and intra-hemispheric EEG coherence in patients with mild cognitive impairment at rest and during working memory task

Objective： To assess functional relationship by calculating inter- and intra-hemispheric electroencephalography （EEG） coherence at rest and during a working memory task of patients with mild cognitive impairment （MCI）. Methods： The sample consisted of 69 subjects： 35 patients （n = 17 males, n = 18 females; 52-71 years old） and 34 normal controls （n = 17 males, n = 17 females; 51 -63 years old）. Mini-mental state examination （MMSE） of two groups revealed that the scores of MCI patients did not differ significantly from those of normal controls （P〉0.05）. In EEG recording, subjects were performed at rest and during working memory task. EEG signals from F3-F4, C3-C4, P3-P4, T5-T6 and O1-O2 electrode pairs are resulted from the inter-hemispheric action, and EEG signals from F3-C3, F4-C4, C3-P3, C4-P4, P3-O1, P4-O2, T5-C3, T6-C4, T5-P3 and T6-P4 electrode pairs are resulted from the intra-hemispheric action for delta （1.0-3.5 Hz）, theta （4.0-7.5 Hz）, alpha-1 （8.0-10.0 Hz）, alpha-2 （10.5-13.0 Hz）, beta-1 （13.5-18.0 Hz） and beta-2 （18.5-30.0 Hz） frequency bands. The influence of inter- and intra-hemispheric coherence on EEG activity with eyes closed was examined using fast Fourier transformation from the 16 sampled channels. Results： During working memory tasks, the inter- and intra-hemispheric EEG coherences in all bands were significantly higher in the MCI group in comparison with those in the control group （P〈0.05）. However, there was no significant difference in inter- and intra-hemispheric EEG coherences between two groups at rest. Conclusion： Experimental results comprise evidence that MCI patients have higher degree of functional connectivity between hemispheres and in hemispheres during working condition, It suggests that MCI may be associated with compensatory processes during working memory tasks between hemispheres and in hemispheres. Moreover, failure of normal cortical connections may exist in MCI patients.

Two-step carbon modification of NaTi_2(PO_4)_3 with improved sodium storage performance for Na-ion batteries

NASICON-type structured NaTi2(PO4)3 has been regarded as a promising anode material for non-aqueous and aqueous Na-ion batteries,whereas its sodium storage performance was greatly restricted by its inherent inferior electronic conductivity.In the present work,a two-step carbon modification method using prefabricated carbon spheres as support and phenolic resin as carbon source was proposed to prepare advanced NaTi2(PO4)3/C.The as-prepared composite with carbon spheres displayed a much higher reversible capacity(126.7 mA?h/g vs 106.7 mA?h/g at 0.5C)than the control sample without carbon spheres.Superior rate capability with discharge capacities of 115.1,95.5,80.8 mAh/g at 1C,10C,20C,respectively and long-term cycling stability with capacity retention of 92.4%after 1000 cycles at 5C were also observed.Owing to the designing of two-step carbon modification,although the as-prepared sample shows much smaller surface area,it possesses much better conductive network and more uniform particle distribution,resulting in higher electronic conductivity and faster ionic conductivity,thereby superior sodium storage ability at high rate.

Influences of melt spinning on electrochemical hydrogen storage performance of nanocrystalline and amorphous Mg_2Ni-type alloys

In order to improve the electrochemical hydrogen storage performance of the Mg2Ni-type electrode alloys, Mg in the alloy was partially substituted by La, and the nanocrystalline and amorphous Mg2Ni-type Mg20-xLaxNi10 （x-=0, 2） alloys were synthesized by melt-spinning technique. The microstructures of the as-spun alloys were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and transmission electron microscopy （TEM）. The electrochemical hydrogen storage properties of the experimental alloys were tested. The results show that no amorphous phase is detected in the as-spun Mg20Ni10 alloy, but the as-spun Mg18La2Ni10 alloy holds a major amorphous phase. As La content increases from 0 to 2, the maximum discharge capacity of the as-spun （20 m/s） alloys rises from 96.5 to 387.1 mA.h/g, and the capacity retaining rate （S20） at the 20th cycle grows from 31.3% to 71.7%. Melt-spinning engenders an impactful effect on the electrochemical hydrogen storage performances of the alloys. With the increase in the spinning rate from 0 to 30 m/s, the maximum discharge capacity increases from 30.3 to 135.5 mA.h/g for the Mg20Ni10 alloy, and from 197.2 to 406.5 mA-h/g for the Mg18La2Ni10 alloy. The capacity retaining rate （S20） of the Mg2oNi10 alloy at the 20th cycle slightly falls from 36.7% to 27.1%, but it markedly mounts up from 37.3% to 78.3% for the Mg18La2Ni10 alloy.

Effects of sodium substitution on properties of LiMn_2O_4 cathode for lithium ion batteries

Na-doped Li1.05Mn2O4 cathodes were synthesized using a sol-gel process.The samples were characterized by X-ray diffractometry(XRD),cyclic voltammetry(CV),electrochemical impedance spectroscopy(EIS)and charge-discharge measurements. The results show that all the samples exhibit the same cubic spinel phase structure without impurity.The lattice constant and unit cell volume decrease with increasing the sodium dopant amount.As the molar ratio of sodium to manganese(x=n(Na)/n(Mn))increases from 0 to 0.03,the initial discharge capacity of the Li1.05Mn2O4 cathodes decreases from 119.2 to 107.9 mA·h/g,and the discharge capability at large current rate and the storage performance decline dramatically,while cycling performance at room temperature and 55℃are improved.The CV and EIS studies indicate that reversibility of Li1.05Mn2O4 cathodes decreases and the electrochemical impedance increases with increasing the sodium dopant amount.

Effect of B and Fe substitution on structure of AB_3-type Co-free hydrogen storage alloy

A series of hydrogen storage Co-free AB3-type alloys were directly synthesized with vacuum mid-frequency melting method,within which Ni of La0.7Mg0.3Ni3 alloy was substituted by Fe,B and(FeB) alloy,respectively.Alloys were characterized by XRD,EDS and SEM to investigate the effects of B and Fe substitution for Ni on material structure.The content of LaMg2Ni9 phase within La0.7Mg0.3Ni3 alloy reaches 37.9% and that of La0.7Mg0.3Ni2.9(FeB)0.1 alloys reduces to 23.58%.Among all samples,ground particles with different shapes correspond to different phases.The major substitution occurs in LaMg2Ni9 phase.Electrochemical tests indicate that substituted alloys have different electrochemical performance,which is affected by phase structures of alloy.The discharge capacity of La0.7Mg0.3Ni3 alloy reaches 337.3 mA·h/g,but La0.7Mg0.3Ni2.9(FeB)0.1 alloy gets better high rate discharge(HRD) performance at the discharge rate of 500 mA/g with a high HRD value of 73.19%.