Characterization of a solid state battery based on polyblend of (PVP+PVA+KBrO3) electrolyte

A potassium ion conducting polyblend electrolyte based on polyvinyl pyrrolidone (PVP) + polyvinyl alcohol (PVA) complexed with KBrO₃ was prepared using solution-cast technique. The electrical conductivity and transference number measurements were performed to characterize the polyblend electrolyte for battery applications. These measurements have shown that the electrolyte is a mixed (ionic + electronic) conductor, the charge transport being mainly ionic (t_ion=0.97). Using the electrolyte, electrochemical cells with configurations K / (PVP+PVA+KBrO₃)/(I₂), K / (PVP+PVA+KBrO₃)/(I₂+C) and K/(PVP+PVA+KBrO₃) / (I₂+C+electrolyte) were fabricated and their discharge characteristics studied. The cell with configuration K / (PVP+PVA+KBrO₃) / (I₂+C+electrolyte) exhibited better discharge characteristics than the other configurations. The other cell parameters like open circuit voltage (OCV), short circuit current (SCC) etc. were evaluated and are reported. Paper presented at the 2nd International Conference of Ionic Devices, Anna University, Chennai, India, Nov. 28–30, 2003.     

Role of composite MnO2 cathode on electrochemical cells based on polymer electrolyte (PEO/NaClO3)

Thin-film sodium-ion-conducting polymer electrolyte based on polyethylene oxide (PEO) system was prepared by solvent casting method. The thin-film electrolytes were characterized by X-ray diffraction (XRD), infrared (IR), cyclic voltammetry (CV) and alternating current conductivity, and Wagner’s polarization method. The complexation of salt with PEO was confirmed by XRD and IR studies. The charge transport of these electrolytes is mainly due to ions, which was confirmed by the transference number experiment. The conductivity studies show that the conductivity value of PEO/NaClO₃ complex increases with the increase of temperature as well as the addition of low molecular weight polyethylene glycol, dimethyl formamide, and propylene carbonate. The electrolyte stability and cell reversibility were analyzed by CV studies. Electrochemical cells have been fabricated with a common cell configuration Na|electrolyte|(MnO₂ + I₂ + C + electrolyte), and their discharge characteristic studies were made through a load 100 kΩ at room temperature. The measured open circuit voltage ranges from 2.80 to 2.54 V with short circuit current ranges from 667 to 1,000 μA and several other cell parameters were evaluated. Finally, the merit of the composite cathode is found with the comparison of the MnO₂ cathode.     

Poly(ethylene glycol)/poly(2-acrylamido-2-methyl-1-propane sulfonic acid) gel electrolytes: a detailed investigation of their conductivity and characterization

Poly(ethylene glycol)/poly(2-acrylamido-2-methyl-1-propane sulfonic acid) (PEG/PAMPS) with a transparent appearance were prepared in the presence of ammonium persulfate (APS) as an initiator at 70 °C for 24 h. PEG/PAMPS-based polymer gel electrolytes in a motionless and uniform state were obtained by adding the required amount of liquid electrolytes to a dry PEG/PAMPS polymer. Liquid electrolytes include organic solvents with high boiling points (-1-methyl-2-pyrrolidone (NMP) and γ-butyrolactone (GBL)) and a redox couple (alkali metal iodide salt/iodine). The optimized conditions for PEG/PAMPS-based gel electrolytes based on the salt type, the concentration of alkali metal iodide salt/iodine, and solvent volume ratio were determined to be NaI, 0.4 M NaI/0.04 M I₂, and NMP:GBL (7:3, v/v), respectively. The highest ionic conductivity and the liquid electrolyte absorbency were 2.58 mS cm^?1 and 3.6 g g^?1 at 25 °C, respectively. The ion transport mechanism in both the polymer gel electrolytes and liquid electrolytes is investigated extensively, and their best fits with respect to the temperature dependence of the ionic conductivity are determined with the Arrhenius equation.     

Evaluation and use of the Pd | SrCe0.95Yb0.05O3| Pd electrochemical reactor for equilibrium-limited hydrogenation reactions

The current — overpotential characteristics of the H₂ - Pd - SCY interphase have been studied at atmospheric total pressure and temparatures between 400 – 550 °C in the single chamber reactor — cell: Pd | SCY | Pd. The results of I−η measurements indicate that the apparent anodic and cathodic charge tranfer coefficients are equal to: α_a=α_c=0.5. The present results are compared to those obtained with the single — chamber reactor cell: Ag | SCY | Ag. A solid state proton (H⁺) conducting reactor — cell with Pd electrodes was tested for the ammonia synthesis from its elements at atmospheric pressure. At 570 °C, over 75% of the ectrochemically supplied hydrogen was converted into NH₃. The thermodynamic requirement for a high pressure process was eliminated. Paper presented at the 5th Euroconference on Solid State Ionics, Benalmádena, Spain, Sept. 13–20, 1998.     

Static moments of 54Fem and perturbed angular distributions with combined dipole and quadrupole interactions

The static moments of a new I^π = (10⁺) isomer in ⁵⁴Fe (E_x = 6528keV; τ = 525 ± 10ns) were measured by the perturbed angular distribution method with the results g = +0.778 ± 0.010, |Q| = 72 ± 7efm². The isomer was then used to study the combined interaction produced by weak randomly-oriented electric field gradients in the presence of a strong magnetic field.     

Channel-combination method for phase-based |B1+| mapping techniques

PurposeThe aim of this study was to propose a channel combination method for |B₁⁺| mapping methods using phase difference to reconstruct |B₁⁺| map.Theory and methodsPhase-based |B₁⁺| mapping methods commonly consider the phase difference of two scans to measure |B₁⁺|. Multiple receiver coils acquire a number of images and the phase difference at each channel is theoretically the same in the absence of noise. Affected by noise, phase difference is approximately governed by Gaussian distribution. Considering data from all channels as samples, estimation can be achieved by maximum likelihood method. With this method, all phase differences at each channel are combined into one. In this study, the proposed method is applied with Bloch-Siegert shift |B₁⁺| mapping method. Simulations are performed to illustrate the phase difference distribution and demonstrate the feasibility and facility of the proposed method. Phantom and vivo experiments are carried out at 1.5 T scanner equipped with 8-channel receiver coil. In all experiments, the proposed method is compared with weighted averaging (WA) method.ResultsSimulations revealed appropriateness of approximating the distribution of phase difference to Gaussian distribution. Compared with WA method, the proposed method reduces errors of |B₁⁺| calculation. Phantom and vivo experiments provide further validation.ConclusionConsidering phase noise distribution, the proposed method achieves channel combination by finding the estimation from data acquired by multiple receivers coil. The proposed method reduces |B₁⁺| reconstruction errors caused by noise.     

Two triple points in the H2O–H2 system

Using a volumetric technique, phase transitions in the H₂O–H₂ system were investigated in the vicinity of two points of an invariant equilibrium, L+I _h+sII and L+sII+C ₁, located at 1.07 kbar and?10 °C and at 3.6 kbar and 1 °C, respectively. Liquid water (L), low-pressure hexagonal ice (I _h) and high-pressure cubic (sII) and rhombohedral (C ₁) clathrate hydrates were in equilibrium with gaseous hydrogen taken in excess.     

Study on the properties and charge generation in dye-sensitized n-TiO2|dye|p-CuI solid state photovoltaic solar cells

Transparent semiconducting copper iodide (CuI) films were prepared by XeCl Excimer laser and their characteristics are investigated. These films exhibited optical transmittance over 80% in the wavelength range from 400 to 900 nm and minimum resistivity of about 2 kΩ cm⁻¹. The optical absorption of the these films shows a remarkable blue shift compared to that of polycrystalline of CuI, which can be explained from the viewpoint formation of ultra fine of CuI grains. The titanium dioxide (TiO₂) films have been prepared by sol-gel method. The properties of pulsed laser deposited CuI and TiO₂ films in power output of n-TiO₂|dye|p-CuI cells is studied. An efficient charge generation is observed through the illumination of TiO₂ layer of the fabricated n-TiO₂|dye|p-CuI solid state photovoltaic solar cells. From the current-voltage characteristics, the fill factor and power conversion efficiency were about of 45 and 3%, respectively. The maximum photo-current of about 12.5 mA/cm² and photo-voltage of 475 mV under AM 1.5 conditions were obtained for the n-TiO₂|dye|p-CuI solid states photovoltaic solar cells with good reproducibility. Adsorbed dye molecules to the TiO₂ surface act as a relay, especially under illumination through TiO₂ layer in the wave range region of 300-400 nm.     

Photovoltaic activity in a ZnSe/PEO–chitosan blend electrolyte junction

Thin films of ZnSe and PEO–chitosan blend polymer doped with NH₄I and iodine crystals were prepared to form the two sides of a semiconductor electrolyte junction. ZnSe was electrodeposited on indium tin oxide (ITO) conducting glass. The polymer is a blend of 50 wt% chitosan and 50 wt% polyethylene oxide. The polymer blend was complexed with ammonium iodide (NH₄I), and some iodine crystals were added to the polymer–NH₄I solution to provide the I⁻/I³⁻redox couple. The room temperature ionic conductivity of the polymer electrolyte is 4.32 × 10⁻⁶ S/cm. The polymer film was sandwiched between the ZnSe semiconductor and an ITO glass to form a ZnSe/polymer electrolyte/ITO photovoltaic cell. The open circuit voltage (V _oc) of the fabricated cells ranges between 200 to 400 mV and the short circuit current between 7 to 10 μA.     

Infrared emission and defect centres in Er and Yb codoped Y3Al5O12 phosphors

YAG phosphor powders doped/codoped with Er³⁺/(Er³⁺ + Yb³⁺) have been synthesised by using the solution combustion method. The effect of direct pumping into the ⁴I_11/2 level under 980 nm excitation of doped/codoped Er³⁺/Yb³⁺−Er³⁺ in Y₃Al₅O₁₂ (YAG) phosphor responsible for an infrared (IR) emission peaking at ∼1.53 μm corresponding to the ⁴I_13/2→⁴I_15/2 transition has been studied. YAG exhibits three thermally-stimulated luminescence (TSL) peaks at around 140°C, 210°C and 445°C. Electron spin resonance (ESR) studies were carried out to identify the centres responsible for the TSL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0176 is identified as O⁻ ion, while centre II with an isotropic g-factor 2.0020 is assigned to an F⁺ centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal-annealing experiments and this centre (assigned to F⁺ centre) seems to originate from an F-centre (oxygen vacancy with two electrons) and these two centres appear to correlate with the observed high-temperature TSL peak in YAG phosphor.     

Bacto agar-based gel polymer electrolyte

The biopolymer of a Bacto agar-based gel polymer electrolyte (GPE) was prepared by addition of NaI and I₂ as redox couple. The prepared GPE was characterized using impedance spectroscopy and X-ray diffraction (XRD) in order to determine its electrical and structural properties, respectively. An optimized ionic conductivity of 12.41 × 10⁻⁴ S cm⁻¹ was achieved for the samples containing 1.6 M NaI and 50 μL I₂. Meanwhile, XRD revealed that the addition of NaI and I₂ altered agar properties and formed an amorphous structure. Linear sweep voltammetry showed that the electrochemical stability window of the sample had a working voltage of 2.0 V.     

100 keV质子辐照对空间GaAs/Ge太阳电池光电效应的影响

利用空间环境模拟设备,用固定能量为100keV、注量为1×10⁹—3×10¹²cm^-2的质子,对空间实用GaAs/Ge太阳电池进行了辐照试验.利用伏安(I-V)特性、光谱响应和光致发光(PL)光谱测试,研究分析了电池的光电效应.试验表明,电池的各种电性能参数如短路电流(I_sc)、开路电压(V_oc)、最大输出功率(P_{m< 关键词： GaAs/Ge太阳电池 质子辐照 光电效应}     

Behavior of mixtures of iodine with anthracene,phenazine and thianthrene

The binary systems I₂-phenazine (I₂P), I₂-anthracene and I₂-thianthrene have been investigated over a wide range of concentrations (0.1 < x_I2 < 1) and over temperatures ranging from 0 to 60°C. EMF measurements were performed in the three systems employing galvanic cells with a silver-ion-conducting solid electrolyte in order to determine the possible compounds and their formation Gibbs energies. Only one compound of stoichiometry I₂P is present in the system I₂phenazine and its formation Gibbs energy can be expressed as follows: Δ_FG⁰(I₂P) = ?20830 + 19.7 T(J mol^?1), 273–333 K. Neither the anthracene nor the thianthrene form compounds or solid solutions in the studied ranges of concentrations and temperatures.     

第I种非对称两态叠加多模叠加态光场的任意不等阶Y压缩

利用多模压缩态理论研究了第种非对称两态叠加多模叠加态光场|Ψ_Iab〉_q的任意不等阶N_j次方Y压缩特性.结果发现:对于任意压缩阶数N_j,态|Ψ_Iab〉_q在一定条件下总可呈现出任意不等阶N_j次方Y混合压缩效应,但在某一压缩阶数区域内并不一定呈现压缩效应;压缩阶数N_j满足特定条件(N_mj=4_mj;4_mj+1;4_mj+2;4_mj+3,其中j=1,2,3,…,…q)时的不等阶N_j次方Y压缩效应仅仅是本文的理论结果在N_j在某一特定条件下的特例.     

A determination of the CKM-matrix element ratio |V ts |/|V cb | from the rareB-decaysB→K *+γ andB→X s +γ

Implications of the recent CLEO observation [1] of the rare decay modeB→K ^*+γ having a combined branching ratio BR(B→K ^*+γ)=(4.5±1.5±0.9)×10^?5 and an improved upper limit on the inclusive branching ratio BR(B→X _s +γ)<5.4×10^?4 (95% C.L.) [2] are discussed in the context of the Standard Model (SM). Using the unitarity of the CKM-matrix and taking into account QCD radiative corrections in the decay rate and the inclusive photon energy spectrum we obtain an improved upper limit on the inclusive branching ratio BR(B→X _s +γ)<4.8×10^?4 (95% C.L.). This can be used to constrain possible non-SM contributions to the inclusive branching ratio, giving BR(B→X _s +γ) (non-SM)<3.0×10^?4 form _t >-108 GeV. Within the SM, we show that the resulting experimental upper limit can be interpreted as a corresponding limit on the CKM-matrix element ratio yielding |V _ts |/|V _cb |<1.67, with the top quark mass assumed to weigh less than 200 GeV. We calculate the relative exclusive to inclusive branching ratioR(K ^*/X _s )≡Γ(B→K ^*+γ)/Γ(B→X _s +γ), based on the inclusive hadronic invariant mass distribution inB→X _s +γ. Estimating theK ^*-contribution from this distribution in the threshold region (m _K +m _π)≤m _{X s} ≤0.97 GeV and using experimental measurements from the semileptonicD-decaysD→K+π+?v _? in the same mass interval, we obtainR(K ^*/X _s )=0.13±0.03. This enables us to put a lower bound on the ratio |V _ts |/|V _cb | from the 95% C.L. lower limit on the branching ratio BR(B→K ^*+γ)>1.6×10^?5 [1,2]. Combining the exclusive and inclusive decay rates, we determine 0.50≤|V _ts |/|V _cb |≤1.67 (at 95% C.L.).     

Investigation of the reaction Dy164 (n, γ) Dy165

The level structure of Dy¹⁶⁵ has been investigated at the Karlsruhe research reactor using thermal neutron capture in Dy¹⁶⁴. The target was Dy₂O₃ enriched to 92.71% Dy¹⁶⁴. Neutrons were either monochromized by Bragg reflection from a lead crystal or transmitted through a bismuth single crystal filter. High-resolution measurements of the capture spectrum have been performed by means of a Ge(Li) 5-detector pair spectrometer and a Ge(Li) anti-Compton assembly. A large number of new lines has been observed. Cascade relationships were studied by using several techniques: a double coincidence apparatus with 4″ Ø×5″ NaI(Tl) detectors, a coincidence system containing a scintillation detector and a 34 cm³ Ge(Li)-diode as well as a two-parameter system involving the pair spectrometer (with NaI (Tl) as the primary detector) and a single 4″Ø×6″ NaI (Tl) counter. In the framework ofNilsson's model and simple microscopic pictures of vibrational states the results are consistent with the following spectroscopic interpretation: 0 keV, 7/2⁺[633]; 108.2 keV, 1/2^?[521]; 184.3 keV, 5/2″[512]; 533.5 keV, 5/2″ [523]; 538.6 keV, 7/2⁺[633] +Q₂₂; 570.3 keV, 5/2^?[512]+Q₂₂+1/2^?[510]; 573.6 keV, 3/2^? [521]+1/2^?[521]+Q₂₂; 1103.3 keV, 1/2^? [521]+Q₂₂+3/2^? [521]. For comparison preliminary results are given for the isotonic nucleus Yb¹⁶⁹.     

弱激光诱导神经元兴奋性改变的实验研究

利用全细胞膜片钳技术研究弱激光诱导下大鼠海马CA3区锥体神经元兴奋性.实验结果显示：弱激光作用使神经元钠通道激活电位向超极化方向移动,钠电流幅度增大,且这种增大作用具有电压依赖性和可逆性.激光作用显著影响钠电流稳态激活与失活特性,对照组和照射组通道半数激活电压分别为(-4414±528)mV和(-5655±614)mV(n=8,P<001),半数失活电压分别为(-6902±1031)mV和(-5660±897)mV(n=8, P<0 关键词： 钠离子通道 膜片钳技术 弱激光 动作电位 神经元     

A 236 GHz Fe3+ EPR Study of Nanoparticles of the Ferromagnetic Room-Temperature Semiconductor Sn1−x Fe x O2 (x = 0.005)

High-frequency (236 GHz) electron paramagnetic resonance (EPR) studies of Fe³⁺ ions at 255 K are reported in a Sn_1?x Fe _x O₂ powder with x = 0.005, which is a ferromagnetic semiconductor at room temperature. The observed EPR spectrum can be simulated reasonably well as the overlap of spectra due to four magnetically inequivalent high-spin (HS) Fe³⁺ ions (S = 5/2). The spectrum intensity is calculated, using the overlap I(BL) + (I(HS1) + I(HS2) + I(HS3) + I(HS4)) × exp(?0.00001B), where B is the magnetic field intensity in Gauss, I represents the intensity of an EPR line (HS1, HS2, HS3, HS4), and BL stands for the baseline (the exponential factor, as found by fitting to the experimental spectrum, is related to the Boltzmann population distribution of energy levels at 255 K, which is the temperature of the sample in the spectrometer). These high-frequency EPR results are significantly different from those at X-band. The large values of the zero-field splitting parameter (D) observed here for the four centers at the high frequency of 236 GHz are beyond the capability of X-band, which can only record spectra of ions with much smaller D values than those reported here.     

Fast diffusion of copper(I) ions in NaI

Results are presented for nmr investigations into the diffusion of Cu⁺ in NaI. The nmr results show that a considerable amount of the copper(I) ions is incorporated interstitially and that the mean jump frequency ν_Cu of the Cu⁺ ions is much higher than that of the host cations: ν_Cu/ν_Na ≈ 820 at 320 °C. Two values for the temperature dependence of ν_Cu are found: E₁ = 1.63 eV (T < 300 °C) and E₂ = 0.61 eV (T > 300 °C). The nature of the mechanism of the Cu⁺-migration in NaI is discussed and a model proposed. The interstitial incorporation and fast diffusion of the Cu⁺ ions is confirmed by a comparison with the results for CdI₂ doped NaI. CdI₂ is incorporated substitutionally and the mean jump frequency ν_Cd is lower than that of the host ions: ν_Cd < 10⁸ s^-1 at 650 °C.For the pure substance conductivity measurements were performed too, for vomparison. The agreement of nmr and conductivity data is good. From both δH_m = 0.59 eV and δH_s = 2.08 eV were calculated in excellent agreement with recently reported data. It is shown that the presence of oxygen in the samples leads to wrong data. A method for removing this impurity is described.     

Effect of plasticizer on electrical conductivity and cell parameters of (PVC+KBrO<Subscript>3</Subscript>) polymer electrolyte system

The effect of a plasticizer dimethyl formamide (DMF) on the properties of a potassium ion conducting electrolyte based on polyvinyl chloride (PVC) complexed with potassium bromate (KBrO₃) prepared using solution-cast technique was investigated. Various experimental techniques, such as electrical conductivity (composition and temperature dependence) and transport number measurements, were used to characterize these polymer electrolyte films. It was found that the addition of plasticizer (DMF) significantly improved the ionic conductivity. Transport number for K⁺ ion ranged from 0.95 to 0.97 depending on the composition and temperature. Electrochemical cells of configuration K/PVC+KBrO₃/(I₂+C+electrolyte) and K/PVC+KBrO₃+plasticizer/(I₂+C+electrolyte) were fabricated. The discharge characteristics of the cells were studied under a constant load of 100 kΩ. The open-circuit voltage, short-circuit current, and discharge time for the plateau region were measured. The PVC+KBrO₃ polymer electrolyte system with added plasticizer showed an increased discharge time with respect to pure PVC+KBrO₃ electrolyte system. The features of complexation of the electrolytes were studied by X-ray diffraction.