Electrical properties of LiBSe ternary system

Amorphous products were obtained in the LiBSe ternary system by quenching melts of Li₂Se, B and Se mixture prepared at 100°C in sealed silica tubes. The vitreous region was slightly lower selenium composition than that of the Li₂SeB₂Se₃ tie-line. The amorphous products were lithium ionic conductors and most of them showed contributions to their total conductivity. The amorphous product of composition Li₂₅B₃₆Se₃₉ has the least electronic contribution to its total conductivity of 6.0 × 10⁻⁶ S/cm at room temperature. A new crystalline compound and crystalline LiBH₄ were also obtained in LiBSe ternary. Both of them were lithium ionic conductors having conductivities of about 1 × 10⁻⁶ S/cm at room temperature.     

大爆炸核合成相关的8Li(d,p)9Li反应截面测量

利用8Li次级束测量了质心系能量7.8 MeV2H(8Li, 9Li)1H反应的角分布，导出了8Li(d, p)9Li反应的天体物理S因子及9Li→8Li+n虚衰变的渐近归一化系数. We have measured the angular distribution of 2H(8Li,9Li)1H at Ecm= 7.8 MeV and deduced the astrophysical S factor of 8Li(d, p)9Li reaction as well as the Asymptotic Normalization Coefficient (ANC) for 9Li → 8Li+n virtual decay.     

同位素7Li和6Li的性质殊异

本文研究了同位素7 Li和6 Li在几个方面的性质差异．用相对论量子力学计算指出,6 Li的电子能级比7 Li的能级低,同时,对电偶极E （1）和磁偶极M （1）的能级跃迁波长,6 Li的跃迁波长都要比7 Li的长．由于7 Li和6 Li的核自旋的大小不同,可以看出在磁场2万高斯和温度100－20 K之间,7 Li的磁极化比6 Li的约大13倍．7 Li和6 Li的磁极化这种差异,也是一种可能的同位素7 Li／6 Li的分离方法．     

Measurement of Angular Distribution for the ^8Li（p,d）^7Li Reaction

The ^8Li（p, d）^7 Li reaction plays an important role in the inhomogeneous Big Bang nucleosynthesis and in the seed-nuclide production phase for the r-process. For the first time, its angular distribution at backward angles was measured in inverse kinematics at Ec.m.=4.0 MeV by using an ^8Li secondary beam. The result of measurement includes the contributions of ^8Li（p, d0）^7Li and ^8Li（p, d1）^7Li^＊. The ^8Li（p, d0）^7Li component is estimated to be 40%-58% in the mixture angular distribution by analysing the measured result.     

Determination of astrophysical ~7Be(p,γ)~8B reaction rates from the ~7Li(d,p)~8Li reaction

The7Be(p,γ)8B reaction plays a central role not only in the evaluation of solar neutrino fluxes but also in the evolution of the first stars.Study of this reaction requires the asymptotic normalization coefficient(ANC) for the virtual decay8 Bg.s.→7Be + p.By using the charge symmetry relation,we obtain this proton ANC with the single neutron ANC of8 Lig.s.→7Li + n,which is determined with the distorted wave Born approximation(DWBA) and adiabatic distorted wave approximation(ADWA) analysis of the7Li(d,p)8Li angular distribution.The astrophysical S-factors and reaction rates of the direct capture process in the7Be(p,γ)8B reaction are further deduced at energies of astrophysical relevance.The astrophysical S-factor at zero energy for direct capture,S17(0),is derived to be(19.9±3.5) e V b in good agreement with the most recent recommended value.The contributions of the1+and 3+resonances to the S-factor and reaction rate are also evaluated.The present result demonstrates that the direct capture dominates the7Be(p,γ)8B reaction in the whole temperature range.This work provides an independent examination to the current results of the7Be(p,γ)8B reaction.     

同位素7Li和6Li 的性质殊异和应用

本文研究了同位素7Li和6Li在几个方面的性质差异。用相对论量子力学计算指出,6Li的电子能级7Li的能级低,同时,对电偶极E（1）和磁偶极M(1)的能级跃迁波长,6Li 的跃迁波长都要比7Li 的长。 非相对论量子力学方法（B3LYP/6-311G**）计算总的核自旋-自旋偶合常数 。由于7Li 和6Li 的核自旋大小不同,当其与其它原子偶合时所导致的偶合常数的差异, 是一种可能的分离同位素7Li/6Li 的方法的础。可以看出在磁场2万高斯和温度100-20 K之间 ,7Li的磁极化比6Li的约大13 倍。7Li 和6Li 的磁极化这种差异,也是一种可能的同位素7Li/6Li 的分离方法。     

同位素7Li和6Li 的性质殊异和应用

本文研究了同位素7Li和6Li在几个方面的性质差异。用相对论量子力学计算指出,6Li的电子能级7Li的能级低,同时,对电偶极E（1）和磁偶极M(1)的能级跃迁波长,6Li 的跃迁波长都要比7Li 的长。 非相对论量子力学方法（B3LYP/6-311G**）计算总的核自旋-自旋偶合常数 。由于7Li 和6Li 的核自旋大小不同,当其与其它原子偶合时所导致的偶合常数的差异, 是一种可能的分离同位素7Li/6Li 的方法的础。可以看出在磁场2万高斯和温度100-20 K之间 ,7Li的磁极化比6Li的约大13 倍。7Li 和6Li 的磁极化这种差异,也是一种可能的同位素7Li/6Li 的分离方法。     

Mixed cationic effect in the Li/AgB2O3P2O5 glasses

Electrical conductivity data have been determined for a series of x Ag₂O(1 − x)Li₂OB₂O₃P₂O₅ glasses. The progressive substitution of Li⁺ by Ag⁺ considerably decreases the ionic conductivity which shows a minimum at Ag/(Ag + Li) = 0.4. This behaviour becomes intense as the temperature is lowered. This mixed cationic effect is further characterised by activation energy and conductivity relaxation time going to a maxima where conductivity minima occurs. ac conductivity and electric modulus response of those glasses are discussed.     

Neutron Spectroscopic Factors of ^7Li and Astrophysical ^6Li（n,γ）^7Li Reaction Rates

Angular distributions of the ^7Li（^6Li, ^6Li）^7Li elastic scattering and the ^7Li（^6Li, ^7Lig.s.）^6Li, ^7Li（^6Li, ^7Li0.48）^6Li transfer reactions at Ec.m. = 23.7 MeV are measured with the Q3D magnetic spectrograph. The optical potential of ^6Li ＋ ^7Li is obtained by fitting the elastic scattering differential cross sections. Based on the distorted wave Born approximation （DWBA） analysis, spectroscopic factors of ^7Li =^6Li n are determined to be 0.73 ± 0.05 and 0.90 ± 0.09 for the ground and first exited states in ^7Li, respectively. Using the spectroscopic factors, the cross sections of the ^6 Li（n, γ0,1）^7 Li direct neutron capture reactions and the astrophysical ^6Li（n, γ）^7 Li reaction rates are derived.     

Global optical model potentials for symmetrical lithium systems: 6Li+6Li, 7Li+7Li at Elab = 5–40 MeV

Angular distributions of ⁶Li+⁶Li elastic scattering were measured for E_lab = 5–40 MeV. An optical model analysis of these data together with older data of ⁷Li+⁷Li elastic scattering taken at E_lab = 8–17 MeV was performed with the aim to search for a “global” OM potential which describes elastic scattering in both LiLi systems in a broad energy range. Both surface and volume absorbing potentials can be found which fulfill this requirement if a linear energy dependence is assumed of the depths of the real as well as the imaginary potential. These depths, if fitted to individual angular distributions, are found to vary in a correlated manner with the beam energy. This is taken as indication of strong coupling between elastic, inelastic, and reaction channels. This is corroborated by the existence of resonances in reaction channels at these energies where the potential depths are most pronouncedly changing.     

电池正极材料中Li+运动特性的7Li NMR研究

利用变温⁷LiNMR实验对Li-电池正极材料LiMn₂O₄和LiCoO₂中Li⁺的运动特性进行了研究,结果表明,随实验温度的提高,LiMn₂O₄的⁷LiNMR谱线窄化,表明其中Li⁺迁移能力增加,而LiCoO₂的谱线无变化.此外随温度提高,LiMn₂O₄的⁷Li的T₁变短,而LiCoO₂的T₁变长,产生这种不同变化趋势的原因在于LiMn₂O₄和LiCoO₂晶相结构的差异造成其中Li⁺迁移能力的差别,它们各自的相关时间τ_c使⁷Li核的T₁分别位于T₁-τ_c曲线极小点两侧.     

Zero resistance above 90K in superconducting oxides ErBaCuO and YbBaCuO

Superconductivity transition has been observed by electrical resistance and a.c. magnetic susceptibility measurements in ErBaCuO and YbBaCuO systems. The highest T_c(ϱ=0) is 90.3K for ErBaCuO and 91K for YbBaCuO.     

Neutrinorückstoßexperiment am Li8

The beta-decay of Li⁸→Be^8*→2α is especially suitable in neutrino recoil experiments on account of the large beta-decay energy available and on account of the subsequent break up of Be^8* into two α-particles. For the angular correlation between the antineutrino and the α-particle one obtains for our counter geometry and a Gamow-Teller interaction the angular distributionw(v)dv=(1+b v/c 0.707 cosv)dv, whereb=?1 for axial vector interaction (A) orb=+1 for tensor interaction (T) and wherev is the angle between the direction of emission of the antineutrino and the α-particle. The measurement of the energy difference of the two α-particles in the Be^8* decay, when the direction of the emission of the beta-particle is fixed, defines the angular correlation coefficientb. In this experiment the value ofb is found to be equal to ?1.12±0.20, which shows axial vector interaction in the Gamow-Teller decay.     

Hypersonic secondary relaxation due to fast ion diffusion modes in xLiCl0.5Li2OB2O3 glasses

The hypersonic attenuation and the sound velocity for a high and a low conducting Li⁺-glass, 0.7LiCl0.5Li₂OB₂O₃ and 0.5Li₂OB₂O₃, respectively, have been measured as functions of temperature by Brillouin scattering. A large excess hypersonic attenuation was found at high temperatures in the LiCl rich glass compared to the low conducting glass. The effect is attributed to structural relaxation of fast ion diffusion modes involving Li⁺ ions jumping between different sites in the glass network. The sound velocity observed for the LiCl doped glass was 10% lower than the value for the undoped glass. This reflects considerable changes in the elastic properties of the glass network in accordance with a model which proposes that the high conductivity in these glasses can be explained by structural changes of the intermediate range order.     

High Tc superconductivity of a TlBaCaCuO compound

A TlBaCaCuO_4.5+x compound has been investigated from the point of view of superconductivity. Depending on the heat treatment, one part of the samples exhibits superconductivity with an onset of 121 K and a zero resistivity of 106 K, while the other part of them shows only a sharp drop in resistivity at 130 K which hints at the existence of superconducting domains. This picture was confirmed by magnetic and ESR measurements giving possibility for estimation of the critical magnetic fields.     

Comment on the7Li(p, γ)8Be reaction at energies of astrophysical interest

The results of two recent publication are reconsidered. These papers argue that the p-wave effects seen in the⁷ Li(p, ) ⁸ Be reaction belowE _p=80 keV can be accounted for by considering the low-energy tail of the p-wave resonance atE _p=441 keV. It is shown that the cross section and analyzing power data require an order-of-magnitude more p-wave strength when considered together.This work was supported by the U.S. Department of Energy, Office of High Energy and Nuclear Physics, under Contract No. DEFG05-91-ER40619.     

Ionic conductivity of ZrF4BaF2MX (M = Li,Na;X = F,Cl) glasses

Glasses were prepared in a wide range of compositions for the two systems oof mixed-cation, ZrF₄BaF₂LiFNaF, and mixed-anion, ZrF₄BaF₂LiFLiCl. Ionic conductivities were measured for these glasses and it was found that these glasses were not only cationic but also anionic conductors depending on the total alkali halide content. Four types of mixed-cation and mixed-anion effects on ionic conductivity were demonstrated for the cation-conducting and anion-conducting glasses. In cation conduction, the cation mixing caused the conductivity decline, whereas the anion mixing led to the conductivity enhancement. In anion conduction, on the other hand, the cation mixing led to the conductivity enhancement, whereas the anion mixing caused the conductivity decline.