G.P.Li
,
D.Li
,
Y.Y.Liu
,
S.X. Guan and Q.J.Wang (Department of Titanium Alloys
,
Institute of Metal Research
,
The Chinese Academy of Sciences
,
Shenyang 110015
,
China)
金属学报(英文版)
TEM examination proves that the second phase particle within the as-forged Ti-55alloy consists of either bright or dark "matrix" (nano-Nd3Sn) and some small dark blocks (SnO) dispersed in the "matrix". The HREM observation shows that the nanoNd3Sn phase is roughly spherical and about 3-15nm in diameter, and the grain boundaries with atout 1nm width are "gas-like" structure.
关键词:
Ti alloy
,
null
,
null
李志宏
,
柳卫平
,
白希祥
,
郭冰
,
连钢
,
颜胜权
,
王宝祥
,
陆昀
,
曾晟
,
苏俊
原子核物理评论
doi:10.3969/j.issn.1007-4627.2005.01.006
利用8Li次级束测量了质心系能量7.8 MeV 2H(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.
关键词:
8Li(d,p)9Li反应
,
角分布
,
天体物理S因子
,
渐近归一化系数
A.H. Salama
材料科学技术(英文)
Li-doped p-type ZnO ceramics were prepared by conventional methods according to the chemical formula Zn1-x LixO2 where x=0.5, 1.0, 1.5 and 2.0 mole fraction, respectively. The crystal structures of the prepared samples were studied by X-ray diffraction analysis. The dielectric properties (including dielectric constant ε'
and dielectric loss ε") and dc-electrical conductivity [σ(Ω-1·cm-1)] were investigated. The dielectric constant ε' was sharply decreased at the low frequency range and independent on frequency at high frequency range. Otherwise, the dielectric loss "00 varied with frequency and showed absorption peak located from 200 Hz to
4 kHz and moved to higher frequency as the concentration of Li+ doped increased. It was found that dc-electrical conductivity log¾ varied from -9 to-5 and the energy gap width were calculated by using Arrhenius equation. The p-type conductivity of Li-doped ZnO may be attributed to the formation of a LiZn-Lii donor complex, which is limited by reducing the amount of Lii.
关键词:
P-type ZnO ceramics
赵中伟
,
刘旭恒
中国有色金属学报
运用同系线性规律对Li-Fe-P-H2O系中缺少的LiFePO4和Li3PO4的△GΘ进行估算.结合已有的热力学数据,运用ψ-pH图的绘制原理,得到25℃时Li-Fe-P-H2O系在不同浓度下的ψ-pH图.结果表明,在水溶液中,LiFePO4具有较大的热力学稳定区域,这对湿法制备LiFePO4很有利.根据所绘制的热力学平衡图,详细讨论了各种LiFePO4软化学制备方法的可行性途径,并就液相法制备LiFePO4可能的技术途径和条件进行分析,为在水溶液中用软化学法制备LiFePO4提供理论依据.
关键词:
Li-Fe-P-H2O系
,
磷酸铁锂
,
热力学
杨昊
,
范广涵
,
李军
材料科学与工程学报
采用基于密度泛函理论的第一性原理赝势法计算了本征ZnO、N掺杂、Li掺杂以及Li、N共掺杂ZnO的能带结构、电子态密度和差分电荷分布.计算结果表明:N掺杂的受主能级局域性较强,导致N溶解度较低,Li替位原子受主能级较浅,但是会受到Li间隙原子的补偿.Li、N共同掺入时,N_o-Li_(Zn)复合受主结构并不是ZnO的主要P型来源,N_o受主可以与间隙原子Li_i形成N_o-Li_i结构,该结构可促进N的掺入,并抑制Li_i施主的补偿效应,因而对实现ZnO的P型非常有利.
关键词:
ZnO
,
第一性原理
,
密度泛函理论
,
双受主共掺杂
曹笃盟
,
李志友
,
周科朝
稀有金属材料与工程
采用固相反应法制备了Li1+xV3-yMyO8(M=Mo,P;0≤y≤0.4),研究了不同Mo和P含量对Li1+xV3O8相的影响,并首次对其进行了高温阴极放电性能的研究.结果表明:Mo和P掺杂量分别为y≤0.2和y<0.2时可获得纯Li1+xV3O8相;Mo掺杂使Li1+xV3O8峰值电压提高0.3 V,比容量提高25%,嵌入的Li+量最高可达x=3.8;P掺杂(y≤0.20)对Li1+xV3O8的峰值电压和比容量影响较小.化学嵌锂实验也证实掺杂后的材料具有更快的Li+嵌入速度.
关键词:
Li1+xV3O8
,
热电池
,
掺杂
,
比容量
陈敬区
,
刘江文
材料导报
评述了国内外Mg-Zn系合金的研究进展.总结了Mg-Zn系合金中时效析出行为和各析出强化相的特征,通过分析铝合金G.P.区的形成规律,探讨了Mg-Zn系合金G.P.区的存在可能性.指出Mg-Zn系合金G.P.区的研究对Mg-Zn合金析出相变理论和发展高强度铗合金具有重要意义.
关键词:
Mg-Zn系合金
,
G.P.区
,
时效
,
析出强化
卢洋藩
,
叶志镇
,
曾昱嘉
,
陈兰兰
,
朱丽萍
,
赵炳辉
无机材料学报
doi:10.3724/SP.J.1077.2006.01511
采用Li-N-H共掺技术在玻璃衬底上生长p型ZnO薄膜. XRD结果表明共掺ZnO薄膜具有高度cll轴取向, Hall测试表明薄膜的电阻率为25.2Ω·cm, Hall迁移率为0.5cm2/(V·s), 空穴浓度为4.92×1017/cm3. 此外, p-ZnO薄膜在可见光区域具有90%的高透射率.
关键词:
p-ZnO
,
magnetron sputtering
,
codoping