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Polyringlpyrrolidoneas a viscosity increaser is used to adjust the viscosity of the sols.When the molar ratio of PVP:Al(OC_3H_7)is up to 1:1,the viscosity of the PVP assisted sol increases from 2.3 to 31.5 mPa·s,and homogeneous,uniform and crack-free 1 mol%Er~(3+)-10 mol%Yb~(3+)codoped Al_2O_3 thin films with the thickness of 1.6μm are formed by 10 dipping and drying cycles sintered at 1000℃.

以聚乙烯吡咯烷酮为增粘剂,调节DCPA改性溶胶的粘度,PVP(K-90):Al_3的摩尔比为1:1时,溶胶粘度由原始溶胶的2.3增加到含PVP溶胶的31.5mPa·s,仅经过10次循环提拉、干燥,1000℃烧结,制备出表面均匀完整,无开裂厚度约为1.6μm的1 mol%Er~(3+)-10 mol%Yb~(3+)共掺杂Al_2O_3薄膜。

The results indicate that rare earth cerium ion dopants do not affect the structure of the material but considerably improves its capacity delivery and cycle performance, which is ascribed to the enhancement of the electronic inductivity and reducing crystal size to nanoscale by ion doping.

研究表明,少量Ce3+的掺杂未影响到LiFePO4的晶体结构,但显著改变了粉体的微观形貌,降低颗粒粒径至纳米级,改善了可逆容量和循环性能。得到的最佳配比正极材料Li0.9975Ce0.0025FePO4,在0.1C的充放电速率下,其初始可逆放电容量达到116 mAh/g。

The influence of this complex on the electrical properties of n-type LEC undoped and compensation in Fe-doped InP is discussed.

讨论了其对未掺杂InP的电子特性和掺Fe的InP的补偿的影响,及其对InP热稳定性的影响。

In chapter II, we calculate the binding energy of a quantum wire in the presence of a strong magnetic field along the wire axis by using the variational method and strong perturbation method.

在第二章中,我们用变分法和强相互作用方法计算了在一个沿着轴向的强磁场下的量子线的束缚能,讨论了束缚能随着量子线的半径,磁场和掺杂浓度的变化。

In order to obtain the high MR value at the room temperature in a low applied magnetic field, several methods have been employed to modify the structure of the compounds, such as introducing the substituting ions or the interstitial atoms into this manganite matrix.

人们致力于通过掺杂、填隙等方法改变材料内部的结构,研究它的电磁输运性质,同时期望在较高的温度以及较小的外加磁场下得到较大的磁电阻效应。

This showed that the electron density of a quinoid ring increased. The peaks of the quaternary carbon atoms of the benzene rings, which were adjacent to the quinoid ring, also shifted to higher field. But the peaks of other C atoms shifted to lower field.

NMR结果表明苯胺低聚体掺杂后主链上的电荷重新分布,环上的H原子上的电子被C原子吸引,电荷密度降低,在〓 NMR中谱峰向低场移动。C原子的谱峰也相应发生变化,醌环上电荷密度增加,全部C原子的峰向高场移动,与醌环相邻苯环受其影响季碳峰移向高场,非季碳峰移向低场。

Theoretical results, which are in good agreement with the experimental work, suggest that the stable ability of doped c-ZrO2 could be described qualitative by the Coulomb repulsive force of neighboring oxygen ions.

即c-ZrO2 的稳定作用可定性描述为近邻氧离子之间Mulliken电荷的库伦排斥力的大小,且此方法也可成功的应用于解释第三相阴离子或阳离子掺杂c-ZrO2复合材料的稳定机理。

And dye. The results from the whole experiments and sensitometric results from these emulsions showed: 1 that sensitization of Zn-EDTA or Cd-EDTA on silver bromide emulsion was affirmed; 2 That a cooperation sensitization of Zn-EDTA or Cd-EDTA, sulfur plus gold, and dye could be carried out to make a higher level of sensitization; 3 That a cooperation sensitization of Zn-EDTA or Cd-EDTA, on the basis of and dye, with oxalate-doped was carried out to make a higher level of sensitization without any increase in the level of fog.

对实验过程的考察和感光性能的测试结果表明,Zn-EDTA或Cd-EDTA对细微粒溴化银颗粒乳剂均有显著的增感效应;Zn-EDTA或Cd-EDTA增感可在传统硫加金增感基础上与光谱增感协同作用,三者具有兼容和可加和性;Zn-EDTA或Cd-EDTA增感可在传统硫加金增感与光谱增感协同作用的基础上,与草酸根内部掺杂增感兼容,实现四者的协同作用,而不引起乳剂灰雾增加。

In this paper, we study the synergetic effects of second ligands and luminescence enhancement effects of doping ions starting from the binary complexes of europium and terbium with inexpensive benzoic acid and its derivatives, and improve the luminescence of complexes step by step.

本文从比较廉价的苯甲酸衍生物配体与稀土铕、铽的二元配合物入手,研究第二配体的协同效应和掺杂离子的荧光增强效应,逐步提高配合物的荧光性能。

It was particularly observed that, with increasing fraction of Q〓 mode Jahn-Teller distortion and decreasing of that of Q〓 mode in the CO state, the magnetic structure evolves from CE-type to C-type, orbital ordering from 3d〓/3d〓 to 3d〓, and crystal structure from tetragonally compressed to tetragonally elongated orthorhombic.

特别是,我们发现〓在电荷有序态下随着Ca〓离子掺杂量从x=0.5增大到x=0.75,合作Jahn-Teller晶格畸变的畸变模式从Q〓模式逐渐转变到Q〓模式,这种晶格畸变模式的转变直接导致了电荷有序态下的磁结构从CE-型转变到C-型,轨道序从3d〓/3d〓转变到3d〓,晶体结构从压缩的正交对称性转变到拉伸的正交对称性。

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随着死亡的吉他手Schuldiner接受主唱的职务,乐队在现实中树立了重要的影响。

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关闭眼睛,深呼吸,一切不再是梦想,犹如。。。。。。