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delocalization相关的网络例句

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与 delocalization 相关的网络例句 [注:此内容来源于网络,仅供参考]

The results showed that a red-shift of the maximum absorption took place when the delocalization of the π electrons in the organic molecules increases.

计算结果表明,随着有机分子的π电子离域结构的增大,最大吸收峰红移。

This behavior is suggested to be originated from delocalization of the localized carriers by thermal activation.

由变温光激萤光光谱,观察到随温度增加能量峰值有下降、上升再下降的现象,此S型行为是因为载子受到温度的活化,脱离原本的局域态而跃迁到高能量能态。

This article argues the delocalization theory has many things to do with the modernization of arbitration law .

于是人们不能不重新审视仲裁地法是否必然适用于仲裁程序。

Furthermore, a theoretical Molecule-In-Molecule approach was used to rationalize the excited state delocalization pathway of cyclophandiene molecules.

透过分子内分子(Molecule-In-Molecule)的方法,可以进一步解环芃二烯在激发态非定域化的途径。

The association chain implied is general reactivity , delocalization, heat of reaction, activation energy, velocity constant

和该量有牵连的因素是一般活性,离域作用,反应热,活化能,速度常数。

Is delocalization the only alternative? Or can a more democratic, more inclusive management of globalization turn it into the most effective tool for dealing with the pressing problems of our time?

或者能否拥有一种更民主,更具有包含性的全球化管理方式,使之成为处理当今所面临问题的有效工具?

RhoA isoprenylation inhibition and its delocalization from the cell membrane may be one of the mechanisms of lovastatin_inhibited anti_proliferation effect in HepG2 cells.

减少RhoA香叶酯化,抑制RhoA的细胞膜锚着可能是洛伐他汀抑制HepG2增殖的机制之一。

The factors such as introduction of aromatic heterocycle with small delocalization energy, formation of acceptor-donor structure, and strong electron-donating or electron-withdrawing abilities of substituents lead to the high third-order nonlinear optical property.

引入离域能小的芳杂环,形成吸供构型,增大取代基的吸或供电子能力等有利于获得较大的三阶非线性光学性能。

In this dissertation, we optimized the thinkness of each layer of TFEL devices using the layered optimization method to obtain ZnS: Ce〓 TFEL devices. Accoding to the energy level structure of Ce〓, two criteria for distinguishing the EL of Ce〓 were found out, from which it was conduded that the TFEL of ZnS: Ce〓 comes from 5d→4f transition of Ce〓. The measurement of brightness waveform showed that the TFEL of ZnS: Ce〓 was the luminescence from independent centers. and there were the field induced-delocalization in this process anf it〓s the cause of low TFEL efficiency of ZnS: Ce〓. In this dissertation, different influence factors on TFEL of ZnS: Ce〓 were sdudied. The influence of different host lattice is different: The blue/green ratio of ZnS: Ce〓 in hexagonal system of ZnS is larger than that in cubic system of ZnS, and the TFEL peaks in hexagonal system of ZnS moves toward longer wavelength compared with that in cubic system of ZnS. The adding buffer layer was used in this stage. The solubility of Ce〓 in ZnS was small and it was another limit to TFEL brightness of ZnS: Ce〓 device. The solubility of Ce〓 increased ten times when using Li ions as flux, so that the TFEL brightness of ZnS: Ce〓 was enhanced. It was found that the appearing of ZnO in active layer improves the TFEL of ZnS: Ce〓: the brightness and the wave range of ZnS: Ce〓TFEL were enhanced.

本文采用TFEL的分层优化方案,优化组合了各膜层厚度,选择最佳制备条件,得到了ZnS:Ce〓的TFEL;根据Ce〓的能级结构,找到了判别Ce〓的EL的两个简单依据,并据此断定ZnS:Ce〓的TFEL的两个发射峰分别属于Ce〓的〓和〓跃迁;亮度波形测量表明ZnS:Ce〓的TFEL属于分立中心发光,分析认为在此过程中存在着较严重的场致离化,这也是ZnS:Ce〓的TFEL效率较低的一个原因;本文考查了影响ZnS:Ce〓的TFEL的各种因素,发现:基质的晶体结构对ZnS:Ce〓的TFEL有所影响,在六角相ZnS中Ce〓的TFEL优于立方相ZnS中Ce〓的TFEL:发射峰的蓝-绿比相对较大,且光谱向短波方向移动,在此项研究中本文采用了在发光层前增镀过渡层的办法,过渡层为六角晶相的ZnO;限制ZnS:Ce〓的TFEL器件亮度的一个原因是Ce〓在ZnS中的溶解度低,本文用Li离子作助溶剂增大了Ce〓的溶解度,增大幅度为一个量级,并且ZnS:Ce〓的TFEL亮度明显提高;从ZnS:Ce〓的TFEL光谱来看ZnS:Ce〓的TFEL波长覆盖范围较小,亮度也不高,达不到做为白色TFEL材料的要求,需要寻找新的白色TFEL材料;在研究ZnS:Ce〓的TFEL中还发现:发光层中ZnO的出现有利于ZnS:Ce〓的TFEL:发射峰变宽、亮度增大。

The smaller fullerenes C2n (2n 60) violating IPR, inevitable suffer large strain energies and show high lability. Besides that, quasi-fullerenes violating the classical definition, contain rings of other size, for example 4 or 7, are expected to suffer extra local strain or/and further loss ofπdelocalization, and thus highly unstable.

碳原子数少于60的小富勒烯,和结构中含有除五元环、六元环之外的其他结构的准富勒烯,由于不满足IPR规则,结构中必然存在较大的张力,因此具有较高的化学活性,难以在实验中合成和分离。

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