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1 INTRODUCTION Silicon is an important kind of semiconductormaterial having been used to produce many sorts ofapparatus, digital and linear integrated circuit andLarge Scale Integrated circuit (LSI), and its clustershave drawn many scientists’ atten… 相似文献
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采用基于密度泛函理论的第一性原理方法系统地研究了Au12M(M=Na,Mg,Al,Si,P,S,Cl)团簇的结构、稳定性和电子性质.对团簇的平均结合能、镶嵌能、垂直离化势、最高占据分子轨道(HOMO)和最低未占据分子轨道(LUMO)的能级差、电荷布居分析、自然键轨道(NBO)进行了计算和讨论.对于Au12M(M=Na,Mg,Al)团簇,它们形成了内含M原子的最稳定的笼状结构.然而对于Au12M(M=Si,P,S,Cl)团簇,它们却形成了以M元素为顶点的稳定锥形结构.在这些团簇中发现Au12S团簇相对是最稳定的,这是由于Au12S团簇形成了稳定的满壳层的电子结构.自然电荷布居分析表明:对于所有的Au12M(M=Na,Mg,Al,Si,P,S,Cl)团簇电荷总是从Au原子转向M原子.自然键轨道和HOMO分析表明Au12M团簇中发生了Au原子的s-d轨道和M原子的p轨道间的杂化现象. 相似文献
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应用密度泛函理论在B3LYP/6 31G*水平上对C40X2 (X=H,F,Cl,Br)进行研究.研究结果表明,C40X2 (X=H,F,C1,Br)在热力学上是稳定的,卤化衍生物的稳定性随卤素原子序数的增大而降低,最有利的衍生化方式是1-4加成,1-2与1-4加成的卤化和氢化衍生物在所研究的分子中较为稳定.这些研究有助于理解富勒烯衍生物的衍生化模式. 相似文献
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利用Gaussian-94计算程序,B3LYP方法,6-311+G(2d)6d基组,对SiOM(M=Li,Be,B,Na,Mg,Al)诸体系的几何结构进行优化.结果表明,M既可与SiO中的Si键合,也可与O键合.第一和第二主族的SiOM体系以折线形构型为最稳定构型,而第三主族则以近直线形或直线形构型为最稳定构型.从Si-O间键长RSiO、力常数fSiO及自然键轨道分析可知,第一主族的SiOLi和SiONa的最稳定构型中SiO-M间的离子键成分较大,可近似看作离子键;而对SiOLi,SiOBe,SiOB和SiOMg体系的以Si为中心的构型,M-SiO间的离子键成分很小,不能看作离子键,可认为M与SiO之间存在着弱相互作用 相似文献
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XU Wen-Guo ZHANG Rui-Chun CHANG Hong-Yan 《结构化学》2009,28(9):1067-1076
Clusters XY2Z species are theoretically investigated with density functional theory (DFT) method. The results show that for LiP2C, LiAs2Ge and KAs2C species, the C2v isomer is the most stable planar structure, while for other species the Cs isomer is the most stable planar structure at the B3LYP/6-311+G* level. Wiberg Bond Index (WBI) and Nucleus-Independent Chemical Shift (NICS) values indicate the existence of delocalization in stable planar structures. A detailed Molecular Orbital (MO) analysis further reveals that planar isomers of these species have strong aromatic character, which strengthens the structural stability and makes them closely connect with the concept of aromaticity. 相似文献
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使用了不同密度泛函方法计算X-H (X = C, N, O, Si, P, S) 键离解能,并分析不同密度泛函方法的计算精度。研究发现大多数密度泛函方法包括B3LYP, B3P86, B3PW91, G96LYP, PBE1PBE,和BH&HLYP都明显低估键离解能13-25 kJ/mol。该现象与是否使用无限基组无关,因为即使使用无限基组键离解能仍然被低估。因此密度泛函方法不适合用于键离解能的估算。其中B3P86方法的偏差最小。进一步分析表明,使用限制性开壳层计算并无任何优势,在大多数情况下非限制性开壳层计算实际上比限制性开壳层计算要好。最后,我们发现了密度泛函方法对键离解能的低估是系统的,因此建议利用校准后的UDFT/6-311++G(d, p)方法计算化学键离解能。 相似文献
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Ab initio valence bond method is employed to quantitatively study the concepts of ionic resonance energy and ionicity of a chemical bond in the cases of hydrides XH(X=Li,Be,B,C,N,O,F) and fluorides XF(X=Li,Be,B),By establishing the relationship between resonance and stability,and comparing the calculated ionicities with Pauling‘s earlier estimations in the above diatomic molecules,the merits of Pauling‘s classical resonance theory were demonstrated at the ab initio level. 相似文献
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(XY)12(X=B,Al;Y=P)团簇的结构与稳定性 总被引:1,自引:0,他引:1
采用B3LYP/6031G*方法,对(XY)12(X=B,Al;Y=P)笼状团簇的同分异构体进行优化,筛选出能量最低的构型.讨论它们的几何构型、HOMO-LUMO能隙、生成焓、核独立化学位移(NICS)和自由能.得到(BP)12和(AlP)12团簇的最稳定构型均为具有Th对称性的四、六元环组成的笼,亚稳态结构中含有五元环。 相似文献
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Three-membered BeXP (X = C, Si, Ge) and CYP (Y = O, S, Se) rings are theoretically investigated using density functional theory (DFT) methods at the B3LYP/6-311+G^* and B3PW91/6-311+G^* levels of theory. The research results show that the size of atoms has a great influence on the structural stability of these species. The wiberg bond indexs (WBIs) suggest the existence of delocalization in these structures. Negative nucleus-independent chemical shift (NICS) values for these species indicate that a strong ring current exists in these three-membered structures (Cs symmetry). A detailed molecular orbital (MO) analysis further reveals that a delocalized π MO strengthens the structural stability and makes these species show strong aromatic characters. 相似文献
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Adjusting magnetic moments of Sc13 and Y13 clusters by doping different X atom (X = Na,Mg, Al,Si, P)
We have investigated the structural and magnetic properties of the doped XM12 and charged M13 (X = Na, Mg, Al, Si, P; M = Sc, Y) clusters using the density‐functional theory with spin‐polarized generalized gradient approximation. It was found that doped atoms can induce significant change of the magnetic moments of Sc13 and Y13 clusters. The total magnetic moments of the NaM12, MgM12, AlM12, SiM12, and PM12 clusters are regular 5, 6 (12), 7, 8, and 9 μb, respectively (but 19 μb for Sc13 and Y13, 12 μb for Y, 18 μb for Sc, Sc, and Y). The doped atom substituting the surface atom of the plausible icosahedral configuration is viewed as the ground‐state structure of the XM12 (X = Na, P; M = Sc, Y) and MgSc12 clusters. While for XM12 (X = Al, Si; M = Sc, Y) and MgY12 clusters, the doped atom occupying the central position of the icosahedral configuration is viewed as the ground‐state structure. The doping and the charging both enhance the stability of the Sc13 and Y13 clusters. These findings should have an important impact on the design of the adjustable magnetic moments systems. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010 相似文献