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首页> 外文期刊>The Journal of Chemical Physics >The accuracy of the pseudopotential approximation. III. A comparison between pseudopotential and all-electron methods for Au and AuH [Review]
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The accuracy of the pseudopotential approximation. III. A comparison between pseudopotential and all-electron methods for Au and AuH [Review]

机译:伪电位近似的精度。三,伪电位法和全电子法对Au和AuH的比较[综述]

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摘要

The quality of the pseudopotential approximation has been tested thoroughly by calculating spectroscopic properties of the gold atom and ground state AuH for eight different effective core potentials using Hartree-Fock, second-order Moller-Plesset and coupled cluster methods. The pseudopotential valence basis set {Phi}(upsilon) for Au was chosen to be identical for all pseudopotentials, a subset of the all-electron basis set {Phi}(upsilon)subset of{Phi}(AE), and the condition was applied that all sets are of near basis set limit quality. The pseudopotential results are compared with data obtained from nonrelativistic, scalar relativistic Douglas-Kroll and fully relativistic four-component all-electron calculations. The variation between the results obtained for all valence electron small-core pseudopotentials and all electron Douglas-Kroll calculations is found to be small (for the Stuttgart pseudopotential Deltar(e)=0.001 Angstrom, DeltaD(e)=0.03 eV, Delta omega (e)=9 cm(-1), Delta mu (e)=0.04 D). Sizable differences to all electron results are only found for the 11 valence electron large-core pseudopotentials. The effects of the basis set superposition error on spectroscopic constants were investigated. Calculated coupled cluster electron affinities and ionization potentials for gold and spectroscopic properties for AuH were found to be in excellent agreement with available experimental data. The variation between the different small-core pseudopotentials for one particular spectroscopic property is shown to be less than the error due to the incompleteness of electron correlation procedure or the basis set and approximately of the same size as the basis set superposition error. The results show that scalar relativistic effects for valence properties are perfectly described by the pseudopotential approximation. (C) 2000 American Institute of Physics. [S0021-9606(00)30741-3]. [References: 110]
机译:通过使用Hartree-Fock,二阶Moller-Plesset和耦合簇方法计算八个不同有效核心电势的金原子和基态AuH的光谱性质,对准电势近似的质量进行了全面测试。选择所有Au的伪电价基集{Phi}(upsilon)对于所有伪电势都是相同的,这是{Phi}(AE)的全电子基集{Phi}(upsilon)子集的子集,条件是适用于所有集合均接近基本集合极限质量。将伪势结果与从非相对论,标量相对论Douglas-Kroll和完全相对论四分量全电子计算获得的数据进行比较。发现所有价电子小核pseudo势与所有电子Douglas-Kroll计算结果之间的差异很小(对于斯图加特pseudo势Deltar(e)= 0.001埃,DeltaD(e)= 0.03 eV,DeltaΩ( e)= 9 cm(-1),Delta mu(e)= 0.04 D)。对于所有电子结果,只有11个价电子大核伪电势存在相当大的差异。研究了基集叠加误差对光谱常数的影响。发现计算出的金的耦合簇电子亲和力和电离势以及AuH的光谱性质与可用的实验数据非常吻合。对于一种特定的光谱特性,不同的小核伪势之间的变化显示为小于误差,这是由于电子相关程序或基集的不完整所致,并且其大小与基团叠加误差大致相同。结果表明,价空间性质的标量相对论效应可以通过伪势近似来完美描述。 (C)2000美国物理研究所。 [S0021-9606(00)30741-3]。 [参考:110]

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