赝势
凝聚态物理
赫巴德模型
晶格常数
态密度
电子结构
局部密度近似
密度泛函理论
电子能带结构
带隙
物理
量子力学
超导电性
衍射
标识
DOI:10.52783/tjjpt.v44.i4.2696
摘要
The most complicated calculation in Density Functional Theory (DFT) is for exchange and correlation potential. In this work “Generalized Gradient Approximation, Perdew-Burke-Ernzerhof and Local density approximation along with Hubbard parameter U functionals are used for exchange and correlation potential approximation. The suitable pseudopotential and Hubbard U value for SnO2 calculation are detected computationally so that the results can be used for further calculation of electronic properties like lattice constant, band plot, TDOS and PDOS plots, magnetic properties etc. From these calculations ultra-soft pseudopotential with Schrodinger relativistic treatment having Hubbard U values Up =7eV and Ud =9eV improved the electronic properties. Utilizing these parameters, the calculated band gap is 3.628 eV with 0.77% of difference in comparison with the experimental data. Then the results from the TDOS and PDOS plots are discussed and analyzed. Symmetry nature of TDOS shows SnO2 has no magnetic behavior.
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