与冰相比,H2O2 () 和H2O2·2H2O () 晶体:DFT功能评估和D3分析
Daniel J Arismendi-Arrieta1, Anik Sen1, Anders Eriksson1
1Department of Chemistry-Ångström, Uppsala University, P.O. Box 530, S-75121 Uppsala, Sweden.
密度函数理论 (DFT) 的计算显示,分散校正,特别是D3校正,显著影响过氧化晶体的晶格能量. optPBEvdW和RPBE-D3功能在这些H2O2 () 和H2O2·2H2O () 系统中表现最好.
科学领域:
- 计算化学计算化学
- 材料科学 材料科学 材料科学
- 固态物理 固态物理
背景情况:
- 过氧化 (H2O2) 分子与水 (H2O) 分子有相似之处.
- 了解过氧化的固态特性对于各种化学和物理应用至关重要.
研究的目的:
- 在H2O2 () 和H2O2·2H2O () 晶体上进行密度函数理论 (DFT) 计算.
- 评估各种分散校正密度函数的性能,重点是D3校正.
- 为了将结果与冰多态的DFT评估进行比较.
主要方法:
- 使用密度函数理论 (DFT) 的计算.
- 评估了各种分散校正密度函数,包括自相一致和事后方法.
- 详细分析了D3调整,特别是它对格子能量的影响.
主要成果:
- D3 校正对格子能量有显著的贡献,约占 H2O2 的总量的 25% (与 PBE 功能).
- D3修正主要归因于高达5 Å的非键相互作用.
- 在被检查的12个函数中,optPBEvdW和RPBE-D3被确定为表现最好的函数.
结论:
- 散射相互作用和DFT的功能限制是影响过氧化晶体晶格能量的关键因素.
- D3修正有效地解决了缺失的分散和其他功能缺陷.
- 对于过氧化晶体的DFT评估方法和结果在很大程度上与使用可比方法的冰多态物相一致.
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