イットリウム添加リチウムおよびカリウムクラスター：磁気スーパーアトムとその水素との相互作用

In this study, we explored the energetic, structural, and magnetic properties of yttrium-doped lithium and potassium clusters using density functional theory combined with Born-Oppenheimer molecular dynamics simulations. The analysis revealed magnetic superatoms such as K₉Y₂ (μ = 5μ_B) with a frontier configuration analogous to Fe⁺. Global reactivity descriptors, particularly the low hardness values (η), identified K₁₂Y, K₁₁Y₂, and K₁₃ as the most reactive potassium clusters, while the analogous Li₁₂Y, Li₁₁Y₂, and Li₁₃ were also selected for subsequent hydrogen interaction analyses. The most stable hydrogen-cluster structures extracted from Born-Oppenheimer molecular dynamics at 300 K were reoptimized including dispersion corrections to compute adsorption and Gibbs free energies. The resulting complexes were analyzed through QTAIM, ELF, and Laplacian electron density maps, complemented by CM5 charge analysis. These results reveal predominant molecular physisorption across the Y-doped systems, with localized polarized chemisorption only in Li₁₂Y. Overall, yttrium doping enhances magnetic polarization, energetic stability, and structural resilience of alkali-metal clusters, which retain their superatomic character and near-icosahedral frameworks under hydrogen exposure.