材料科学
空位缺陷
二聚体
磁铁
磁各向异性
凝聚态物理
Atom(片上系统)
双金属片
各向异性
磁存储器
密度泛函理论
结晶学
磁场
核磁共振
金属
计算化学
磁化
物理
量子力学
计算机科学
冶金
嵌入式系统
化学
作者
Jan Navrátil,Michal Otyepka,Piotr Błoński
标识
DOI:10.1088/1361-6528/ac53d5
摘要
Abstract The growing gap between the volume of digital data being created and the extent of available storage capacities stimulates intensive research into surface-supported, well-ordered array of atom-sized magnets that represents the ultimate limit of magnetic data storage. Anchoring transition metal heterodimers in vacancy defects in the graphene lattice has been identified as a vivid strategy to achieve large magnetic anisotropy energy (MAE) up to 80 meV with an easy axis aligned along the dimer bond. In this paper we have made a significant leap forward finding out MAE of 119 meV for an OsPt dimer and 170 meV for an OsPd dimer bound to a single nitrogen-decorated vacancy defect. The system with the highest MAE and with the theoretical storage density of 490 Tb inch -2 pushes the current limit of theoretical blocking temperature in graphene-supported transition-metal dimers from ~20 K to ~44 K assuming the relaxation time of 10 years. The mechanism of the enhanced MAE is discussed.
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