Center for Nanophase Materials Sciences, Oak Ridge National Laboratory , Oak Ridge, Tennessee 37831, United States.
Nano Lett. 2017 Jan 11;17(1):292-298. doi: 10.1021/acs.nanolett.6b04062. Epub 2016 Dec 6.
Controlling the spin states of the surface and interface is key to spintronic applications of magnetic materials. Here, we report the evolution of surface magnetism of Co nanoislands on Cu(111) upon hydrogen adsorption and desorption with the hope of realizing reversible control of spin-dependent tunneling. Spin-polarized scanning tunneling microscopy reveals three types of hydrogen-induced surface superstructures, 1H-(2 × 2), 2H-(2 × 2), and 6H-(3 × 3), with increasing H coverage. The prominent magnetic surface states of Co, while being preserved at low H coverage, become suppressed as the H coverage level increases, which can then be recovered by H desorption. First-principles calculations reveal the origin of the observed magnetic surface states by capturing the asymmetry between the spin-polarized surface states and identify the role of hydrogen in controlling the magnetic states. Our study offers new insights into the chemical control of magnetism in low-dimensional systems.
控制表面和界面的自旋状态是磁性材料用于自旋电子学的关键。在这里,我们报告了 Co 纳米岛在 Cu(111)表面上的磁性质随氢吸附和脱附的演变,以期实现对自旋相关隧穿的可逆控制。自旋极化扫描隧道显微镜揭示了三种类型的氢诱导表面超结构,1H-(2×2)、2H-(2×2)和 6H-(3×3),随着 H 覆盖度的增加。Co 的显著磁表面态在低 H 覆盖度下得以保留,但随着 H 覆盖度的增加而被抑制,随后通过 H 脱附可以恢复。第一性原理计算通过捕捉自旋极化表面态之间的不对称性,揭示了观察到的磁表面态的起源,并确定了氢在控制磁态方面的作用。我们的研究为低维系统中化学控制磁体提供了新的见解。