论文标题
对称介导的可调分子磁性在2D材料上
Symmetry mediated tunable molecular magnetism on a 2D material
论文作者
论文摘要
通过扭曲两层石墨烯的诱导诱导非常规的超导性,这是开创性的1,此后引起了人们对二维(2D)材料之间晶格或角度不匹配引起的新现象的广泛关注。尽管许多研究涉及分层2D材料之间的角度不匹配的影响3-5,但尚未详细研究吸收比对对平面分子物理特性对2D底物的物理性能的影响。使用扫描探针显微镜(SPM),我们表明,当分子和底物的对称轴相对于彼此而扭曲时,在分层超导体2H-NBSE2上吸附的单个钴分子(COPC)分子在分层超导体2H-NBSE2上吸附。 COPC从在气相6中发现的有效自旋1/2变为具有非磁基态的分子。在后者上,我们观察到一个单线 - 三个旋转过渡,该转变源自中央离子自旋与分子配体上的分布式磁矩之间的抗磁相互作用。因为Ising超导体2H-NBSE2缺乏反转对称性,并且具有大型自旋轨道耦合7,这种分子内磁交换具有明显的非共同dzyaloshinskii-moriya(DM)8,9的贡献。
The induction of unconventional superconductivity by twisting two layers of graphene a small angle was groundbreaking1, and since then has attracted widespread attention to novel phenomena caused by lattice or angle mismatch between two-dimensional (2D) materials2. While many studies address the influence of angle mismatch between layered 2D materials3-5 , the impact of the absorption alignment on the physical properties of planar molecules on 2D substrates has not been studied in detail. Using scanning probe microscopy (SPM) we show that individual cobalt phthalocyanine (CoPc) molecules adsorbed on the layered superconductor 2H-NbSe2 change drastically their charge and spin state when the symmetry axes of the molecule and the substrate are twisted with respect to each other. The CoPc changes from an effective spin-1/2 as found in gas-phase6 to a molecule with non-magnetic ground-state. On the latter we observe a singlet-triplet transition originating from an antiferromagnetic interaction between the central-ion spin and a distributed magnetic moment on the molecular ligands. Because the Ising superconductor 2H-NbSe2 lacks inversion symmetry and has large spin-orbit coupling7 this intramolecular magnetic exchange has significant non-collinear Dzyaloshinskii-Moriya (DM)8, 9 contribution.