论文标题
设计师的旋转订单
Designer spin order in diradical nanographenes
论文作者
论文摘要
碳材料的磁性特性目前是由于它们在旋转和量子计算中的潜在应用,因此在物理,化学和材料科学方面进行了强烈的研究工作的重点。尽管最近已经确认了在开放式纳米仪中旋转的存在,但控制磁耦合符号的能力仍然难以捉摸,但最可取的能力。在这里,我们使用组合的扫描探针技术和均值场式Hubbard模型计算在原子上精确的开放式双方/非双方纳米仪中进行了工程磁接地态的有效方法。两个旋转之间的磁耦合符号已通过破坏纳米仪的两分晶格对称性来控制。此外,两个自旋之间的交换强度通过精细定制其旋转密度重叠来广泛调节,从而实现了42 MeV的较大交换强度。我们的演示方法为设计师的室温高温磁相和石墨烯纳米材料的功能提供了足够的机会。
The magnetic properties of carbon materials are at present the focus of an intense research effort in physics, chemistry and materials science due to their potential applications in spintronics and quantum computations. Although the presence of spins in open-shell nanographenes has been recently confirmed, the ability to control magnetic coupling sign has remained elusive, but the most desirable. Here, we demonstrate an effective approach of engineering magnetic ground states in atomically precise open-shell bipartite/nonbipartite nanographenes using combined scanning probe techniques and mean-field Hubbard model calculations. The magnetic coupling sign between two spins has been controlled via breaking bipartite lattice symmetry of nanographenes. In addition, the exchange-interaction strength between two spins has been widely tuned by finely tailoring their spin density overlap, realizing a large exchange-interaction strength of 42 meV. Our demonstrated method provides ample opportunities for designer above-room-temperature magnetic phases and functionalities in graphene nanomaterials.