Proximity coupling of magnetic and helical molecules to 2D spin-polarized electron gases – a surface transport study

磁性分子和螺旋分子与二维自旋极化电子气的邻近耦合——表面传输研究

• 批准号: 430575550
• 负责人: Professor Dr. Christoph Tegenkamp
• 金额: --
• 依托单位: Professur Analytik an Festkörperoberflächen
• 依托单位国家: 德国
• 项目类别: Research Grants
• 资助国家: 德国
• 项目状态: 未结题
• 来源: https://gepris.dfg.de/gepris/projekt/430575550?language=en
• 关键词: Proximity; coupling; magnetic; helical; molecules

Proximity coupling is a promising approach to tailor the band structures and to tune transport properties in a host material. Thereby, the quantum nature of the bans structure shall be modified while band filling and charge carrier mobilities should be unaffected. This demands a well-balanced interaction between the template and adsorbate, which can be controlled in detail by a surface science approach. In detail, we want to study spin-proximity effects of magnetic and helical organic molecules (functionalized porphyrins (Ph), phthalocyanines (Pc)), polyalanine (PA) towards 2D spin polarized electron gases (Bi(111), TIs) by means of surface transport. The goal is tounderstand the screening of (localized) magnetic moments and impact towards the spin orbit scattering of (delocalized) spin-polarized electrons. The systematic variation of the molecules with respect to their coupling strength and spin moments will enable us to understand atomistic details of proximity-coupling, including the spin state, charge transfer and break of symmetry. The transport experiments will be systematically performed as a function of magnetic field (0-4 T), temperature (10-300 K) and molecular coverage (0.001-1 ML). The transport measurements are complemented by low temperature STM and STS measurements. As substrate, mainly epitaxial Bi(111) films grown on Si(111), but also topological insulators, epitaxial Ag and films as well as graphene are used. The class of Ph- and Pc-molecules allow to change gradually the local spin-moment (different transition metal core atoms) as well as the coupling strengths (e.g. H-, F-terminated side groups). Moreover, the achiral molecule reveal chiral adsorption geometries, giving rise to break time reversal symmetry without external magnetic fields. This concept will be tested in detail using helical -L polyalanine molecules for anomalous Hall effect studies. Our results will provide new concepts for 2D spintronic devices.

近距离耦合是一种很有前途的方法来定制能带结构和调整宿主材料中的输运性质。因此，在不影响带填充和载流子迁移率的情况下，应改变禁带结构的量子性质。这需要模板和吸附物之间的良好平衡的相互作用，这可以通过表面科学方法进行详细控制。详细地，我们想研究磁性和螺旋有机分子（功能化卟啉（Ph），酞菁（Pc）），聚丙氨酸（PA）)通过表面输运对二维自旋极化电子气体（Bi(111), TIs）的自旋接近效应。目的是了解（局域）磁矩的筛选和对（非局域）自旋极化电子自旋轨道散射的影响。分子在耦合强度和自旋矩方面的系统变化将使我们能够理解原子的接近耦合细节，包括自旋态、电荷转移和对称性的破坏。输运实验将以磁场（0-4 T）、温度（10-300 K）和分子覆盖率（0.001-1 ML）为函数系统地进行。输运测量由低温STM和STS测量补充。作为衬底，主要使用生长在Si（111）上的外延Bi（111）薄膜，但也使用拓扑绝缘体、外延Ag和薄膜以及石墨烯。Ph-和pc -类分子允许逐渐改变局部自旋力矩（不同的过渡金属核心原子）以及耦合强度（例如H-， f端侧基）。此外，非手性分子表现出手性吸附几何形状，在没有外加磁场的情况下产生破缺时间反转对称性。这个概念将被详细测试使用螺旋-L聚丙氨酸分子异常霍尔效应的研究。我们的研究结果将为二维自旋电子器件提供新的概念。