International Center for Young Scientists (ICYS), National Institute for Materials Science , 1-1, Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Department of Materials Engineering, The University of Tokyo , 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
Nano Lett. 2017 Apr 12;17(4):2287-2293. doi: 10.1021/acs.nanolett.6b05010. Epub 2017 Mar 30.
Self-assembled organic molecules can potentially be an excellent source of charge and spin for two-dimensional (2D) atomic-layer superconductors. Here we investigate 2D heterostructures based on In atomic layers epitaxially grown on Si and highly ordered metal-phthalocyanine (MPc, M = Mn, Cu) through a variety of techniques: scanning tunneling microscopy, electron transport measurements, angle-resolved photoemission spectroscopy, X-ray magnetic circular dichroism, and ab initio calculations. We demonstrate that the superconducting transition temperature (T) of the heterostructures can be modified in a controllable manner. Particularly, the substitution of the coordinated metal atoms from Mn to Cu is found to reverse the T shift from negative to positive directions. This distinctive behavior is attributed to a competition of charge and spin effects, the latter of which is governed by the directionality of the relevant d-orbitals. The present study shows the effectiveness of molecule-induced surface doping and the significance of microscopic understanding of the molecular states in these 2D heterostructures.
自组装有机分子有可能成为二维(2D)原子层超导体中电荷和自旋的极好来源。在这里,我们通过多种技术研究了基于在 Si 上外延生长的 In 原子层和高度有序的金属酞菁(MPc,M=Mn,Cu)的 2D 异质结构:扫描隧道显微镜、电子输运测量、角分辨光发射谱、X 射线磁圆二色性和从头算计算。我们证明了异质结构的超导转变温度(T)可以以可控的方式进行修饰。特别地,发现从 Mn 到 Cu 的配位金属原子的取代将 T 位移从负向正向方向反转。这种独特的行为归因于电荷和自旋效应的竞争,后者受相关 d 轨道的方向性控制。本研究表明了分子诱导表面掺杂的有效性以及对这些 2D 异质结构中分子态微观理解的重要性。