Sebastian Schimmel

Topological superconductivity is a promising concept for generating fault-tolerant qubits. Early experimental studies looked at hybrid systems and doped intrinsic topological or superconducting materials at very low temperatures. However, higher critical temperatures are indispensable for technological exploitation. Recent angle-resolved photoemission spectroscopy results have revealed that superconductivity in the type-I Weyl semimetal—trigonal PtBi₂ (t-PtBi₂)—is located at the Fermi-arc surface states, which renders the material a potential candidate for intrinsic topological superconductivity. Here we show, using scanning tunnelling microscopy and spectroscopy, that t-PtBi₂ presents surface superconductivity at elevated temperatures (5 K). The gap magnitude is elusive: it is spatially inhomogeneous and spans from 0 to 20 meV. In particular, the large gap value and the shape of the quasiparticle excitation spectrum resemble the phenomenology of high-T_c superconductors. To our knowledge, this is the largest superconducting gap so far measured in a topological material. Moreover, we show that the superconducting state at 5 K persists in magnetic fields up to 12 T.

Magnetic hysteresis is demonstrated for monolayers of the single‐molecule magnet (SMM) Dy₂ScN@C₈₀ deposited on Au(111), Ag(100), and MgO|Ag(100) surfaces by vacuum sublimation. The topography and electronic structure of Dy₂ScN@C₈₀ adsorbed on Au(111) were studied by STM. X‐ray magnetic CD studies show that the Dy₂ScN@C₈₀ monolayers exhibit similarly broad magnetic hysteresis independent on the substrate used, but the orientation of the Dy₂ScN cluster depends strongly on the surface. DFT calculations show that the extent of the electronic interaction of the fullerene molecules with the surface is increasing dramatically from MgO to Au(111) and Ag(100). However, the charge redistribution at the fullerene‐surface interface is fully absorbed by the carbon cage, leaving the state of the endohedral cluster intact. This Faraday cage effect of the fullerene preserves the magnetic bistability of fullerene‐SMMs on conducting substrates and facilitates their application in molecular spintronics.