Locally varying formation of nanoclusters across a low-intensity ultra-short laser spot.

Ultra-short laser illumination is an intriguing tool for engineering material by light. It is usually employed at or above the ablation threshold. Practical applications profit from tailoring surface properties, for instance, by structural changes to the surface layer of an irradiated target.

Moiré Superlattice-Induced Superconductivity in One-Unit-Cell FeTe.

In this work, we demonstrate that the nonsuperconducting single-layer FeTe can become superconducting when its structure is properly tuned by epitaxially growing it on BiTe thin films. The properties of the single-layer FeTe deviate strongly from its bulk counterpart, as evidenced by the emergence of a large superconductivity gap (3.3 meV) and an apparent 8 × 2 superlattice (SL).

Superconductivity in Single-Quintuple-Layer BiTe Grown on Epitaxial FeTe.

How an interfacial superconductivity emerges during the nucleation and epitaxy is of great importance not only for unveiling the physical insights but also for finding a feasible way to tune the superconductivity via interfacial engineering. In this work, we report the nanoscale creation of a robust and relatively homogeneous interfacial superconductivity ( ≈ 13 K) on the epitaxial FeTe surface, by van der Waals epitaxy of single-quintuple-layer topological insulator BiTe. Our study suggests that the superconductivity in the BiTe/FeTe heterostructure is generated at the interface and that the superconductivity at the interface does not enhance or weaken with the increase of the BiTe thickness beyond 1 quintuple layer (QL).

Non-local atomic manipulation on semiconductor surfaces in the STM: the case of chlorobenzene on Si(111)-7×7.

Control over individual atoms with the scanning tunnelling microscope (STM) holds the tantalising prospect of atomic-scale construction, but is limited by its "one atom at a time" serial nature. "Remote control" through non-local STM manipulation-as we have demonstrated in the case of chlorobenzene on Si(111)-7×7-offers a new avenue for future "bottom-up" nanofabrication, since hundreds of chemical reactions may be carried out in parallel. Thus a good understanding of the non-local manipulation process, as provided by recent experiments, is important.

Quantum chemical cluster models for chemi- and physisorption of chlorobenzene on Si(111)-7×7.

Motivated by recent atomic manipulation experiments, we report quantum chemical calculations for chemi- and physisorption minima of chlorobenzene on the Si(111)-7×7 surface. A density functional theory cluster approach is applied, using the B3LYP hybrid functional alongside Grimme's empirical dispersion corrections (D3). We were able to identify chemisorption sites of binding energies of 1.