Eric Salomon

24 h stability of thick multilayer silicene in air

Thick epitaxial multilayer silicene films with a root 3 x root 3R(30 degrees) surface structure show only mild surface oxidation after 24 h in air, as measured by Auger electron spectroscopy. X-ray diffraction and Raman spectroscopy measurements performed in air without any protective capping, as well as, for comparison, with a thin Al2O3 cap, showed the (002) reflection and the G, D and 2D Raman structures, which are unique fingerprints of thick multilayer silicene.

Growth and structural properties of silicene at multilayer coverage

At monolayer coverage, silicene on Ag(1 1 1) may present different structural phases depending on the growth conditions. At multilayer coverage, only one structural phase has been reported: the [Formula: see text] phase. However, no link between the structural arrangement of the monolayer and that of the multilayer has been addressed. In this paper, reporting experimental work based on low-energy electron diffraction and scanning tunneling microscopy, we focus on the structural aspects of a multilayer film of silicene. We demonstrate that it exhibits one structural arrangement, namely the [Formula: see text] form, but with different domain orientations resulting from the structural properties of the initial wetting monolayer.

Multilayer silicene: clear evidence

One year after the publication of the seminal paper on monolayer 3 by 3 reconstructed silicene grown on a silver (111) substrate, evidence of the synthesis of epitaxial root3 by root3 reconstructed multilayer silicene hosting Dirac fermions was presented. Although a general consensus was immediately reached in the former case, in the latter one, the mere existence of multilayer silicene was questioned and strongly debated. Here, we demonstrate by means of a comprehensive x-ray crystallographic study, that multilayer silicene is effectively realized upon growth at rather low growth temperatures (~200{\deg}C), while, instead, 3D growth of silicon crystallites takes place at higher temperatures, (~300{\deg}C). This transition to bulk like silicon perfectly explains the various data presented and discussed in the literature and solves their conflicting interpretations.

On-surface synthesis of aligned functional nanoribbons monitored by scanning tunnelling microscopy and vibrational spectroscopy

In the blooming field of on-surface synthesis, molecular building blocks are designed to self-assemble and covalently couple directly on a well-defined surface, thus allowing the exploration of unusual reaction pathways and the production of specific compounds in mild conditions. Here we report on the creation of functionalized organic nanoribbons on the Ag(110) surface. C–H bond activation and homo-coupling of the precursors is achieved upon thermal activation. The anisotropic substrate acts as an efficient template fostering the alignment of the nanoribbons, up to the full monolayer regime. The length of the nanoribbons can be sequentially increased by controlling the annealing temperature, from dimers to a maximum length of about 10 nm, limited by epitaxial stress. The different structures are characterized by room-temperature scanning tunnelling microscopy. Distinct signatures of the covalent coupling are measured with high-resolution electron energy loss spectroscopy, as supported by density functional theory calculations.

The Rise of Elemental Two-Dimensional Materials Beyond Graphene

Following the publication in 2012 of the first compelling evidence of the synthesis of silicene, the silicon based counterpart of graphene, the last two years have seen a surge of articles on elemental, novel two-dimensional materials beyond graphene. Here, research in this burgeoning field is highlighted

Increasing the lego of 2D electronics materials: silicene and germanene, graphene's new synthetic cousins

The realization of the first Field Effect Transistors operating at room temperature, based on a single layer silicene channel, open up highly promising perspectives, e.g., typically, for applications in digital electronics. Here, we describe recent results on the growth, characterization and electronic properties of novel synthetic two-dimensional materials beyond graphene, namely silicene and germanene, its silicon and germanium counterparts.

The Orientation of Silver Surfaces Drives the Reactivity and the Selectivity in Homo-Coupling Reactions

Original reaction pathways can be explored in the on-surface synthesis approach where small aromatic precursors are confined to the surface of single crystal metals. The bis-indanedione molecule reacted with itself on silver surfaces in different ways, through a Knoevenagel reaction or an oxidative coupling, leading to the formation of a variety of new molecular compounds and covalently-linked 1D or 2D networks. Noteworthy, original reaction products were obtained that cannot be synthesized in traditional solvent-based chemistry. The lowest activation temperature for the homo-coupling reactions was found on the Ag(111) surface. The Ag(110) was highly selective in terms of coupling reaction type, while on Ag(100) the temperature could finely control the selectivity. The on-surface synthesis approach is shown here to be particularly efficient to produce original compounds in mild conditions, using activation temperatures as low as 200 °C. The different structures were characterized by scanning tunnelling microscopy (STM) together with X-ray photoelectron emission spectroscopy (XPS) and high-resolution electron energy loss spectroscopy (HREELS).

Elemental two-dimensional materials beyond graphene

Abstract This review article summarizes a few of the papers presented during Symposium II of the International Conference of Pure and Applied Chemistry in July 2016. Properties of monolayers of silicene are first addressed, followed by multilayer silicene and, at the end, a discussion on germanene.

11. Elemental Two-Dimensional Materials Beyond Graphene

This review article summarizes a few of the papers presented during Symposium II of the International Conference of Pure and Applied Chemistry in July 2016. Properties of monolayers of silicene are first addressed, followed by multilayer silicene and, at the end, a discussion on germanene.