Abstract
With progress in the extreme miniaturisation of electronic components and the discovery of low-dimensional conductive materials, it is now possible to assemble field-effect transistors (FETs) that can incorporate single-molecule components as a channel or gate1,2. Such types of FETs have been recently used to detect and study various fundamental mechanisms at the single-molecule scale, among which the folding and unfolding of molecules, hybridization mechanisms, charge transport or chemical reactions1–5. In these experiments, devices were typically fabricated using architectures based on individual 1D materials, such as carbon nanotubes (CNTs) and silicon nanowires. The 1D topology facilitates the isolation of individual molecules in the circuit, but present drawbacks in scalability due to challenges in the growth, purification and/or assembling of such 1D materials into FET circuits. Here, we present new top-down approaches for the fabrication of single-molecule FETs, based on 2D graphene architectures. As CNTs, graphene is made of an hexagonal carbon lattice enabling excellent conductivity as well as carbon-based chemistry to anchor individual molecules, yet its 2D topology is more compatible with wafer-scale fabrication processes. First, we report the fabrication of large arrays of FETs based on graphene ribbons with controlled electrical properties. These arrays were built from high-quality large area graphene synthesized by chemical vapor deposition (CVD), followed by patterning steps using photolithography and plasma etching processes. Then, we report the design of two different architectures for single-molecule experiments: nanoconstrictions and nanogaps. Nanoconstrictions were achieved using electron-beam lithography (EBL), allowing to pattern high-resolution features (50nm) in the graphene channel. Nanogaps were obtained using the electroburning technique to open a gap of a few nanometers in the graphene channel6. We will present the design and fabrication process of these architectures, as well as their characterization using high-resolution microscopy (SEM/AFM) and transport measurements. Finally, we will discuss approached for the single-molecule functionalization for these architectures and their application in conductance-based single-molecule measurements.
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