Abstract

We report on the fabrication of molybdenum (Mo) nanopillar (NP) arrays with NP diameters down to 75 nm by means of deep-reactive ion etching at cryogenic temperatures. A variable-thickness Mo metal layer sputtered onto a Si3N4/Si substrate makes possible NPs with different lengths in a controllable manner. We demonstrate how our fabrication strategy leads to tunable cross-sections with different geometries, including hexagonal, cylindrical, square and triangular shapes, by using electron beam lithography on hydrogen silsesquioxane negative tone resist. To ensure well-defined facets and surfaces, we employ deep-reactive ion etching in a gas mixture of SF6 and O2 at cryogenic temperatures in an inductively coupled plasma reactive ion etching (ICP-RIE) system. These results represent an attractive route towards the realization of high-density Mo NP arrays for applications from nanoelectronics to quantum sensing and hydrogen evolution reaction catalysis.

Highlights

  • One-dimensional (1D) Molybdenum (Mo) nanostructures have garnered significant attention recently due to their potential uses in a wealth of applications from interconnects in nanoelectronic devices to promoting the hydrogen evolution reaction [1,2,3,4,5,6]

  • We report on the fabrication of molybdenum (Mo) nanopillar (NP) arrays with NP diameters down to 75 nm by means of deep-reactive ion etching at cryogenic temperatures

  • We have demonstrated the feasibility of a novel strategy for the top-down large-scale fabrication of geometric arrays of Mo NPs with different cross-sectional shapes as well as of nanocones

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Summary

Introduction

One-dimensional (1D) Molybdenum (Mo) nanostructures have garnered significant attention recently due to their potential uses in a wealth of applications from interconnects in nanoelectronic devices to promoting the hydrogen evolution reaction [1,2,3,4,5,6]. This potential stems from their remarkable properties, such as efficient electron emission and structural stability. These approaches have some limitations in terms of scalability as well as concerning the control on the orientation, shape, and density of the 1D nanostructures at spatially well-defined locations

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