Affiliation:
1. National Isotope Centre GNS Science 30 Gracefield Road Lower Hutt 5010 New Zealand
2. School of Chemical Sciences The University of Auckland Auckland 1010 New Zealand
3. Electron Microscopy Centre University of Wollongong Innovation Campus Squires Way Wollongong 2519 Australia
4. The MacDiarmid Institute for Advanced Materials and Nanotechnology School of Chemical and Physical Sciences Victoria University of Wellington Wellington 6040 New Zealand
Abstract
AbstractMolybdenum carbides are promising low‐cost electrocatalysts for electrolyzers, fuel cells, and batteries. However, synthesis of ultrafine, phase‐pure carbide nanoparticles (diameter < 5 nm) with large surface areas remains challenging due to uncontrollable agglomeration that occurs during traditional high temperature syntheses. This work presents a scalable, physical approach to synthesize molybdenum carbide nanoparticles at room temperature by ion implantation. By tuning the implantation conditions, various molybdenum carbide phases, stoichiometries, and nanoparticle sizes can be accessed. For instance, molybdenum ion implantation into glassy carbon at 30 keV energy and to a fluence of 9 × 1016 at cm−2 yields a surface η‐Mo3C2 with a particle diameter of (10 ± 1) nm. Molybdenum implantation into glassy carbon at 60 keV to a fluence of 6 × 1016 at cm−2 yields a buried layer of ultrafine γ’‐MoC/η‐MoC nanoparticles. Carbon ion implantation at 20 keV into a molybdenum thin film produces a 40 nm thick layer primarily composed of β‐Mo2C. The formation of nanoparticles in each molybdenum carbide phase is explained based on the Mo‐C phase diagram and Monte‐Carlo simulations of ion‐solid interactions invoking the thermal spike model. The approaches presented are widely applicable for synthesis of other transition metal carbide nanoparticles as well.
Funder
Royal Society Te Apārangi
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
3 articles.
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