Journal
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 45, Issue 37, Pages 18602-18611Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.10.131
Keywords
DFT; h-AlC ML; Adsorption; Hydrogen evolution reaction (HER); Work function
Categories
Funding
- Department of Science and Technology (DST), New Delhi [DST/INT/SL/P-21/2016]
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The hydrogen due to its high mass energy density is a new renewable, economically viable and clean resource. The most eco-friendly and economical approaches for the generation of hydrogen through hydrogen evolution is electrochemical water splitting. The two-dimensional (2D) nanomaterials have been recently found as potential candidates as non-noble metal catalyst for hydrogen evolution. In this work, we have systematically studied the structural and electronic properties of the newly predicted hexagonal-aluminium carbide monolayer (h-AlC ML) under the framework of dispersion-corrected density functional theory (DFT) calculations. The calculated electronic total density of states (TDOS) of h-AlC ML predict its metallic nature in contrast to other polar honeycomb 2D materials which are either semiconducting or semimetallic. The metallic behavior of h-AlC monolayer which motivates us to investigate its HER activity results due to the presence of delocalized charge density near Fermi level. Thus, we have investigated the HER activity of h-AlC ML by calculating hydrogen (H) adsorption energy (Delta G(H)) and Gibbs free energy (Delta G(H)) at three different sites of the 3 x 3 and 4 x 4 supercells of h-AlC ML; top of carbon atom (EH-C), top of aluminium atom (EH-Al) and hollow site (EH-Hollow). Our results show that the hollow site is most catalytically active site in both supercells of h-AlC ML. We believe that our results will inspire experimentalists to fabricate this new 2D material for achieving the desired range of HER activity. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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