Affiliation:
1. The Molecular Foundry Lawrence Berkeley National Laboratory Berkeley CA 94720 USA
2. Lawrence Livermore National Laboratory 7000 East Avenue Livermore CA 94550 USA
3. Sandia National Laboratories Livermore CA 94550 USA
Abstract
AbstractMetal amides are attractive candidates for hydrogen storage due to their high volumetric and gravimetric hydrogen densities. However, the sluggish kinetics and competing side reactions during hydrogen uptake and release limit their practical use. Here, a novel nanoconfined Li2Mg(NH)2@reduced graphene oxide (rGO) composite is presented, which is fabricated using a melt‐infiltration method with a minimum weight penalty of only 2 wt.%. The presence of rGO ensures close contact between the active phases, effectively preventing aggregation during cycling process. As a result, the reversible capacity of Li2Mg(NH)2@rGO reaches 4.42 wt.%, with no capacity degradation observed after multiple cycling. Theoretical calculations show that rGO catalyzes the hydrogen bond cleavage at the Mg‐amide/Li hydride interface, leading to local dehydrogenation hotspots and significantly improves kinetics of dehydrogenation compared to the bulk counterpart. This study provides a promising strategy for designing metal imide‐based composites to overcome the kinetic limitations and improve their reversible hydrogen storage performance.
Funder
U.S. Department of Energy
Lawrence Livermore National Laboratory
Office of Energy Efficiency and Renewable Energy
Hydrogen and Fuel Cell Technologies Office
Subject
Mechanical Engineering,Mechanics of Materials
Cited by
2 articles.
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