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Electrodeposited Magnesium Nanoparticles Linking Particle Size to Activation Energy
- Source :
- Energies, Vol 9, Iss 12, p 1073 (2016)
- Publication Year :
- 2016
- Publisher :
- MDPI AG, 2016.
-
Abstract
- The kinetics of hydrogen absorption/desorption can be improved by decreasing particle size down to a few nanometres. However, the associated evolution of activation energy remains unclear. In an attempt to clarify such an evolution with respect to particle size, we electrochemically deposited Mg nanoparticles on a catalytic nickel and noncatalytic titanium substrate. At a short deposition time of 1 h, magnesium particles with a size of 68 ± 11 nm could be formed on the nickel substrate, whereas longer deposition times led to much larger particles of 421 ± 70 nm. Evaluation of the hydrogen desorption properties of the deposited magnesium nanoparticles confirmed the effectiveness of the nickel substrate in facilitating the recombination of hydrogen, but also a significant decrease in activation energy from 56.1 to 37.8 kJ·mol−1 H2 as particle size decreased from 421 ± 70 to 68 ± 11 nm. Hence, the activation energy was found to be intrinsically linked to magnesium particle size. Such a reduction in activation energy was associated with the decrease of path lengths for hydrogen diffusion at the desorbing MgH2/Mg interface. Further reduction in particle size to a few nanometres to remove any barrier for hydrogen diffusion would then leave the single nucleation and growth of the magnesium phase as the only remaining rate-limiting step, assuming that the magnesium surface can effectively catalyse the dissociation/recombination of hydrogen.
- Subjects :
- hydrogen storage
magnesium
particle size
nanosize
activation energy
Technology
Subjects
Details
- Language :
- English
- ISSN :
- 19961073
- Volume :
- 9
- Issue :
- 12
- Database :
- Directory of Open Access Journals
- Journal :
- Energies
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.458fe0ccf8094f459f04dee90ded5209
- Document Type :
- article
- Full Text :
- https://doi.org/10.3390/en9121073