Tuning of Hydrogen Storage Property of Multi-walled Carbon Nanotube by Decorating Ni, Cu and Fe Nanoparticles

Author(s): Jyoti Prakash , B.M. Tripathi , Kinshuk Dasgupta , J.K. Chakravartty , M.R. Pai , Asheesh Kumar , S. R. Bharadwaj .

Journal Name: Current Nanomaterials

Volume 1 , Issue 2 , 2016

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Abstract:

Background: Since last two decades, there has been rigorous efforts are going on to develop a hydrogen storage system for large-scale application in fuel cells, mobiles and for automotive uses. The early experimental data on hydrogen storage using CNTs contradicted theoretical calculations, and there has been a large variation in the CNT hydrogen storage capacity reported by various research groups. In present work, a comparative study on hydrogen storage and release characteristics of bare as well as three transition metals viz. Ni, Cu & Fe nanoparticles decorated MWCNT at ambient temperature i.e. 298K and pressure range of 9-16 atm has been studied.

Methods: Synthesis, characterization and hydrogen adsorption-desorption behavior of bare as well as transition metal (Ni, Cu and Fe) decorated multiwalled carbon nanotubes has been studied systematically.

Results: The maximum hydrogen storage capacities of finely dispersed Ni, Cu, and agglomerated Fe decorated and bare multiwalled carbon nanotubes measured at 298K were 0.812 wt% (at 15.85 atm), 2.59 wt% (at 12.64 atm), 0.909 wt % (at 15.45atm) and 0.654 wt% (at 12.84 atm) respectively. A mechanism invoking metal nanoparticle mediated dissociation of hydrogen molecule and its subsequent storage in carbon structure as well as defect sites has been proposed to explain hydrogen storage and release behavior of metal-decorated multiwalled carbon nanotubes.

Conclusion: The nature and morphology of metal nanoparticle has significant role in controlling hydrogen adsorption-desorption characteristic of decorated multiwalled carbon nanotubes.

Keywords: MWCNT, decorated MWCNT, adsorption, hydrogen storage, CNTs, s–p–d hybridization.

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Article Details

VOLUME: 1
ISSUE: 2
Year: 2016
Page: [124 - 131]
Pages: 8
DOI: 10.2174/2405461501666160808164652

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