Journal
TOPICS IN CATALYSIS
Volume 60, Issue 15-16, Pages 1251-1259Publisher
SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11244-017-0806-0
Keywords
Ammonia decomposition; Nitrogen-doped CNT; Ruthenium; In situ H-2 production; Nitrogen; N-CNT
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Funding
- UK Engineering and Physical Science Research Council [EP/L020432/2]
- Department of Chemical Engineering and Biotechnology at the University of Cambridge
- SASOL UK Ltd
- EPSRC [EP/L020432/2] Funding Source: UKRI
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The use of ammonia as a hydrogen vector has the potential to unlock the hydrogen economy. In this context, this paper presents novel insights into improving the ammonia decomposition activity of ruthenium nanoparticles supported on carbon nanotubes (CNT) by nitrogen doping. Our results can be applied to develop more active systems capable of delivering hydrogen on demand, with a view to move towards the low temperature target of less than 150 degrees C. Herein we demonstrate that nitrogen doping of the CNT support enhances the activity of ruthenium nanoparticles for the low temperature ammonia decomposition with turnover frequency numbers at 400 degrees C of 6200 LH2 mol(Ru)(-1) h(-1), higher than the corresponding value of unmodified CNT supports under the same conditions (4400 LH2 mol(Ru)(-1) h(-1)), despite presenting similar ruthenium particle sizes. However, when the nitrogen doping process is carried out with cetyltrimethylammonium bromide (CTAB) to enhance the dispersion of CNTs, the catalyst becomes virtually inactive despite the small ruthenium particle size, likely due to interference of CTAB, weakening the metal-support interaction. Our results demonstrate that the low temperature ammonia decomposition activity of ruthenium can be enhanced by nitrogen doping of the CNT support due to simultaneously increasing the support's conductivity and basicity, electronically modifying the ruthenium active sites and promoting a strong metal-support interaction.
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