Interestingly, the most active catalyst in this study, Ru/N-CNT1, presents a ruthenium particle size outside of this optimum range (based on both TEM and CO chemisorption estimates), suggesting that the electronic modification of the support by the presence of nitrogen plays a highly significant role in enhancing the low temperature ammonia decomposition activity.
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Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports.
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