Strong activation effect on a ru-co-c thin film catalyst for the hydrolysis of sodium borohydride

Autor: Arzac, G. M., Paladini, M., Fortio Godinho, Vanda Cristina, Beltrán, Ana M., Jiménez de Haro, María del Carmen
Přispěvatelé: Universidad de Sevilla. Departamento de Ingeniería y Ciencia de los Materiales y del Transporte, Universidad de Sevilla. TEP123: Metalurgia e Ingeniería de los Materiales
Jazyk: angličtina
Rok vydání: 2018
Zdroj: idUS. Depósito de Investigación de la Universidad de Sevilla
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Popis: In this work, we prepared a series of Ni foam supported Ru-Co, Ru-Co-B and Ru-Co-C catalysts in the form of columnar thin films by magnetron sputtering for the hydrolysis of sodium borohydride. We studied the activity and durability upon cycling. We found a strong activation effect for the Ru-Co-C sample which was the highest ever reported. This catalyst reached in the second cycle an activity 5 times higher than the initial (maximum activity 9310 ml.min−1.gCoRu−1 at 25 °C). Catalytic studies and characterization of the fresh and used samples permitted to attribute the strong activation effect to the following factors: (i) small column width and amorphous character (ii) the presence of Ru and (iii) dry state before each cycle. The presence of boron in the initial composition is detrimental to the durability. Our studies point out to the idea that after the first cycle the activity is controlled by surface Ru, which is the most active of the two metals. Apart from the activation effect, we found that catalysts deactivated in further cycles. We ascribed this effect to the loss of cobalt in the form of hydroxides, showing that deactivation was controlled by the chemistry of Co, the major surface metal component of the alloy. Alloying with Ru is beneficial for the activity but not for the durability, and this should be improved. Ministerio de Economía (España): grant MAT2015-69035-REDC, EU co-financed by FEDER Ministerio de Economía (España): grant CTQ2015-65918-R, EU co-financed by FEDER Junta de Andalucía: grant PE2012-TEP862, EU co-financed by FEDER CSIC (España): PIE-201760E002
Databáze: OpenAIRE