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Magnetic Co-Pd/C Nanocomposites for Hydrogen Evolution upon the Hydrolytic Dehydrogenation of NH3BH3, NaBH4, and Me2NHBH3
Owing to the high price and rareness of noble metals (including Pd, Rh, and Pt), the design and synthesis of bimetallic nanocomposites, by alloying a noble transition metal with an earth abundant and a cheap metal, for synergistically promoting hydrogen evolution are highly desirable. To meet the re...
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Published in: | ACS applied nano materials 2021-07, Vol.4 (7), p.7479-7485 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Owing to the high price and rareness of noble metals (including Pd, Rh, and Pt), the design and synthesis of bimetallic nanocomposites, by alloying a noble transition metal with an earth abundant and a cheap metal, for synergistically promoting hydrogen evolution are highly desirable. To meet the requirement, in this work, magnetic Co-Pd/C nanocomposites have been designed and constructed, by simply alloying Pd/C with Co, for synergistically promoting H2 evolution upon the hydrolytic dehydrogenation of NH3BH3, NaBH4, and Me2NHBH3 for the first time. Transmission electron microscopy and energy-dispersive X-ray spectroscopy have shown that magnetic Co-Pd/C nanocomposites have a possible core/shell structure. The Co-Pd/C has shown superior catalytic performance in H2 evolution, with the turnover frequency (TOF) of 263.39 mol(H2)·molcat –1·min–1, which is 10 times as that of Pd/C (only 26.97 mol(H2)·molcat –1·min–1). Gratifyingly, Co-Pd/C also provides 20-fold and 7-fold TOF values as that of Pd/C in the hydrolysis of NaBH4 and Me2NHBH3, respectively. Indeed, the activation energy of the hydrolytic dehydrogenation of NH3BH3 has been significantly decreased from 57.92 kJ/mol (Pd/C) to 35.70 kJ/mol (Co-Pd/C). |
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ISSN: | 2574-0970 2574-0970 |
DOI: | 10.1021/acsanm.1c01500 |