dc.contributor.author | Lu, Dongsheng | |
dc.contributor.author | Liao, Jinyun | |
dc.contributor.author | Li, Hao | |
dc.contributor.author | Ji, Shan | |
dc.contributor.author | Pollet, Bruno | |
dc.date.accessioned | 2019-08-27T12:10:06Z | |
dc.date.available | 2019-08-27T12:10:06Z | |
dc.date.created | 2019-08-24T14:43:57Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 2168-0485 | |
dc.identifier.uri | http://hdl.handle.net/11250/2611214 | |
dc.description.abstract | Dehydrogenation of ammonia borane (AB) is a promising approach for the production and use of hydrogen for industrial and fuel cell applications. The development of low-cost and highly active catalysts is critical for these practical applications. In this study, low-cost Co3O4/CuMoO4 hybrid microflowers composed of nanorods with rich particle boundaries were synthesized. Co3O4/CuMoO4 was used as a catalyst for the dehydrogenation of AB and showed a high catalytic activity with a turnover frequency (TOF) of 129.15 molhydrogenmolcat-1 min-1 at room temperature. The apparent activation energy (Ea) of the catalyst was found to be as low as 23.2 kJ mol-1. It was revealed that the synergistic effect between Co3O4 and CuMoO4 played a critical role in improving the catalytic activity. Co3O4 is relatively active, but a long induction time is needed when it acts as a catalyst in AB hydrolysis. In contrast, CuMoO4 is less active, but it can immediately catalytically initiate the hydrolytic reaction. When these two compound are combined as a hybrid catalyst, its catalytic performance is significantly improved. These findings can provide some new insight for those who are trying to design some noble-metal-free hybrid catalyst with high catalytic activity towards AB hydrolysis. | nb_NO |
dc.language.iso | eng | nb_NO |
dc.publisher | American Chemical Society | nb_NO |
dc.title | Co3O4/CuMoO4 Hybrid Microflowers Composed of Nanorods with Rich Particle Boundaries as a Highly Active Catalyst for Ammonia Borane Hydrolysis | nb_NO |
dc.type | Journal article | nb_NO |
dc.type | Peer reviewed | nb_NO |
dc.description.version | acceptedVersion | nb_NO |
dc.source.journal | ACS Sustainable Chemistry and Engineering | nb_NO |
dc.identifier.doi | 10.1021/acssuschemeng.9b03698 | |
dc.identifier.cristin | 1718449 | |
dc.description.localcode | This document is the Accepted Manuscript version of a Published Work that appeared in final form in [ACS Sustainable Chemistry and Engineering], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see [insert ACS Articles on Request author-directed link to Published Work, see http://pubs.acs.org/page/policy/articlesonrequest/index.html].” | nb_NO |
cristin.unitcode | 194,64,25,0 | |
cristin.unitname | Institutt for energi- og prosessteknikk | |
cristin.ispublished | true | |
cristin.fulltext | postprint | |
cristin.qualitycode | 1 | |