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dc.contributor.authorLu, Dongsheng
dc.contributor.authorLiao, Jinyun
dc.contributor.authorLi, Hao
dc.contributor.authorJi, Shan
dc.contributor.authorPollet, Bruno
dc.date.accessioned2019-08-27T12:10:06Z
dc.date.available2019-08-27T12:10:06Z
dc.date.created2019-08-24T14:43:57Z
dc.date.issued2019
dc.identifier.issn2168-0485
dc.identifier.urihttp://hdl.handle.net/11250/2611214
dc.description.abstractDehydrogenation 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.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleCo3O4/CuMoO4 Hybrid Microflowers Composed of Nanorods with Rich Particle Boundaries as a Highly Active Catalyst for Ammonia Borane Hydrolysisnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.journalACS Sustainable Chemistry and Engineeringnb_NO
dc.identifier.doi10.1021/acssuschemeng.9b03698
dc.identifier.cristin1718449
dc.description.localcodeThis 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.unitcode194,64,25,0
cristin.unitnameInstitutt for energi- og prosessteknikk
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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