Synergistic Pt-WO3 Dual Active Sites to Boost Hydrogen Production from Ammonia Borane
Development of synergistic heterogeneous catalysts with active sites working cooperatively has been a pursuit of chemists. Herein, we report for the first time the fabrication and manipulation of Pt-WO3 dual-active-sites to boost hydrogen generation from ammonia borane. A combination of DFT calculat...
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Published in | iScience Vol. 23; no. 3; p. 100922 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
27.03.2020
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Development of synergistic heterogeneous catalysts with active sites working cooperatively has been a pursuit of chemists. Herein, we report for the first time the fabrication and manipulation of Pt-WO3 dual-active-sites to boost hydrogen generation from ammonia borane. A combination of DFT calculations, structural characterization, and kinetic (isotopic) analysis reveals that Pt and WO3 act as the active sites for ammonia borane and H2O activation, respectively. A trade-off between the promoting effect of WO3 and the negative effect of decreased Pt binding energy contributes to a volcano-shaped activity, and Pt/CNT-5W delivers a 4-fold increased activity of 710.1 molH2·molPt−1·min−1. Moreover, WO3 is suggested to simultaneously act as the sacrificial site that can divert B-containing by-products away from Pt sites against deactivation, yielding an increase from 24% to 68% of the initial activity after five cycles. The strategy demonstrated here could shed a new light on the design and manipulation of dual-active-site catalysts.
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•Mechanism-guided design of Pt-WO3 dual active sites boosts H2 generation•A trade-off between WO3 loading and Pt B.E. yields a volcano-shaped activity•WO3 acts as the sacrificial site to divert by-products against deactivation•Multifunctional Pt-MO/C catalysts achieve enhanced activity and durability
Inorganic Chemistry; Catalysis; Nanomaterials |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Lead Contact |
ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2020.100922 |