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首页> 外文期刊>International journal of hydrogen energy >Hydrogen generation rate enhancement by in situ Fe(0) and nitroarene substrates in Fe_3O_4@Pd catalyzed ammonia borane hydrolysis and nitroarene reduction tandem reaction
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Hydrogen generation rate enhancement by in situ Fe(0) and nitroarene substrates in Fe_3O_4@Pd catalyzed ammonia borane hydrolysis and nitroarene reduction tandem reaction

机译:通过原位Fe(0)和硝基丙烯衬底在Fe_3O_4致催化氨基硼烷水解和硝基酮还原串联反应中提高氢生成率

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We report the catalytic enhancement of hydrogen generation by 1) in situ Fe(0) formed and 2) nitroarenes substrates during Fe3O4@Pd core-shell nanoparticles catalyzed tandem reaction. The active hydrogen species are generated in Pd shell, which either combine to form H-2 gas or take part in relatively faster nitroarene reduction reaction. The rate of hydrogen generation from ammonia borane is dependent on the nitroarene substrate and is higher when 4-nitrophenol is used. This is due to the difference in ammonia borane adsorption on the surface of the catalyst. During recyclability, the H-2 generation rate of 2 wt% Pd loaded samples is higher than other compositions. Such an enhancement has been attributed to the formation of Fe(0) via gamma-FeOOH mediated by Pd species, presumably through Pd(OH)(2). The electronic connection between Fe and Pd interface is thus shown to play an important role in the catalytic enhancement of the tandem reaction. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:我们在Fe3O4核 - 核 - 壳纳米颗粒催化串联反应期间报道了在Fe3O4核 - 壳纳米颗粒催化串联反应的原位Fe(0)中以1)的催化增强。在Pd壳中产生活性氢物质,其组合以形成H-2气体或参与相对更快的硝基烷还原反应。氨气硼烷的氢气率取决于硝基烯基材,当使用4-硝基苯酚时较高。这是由于催化剂表面上的氨硼烷吸附的差异。在再循环期间,2wt%Pd加载样品的H-2生成率高于其他组合物。这种增强已经归因于通过Pd物种介导的γ-FeOOH形成Fe(0),推测通过Pd(OH)(2)。因此,Fe和Pd界面之间的电子连接在串联反应的催化增强中起着重要作用。 (c)2021氢能出版物LLC。 elsevier有限公司出版。保留所有权利。

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