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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Ceria-supported ruthenium nanoparticles as highly active and long-lived catalysts in hydrogen generation from the hydrolysis of ammonia borane
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Ceria-supported ruthenium nanoparticles as highly active and long-lived catalysts in hydrogen generation from the hydrolysis of ammonia borane

机译:二氧化铈负载的钌纳米颗粒作为氨硼烷水解产生氢气中的高活性和长寿命催化剂

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Ruthenium(0) nanoparticles supported on ceria (Ru-0/CeO2) were in situ generated from the reduction of ruthenium(III) ions impregnated on ceria during the hydrolysis of ammonia borane. Ru-0/CeO2 was isolated from the reaction solution by centrifugation and characterized by ICP-OES, BET, XRD, TEM, SEM-EDS and XPS techniques. All the results reveal that ruthenium(0) nanoparticles were successfully supported on ceria and the resulting Ru-0/CeO2 is a highly active, reusable and long-lived catalyst for hydrogen generation from the hydrolysis of ammonia borane with a turnover frequency value of 361 min(-1). The reusability tests reveal that Ru-0/CeO2 is still active in the subsequent runs of hydrolysis of ammonia borane preserving 60% of the initial catalytic activity even after the fifth run. Ru-0/CeO2 provides a superior catalytic lifetime (TTO = 135 100) in hydrogen generation from the hydrolysis of ammonia borane at 25.0 +/- 0.1 degrees C before deactivation. The work reported here includes the formation kinetics of ruthenium(0) nanoparticles. The rate constants for the slow nucleation and autocatalytic surface growth of ruthenium(0) nanoparticles were obtained using hydrogen evolution as a reporter reaction. An evaluation of rate constants at various temperatures enabled the estimation of activation energies for both the reactions, E-a = 60 +/- 7 kJ mol(-1) for the nucleation and E-a = 47 +/- 2 kJ mol(-1) for the autocatalytic surface growth of ruthenium(0) nanoparticles, as well as the activation energy of E-a = 51 +/- 2 kJ mol(-1) for the catalytic hydrolysis of ammonia borane.
机译:负载在二氧化铈上的钌(0)纳米粒子(Ru-0 / CeO2)是通过氨硼烷水解过程中浸渍在二氧化铈上的钌(III)离子还原而原位生成的。通过离心从反应溶液中分离Ru-0 / CeO2,并通过ICP-OES,BET,XRD,TEM,SEM-EDS和XPS技术对其进行表征。所有结果表明,钌(0)纳米颗粒已成功负载在二氧化铈上,所得的Ru-0 / CeO2是一种高活性,可重复使用且长寿命的催化剂,用于氨硼烷水解产生氢气,周转频率值为361 min(-1)。可重用性测试表明,Ru-0 / CeO2在氨硼烷的后续水解过程中仍然具有活性,即使在第五次操作后仍保留了60%的初始催化活性。在停用之前,Ru-0 / CeO2在25.0 +/- 0.1摄氏度下通过氨硼烷的水解产生氢气时,提供了卓越的催化寿命(TTO = 135100)。此处报道的工作包括钌(0)纳米粒子的形成动力学。钌(0)纳米粒子的缓慢成核和自催化表面生长的速率常数是使用析氢作为报告反应获得的。评估不同温度下的速率常数可以估算两个反应的活化能,对于成核,Ea = 60 +/- 7 kJ mol(-1),对于反应,Ea = 47 +/- 2 kJ mol(-1)钌(0)纳米粒子的自催化表面生长以及氨硼烷的催化水解Ea = 51 +/- 2 kJ mol(-1)的活化能。

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