首页> 外文期刊>Journal of Catalysis >Highly active and stable MgAl_2O_4-supported Rh and Ir catalysts for methane steam reforming: A combined experimental and theoretical study
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Highly active and stable MgAl_2O_4-supported Rh and Ir catalysts for methane steam reforming: A combined experimental and theoretical study

机译:用于甲烷蒸汽重整的高活性且稳定的MgAl_2O_4负载Rh和Ir催化剂:结合实验和理论研究

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In this work, we present a combined experimental and theoretical investigation of stable MgAl_2O_4- supported Rh and Ir catalysts for the steam methane reforming (SMR) reaction. Catalytic SMR performance for a series of noble metal catalysts supported on MgAl_2O_4 spinel has been evaluated at 873-1123 K. The turnover rate at 873 K follows the order: Pd > Ir > Pt ~ Rh > Ru > Ni. However, Rh and Ir are found to have the best combination of activity and stability for SMR in the presence of simulated biomass-derived syngas where highly dispersed ~2 nm Rh and ~1 nm Ir clusters are identified on the MgAl_2O_4 spinel support. Scanning Transmission Electron Microscopy (STEM) images show that this excellent dispersion is maintained even under high-temperature conditions (e.g., at 1123 K in the presence of steam), while larger particle sizes of Rh and particularly Ir are observed when supported on Al_2O_3. These observations are further confirmed by ab initio molecular dynamic (AIMD) simulations, which find that ~1 nm Rh and Ir particles (50-atom cluster) bind strongly to the MgAl_2O_4 surface via a redox process. The strong metal-support interaction between the spinel support and Rh or Ir helps anchor the metal clusters and reduce the tendency to form larger particle sizes. Density functional theory (DFT) calculations suggest that these supported smaller Rh and Ir particles have a lower work function than larger more bulk-like ones, which enables them to activate both water and methane more effectively than larger particles, yet have a minimal influence on the relative stability of coke precursors. In addition, theoretical mechanistic studies are used to probe the relationship between structure and reactivity. Consistent with the experimental observations, our theoretical modeling results also suggest that the small spinel-supported Ir catalyst is more active than the counterpart Rh catalyst for SMR.
机译:在这项工作中,我们提供了稳定的MgAl_2O_4负载的Rh和Ir催化剂用于蒸汽甲烷重整(SMR)反应的组合实验和理论研究。负载在MgAl_2O_4尖晶石上的一系列贵金属催化剂的催化SMR性能已评估为873-1123K。873K处的周转率遵循以下顺序:Pd> Ir> Pt〜Rh> Ru> Ni> Ni。然而,在模拟生物质衍生的合成气存在下,发现Rh和Ir具有SMR活性和稳定性的最佳组合,其中在MgAl_2O_4尖晶石载体上鉴定出高度分散的〜2 nm Rh和〜1 nm Ir团簇。扫描透射电子显微镜(STEM)图像显示,即使在高温条件下(例如,在蒸汽存在下在1123 K下)也保持了这种优异的分散性,而当负载在Al_2O_3上时观察到较大的Rh和特别是Ir的颗粒尺寸。从头算分子动力学(AIMD)模拟进一步证实了这些观察结果,该模拟发现〜1 nm的Rh和Ir粒子(50原子簇)通过氧化还原过程与MgAl_2O_4表面牢固结合。尖晶石载体和Rh或Ir之间强烈的金属-载体相互作用有助于锚定金属簇,并减少形成较大粒径的趋势。密度泛函理论(DFT)计算表明,与较大的大块状颗粒相比,这些负载的较小的Rh和Ir颗粒的功函数较低,这使它们比较大的颗粒更有效地活化水和甲烷,但对较大的颗粒影响最小焦炭前体的相对稳定性。另外,理论机制研究用于探究结构与反应性之间的关系。与实验观察结果一致,我们的理论建模结果也表明,尖晶石负载的Ir催化剂比SMR的Rh催化剂更具活性。

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