High-Performance Rh@MgO Catalysts for Complete Dehydrogenation of Hydrazine Borane: A Comparative Study

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2024-11-21 DOI:10.1039/d4qi02575j
Ahmet Bulut, Mustafa Erkartal, Mehmet Yurderi, Tuba Top, Mehmet Zahmakiran
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Abstract

Hydrazine borane (HB) has great potential as a safe and convenient hydrogen carrier material due to its high hydrogen capacity (15.4 % wt) and good stability under ambient conditions. However, efficient hydrogen production through the complete decomposition of hydrazine borane at low temperatures (< 373 K) constitutes a major challenge. Herein, we report the successful immobilization of monodisperse Rh nanoparticles on MgO solid support, leading to the formation of the Rh@MgO catalyst. This developed catalyst exhibits outstanding catalytic performance in the dehydrogenation of HB, achieving a remarkable turnover frequency (TOF) of 2005.34 h⁻¹ at 50 °C with 100% H₂ selectivity, despite containing only 2 wt% Rh. Comparative experiments with Rh on various metal-oxide nanoparticles, other transition metal catalysts on MgO, and Ni grown on MgO in both single-phase and bimetallic forms reveal that Rh@MgO consistently outperforms these alternatives. The exceptional catalytic activity is attributed to the synergistic interaction between Rh and MgO, which involves several key factors: the homogeneous dispersion of ultrafine, monodisperse Rh particles enhances catalytic efficiency; the proximity of the work functions of Rh and MgO results in a low-energy Schottky barrier that facilitates electron transfer; and the localization of electrons in surface defects of MgO aligns with the Fermi level of Rh, further promoting electron transfer through Fermi Level Pinning (FLP). The combination of low Rh content and cost-effective MgO support presents a promising pathway for both laboratory-scale research and practical industrial applications, highlighting the potential of the Rh@MgO catalyst as an efficient and economically viable solution for catalytic processes.
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用于肼硼烷完全脱氢的高性能 Rh@MgO 催化剂:比较研究
肼硼烷(HB)具有很高的氢容量(15.4 % wt),并且在环境条件下具有良好的稳定性,因此作为一种安全方便的氢载体材料具有很大的潜力。然而,在低温(373 K)下通过肼硼烷的完全分解高效制氢是一项重大挑战。在此,我们成功地将单分散 Rh 纳米颗粒固定在氧化镁固体载体上,从而形成了 Rh@MgO 催化剂。这种催化剂在 HB 的脱氢反应中表现出卓越的催化性能,尽管只含有 2 wt% 的 Rh,但在 50 °C条件下的翻转频率 (TOF) 达到了 2005.34 h-¹,H₂ 选择性达到 100%。与各种金属氧化物纳米颗粒上的 Rh、氧化镁上的其他过渡金属催化剂以及生长在氧化镁上的单相和双金属形式的 Ni 进行的比较实验表明,Rh@MgO 始终优于这些替代品。超凡的催化活性归功于 Rh 和氧化镁之间的协同作用,其中涉及几个关键因素:超细、单分散的 Rh 粒子的均匀分散提高了催化效率;Rh 和氧化镁的功函数接近,形成了低能肖特基势垒,促进了电子转移;氧化镁表面缺陷中的电子定位与 Rh 的费米级一致,通过费米级钉化(FLP)进一步促进了电子转移。低 Rh 含量与经济高效的氧化镁支撑相结合,为实验室规模的研究和实际工业应用提供了一条前景广阔的途径,凸显了 Rh@MgO 催化剂作为一种高效且经济可行的催化过程解决方案的潜力。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
期刊最新文献
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