From “Single Sites” to Stable Nanoparticles Derived from Spray-Flame Synthesized Solid Solutions of Cobalt in MgO for Ammonia Decomposition

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Barış Alkan, Liseth Duarte-Correa, Frank Girgsdies, Gregor Koch, Jutta Kröhnert, Mervan Ertegi, Shan Jiang, Thomas Lunkenbein and Annette Trunschke*, 
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Abstract

Chemical energy storage, in particular, the storage of hydrogen in carbon-free molecules such as ammonia, is being considered as an essential element in the transformation of our future energy system. In the present work, cobalt catalysts were investigated as alternatives to Ru- and Ni-based materials for the decomposition of ammonia. Spray-flame synthesis (SFS) was used to prepare metastable, phase-pure solid solutions Mg1–xCoxO, 0.03 ≤ x ≤ 0.47, as catalyst precursors composed of oxide nanoparticles with a particle size of 7–8 nm. In situ and operando XRD, H2-TPR studies, electron microscopy, Raman spectroscopy, and FTIR spectroscopy of adsorbed CO were applied to characterize the nanostructure of the host oxides and catalysts generated by exsolution of Co under reductive conditions. Calcination at 600 °C causes partial segregation of a Co3O4 spinel phase at a higher Co content (x ≥ 0.24). Small Co clusters are formed by exsolution from the solid solution, while the reduction of the spinel component yields Co nanoparticles of 3.3–8.5 nm. Very high space-time yields of 19 mmolH2·gcat–1·min–1 at 500 °C can be achieved due to the high dispersion of metallic cobalt. The turnover frequency (TOF) for metallic nanoparticles in the range between 1 and 5 nm remains constant at about 0.2 s–1, suggesting a structure insensitivity of the reaction in this size range at industrially relevant reaction conditions (500 °C, 100% NH3, WHSV of 36,000 N mL·g–1·h–1, 1 atm) caused by structural dynamics. Only atomically dispersed cobalt shows a TOF of about 0.5 s–1. The Co/Mg1–xCoxO catalysts exhibit very good stability even at high Co contents under the harsh conditions of ammonia decomposition due to strong metal–support interaction, making continuous SFS, which is potentially scalable, an attractive method for preparing cost-effective and resource-saving catalysts for ammonia decomposition.

从“单位点”到稳定的纳米颗粒,用喷雾火焰合成氧化镁中钴的固溶解氨
化学能量储存,特别是氢在无碳分子(如氨)中的储存,被认为是我们未来能源系统转型的一个基本要素。在本工作中,研究了钴催化剂作为Ru基和ni基材料的替代品,用于氨的分解。采用喷雾火焰合成(SFS)法制备了Mg1-xCoxO(0.03≤x≤0.47)为催化剂前驱体的亚稳相纯固溶体,前驱体由粒径为7 ~ 8 nm的氧化纳米颗粒组成。采用原位和操作氧化物XRD、H2-TPR、电子显微镜、拉曼光谱和FTIR光谱对吸附CO在还原条件下析出生成的主氧化物和催化剂的纳米结构进行了表征。在600°C下煅烧导致Co含量较高(x≥0.24)的Co3O4尖晶石相部分偏析。在固溶体中析出形成小的Co团簇,而尖晶石组分的还原得到了3.3 ~ 8.5 nm的Co纳米颗粒。由于金属钴的高度分散,在500°C时可以达到19 mmolH2·gcat-1·min-1的高时空产率。1 ~ 5 nm范围内的金属纳米颗粒的周转频率(TOF)保持在0.2 s-1左右,表明在工业相关的反应条件下(500℃,100% NH3, WHSV为36,000 N mL·g-1·h - 1,1 atm),结构动力学导致该尺寸范围内的反应结构不敏感。只有原子分散的钴显示出约0.5 s-1的TOF。Co/ Mg1-xCoxO催化剂即使在高Co含量条件下,在氨分解的恶劣条件下,由于强金属-载体相互作用,也表现出非常好的稳定性,使得连续SFS具有潜在的可扩展性,是一种有吸引力的制备高成本和资源节约的氨分解催化剂的方法。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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