Constructing the Ni-O-Ce interface to enhance the activity and stability for partial oxidation of methane to syngas under high temperatures

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Catalysis Pub Date : 2024-05-12 DOI:10.1016/j.jcat.2024.115545
Yuanjie Xu , Rong Chen , Hongqiao Lin , Qian Lv , Bo Liu , Lizhi Wu , Li Tan , Yihu Dai , Xupeng Zong , Yu Tang
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Abstract

Catalyst interface determines the activity and stability of partial oxidation of methane (POM) toward syngas under high temperatures crucially. Herein, Ni catalysts supported on CeO2 were prepared under different pretreatment atmospheres to construct an optimal and robust interface. Ni/CeO2 catalyst pretreated in H2 (Ni/CeO2-H2) exhibits the higher activity and the better stability than Ni/CeO2-Ar and Ni/CeO2-air catalysts. The Ni-O-Ce interfacial site in Ni/CeO2-H2 catalyst shows the lower reduction temperature, indicating the enhanced H-spillover effect and enhanced oxidation resistance of Ni under POM conditions. Moreover, the XPS and in situ Raman results show that Ni/CeO2-H2 contains more surface oxygen vacancies for adsorbing and activating oxygen, further contributing to the reaction activity. The in situ DRIFTS results indicate that the CH4 could react with the lattice oxygen to form formate and carbonate, and further decompose to CO and CO2. These findings deepen the fundamental understanding of Ni/CeO2 catalysts for POM reaction.

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构建 Ni-O-Ce 界面,提高高温下甲烷部分氧化为合成气的活性和稳定性
催化剂界面对高温条件下甲烷部分氧化(POM)转化为合成气的活性和稳定性起着至关重要的作用。在此,我们在不同的预处理气氛下制备了以 CeO2 为载体的 Ni 催化剂,以构建一个最佳的稳健界面。与 Ni/CeO2-Ar 和 Ni/CeO2-air 催化剂相比,在 H2 中预处理的 Ni/CeO2 催化剂(Ni/CeO2-H2)具有更高的活性和更好的稳定性。Ni/CeO2-H2 催化剂中的 Ni-O-Ce 界面位点显示出较低的还原温度,表明在 POM 条件下 H 溢出效应增强,Ni 的抗氧化性增强。此外,XPS 和原位拉曼结果表明,Ni/CeO2-H2 表面含有更多的氧空位,可吸附和活化氧,进一步提高了反应活性。原位 DRIFTS 结果表明,CH4 可与晶格氧反应生成甲酸盐和碳酸盐,并进一步分解为 CO 和 CO2。这些发现加深了人们对用于 POM 反应的 Ni/CeO2 催化剂的基本认识。
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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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