催化作用
无机化学
化学
煅烧
氨
氧气
氢
分解
制氢
铈
X射线光电子能谱
X射线吸收精细结构
拉曼光谱
氧化铈
化学工程
有机化学
光谱学
工程类
物理
光学
量子力学
作者
Wenying Wu,Wenhao Yao,Yitong Liu,Senliang Xi,Teng Zhang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2025-05-23
卷期号:30 (11): 2301-2301
被引量:8
标识
DOI:10.3390/molecules30112301
摘要
Ammonia is a promising hydrogen storage material because it is easy to store and decompose into COX-free hydrogen. A Ru-based catalyst exhibits good catalytic performance in ammonia decomposition, and enhancing the interaction between the Ru atoms and the support is an important way to further improve its catalytic activity. In this study, CeO2 was prepared by calcination using a cerium-based metal–organic framework (MOF) as the precursor, and the number of oxygen vacancies on the surface of CeO2 was regulated by hydrogen reduction. The XPS and Raman results showed that abundant oxygen vacancies were formed on the surface of these CeO2, and their number increased with an increase in the reduction time. The Ru/CeO2-4 h catalyst, using CeO2 reduced for 4 h as the support, exhibited good catalytic activity in ammonia decomposition, reaching 98.9% ammonia conversion and 39.74 mmol gcat−1 min−1 hydrogen yield under the condition of GHSV = 36,000 mL gcat−1 h−1 at 500 °C. The XAFS results demonstrated that Ru was stably anchored with oxygen vacancies on the surface of CeO2 via Ru-O-Ce bonds. Density functional theory calculations further showed that these bondings lower the reaction energy barrier for N-H bond cleavage, thereby significantly enhancing the catalytic activity.
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