催化作用
集聚经济
空间速度
纳米颗粒
氨
材料科学
分解
金属
化学工程
X射线光电子能谱
氢
氧化物
无机化学
化学
纳米技术
冶金
有机化学
工程类
选择性
作者
Jiaxin Li,Junhui Liang,Xin Yao,Hongming Liu,Yuhui Du,Huayu Chen,Hangning Chen,Chenhao Du,Liuqi Wang,Yincheng Li,Yuexiang Huang,Da Chen
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2025-01-01
标识
DOI:10.1021/acsanm.4c05957
摘要
The development of low-temperature, nonprecious metal thermocatalysts for ammonia decomposition holds significant promise for advancing the green hydrogen industry. LaNiO3 catalysts, with their perovskite structure (ABX3), are notable for enabling in situ growth of active metal Ni on reduced oxide supports during ammonia decomposition reactions (ADRs). However, unintentional in situ growth can lead to uncontrolled reactions and metal particle agglomeration. To address this, we employed a straightforward high-temperature and pressure hydrogenation pretreatment process to enhance the interaction between the active metal and the support, thereby suppressing the agglomeration of the active metal during the ADR process. Our results indicate that the hydrogenation pretreatment catalyst exhibits finer Ni metal nanoparticles, with an average size of approximately 8 nm. Under a gas hourly space velocity (GHSV) of 18,000 mL gcat–1 h–1 and at 550 °C, the NH3 conversion efficiency reaches 90%, which exhibited excellent stability over a period of 100 h. Additionally, we utilized TEM, XPS, EPR, NH3-TPD, and H2-TPR techniques to elucidate the intrinsic mechanisms related to the enhanced catalytic activity. This study addresses the issue of active metal nanoparticle agglomeration through hydrogenation pretreatment.
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