Ru nanoparticles embedded in Ru/SiO2@N-CS for boosting hydrogen production via ammonia decomposition with robust lifespan

被引:3
|
作者
Huang, Yunyun [1 ,2 ]
Ren, Hongju [1 ]
Fang, Huihuang [1 ,2 ,3 ]
Ouyang, Dong [1 ]
Chen, Chongqi [1 ,2 ,3 ]
Luo, Yu [1 ,2 ,3 ]
Lin, Li [1 ,2 ,3 ]
Wang, Dabiao [1 ,2 ,3 ]
Jiang, Lilong [1 ,2 ]
机构
[1] Fuzhou Univ, Natl Engn Res Ctr Chem Fertilizer Catalyst NERC CF, Sch Chem Engn, Fuzhou 350002, Peoples R China
[2] Qingyuan Innovat Lab, Quanzhou 362801, Fujian, Peoples R China
[3] Fuda Zijin Hydrogen Energy Sci & Technol Co Ltd, Fuzhou 362801, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Ammonia decomposition; Ruthenium; N-doped carbon; Stability; COX-FREE HYDROGEN; CARBON NANOTUBES; HIGH DISPERSION; CATALYST; GENERATION; SUPPORT; OXIDATION; ELECTROCATALYSTS; MICROSPHERES; RU/CNTS;
D O I
10.1016/j.apsusc.2024.160517
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ammonia decomposition for onsite hydrogen production has been regarded as an important reaction which links to efficient hydrogen storage, transport and utilization. However, it still remains challenging to develop efficient catalysts with robust stability for ammonia decomposition. Herein, an integrated strategy was employed to synthesize Ru/SiO2@N-CS via wrapping a thin layer of N-doped carbon onto the SiO2 sphere, following the anchor of Ru nanoparticles (NPs) onto the support. The obtained Ru/SiO2@N-CS (Ru loading: 1 wt%) shows a promising performance for ammonia decomposition, reaching 94.5 % at 550 degrees C with a gas hourly space velocity (GHSV) of 30 000 mL gcat-1 h- 1. The combination of the SiO2 as the core prevents the degradation of N-doped carbon layers and then enhance the durability of the catalysts, remaining stable after 50 h at evaluated temperatures. Adequate characterizations were used to illustrate the effect of microchemical environment on ammonia decomposition activity of Ru/SiO2@N-CS catalyst under different calcination atmosphere and the correlation between structure and performance.
引用
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页数:9
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