Supported nickel-iron nanocomposites as a bifunctional catalyst towards hydrogen generation from N2H4•H2O

被引:81
作者
Gao, Wa [1 ]
Li, Changming [1 ]
Chen, Hao [1 ]
Wu, Min [2 ]
He, Shan [1 ]
Wei, Min [1 ]
Evans, David G. [1 ]
Duan, Xue [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
LAYERED DOUBLE-HYDROXIDE; MG-AL HYDROTALCITE; HIGHLY EFFICIENT CATALYST; ROOM-TEMPERATURE; SOLID BASE; OXIDATION; HYDRAZINE; NANOPARTICLES; DECOMPOSITION; CONVERSION;
D O I
10.1039/c3gc41939h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen represents an important alternative energy feedstock for both environmental and economic reasons. Development of highly selective, efficient and economical catalysts towards H-2 generation from hydrogen storage materials (e. g., hydrous hydrazine, N2H4 center dot H2O) has been one of the most active research areas. In this work, a bifunctional NiFe-alloy/MgO catalyst containing both an active center and a solid base center was obtained via a calcination-reduction process of NiFeMg-layered double hydroxides (LDHs) precursor, which exhibits 100% conversion of N2H4 center dot H2O and up to 99% selectivity towards H-2 generation at room temperature, comparable to the most reported noble metal catalysts (e. g., Rh, Pt). The XRD, HRTEM and HAADF-STEM results confirm that well-dispersed NiFe alloy nanoparticles (NPs) with diameters of similar to 22 nm were embedded in a thermally stable MgO matrix. The EXAFS verifies the electronic interaction between nickel and iron elements in NiFe alloy NPs, accounting for the significantly enhanced low-temperature activity. The CO2-TPD results indicate that the strong basic sites on the surface of the NiFe-alloy/ MgO catalyst contribute to the high H-2 selectivity.
引用
收藏
页码:1560 / 1568
页数:9
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