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Enhanced catalytic performance of cobalt ferrite by a facile reductive treatment for H2 release from ammonia borane
被引:14
作者:
Wang, Yi
[1
]
Liu, Xiang
[1
,2
]
机构:
[1] China Three Gorges Univ, Coll Mat & Chem Engn,Minist Educ, Engn Res Ctr Ecoenvironm Three Gorges Reservoir R, Key Lab Inorgan Nonmetall Crystalline & Energy Co, Yichang 443002, Hubei, Peoples R China
[2] Hubei Three Gorges Lab, Yichang 443007, Hubei, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Ammonia borane;
Cobalt ferrite;
H-2;
evolution;
Reduction;
Oxygen vacancy;
HYDROGEN GENERATION;
REUSABLE CATALYST;
HYDROLYTIC DEHYDROGENATION;
OXYGEN REDUCTION;
HIGHLY EFFICIENT;
NANOPARTICLES;
EVOLUTION;
ELECTROCATALYSTS;
COFE2O4;
PHOTOCATALYST;
D O I:
10.1016/j.molliq.2021.117697
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:
Although magnetic cobalt ferrite (CoFe2O4) has been applied as support to gain magnetically separable nanocomposites for H-2 evolution upon the hydrolytic dehydrogenation of ammonia borane (AB), none of them find that only CoFe2O4 could be used as the efficient catalyst for the H-2 evolution. Herein, we report a facile reduction strategy to significantly improve the catalytic activity of CoFe2O4 by producing more oxygen vacancies and enhencing surface adsorbed oxygen species. The reduced CoFe2O4 catalyst exhibited superior catalytic activity for H-2 evolution upon hydrolytic dehydrogenation of AB, with a TOF of 245 mol(H-2).mol(H-2).mol(cat)(-1).h(-1), whereas the pristine CoFe2O4 does not work. Interestingly the TOF of reduced CoFe2O4 in the H-2 evolution increased sharply from 245 to 390 mol(H-2).mol(cat)(-1).h(-1) in the presence of NaOH. In addition, as-prepared reduced CoFe2O4 has been successfully reused at least 5 cycles without any catalytic activity loss in the hydrolytic dehydrogenation of AB. (C) 2021 Elsevier B.V. All rights reserved.
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