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Tailoring the oxidation state of cobalt through halide functionality in sol-gel silica
被引:15
|作者:
Olguin, Gianni
[1
,2
]
Yacou, Christelle
[1
]
Smart, Simon
[1
]
da Costa, Joao C. Diniz
[1
]
机构:
[1] Univ Queensland, FIMLab Films & Inorgan Membrane Lab, Sch Chem Engn, Brisbane, Qld 4072, Australia
[2] Pontificia Univ Catolica Valparaiso, Escuela Ingn Quim, Valparaiso, Chile
来源:
SCIENTIFIC REPORTS
|
2013年
/
3卷
基金:
澳大利亚研究理事会;
关键词:
CATALYSTS;
METAL;
OXIDE;
HYDROCARBONS;
MEMBRANES;
XEROGELS;
CO;
D O I:
10.1038/srep02449
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The functionality or oxidation state of cobalt within a silica matrix can be tailored through the use of cationic surfactants and their halide counter ions during the sol-gel synthesis. Simply by adding surfactant we could significantly increase the amount of cobalt existing as Co3O4 within the silica from 44% to 77%, without varying the cobalt precursor concentration. However, once the surfactant to cobalt ratio exceeded 1, further addition resulted in an inhibitory mechanism whereby the altered pyrolysis of the surfactant decreased Co3O4 production. These findings have significant implications for the production of cobalt/silica composites where maximizing the functional Co3O4 phase remains the goal for a broad range of catalytic, sensing and materials applications.
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页数:5
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