Performance of MOF-Derived Spinel Type NixCo3-xO4-y Nanocages in Efficient Methanol Electro-Oxidation

被引:32
作者
Antony, Rajini P. [1 ]
Satpati, Ashis K. [2 ]
Jagatap, Bhagawantrao N. [3 ]
机构
[1] Bhabha Atom Res Ctr, Chem Div, Bombay 400085, Maharashtra, India
[2] Bhabha Atom Res Ctr, Analyt Chem Div, Bombay 400085, Maharashtra, India
[3] Indian Inst Technol, Dept Phys, Bombay 400076, Maharashtra, India
关键词
electrocatalysis; metal-organic framework; nickel cobalt oxides; direct methanol fuel cells; electrochemical impedance spectroscopy; GLASSY-CARBON ELECTRODE; ELECTROCATALYTIC OXIDATION; FUEL-CELLS; ORGANIC-COMPOUNDS; FACILE SYNTHESIS; NANOWIRE ARRAYS; NICO2O4; GRAPHENE; CO3O4; NANOPARTICLES;
D O I
10.1002/celc.201700832
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The present study reports electrocatalytic activity towards methanol oxidation of mesoporous NixCo3-xO4-y fabricated through a metal-organic framework (MOF) template route. MOF-derived NixCo3-xO4-y nanocages exhibit a methanol oxidation reaction (MOR) current of approximately 200 Ag-1 at 0.55 V versus Hg-HgOx which is around 12 times higher than that from Co3O4. Improve(d) activity for the catalyst is ascribed to its higher number of catalytic active sites and non-stoichiometry in the composition. The improved charge-transfer kinetics for the MOR is evident from the electrochemical impedance measurements, where a lower charge-transfer resistance is observed for NixCo3-xO4-y nanocages and the trend is consistent with the MOR results. The potential-dependent impedance measurements suggest that direct electrochemical MOR is facilitated through a surface intermediate, where the surface intermediates (CH3OH or CO) are adsorbed on low coordinated Ni and Co sites, respectively.
引用
收藏
页码:2989 / 2996
页数:8
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