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High Power Density of a Hydrogen Peroxide Fuel Cell Using Cobalt Chlorin Complex Supported on Carbon Nanotubes as a Noncorrosive Anode
被引:0
|作者:
Hashimoto, Kazuki
[1
]
Nakazono, Takashi
[2
]
Yamada, Yusuke
[1
,2
]
机构:
[1] Osaka Metropolitan Univ, Grad Sch Engn, Dept Chem & Bioengn, Sumiyoshi, Osaka 5588585, Japan
[2] Osaka Metropolitan Univ, Res Ctr Artificial Photosynth ReCAP, Sumiyoshi, Osaka 5588585, Japan
关键词:
PRUSSIAN-BLUE;
H2O2;
PERFORMANCE;
REDUCTION;
CATALYST;
ACID;
PHTHALOCYANINE;
DIOXYGEN;
CATHODE;
DERIVATIVES;
D O I:
10.1021/acs.inorgchem.3c03857
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Hydrogen peroxide fuel cells (HPFCs) have attracted much attention due to their simple one-compartment structures and high availability under harsh conditions such as an anaerobic environment; however, catalysis improvement is strongly demanded for both anodes and cathodes in terms of activity and durability. Herein, we report the high catalytic activity of Co-II chlorin [Co-II(Ch)] for hydrogen peroxide (H2O2) oxidation with a low overpotential (0.21 V) compared to that of the Co-II phthalocyanine and Co-II porphyrin complexes, which have previously been reported as active anode catalysts. Linear sweep voltammograms and differential pulse voltammograms of the Co-II complexes ((CoL)-L-II) and the corresponding ligands clearly showed that the (CoL)-L-III species are the active species for H2O2 oxidation. Then, one-compartment HPFCs were constructed with Co-II(Ch) supported on multiwalled carbon nanotubes (CNTs) as the anode together with Fe-3(II)[Co-III(CN)(6)](2) supported on CNTs as the cathode. The maximum power density of the HPFCs reached 151 mu W cm(-2) with an open circuit potential of 0.33 V when the coverage of CNT surfaces with Co-II(Ch) exceeded similar to 60% at the anode.
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页码:1347 / 1355
页数:9
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