Hybrid electrocatalysts for oxygen reduction reaction: Integrating enzymatic and non-platinum group metal catalysis

被引:12
|
作者
Rojas-Carbonell, Santiago [1 ]
Babanova, Sofia [1 ]
Serov, Alexey [1 ]
Ulyanova, Yevgenia [2 ]
Singhal, Sameer [2 ]
Atanassov, Plamen [1 ]
机构
[1] Univ New Mexico, Chem & Biol Engn Dept, CMEM, Adv Mat Lab, 1001 Univ Blvd SE Suite 103,MSC 04 2790, Albuquerque, NM 87131 USA
[2] CFD Res Corp, 701 McMillian Way Northwest, Huntsville, AL 35806 USA
关键词
Oxygen reduction reaction; Bilirubin oxidase; Non-platinum group metal catalyst; Iron aminoantipyrine; DIRECT ELECTRON-TRANSFER; BILIRUBIN OXIDASE; FUEL-CELLS; IRON; PERFORMANCE; NANOTUBES; ENZYMES;
D O I
10.1016/j.electacta.2016.01.030
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
For the first time, oxygen reduction reaction has been demonstrated on a system which integrates enzymatic and non-platinum based catalysts simultaneously. This achievement is of a great importance as it offers the possibility of exploring concomitantly two very different types of catalysts, combining the advantages of both in enhancing oxygen reduction reaction rate. The engineered catalytic hybrid material not only possesses lower overpotentials compared to the purely non-PGM catalyst, but also is capable of achieving higher current densities in comparison to purely enzymatic catalyst. The hybrid catalyst undergoes oxygen reduction with the desired 4 electron transfer process, leading to the formation of water as a final product. The achieved current density of 1.2 mA cm(-2) is believed to be the highest reported for bilirubin oxidase-based gas-diffusion cathode reported so far. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:504 / 510
页数:7
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