Oxygen Reduction and Evolution on Ni-modified Co3O4(111) Cathodes for Zn-Air Batteries: A Combined Surface Science and Electrochemical Model Study

被引:35
作者
Buchner, Florian [1 ]
Eckardt, Markus [1 ,2 ,3 ]
Boehler, Timo [1 ]
Kim, Jihyun [1 ]
Gerlach, Jasmin [1 ]
Schnaidt, Johannes [2 ,3 ]
Behm, R. Juergen [1 ,2 ]
机构
[1] Ulm Univ, Inst Surface Chem & Catalysis, Albert Einstein Allee 47, Ulm 89081, Germany
[2] Helmholtz Inst Ulm Electrochem Energy Storage HIU, Helmholtzstr 11, Ulm 89081, Germany
[3] Karlsruhe Inst Technol KIT, POB 3640, Karlsruhe 76021, Germany
关键词
electrochemistry; oxygen evolution reaction; oxygen reduction reaction; surface chemistry; thin films; BIFUNCTIONAL CATALYST; METAL; OXIDE; PERFORMANCE; NICO2O4; CO; REDUCTION/EVOLUTION; NANOCRYSTALS; ADSORPTION; ELECTRODES;
D O I
10.1002/cssc.202000503
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The performance of structurally and chemically well-defined Ni-free and Ni-modified single-crystalline Co3O4(1 1 1) thin-film electrodes in the oxygen reduction and evolution reactions (ORR and OER) was investigated in a combined surface science and electrochemistry approach. Pure and Ni-modified Co3O4(1 1 1) film electrodes were prepared and characterized under ultrahigh-vacuum conditions by scanning tunneling microscopy and X-ray photoelectron spectroscopy. Both Ni decoration (by post-deposition of Ni) and Ni doping (by simultaneous vapor deposition of Ni, Co, and O-2) induced distinct differences in the base cyclic voltammograms in 0.5 m KOH at potentials higher than 0.7 V compared with Co3O4(1 1 1) electrodes. Also, all oxide film electrodes showed a higher overpotential for the ORR but a lower one for the OER than polycrystalline Pt. Ni modification significantly improved the ORR current densities by increasing the electrical conductivity, whereas the OER onset of approximately 1.47 V-RHE (RHE: reversible hydrogen electrode) at 0.1 mA cm(-2) was almost unchanged.
引用
收藏
页码:3199 / 3211
页数:13
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