Electrocatalytic Oxidation of Hydroxide Ions by Co3O4 and Co3O4@SiO2 Nanoparticles Both at Particle Ensembles and at the Single Particle Level

被引:14
作者
Xie, Ruo-Chen [1 ]
Volokhova, Maria [2 ]
Boldin, Aleksei [2 ]
Seinberg, Liis [2 ]
Tsujimoto, Masahiko [3 ]
Yang, Minjun [1 ]
Rasche, Bertold [1 ]
Compton, Richard G. [1 ]
机构
[1] Univ Oxford, Phys & Theoret Chem Lab, Dept Chem, South Parks Rd, Oxford OX1 3QZ, England
[2] NICPB, Chem Phys Lab, Akad Tee 23, EE-12618 Tallinn, Estonia
[3] KUIAS, Inst Integrated Cell Mat Sci iCeMS, Sakura Ku, Yoshida Ushinomiya Cho, Kyoto 6068501, Japan
基金
英国工程与自然科学研究理事会;
关键词
cobalt (II) dicobalt (III) oxide nanoparticles; core-shell nanoparticles; electrocatalysis; hydroxide ion oxidation; nano-impacts; ANODIC-STRIPPING VOLTAMMETRY; OXYGEN REDUCTION REACTION; AQUEOUS-SOLUTIONS; SILVER NANOPARTICLES; CATALYTIC-ACTIVITY; EVOLUTION; NANOCRYSTALS; WATER; DECOMPOSITION; INSIGHTS;
D O I
10.1002/celc.202000230
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We report that the Co3O4 nanoparticle-mediated electrochemical oxidation under alkaline conditions of the hydroxide ion on a glassy carbon macroelectrode leads to hydrogen peroxide as the initial oxidation product of electron transfer. The latter is inferred to subsequently partially decompose to dioxygen by catalytic chemical reaction at the nanoparticles. At the single particle level, electrochemical particle-electrode impacts point out the rate-determining step and the limiting kinetics of the reaction. Furthermore, particles with a core-shell structure of a Co3O4 core and SiO2 shell are synthesised, and their electrochemical behaviour is studied and compared with bare Co3O4 nanoparticles, suggesting the very likely broken or highly porous state of the silica shell, which is not otherwise easily distinguished, for example, by electron microscopy.
引用
收藏
页码:1261 / 1276
页数:16
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