Electrochemistry at nanoporous interfaces: new opportunity for electrocatalysis

被引:166
作者
Bae, Je Hyun [1 ]
Han, Ji-Hyung [1 ]
Chung, Taek Dong [1 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
基金
新加坡国家研究基金会;
关键词
OXYGEN REDUCTION REACTION; ORDERED MESOPOROUS CARBONS; QUARTZ-CRYSTAL MICROBALANCE; ELECTRON-TRANSFER KINETICS; PHASE LIQUID-CHROMATOGRAPHY; LINEAR-SWEEP VOLTAMMETRY; DOUBLE-LAYER CAPACITANCE; POROUS FILM ELECTRODES; SURFACE-DIFFUSION; ACTIVATED CARBON;
D O I
10.1039/c1cp22927c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Physical and electrochemical features of nanoporous electrodes arising from their morphology are presented in this perspective. Although nanoporous electrodes have been used to enhance electrocatalysis for several decades, the origin of their capability was understood on the basis of enlarged surface area or crystalline facet. However, considerable attention should be paid to the fact that nano-confined space of nanoporous electrodes can significantly affect electrochemical efficiency. Molecular dynamics in nano-confined spaces is capable of offering much more chances of interaction between a redox molecule and an electrode surface. The mass transport in the nanoporous electrode depends on various pore characteristics such as size, shape, charge, connectivity, and symmetry as well as molecular properties such as size, charge, and kinetics. Moreover, when the pore size is comparable to the thickness of an electric double layer (EDL), the EDLs overlap in the porous structure so that electrochemically effective surface area is not the same as that of the real electrode surface. These unique properties come from simply nanoporous structure and suggest new opportunity to innovative electrocatalysts in the future.
引用
收藏
页码:448 / 463
页数:16
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