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Redox competition mode of scanning electrochemical microscopy (RC-SECM) for visualisation of local catalytic activity

扫描电化学显微镜 催化作用 氧化还原 化学 铂金 电化学 氧气 分析化学(期刊) 纳米技术 电极 材料科学 无机化学 色谱法 物理化学 有机化学
作者
Kathrin Eckhard,Xingxing Chen,Florin Turcu,Wolfgang Schuhmann
出处
期刊:Physical Chemistry Chemical Physics [The Royal Society of Chemistry]
卷期号:8 (45): 5359-5359 被引量:198
标识
DOI:10.1039/b609511a
摘要

In order to locally analyse catalytic activity on modified surfaces a transient redox competition mode of scanning electrochemical microscopy (SECM) has been developed. In a bi-potentiostatic experiment the SECM tip competes with the sample for the very same analyte. This leads to a current decrease at the SECM tip, if it is positioned in close proximity to an active catalyst site on the surface. Specifically, local catalytic activity of a Pt-catalyst modified sample with respect to the catalytic reduction of molecular oxygen was investigated. At higher local catalytic activity the local 02 partial pressure within the gap between accurately positioned SECM tip and sample is depleted, leading to a noticeable tip current decrease over active sites. A flexible software module has been implemented into the SECM to adapt the competition conditions by proper definition of tip and sample potentials. A potential pulse profile enables the localised electrochemically induced generation of molecular oxygen prior to the competition detection. The current decay curves are recorded over the entire duration of the applied reduction pulse. Hence, a time resolved processing of the acquired current values provides movies of the local oxygen concentration against x,y-position. The SECM redox competition mode was verified with a macroscopic Pt-disk electrode as a test sample to demonstrate the feasibility of the approach. Moreover, highly dispersed electro-deposited spots of gold and platinum on glassy carbon were visualised using the redox competition mode of SECM. Catalyst spots of different nature as well as activity inhomogeneities within one spot caused by local variations in Pt-loading were visualised successfully.
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