Scanning electrochemical microscopy
Scanning electrochemical microscopy
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DOI:
10.1021/ac00194a002
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发表时间:
1989-10
影响因子:
7.4
通讯作者:
R. Engstrom;C. Pharr
中科院分区:
文献类型:
--
作者:
R. Engstrom;C. Pharr
Modern electroanalytical chemistry re-lies on increasingly complicated inter-facial designs to achieve improved se-lectivity, sensitivity, and adaptability. Chemical modifications, polymer films, composite materials, and micro-electrode arrays are examples of schemes in which the electrode-solu-tion interface possesses spatial heterogeneity on a dimensional level ranging from the microscopic to the atomic. The chemical and physical structure of such surfaces can now be characterized with spatial resolutions ranging from the micrometer to the atomic levels us-ing techniques such as optical and electron microscopy, ESCA, Raman microprobe, and scanning tunneling micros-f= acus copy (STM). However, these techniques do not directly provide information about electrochemical activity. Knowl-edge of structure-activity relationships could ultimately lead to optimized designs of electroanalytical devices and increase our ability to interpret data generated with complicatedelectrode designs.There are many examples of ques-tions related to thespatial distribution of electrochemical activity. For in-stance, what fraction of a composite electrode surface is in electrochemical communication with thesolution? Are electrochemical “hot spots” present on surfaces where events such as nucleation occur? Do defects existin a poly-