In the mid-1970s, surface-enhanced Raman scattering (SERS) was discovered which impacted on surface science and spectroscopy because of its extremely high surface sensitivity. However, SERS had not developed as many people had hoped to be a powerful surface diagnostic technique that can be widely used because of some obstacles. For example, only three noble metals Au, Ag, and Cu could provide large enhancement, severely limiting the widespread applications involving other metallic materials of both fundamental and practical importance. In this article, emphasis is put on the recent work of our group to directly generate SERS on net transition metals (e.g., Pt, Ru, Rh, Pd, Fe, Co, Ni, and their alloys) by developing various roughening procedures and optimizing the performance of the confocal Raman microscope. An approach of replacing the randomly roughened surface with ordered nanorod arrays of transition metals is introduced as a promising class of highly SERS-active substrates. The surface enhancement factor for transition metals was calculated, which ranged from 1 to 4 orders of magnitude. The applications of SERS in surface adsorption, electro-catalysis, and corrosion of transition-metal-based systems demonstrated several advantages of in situ surface Raman spectroscopy. A preliminary theoretical approach, considering the electromagnetic and chemical contributions, is presented to explain the SERS behavior of transition metal electrodes and nanorod arrays. It has been shown that SERS together with other surface-enhanced optical phenomena could be one of important issues not only in surface science but also in nanoscale science. Prospects and further developments in this exciting field are discussed with emphasis on the emerging experimental methodology.
Surface-enhanced Raman spectroscopy (SERS) has long been considered as a noninvasive technique that can obtain the fingerprint vibrational information of surface species. We demonstrated in this paper that a laser with a power level considered to be low in the traditional SERS measurement can already lead to a significant surface reaction. para-Aminothiophenol, an important probe molecule in SERS, was found to be oxidized to form 4,4'-dimercaptoazobenzene (DMAB) on a roughened silver surface during the SERS measurement. The assumption was confirmed experimentally by surface mass spectroscopy and SERS as well as electrochemistry of the synthesized DMAB, which agrees well with theoretical calculations. A defocusing method was used to avoid the laser induced surface reaction and perform reliable SERS characterization and identification, which can effectively avoid erroneous interpretation of the distorted experimental result.
This tutorial review first describes the early history of SERS as the first SERS spectra were obtained from an electrochemical cell, which led to the discovery of the SERS effect in mid-1970s. Up to date, over 500 papers have been published on various aspects of SERS from electrochemical systems. We then highlight important features of electrochemical SERS (EC-SERS). There are two distinctively different properties of electric fields, the electromagnetic field and static electrochemical field, co-existing in electrochemical systems with various nanostructures. Both chemical and physical enhancements can be influenced to some extent by applying an electrode potential, which makes EC-SERS one of the most complicated systems in SERS. Great efforts have been made to comprehensively understand SERS and analyze EC-SERS spectra on the basis of the chemical and physical enhancement mechanisms in order to provide meaningful information for revealing the mechanisms of electrochemical adsorption and reaction. The EC-SERS experiments and applications are then discussed from preparation of nanostructured electrodes to investigation of SERS mechanisms and from characterization of adsorption configuration to elucidation of electrochemical reaction mechanisms. Finally, prospective developments of EC-SERS in substrates, methods and theory are discussed.
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