首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Potential-dependant SERS interaction of ortho-substituted N-benzylamino(boronphenyl)methylphosphonic acid with Ag,Au, and Cu electrode surfaces
Institution:1. Institute of Nuclear Physics Polish Academy of Sciences, PL-31342 Krakow, Poland;2. Spectroscopy Product Division, Renishaw Sp. z o o, 02-823 Warszawa, Poland;3. Department of Ophthalmology, 5th Military Hospital with Polyclinic in Krakow, Wroclawska 1-3, 30-091 Kraków, Poland;4. Department of Ophthalmology, Military Medical Institute, Szaserów 128, 04-141 Warszawa, Poland;5. Department of Histology, Jagiellonian University Medical College, Kopernika 7, 31-034 Krakow, Poland
Abstract:In this study we present surface-enhanced Raman spectroscopy (SERS) investigations of ortho-substituted N-benzylamino(boronphenyl)methylphosphonic acid (N-benzylamino-(2-boronphenyl)-R-methylphosphonic acid; o-PhR) adsorbed onto a roughened in oxidation–reduction cycles (ORC) Ag, Au, and Cu electrode surfaces at different applied electrode potentials. Based on the spectral changes in bandwidth and wavenumber of selected bands upon the alternation of the applied electrodes potential the manner and differences in the interaction of o-PhR with the Ag, Au, and Cu electrode surfaces were determined. Briefly, the spectral patterns on Ag and Au suggest that, generally, the both aromatic rings are involved in the o-PhR/electrode interaction, whereas the boronophenyl ring only interacts with Cu. Also, the boronic acid and phosphonic acid groups participate in the o-PhR interaction with all the types of electrodes. However, the type of the used electrode material and the applied electrode potential have influence onto the mode of adsorption.
Keywords:Surface-enhanced raman spectroscopy  SERS  Ag  Au  Cu electrodes
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号