Electrodeposition of Au from [EMIm][TFSA] room-temperature ionic liquid: An electrochemical and Surface-Enhanced Raman Spectroscopy study

被引:15
作者
Bozzini, Benedetto [1 ]
Tondo, Elisabetta [1 ]
Bund, Andreas [2 ]
Ispas, Adriana [2 ]
Mele, Claudio [1 ]
机构
[1] Univ Salento, Dipartimento Ingn Innovaz, I-73100 Lecce, Italy
[2] Tech Univ Dresden, D-01062 Dresden, Germany
关键词
Ionic liquid; EMIm][TFSA; Au; Electrodeposition; SERS; FREQUENCY GENERATION SPECTROSCOPY; SPECTROELECTROCHEMICAL CHARACTERIZATION; BIS(TRIFLUOROMETHANESULFONYL) IMIDE; GLASSY-CARBON; GOLD; WATER; SILVER; CHLORIDE; ANION; DEPOSITION;
D O I
10.1016/j.jelechem.2010.11.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this paper we report in situ Surface-Enhanced Raman Scattering (SERS) experiments carried out during the electrochemical deposition of gold from Au(I) cyanocomplexes in the room-temperature ionic liquid (RTIL) 1-ethyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl) amide ([EMIn][TFSA]). The obtained SERS spectra indicated the co-adsorption of CN- and both anions and cations of the RTIL in the range from -1.8 to +0.3 V vs. an Au quasi-reference electrode (QRE). The surface CN- peak exhibits a Stark tuning of ca. 28 cm(-1) V-1. The oxidation of CN- to OCN- was observed at potentials more anodic than 0.3 V. The study was complemented by cyclic voltammetry, pinpointing RTIL reactivity at an Au electrode as well as CN- adsorption effects and Au(I) reduction. SEM observations allowed to identify the conditions for the achievement of continuous Au films as well as the morphological peculiarities of Au electrodeposited from [EMIm][TFSA]. XPS measurements proved that no RTIL is incorporated into the Au film, under the investigated conditions. (c) 2010 Elsevier B.V. All rights reserved.
引用
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页码:1 / 11
页数:11
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