Palladium electrochemistry in the choline chloride-urea deep eutectic solvent at gold and glassy carbon electrodes

被引:18
作者
Soma, Fousseni [1 ,2 ]
Rayee, Quentin [1 ]
Bougouma, Moussa [2 ]
Baustert, Christophe [1 ]
Buess-Herman, Claudine [1 ]
Doneux, Thomas [1 ]
机构
[1] Univ Libre Bruxelles ULB, Chem Surfaces Interfaces & Nanomat ChemSIN, Blvd Triomphe 2,CP 255, B-1050 Brussels, Belgium
[2] Univ Norbert ZONGO, Lab Chim Mat & Environm LCME, UFR Sci & Technol ST, Ave Maurice Yameogo,BP 376, Koudougou, Burkina Faso
关键词
Deep eutectic solvent; Palladium; Electrodeposition; Nucleation; Growth; SURFACE-MORPHOLOGY; INITIAL-STAGES; PD; DEPOSITION; PERFORMANCE; NUCLEATION; REDUCTION; MIXTURES; GROWTH; FILMS;
D O I
10.1016/j.electacta.2020.136165
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemical behaviour of Pd(II) in choline chloride-urea eutectic (ChCl-U) has been investigated at polycrystalline gold and glassy carbon electrodes at 60 degrees C using voltammetry (cyclic and hydrodynamic) and chronoamperometry. The voltammograms recorded at Au in the palladium solution show three reduction signals, assigned to Pd bulk deposition (around -0.2 V vs. Ag QRE), the formation of palladium hydrides PdHx (around -0.4 V vs. Ag QRE) and an underpotential deposition (upd) of Pd (around 0 V vs. Ag QRE). Two anodic peaks present in the cyclic voltammograms correspond to the oxidation of Pd hydrides and Pd deposits. In contrast to the results obtained at Au, no upd response is observed at a GC electrode and a crossover between the forward and backward scan, characteristic of a kinetic control by nucleation and growth, is clearly evidenced. Typical peaked transients are observed whose analysis unambiguously demonstrates that the deposition occurs through a 3D progressive nucleation mechanism. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:7
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