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Monitoring charge transfer at polarisable liquid/liquid interfaces employing time-resolved Raman spectroelectrochemistry
被引:15
作者:
Ibanez, D.
[1
]
Plana, D.
[2
]
Heras, A.
[1
]
Fermin, D. J.
[2
]
Colina, A.
[1
]
机构:
[1] Univ Burgos, Dept Chem, E-09001 Burgos, Spain
[2] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
基金:
英国工程与自然科学研究理事会;
关键词:
Liquid/liquid interfaces;
Ion transfer;
Electron transfer;
In-situ Raman spectroscopy;
SUM-FREQUENCY SPECTROSCOPY;
ELECTRON-TRANSFER;
LIQUID INTERFACE;
NANOPARTICLES;
ADSORPTION;
D O I:
10.1016/j.elecom.2015.02.012
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
In-situ Raman spectroscopy is implemented for the first time to monitor dynamic charge transfer processes at polarisable interfaces between two immiscible electrolyte solutions (ITIES) in real time. A custom-designed new electrochemical cell is described which allows probing the Raman signals of ferroin ions as a function of the potential applied across the water vertical bar 1,2-dichlorobenzene (DCB) interface. This approach is also used for investigating the heterogeneous electron transfer reaction involving dimethylferrocene in DCB and potassium hexacyanoferrate (II/III) in the aqueous phase. The evolution of the Raman signals during potentiodynamic measurements is recorded in real-time with a resolution of a few seconds. (C) 2015 Elsevier B.V. All rights reserved.
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页码:14 / 17
页数:4
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