Beijing National Laboratory
for Molecular Sciences lead by Prof. Yuanhua Shao's group have recently
studied the kinetics of several ion transfer (IT) reactions at the water/1,2-dichloroethane
(W/DCE) interface by nanopipette voltammetry collaborated with Prof. Hubert
H. Girault (EPFL, Switzerland). This work is important in understanding the
mechanism of IT processes at soft interfaces, chemical analysis and biological
sensing on the molecular scale. (Sees Angew. Chem. Int. Ed., 2009, 48, 43, 8010-8013).
 | | Schematic representation of the experimental setup |
The kinetics of IT reactions at liquid/liquid interfaces has been the central
focus in the past few decades, and is often very fast and difficult to measure.
Many electrochemical methods including chronocoulometry, a.c. impedance, and
cyclic voltammetry have been extensively used to probe kinetics of IT processes.
Unfortunately, measurements by these conventional electrochemical methods at
macroscopic (e.g., mm-sized) liquid/liquid interface are easily affected by
uncompensated ohmic potential drop (iR-drop), capacitive currents and deficient
mass-transport rate (m0). To minimize those effects, Girault et al. introduced
in 1986 a micro-sized liquid/liquid (µ-L/L) interface supported at the
tip of a pulled glass micropipette and in 1997 Shao et al. further reduced the
liquid/liquid interface to the nanometer-range using nanopipettes. Nanopipette
voltammetry and scanning electrochemical microscopy (SECM) are currently the
most reliable techniques which can be used to extract the fast kinetic rate
constants of IT reactions at a liquid/liquid interface. The fastest rate constants
reported so far are in the range of a few cm/s.
The configuration of the experimental setup is illustrated in Figure A. We
employ nanopipettes with r less than 5 nm (which has never been reported) for
the kinetic study in this work. Because nanopipettes are insulator and hard
to be characterized by SEM, the empirical equation proposed by Girault et al.
is utilized to characterize the nanopipettes using facilitated ion transfer
(FIT) of potassium by dibenzo-18-crown-6 (DB18C6) at a W/DCE interface. By optimization
of experimental conditions and background subtraction, well-defined steady state
voltammograms for the transfers of TEA+ (Figure B), ClO4–, and FIT of
K+ by DB18C6 could be obtained. Based on the three-point method developed by
Bard and Mirkin, the kinetic parameters can be extracted. The mean values of
k0 and charge transfer coefficient(a)of three IT reactions are 110 ±
23.2, 94.9 ± 30.6, 27.1 ± 6.4 cm s-1 and 0.57 ± 0.08, 0.56
± 0.13, 0.65 ± 0.09, respectively. These values are the highest
rate constants reported so far for charge processes at a liquid/liquid interface.
Furthermore, we have discussed the rationality of the obtained values in details.
Two equations based on different theoretical models have also been proposed
to explain the steady-state current for ion egress reactions at the nano-liquid/liquid
interface supported at nanopipettes.
Posted November 24th, 2009
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