A |
area (cm2) |
C* |
bulk concentration (mol cm-3) |
Cj* |
bulk concentration of species j (mol cm-3) |
D |
diffusion coefficient (cm2 s-1) |
Dj |
diffusion coefficient of species j (cm2 s-1) |
E |
electrode potential versus some reference electrode (V) |
E1/2 |
half-wave potential (V) |
E0' |
formal potential (V) |
Ep |
peak potential (V) |
Ep/2 |
potential at i = ip/2 (V) |
Epa |
anodic peak potential (V) |
Epc |
cathodic peak potential (V) |
Eeq |
equilibrium potential in a solution containing a redox couple (V) |
F |
Faraday constant (96485 C) |
i |
current (A) |
i(t) |
current as a function of time (A) |
ip |
peak current (A) |
ip/2 |
half-peak peak current (A) |
ipa |
anodic peak current (A) |
ipc |
cathodic peak current (A) |
isp |
current at the switching potential (A) |
ila |
anodic limiting current (A) |
ilc |
cathodic limiting current (A) |
ik |
kinetically limited current (A) |
j |
current density (A cm-2) |
jm |
maximum current density (A cm-2) |
kf(E) |
potential dependent heterogeneous rate constant for forward reaction (cm s-1) |
k0 |
standard heterogeneous rate constant (cm s-1) |
n |
number of electrons in an electrode reaction |
R |
molar gas constant (8.314 J mol-1 K-1) |
T |
absolute temperature (K) |
t |
time (s) |
tm |
time at maximum current density (s) |
t0 |
nucleation delay time (s) |
t' |
corrected time = t – t0 (s) |
tm' |
corrected time = tm – t0 (s) |
υ |
kinematic viscosity (cm2 s-1) |
x |
dimensionless time of the maximum |
α |
(i) dimensionless parameter; (ii) transfer coefficient |
η |
overpotential (V) |
ν |
potential scan rate (V s-1) |
ω |
angular frequency of rotation (s-1) REFERENCES |
1
K. R. Seddon, Nature Mater. 2 (2003) 363. 2
R. D. Rogers and K. R. Seddon, Science 302 (2003) 792. 3
J. S. Wilkes, Green Chem. 4 (2002) 73. 4
K. Ui, M. Ueda, R. Hagiwara, and M. Mizuhata, Molten Salts 47 (2004) 114 (in Japanese). 5 V. C. Reinsborough, Rev. Pure and Appl. Chem. 18 (1968) 281.
6
H. L. Chum and R. A. Osteryoung, “Chemical and Electrochemical Studies in Room Temperature Aluminum-Halide-Containing Melts,” in: Ionic Liquids, p. 407, D. Inman and D. G. Lovering, eds., Plenum Press, New York, 1981. 7
C. L. Hussey, “Room Temperature Molten Salt Systems,” in: Advances in Molten Salt Chemistry, Vol. 5, p. 185, G. Mamantov and C. B. Mamantov, eds., Elsevier, Amsterdam, 1983. 8
D. G. Lovering and R. J. Gale, “Introduction,” in: Molten Salt Techniques, Vol. 1, p. 1, D. G. Lovering and R. J. Gale, eds., Plenum Press, New York, 1983. 9
R. J. Gale and R. A. Osteryoung, “Haloaluminates,” in: Molten Salt Techniques, Vol. 1, p. 55, D. G. Lovering and R. J. Gale, eds., Plenum Press, New York, 1983. 10 P. Tissot, “Ionized Organic Salts,” in: Molten Salt Techniques, Vol. 1, p. 137, D.
G. Lovering and R. J. Gale, eds., Plenum Press, New York, 1983. 11
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