|
|
| Line 1: |
Line 1: |
| [[Image:Dielectric responses.svg|thumb|right|454px|A dielectric permittivity spectrum over a wide range of frequencies. The real and imaginary parts of permittivity are shown, and various processes are depicted: ionic and dipolar relaxation, and atomic and electronic resonances at higher energies. From the [http://www.psrc.usm.edu/mauritz/dilect.html Dielectric spectroscopy] page of the research group of [http://www.psrc.usm.edu/mauritz/mauritz.html Dr. Kenneth A. Mauritz].]]
| | My name is Meri from Stolk studying English Literature. I did my schooling, secured 74% and hope to find someone with same interests in Shortwave listening.<br><br>Feel free to visit my homepage - [http://harlesflowers.com/2013/10/29/hello-world/ FIFA coin generator] |
| | |
| '''Dielectric spectroscopy''' (sometimes called '''impedance spectroscopy'''), and also known as '''electrochemical impedance spectroscopy (EIS)''', measures the [[dielectric]] properties of a medium as a function of [[frequency]].<ref name="Kremer F. 2002">Kremer F., Schonhals A., Luck W. Broadband Dielectric Spectroscopy. – Springer-Verlag, 2002.</ref><ref>Sidorovich A. M., Dielectric Spectrum of Water. – Ukrainian Physical Journal, 1984, vol. 29, No 8, p. 1175-1181 (In Russian).</ref><ref>Hippel A. R. Dielectrics and Waves. – N. Y.: John Willey & Sons, 1954.</ref><ref>Volkov A. A., Prokhorov A. S., Broadband Dielectric Spectroscopy of Solids. – ''[http://www.springer.com/astronomy/journal/11141 Radiophysics and Quantum Electronics]'', 2003, vol. 46, Issue 8, p. 657–665.</ref> It is based on the interaction of an external field with the electric [[Electric dipole moment|dipole moment]] of the sample, often expressed by [[permittivity]].
| |
| | |
| It is also an experimental method of characterizing electrochemical systems. This technique measures the [[Electrical impedance|impedance]] of a system over a range of frequencies, and therefore the frequency response of the system, including the energy storage and dissipation properties, is revealed. Often, data obtained by EIS is expressed graphically in a [[Bode plot]] or a [[Nyquist plot]].
| |
| | |
| Impedance is the opposition to the flow of [[alternating current]] (AC) in a complex system. A passive complex electrical system comprises both energy dissipater ([[resistor]]) and energy storage ([[capacitor]]) elements. If the system is purely resistive, then the opposition to AC or [[direct current]] (DC) is simply [[Electrical resistance|resistance]].
| |
| | |
| Almost any physico-chemical system, such as [[electrochemical cell]]s, [[mass-beam oscillator]]s, and even biological tissue possesses energy storage and dissipation properties. EIS examines them.
| |
| | |
| This technique has grown tremendously in stature over the past few years and is now being widely employed in a wide variety of scientific fields such as [[fuel cell]] testing, biomolecular interaction, and microstructural characterization. Often, EIS reveals information about the reaction mechanism of an electrochemical process: different reaction steps will dominate at certain frequencies, and the frequency response shown by EIS can help identify the rate limiting step.
| |
| | |
| == Dielectric mechanisms ==
| |
| | |
| There are a number of different dielectric mechanisms, connected to the way a studied medium reacts to the applied field (see the figure illustration). Each dielectric mechanism is centered around its characteristic frequency, which is the reciprocal of the [[characteristic time]] of the process. In general, dielectric mechanisms can be divided into [[dielectric relaxation|relaxation]] and [[resonance]] processes. The most common, starting from high frequencies, are:
| |
| | |
| === Electronic polarization ===
| |
|
| |
| This resonant process occurs in a neutral [[atom]] when the electric field displaces the [[electron density]] relative to the [[Atomic nucleus|nucleus]] it surrounds.
| |
| | |
| This displacement occurs due to the equilibrium between restoration and electric forces.
| |
| Electronic polarization may be understood by assuming an atom as a point nucleus surrounded by spherical electron cloud of uniform charge density.
| |
| | |
| === Atomic polarization ===
| |
| | |
| Atomic polarization is observed when the nucleus of the atom reorients in response to the electric field. This is a resonant process. Atomic polarization is intrinsic to the nature of the atom and is a consequence of an applied field. Electronic polarization refers to the electron density and is a consequence of an applied field. Atomic polarization is usually small compared to electronic polarization.
| |
| | |
| === Dipole relaxation ===
| |
| | |
| This originates from permanent and induced [[dipole]]s aligning to an electric field. Their orientation polarisation is disturbed by thermal noise (which mis-aligns the dipole vectors from the direction of the field), and the time needed for dipoles to relax is determined by the local [[viscosity]]. These two facts make dipole relaxation heavily dependent on [[temperature]], [[pressure]]<ref>Floudas G., Paluch, M., Grzybowski A., Ngai K. L. Molecular Dynamics of Glass-Forming Systems - Effects of Pressure. Springer-Verlag, 2011.</ref> and chemical surrounding.
| |
| | |
| === Ionic relaxation ===
| |
| | |
| Ionic relaxation comprises [[ionic conductivity]] and interfacial and space charge relaxation. Ionic conductivity predominates at low frequencies and introduces only losses to the system. Interfacial relaxation occurs when charge carriers are trapped at interfaces of heterogeneous systems. A related effect is [[Maxwell-Wagner-Sillars polarization]], where charge carriers blocked at inner dielectric boundary layers (on the mesoscopic scale) or external electrodes (on a macroscopic scale) lead to a separation of charges. The charges may be separated by a considerable distance and therefore make contributions to the dielectric loss that are orders of magnitude larger than the response due to molecular fluctuations.<ref name="Kremer F. 2002"/>
| |
| | |
| === Dielectric relaxation ===
| |
| | |
| [[Dielectric relaxation]] as a whole is the result of the movement of dipoles (dipole relaxation) and electric charges (ionic relaxation) due to an applied alternating field, and is usually observed in the frequency range 10<sup>2</sup>-10<sup>10</sup> Hz. Relaxation mechanisms are relatively slow compared to resonant electronic transitions or molecular vibrations, which usually have frequencies above 10<sup>12</sup> Hz.
| |
| | |
| == Principles ==
| |
| === Steady-state ===
| |
| | |
| For a redox reaction
| |
| R <math> \leftrightarrow </math> O + e, without mass-transfer limitation, the relationship between the current density and the electrode overpotential is given by the [[Butler-Volmer equation]]:
| |
| | |
| <math>
| |
| j_{\text{t}}=j_0\left(\exp(\alpha_{\text{o}}\,f\, \eta)-\exp(-\alpha_{\text{r}}\,f\,\eta)\right)
| |
| </math>
| |
| | |
| with | |
| | |
| <math> \eta=E-E_{\text{eq}} ,\;f=F/(R\,T),\;\alpha_{\text{o}}+\alpha_{\text{r}}=1</math>.
| |
| <math>j_0</math> is the exchange current density and <math>\alpha_{\text{o}}</math> and <math>\alpha_{\text{r}}</math> are the symmetry factors.
| |
| | |
| [[Image:ButlerVolmer1.png|thumb|300px|Fig. 1 : Steady-state current density vs. overpotential for a redox reaction.]]
| |
| | |
| The curve <math> j_{\text{t}}\; vs.\; E </math> is not a straight line (Fig. 1), therefore a redox reaction is not a linear system.<ref>[http://www.bio-logic.info/potentiostat/notes/Application%20note%209.pdf Linear vs. non-linear systems in impedance measurements]{{dead link|date=November 2011}}</ref>
| |
| | |
| === Dynamic behavior ===
| |
| ==== Faradaic impedance ====
| |
| | |
| Let us suppose that the Butler-Volmer relationship correctly describes the dynamic behavior of the redox reaction :
| |
| | |
| <math>
| |
| j_{\text{t}}(t)=j_{\text{t}}(\eta(t))=j_0\,\left(\exp(\alpha_{\text{o}}\,f\, \eta(t))-\exp(-\alpha_{\text{r}}\,f\,\eta(t))\right)
| |
| </math>
| |
| | |
| Dynamic behavior of the redox reaction is characterized by the so-called charge transfer resistance defined by :
| |
| | |
| <math>
| |
| R_{\text{ct}}=\frac{1}{\partial j_{\text{t}}/\partial \eta }=
| |
| \frac{1}{f\,j_0\,\left(\alpha_{\text{o}}\,\exp(\alpha_{\text{o}}\,f\, \eta)+\alpha_{\text{r}}\,\exp(-\alpha_{\text{r}}\,f\, \eta) \right)}
| |
| </math>
| |
| | |
| The value of the charge transfer resistance changes with the overpotential. For this simplest example the Faradaic impedance is reduced to a resistance. It is worthwhile to notice that:
| |
| | |
| <math>
| |
| R_{\text{ct}} = \frac{1}{f\,j_0}
| |
| </math>
| |
| | |
| for <math> \eta = 0</math> .
| |
| | |
| ==== Double layer capacitance ====
| |
| | |
| An electrode <math> | </math> electrolyte interface behaves like a capacitance called [[Electrical double layer|electrochemical double-layer]] capacitance <math> C_{\text{dl}}</math>. The [[equivalent electrical circuit]] for the redox reaction taking account of the double-layer capacitance is shown in Fig. 2. Another analog circuit commonly used to model the electrochemical double-layer is called a [[constant phase element]].
| |
| | |
| [[Image:CircuitRctCdlparallele.png|thumb|300px|Fig. 2 : Equivalent circuit for a redox reaction without mass-transfer limitation.]]
| |
| | |
| The electrical impedance of this circuit is easily obtained remembering the impedance of a capacitance which is given by :
| |
| | |
| <math>
| |
| Z_{\text{dl}}(\omega) =\frac{1}{\text{i}\,\omega\, C_{\text{dl}}}
| |
| </math>
| |
| | |
| where <math> \omega </math> is the angular frequency of a sinusoidal signal (rd/s), and <math>\scriptstyle{ \text{i}=\sqrt{-1}} </math>.
| |
| It is obtained:
| |
| | |
| <math>
| |
| Z(\omega)=\frac{R_{\text{t}}}{1+R_{\text{t}}\,C_{\text{dl}}\,\text{i} \,\omega}
| |
| </math>
| |
| | |
| Nyquist diagram of the impedance of the circuit shown in Fig. 3 is a semicircle with a diameter <math>\scriptstyle{R_{\text{t}}} </math> and an angular frequency at the apex equal to <math>\scriptstyle{1/(R_{\text{t}}\,C_{\text{dc}})}</math> (Fig. 3). Others representations, [[Bode plot|Bode]] or Black plans can be used.<ref>{{cite web|url=http://www.bio-logic.info/potentiostat/notes/Application%20note%204.pdf |title=Potentiostat stability mystery explained |format=PDF |date= |accessdate=2011-11-08}}{{dead link|date=January 2014}}</ref>
| |
| | |
| [[Image:ZRctCdlparallele.png|thumb|300px|Fig. 3 : Electrochemists Nyquist diagram of a RC parallel circuit. The arrow indicates increasing angular frequencies.]]
| |
| | |
| ==== Ohmic resistance ====
| |
| | |
| The ohmic resistance <math> R_\Omega </math> appears in series with the electrode impedance of the reaction and the Nyquist diagram is translated to the right.
| |
| | |
| == Measurement of the impedance parameters ==
| |
| | |
| Plotting the Nyquist diagram with a [[potentiostat]]<ref>[http://www.bio-logic.info/potentiostat/notes/20101105%20-%20application%20note%208.pdf Impedance, admittance, Nyquist, Bode, Black, etc.]{{dead link|date=January 2014}}</ref> and an [[impedance analyzer]], most often included in modern potentiostats, allows the user to determine charge transfer resistance, double layer capacitance and ohmic resistance. The exchange current density <math>j_0</math> can be easily determined measuring the impedance of a redox reaction for <math>\eta=0</math>.
| |
| | |
| Nyquist diagrams are made of several arcs for reaction more complex than redox reaction and with mass-transfer limitation.
| |
| | |
| == See also ==
| |
| *[[loss tangent]]
| |
| * [[Debye relaxation]]
| |
| * [[Ellipsometry]]
| |
| * [[Linear response function]]
| |
| * [[Kramers–Kronig relation]]
| |
| * [[Green–Kubo relations]]
| |
| * [[Electrochemistry]]
| |
| * [[Potentiostat]]
| |
| | |
| == References ==
| |
| {{reflist}}
| |
| | |
| {{DEFAULTSORT:Dielectric Spectroscopy}}
| |
| [[Category:Spectroscopy]]
| |
| [[Category:Electric and magnetic fields in matter]]
| |
| [[Category:Electrochemistry]]
| |