Classifications

• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
  • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
  • G01N27/28—Electrolytic cell components
  • G01N27/30—Electrodes, e.g. test electrodes; Half-cells
  • G01N27/301—Reference electrodes

Definitions

• the invention relates to a miniature reference electrode for measuring potentials in electrochemical systems.
• a reference electrode is the measurement of electrode potentials in electrochemical systems.
• the potential of a working electrode in an electrochemical cell is defined relative to the reference electrode, by measuring the voltage between the working electrode and the reference electrode.
• the reference electrode mainly comprises a pair of oxidation-reduction materials having a constant potential and an internal electrolyte.
• the silver / silver chloride (Ag / AgCl) pair is widely used because of its high stability and reversibility of reaction.
• the electrolyte is a saturated solution of potassium chloride (KCl) or sodium chloride (NaCl). Since the potential of the electrode varies as a function of the concentration of chloride ions contained in the electrolyte, it must be as stable as possible.
• a porous membrane called a liquid junction, is conventionally used to separate the internal electrolyte from the electrolyte of the cell. This membrane allows the exchange of protons (H + ) between the two electrolytes. It slows the diffusion of the ions (K + , Na + , CI " ...) between the cell and the reference electrode, to maintain a constant reference potential.
• FIG. 1 shows an exploded view of a miniature reference electrode as described in US6419809.
• This electrode consists of thin layers deposited successively on a glass substrate 2.
• the electrode comprises a layer 4 of silver of which a portion 4 'is converted into silver chloride AgCl.
• the portion 4 ' is in contact with an electrolyte layer 6 through a slot 8 formed in a polyimide layer 10.
• the layer 6 is impregnated with a saturated solution of potassium chloride (KCl).
• the layer 10 comprises a recess at one of its ends for housing a membrane 12 of hydrophilic and porous polymeric material. A portion of the membrane 12 is covered with the electrolyte layer 6.
• the porous membrane 12 is impregnated with the KCl electrolyte.
• an end of the membrane 12 is immersed in an aqueous solution 14 constituting the electrolyte of the cell. A proton transfer between the internal electrolyte 6 and the electrolyte 14 of the cell is then possible via the membrane 12.
• Nafion membranes are used in a similar manner in PEMFC fuel cells (Proton Exchange Membrane Fuel Cell) between two catalytic layers, which are the seat of oxidation and reduction reactions.
• the membrane separates the two compartments of the cell and allows only the protons to pass through.
• the Nafion membrane is effective only for a short time, given its small thickness. The use of a greater thickness of Nafion is constrained by the effort of miniaturization and a significant cost of the material.
• the miniature reference electrode can be incorporated into batteries for health monitoring or control of charge and discharge cycles. Batteries having a life span of up to several years, it is sought to obtain a reference electrode which remains reliable over such a long period.
• a reference electrode comprising a reference electrolyte and a proton exchange membrane arranged to separate the reference electrolyte from an external medium to the electrode, the proton exchange membrane comprising particles of acid-doped polyaniline distributed in a binder polymer material.
• the method comprises the steps of making a mixture of an acid-doped polyaniline powder and a polymerizable liquid material, depositing a layer of the mixture on a reference electrolyte layer and polymerization of the mixture.
• FIG. 1 previously described, represents a an exploded view of a miniature reference electrode according to the prior art
• FIG. 2 diagrammatically represents a test cell of a proton exchange membrane used in a miniature reference electrode according to the invention
• FIG. 3 represents the impedance modules of an electrode according to the invention and of several electrodes.
• FIG. 4 represents a sectional view of an electrode embodiment according to the invention
• FIGS. 5 and 6 show, respectively in sectional view and in diagrammatic top view, a half -electrode according to an alternative embodiment
• Figure 7 shows schematically an assembly of two half-electrodes according to Figures 5 and 6.
• polyaniline-based separating membrane PANI
• acid-doped polyaniline means a salt resulting from the reaction of the polyaniline with an acid.
• This form of polyaniline has good proton conductivity.
• it is perfectly adapted to the conditions of use in a reference electrode. On the one hand, it is insoluble in water, alkaline or acid solutions and most organic solvents. On the other hand, it resists oxidation and reduction reactions, especially with oxygen in the atmosphere. Subsequently, the terms "PANI” or "polyaniline” will be used to denote acid-doped polyaniline.
• Polyaniline is an electrically conductive polymer that can be used as an electrode.
• its use as a proton exchange membrane in PEMFC cells is not possible since a short circuit would be caused between the electrodes of the battery.
• polyaniline in a reference electrode as a membrane.
• the polyaniline is in the form of particles and the membrane comprises a polymer matrix in which the particles are dispersed.
• the ratio of the mass of polyaniline to the polymer mass is advantageously between 1 and 2. The membrane thus obtained is then compact and non-porous, unlike conventional membranes.
• the porosity with water and sulphate ions which corresponds to the permeability of the membrane, can be evaluated as follows: a tube containing a solution of sulfuric acid of 5 mol / L (5 MH 2 SO 4) and closed by a membrane based on PA I is immersed in a beaker containing deionized water. The pH of the water is measured a few minutes after plunging the membrane into the water and then after one week. The pH remains constant, indicating that the PANI-based membrane is impervious to sulfate ions (SO4 2 " , HS0 4 " ) -
• the proton conductivity is the magnitude characterizing the ability of the membrane to allow the passage of protons. It is directly related to the electrical resistance of the membrane. Moreover, the membrane is generally the most resistive element of the reference electrode and a high resistance of the electrode leads to an error in the potential measurements. So we try to minimize this resistance.
• PANI-based membrane being non-porous, it is proposed to evaluate its impedance to verify its ability to be part of a reference electrode.
• FIG. 2 represents an experimental electrochemical cell making it possible to determine the impedance of a PANI-based membrane.
• the cell comprises a tube 14 approximately 8 mm in diameter. One end of the tube 14 is sealed with a membrane 16 made of epoxy resin and PANI (1: 1 ratio), about 1 mm thick.
• a lead wire 18 in the form of spirals is disposed inside the tube and partially immersed in an electrolyte 20 of 5 M H2SO4. The tube 14 is then immersed in the same electrolyte 20, so that the membrane 16 is completely immersed. The lead wire 18 then constitutes a working electrode.
• the cell is completed by a platinum counter-electrode 24 immersed in the electrolyte 20. In this configuration, the membrane 16 is the most resistive element of the cell.
• the impedance of the membrane 16 can be determined by measuring the impedance of the electrochemical cell of FIG. 2. Indeed, these are substantially identical since the membrane is on each side in contact with the electrolyte 20 and in the immediate vicinity of the conductive parts. The ohmic drop due to the H2SO4 electrolyte is negligible.
• the method used is impedance spectroscopy over a frequency range from 0.1 Hz to 65 kHz using a sinusoidal signal with an amplitude between 5 and 10 mV.
• FIG. 3 represents the impedance (expressed by its module) of the cell of FIG. 2 (Pb / H 2 SO 4 + PANI).
• Conventional electrodes using porous membranes were measured for comparison, including Ag Ag2S0 electrodes 4 and Hg / Hg2S0 4 with membranes of graphite or ceramic.
• Two types of graphite are used: a graphite of high porosity (A) and a graphite of low porosity (B).
• the ohmic resistance of the PANI membrane reaches values between those of the conventional electrodes Hg / Hg 2 S0 4 and Ag / Ag 2 S0 4 .
• the PANI-based membrane thus achieves similar performance in terms of strength. Its use to form a precise reference electrode is therefore possible.
• the realization of a membrane based on PANI can pose some difficulties.
• the acid-doped polyaniline is generally obtained by electrochemical synthesis. It is then in the form of an electrolytic deposit on electrodes.
• the material obtained is hard and friable, which makes it difficult to use in the form of a membrane.
• the polyaniline is also synthesized electrochemically. It is possible, for example, to obtain a layer of approximately 1.5 mm PANI on graphite electrodes immersed in a bath comprising aniline sulphate solution (0.15 mol / L) and a sulfuric acid electrolyte. (0.25 mol / L), applying a current of the order of 1 mA.crr ⁇ 2 for a period of 300h.
• the deposit thus formed is ground in the form of a powder.
• the particle size of the powder is variable.
• the PANI powder is then mixed with a polymerizable material in liquid form to form a paste.
• the paste is deposited in the form of a layer.
• the polymerization of the paste is carried out, preferably by heat treatment at a temperature between 60 ° C and 80 ° C or by ultraviolet irradiation. A dense and non-porous structure due to the polymerization process is then obtained.
• the polymerizable material is preferably an acid or radical activated prepolymer. It is also preferable that the material is stable in the acid electrolytes and that it preserves the proton conductivity of the PANI. Pre-polymers based on phenol-furfural, phenol-formaldehyde, methyl methacrylate or acid-hardened epoxy resin meet these criteria. In addition, with these prepolymers, the paste is perfectly suited to inexpensive printing technologies, including screen printing.
• the electrochemical synthesis of the polyaniline can be adapted to the desired type of electrode.
• a precursor (the source of aniline) and an electrolyte are preferably chosen depending on the oxidation-reduction torque and the nature of the internal electrolyte.
• the electrode is Ag / Ag2SO4 H2SO4
• the precursor may be aniline sulfate and the electrolyte may be H2SO4.
• the precursor contains an ion identical to one of the ions of the internal electrolyte and the electrolyte of the synthesis is of the same nature as the internal electrolyte.
• the polyaniline is doped with the same ion as one of the ions of the internal electrolyte.
• it is the sulfate ion, also present in the salt of the redox couple. It minimizes the exchanges between anions at the interface between the PANI and the electrolyte, these exchanges usually creating a harmful interface potential.
• FIG. 4 shows an embodiment of a miniature reference electrode provided with a PANI-based membrane.
• the electrode is formed on a substrate 2 made of glass or silicon covered with a passivation layer of a thickness of about 1 mm.
• the layers constituting the electrode are preferably deposited by screen printing.
• a cavity having a depth of approximately 300 ⁇ m is first etched in the substrate 2.
• a silver layer 4, approximately 30 ⁇ m thick, is then deposited at the bottom of the cavity.
• a layer 4 'of silver sulphate, approximately 60 ⁇ m thick, is deposited on a portion of the layer 4.
• An electrical contact pad 26, for example copper, is also formed on the silver layer 4 , at one end of the electrode.
• a layer 6, for example glass microfibers, is then deposited on the entire layer 4 '. Its thickness is of the order of 210 pm.
• An electrically insulating layer 28, preferably of polymer, covers the pad 26 and a portion of the layer 4 located between the pad and the layer 4 '. A side face of the pad 26 corresponding to the edge of the electrode is exposed to the ambient environment.
• an electrolytic solution (H2SO4) is inserted into the layer 6 to form the electrolyte layer. This insertion can be performed by inkjet printing or using a micro-syringe.
• the substrate 2, the electrolyte layer 6 and the insulating layer 28 form a surface, preferably flat, on which is deposited a layer of PANI-based paste, so as to completely seal the electrolyte 6.
• the paste is then polymerized to form the membrane 16.
• the thickness of the membrane 16 is preferably between 0.5 and 1 mm. The short circuits between the pad 26 and the layer 6 and between the pad 26 and the membrane 16 are avoided by the insulating layer 28.
• the membrane 16 comprises, by mass, twice as much PANI as polymer.
• a metal current collector is fixed to the contact pad 26, for example by welding.
• the reference electrode is, moreover, covered by a protective envelope, plastic for example.
• the envelope preferably covers the whole of the electrode except for a portion of the membrane 16, placed directly above the layer 4 '.
• This reference electrode has a large contact area between the electrolyte of the cell and the membrane 16, which decreases the electrical resistance of the latter.
• Figures 5 to 7 illustrate an alternative embodiment of a reference electrode, composed of two identical halves which are then glued.
• Figures 5 and 6 show, respectively in sectional view and diagrammatic top view, a half electrode while Figure 7 shows the assembled reference electrode.
• Each half electrode comprises a substrate 2 in which are formed two distinct cavities with a depth of about 300 ⁇ m, each cavity opening on one end of the electrode.
• a cavity (on the right in FIGS. 5 and 6) is filled by the contact pad 26.
• a first layer 6a of glass microfibers, the 4 'layer of silver sulphate (50-100 ⁇ m thick) and the layer 4 of silver (20-50 ⁇ m thick) are deposited successively in the other cavity (left).
• the layer 4 covers the layer 4 ', the pad 26 and the portion of the substrate located between the two.
• a second layer 6b of glass microfibers and the membrane 16 (300 ⁇ m thick) are deposited at the end opposite the pad 26, preferably up to the level of the layer 4.
• the polymerization of the membrane is carried out as described above, as is the filling of the microfiber layers 6a and 6b with the liquid electrolyte.
• FIG. 6 shows that the glass microfibers layer is preferably divided into two parts 6c and 6d separated by the membrane 16. Part 6c, at the end of the electrode, protects the membrane 16 from contact direct with the other electrodes of the cell.
• the layers 4 and 4 ' can be arranged as laterally spaced strips in the portion 6d of about 50 ⁇ m. In this way, the step of filling the portion 6d with the internal electrolyte is facilitated.
• the two half-electrodes are secured by their layers 4 in a sealed manner, by example by gluing.
• a current collector and a protective envelope are attached to the electrode, as described in connection with FIG. 4.
• the unprotected portion of the electrode corresponds to the portion 6c of the electrolyte layer, which is in contact with the electrode. electrolyte of the cell.
• the method for producing the reference electrode described above may comprise steps common with other methods of producing electrodes.
• a reference electrode, a working electrode and a counter-electrode can be produced on a large scale simultaneously on the same substrate.
• a complete electrochemical device, for example a chemical detector, can thus be produced by these simple and inexpensive techniques.
• the embodiment has been described in relation to the silver / silver sulphate pair and the H2SO4 electrolyte.
• the invention is not limited to a particular type of electrodes. Ag / AgCl, Ag / AgBr, Ag / Ag and the electrolytes HCI, HBr, H1 can also be used.
• other porous (solid) materials serving as a container for the electrolyte internal (liquid), can be used, including glass in the form of microbeads made porous by chemical etching and acting as a reservoir.

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• 2010
  • 2010-07-16 FR FR1003007A patent/FR2962806B1/fr not_active Expired - Fee Related
• 2011
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