Title of Invention


Abstract This method for fabricating an electrode for electrochemical reactor, in which the said electrode comprises a diffusion layer and a catalyst layer, consists in that the step of depositing the catalyst on the diffusion layer is carried out by the DLI-MOCVD process, the diffusion layer being made of porous carbon.
Full Text FORM 2
THE PATENTS ACT, 1970 (39 of 1970)
[See section 10, Rule 13]


28 JUL 2008

The invention relates to the field of electrochemical reactors such as fuel cells and storage batteries and more particularly the field of electrodes used in such cells. It relates more specifically to the deposition of catalyst particles constituting the active part of the electrodes of fuel cells, of the PEMFC (Proton Exchange Membrane Fuel Cell) type.
According to the invention, this deposition is carried out by the DLI-MOCVD (Direct Liquid Metal Organic Chemical Vapour Deposition) process, making it possible to immobilise the catalyst particles directly on the electron conductor support components (GDL for Gas Diffusion Layer), and thereby to optimise the use of the immobilised catalyst load and to favour the organisation of the catalyst layer for electrocatalysis.
This method, which serves to control the load of immobilised catalyst particles and the morphology of the particles, can be industrialised easily and developed for mass production of electrodes for fuel cells because it is compatible with continuous deposition processes.
The electrodes thereby obtained have a unique structure, the catalyst being in the form of nanoparticles directly dispersed on the diffusion layer.
Broadly speaking, the invention relates to any electrode material used for fuel cell and battery systems in power generation.
The material constituting the electrodes of a fuel cell operating at low temperature (PEMFC, DMFC, alkaline solid membrane battery) is produced on a carbon support based on fabric, paper or felt, which plays the role of support for the diffusion layer and ensures the mechanical strength of the electrode.
The electron conducting properties of the electrode material and of the gas diffusion material derive from this support material and from the carbon inks or pastes introduced mechanically or sprayed on the surface of the support of the diffusion layer to form the charge percolation network.

Figure 1 shows a schematic view of an assembly of an electrode of the type in question of the prior art. Microporous carbon 1 is generally sprayed on one of the faces of the diffusion layer to support the catalyst layer and to ensure good gas diffusion.
The catalyst layer is a fundamental element of the membrane-electrode assembly. Due to the presence of the catalyst particles 2 (platinum or other noble metals), the hydrogen oxidation and oxygen reduction reactions implemented in the fuel cells occur on either side of the proton conducting separating membrane 3 and thereby permit the generation of electrons.
The formulation of the catalyst layer with low loads of noble metals is one of the key factors in the development of PEMFC type fuel cell. In fact, several economic studies conducted in the early 2000s have demonstrated that the platinum introduced in the catalyst layers and the forming thereof constituted the second most costly component in the cell. A knowledge of physicochemical and electrochemical transfers occurring in the electrode materials shows that the catalyst particle content in the cell can only be reduced by optimising the morphology of the catalyst zone.
The active layer forming methods most commonly reported in the literature are based on the principle of deposition, on the diffusion layer, of a spray of C/Pt particles placed in suspension in a light solvent, such as alcohol, and incorporating a polymer binder, the latter ensuring the mechanical strength and the water management. Over the last twenty years, a sharp decrease in platinum loads in the electrode material has been achieved.
This decrease was associated with the combination of platinum nanoparticles immobilised on carbon 5 and the use of a proton conducting impregnating film 4. Thus, the catalytic site becomes active as it integrates the proton conduction network and the electron charge percolation network directly in contact with the particle. This zone is active to the extent of the accessibility of the fuel or the oxidising gas, that is, it is limited by the material input.
In present embodiments, as illustrated in Figure 1, the morphology of the active layer is unfortunately not optimal. In fact, only 50 to 75% of the platinum introduced into these active layers is recognised as electroactive. This loss of electroactivity is associated with the poor distribution of the catalyst. The various limitations have the following causes: - non-optimal electron charge transfer, the carbon percolation network then not
being continuous from the C/Pt particle to the diffusion layer and through the
diffusion layer to the bipolar plates;

or by limiting material transport, the catalyst particle no longer being reached by the gas (if for example the platinum is located opposite the carbon particle); or by a proton conduction network (obtained by impregnation with a proton conducting solution or by contact of the electrode with the membrane) preventing access to the catalyst particle.
Optimal formulations of active layers on diffusion layer support have been described. More particularly, the formulation of E-Tek electrodes, sold by DeNora, is reported in documents EP-A-0 872 906 and EP-A-0 928 036.
The literature reports the possibility of improving the performance of the cells by adjusting the methods of incorporation of the proton conductor. By optimising the Nation content incorporated in the active layer, the kinetic operating range of the fuel cell (low current density range) can be improved. However, for very low platinum loads, this improvement occurs to the detriment of the high current density range, with a limitation by mass transfer being reached more rapidly and an increase in electrode-membrane interface resistance.
The active layers have been the subject of several modelings aimed to determine their optimal organisation, by increasing the geometric surface area of the platinum developed and by minimising the resistance effects associated with the proton conductor and the carbon. Based on these modelings, new structures have been tested, either introducing multilayer structures (alternating catalyst layer and proton conducting film), or fibres impregnated with proton conductor, or porophores. The most satisfactory results were obtained by the introduction of porophoric systems into the active layers, as described in document US 2001/0031389. The mass transfer is improved, thereby serving to meet the demand for operating applications of the cells in air.
In conjunction with the idea of a more open active layer to avoid limiting material transport and to reinforce the electron charge percolation network, the possibility has been developed of directly immobilising the catalyst particles on the diffusion layer support.
This type of operation is reported in the literature with various techniques: pulsed electrodeposition, microemulsion, spray coating, vacuum deposition (EBPVD in document US - 6 610 436, CCVD described in document WO 03/015199). However, these various techniques have non-negligible drawbacks.
Microemulsion processes are not suitable for obtaining a controlled particle distribution if directly deposited on the diffusion layer.

In the case of deposits by electrodeposition, the particle size obtained is generally higher than 50 nm and therefore has low electroactivity.
For deposits by PVD, the limitation to this type of process resides in the difficulty of obtaining nanodispersions of catalyst nanoparticles and of locating the catalysts close to the membrane, without losing some depth in order to respond to a higher catalytic activity during power draws.
The ion-beam processes, as described in document US-6 673 127, do not allow a dispersion in depth, in more than 5 nm of the thickness of the diffusion layer.
The standard CVD deposition process has a particle growth yield that is too low for the deposition temperatures required by electrode supports (T It therefore clearly appears that the catalyst layers currently present in PEMFC type fuel cells, shown in Figure 1, have the drawback of immobilising a high catalyst load which remains inaccessible to the proton conduction and gas diffusion network, or blocks the electron conduction.
An obvious need therefore exists to obtain novel catalyst layer structures not having all the above drawbacks and hence to identify a deposition technology suitable for producing such structures.
Thus, according to a first aspect, the invention relates to a method for fabricating electrodes of fuel cells.
Fuel cell electrodes are defined as the seat of electrochemical reactions (oxidation of the anode and reduction of the cathode), the said reactions only being possible in the presence of a catalyst. In practice, such electrodes comprise a support ensuring the mechanical strength, comprising at least one electron conducting microporous layer, also called diffusion layer, and covered with a catalyst layer and optionally in contact with a proton conducting film.

The method according to the invention is characterized in that the step of depositing the catalyst on the diffusion layer is carried out by DLI-MOCVD, and in that the said diffusion layer is made of porous carbon.
The implementation of the DLI-MOCVD process has certainly been reported in the journal Microelectronic Engineering (64 (2002) pp 457-463), but only for obtaining continuous platinum films for applications related to ferroelectricity.
On the other hand, and in the context of the invention, this technology generates catalyst nanoparticles in a nanometric dispersion and with a rapid growth rate, which prior deposition techniques did not serve to obtain. Accordingly, according to a second aspect, the invention also relates to electrodes for fuel cells having catalyst nanoparticles dispersed in direct contact with the diffusion layer.
In the context of the invention, the type of support on which these nanoparticles are formed is important for preventing the formation of a continuous film. More particularly, the microporosity of the surface layers of the gas diffusion electrodes must be taken into account for the final structure of the electrode material.
Thus, the porous carbon of the diffusion layer on which the deposition is carried out is made for example of carbon, graphite or nanotubes. The carbon may be of the Vulcan XC 72 or Shawanagan type.
To ensure good electrochemical operation, the proton conductor must also be brought into contact with the catalyst. In the prior art, to finalise the fabrication of the electrode material, the proton conductor is sprayed into an alcohol-containing solution thereby covering the catalyst particle distribution zones. According to the invention, the catalyst particles can be deposited on a microporous layer having a proton conductor. For example, platinum particles were deposited by DLI-MOCVD on a carbon layer having an equivalent Nation® load of 0.4 mg/cm2 via a Pt(COD) with a precursor diluted in a solvent (toluene) at a temperature of 210°C. This microporous layer can be deposited by spraying a solution of carbon particles mixed with a solubilised proton conductor. The film-forming proton conductor may or may not have the same structure as the separating membrane in the cell.
Conventionally, the catalyst is advantageously selected from the group of noble metals, preferably platinum (Pt). The catalyst particles deposited are preferably monometallic.

iFurthermore, the immobilisation of platinum nanoparticles by the method of injecting organometallic liquid by CVD (DLI-MOCVD) can be carried out at high temperature, thereby providing a good bonding of the particles to the substrate. According to the invention, the deposition is therefore carried out at a temperature of preferably between 200 and 350°C.
In fact, for electrode materials, the problem arises of their aging and of the adhesion of the deposit. Studies have shown that the aging of the materials is reflected by a loss of catalyst by elution. The interface of the fuel cell electrodes being in contact with a water flow issuing either from the catalysis of the oxygen reduction, or the humidification of the gases, it is necessary to ensure the adhesion of the platinum particles. Since the production of active layers by spraying is carried out at fairly low temperatures ( The presence on the diffusion layer of a proton conductor, a material which has a well known sensitivity to temperature, implies that the method for immobilising the catalyst layer makes use of low temperature deposition, either by the use of specific low temperature precursors, or by the use of the plasma enhanced chemical vapour deposition (PECVD) process.
The principle of DLI-MOCVD is derived from conventional CVD systems. The reactive species are provided in liquid form and injected at high pressure by injectors. Thus, starting with a dilute precursor solution, the product consumption is reduced and can be controlled in volume or mass. This method therefore serves to control the morphology of the particles according to the preparation parameters (the mass of product injected, the injection frequency, the solvent of the precursor and the deposition time) and ensures a rapid and industrialisable production.
In practice, the catalyst nanoparticles are synthesised by DLI-MOCVD at atmospheric pressure or under vacuum (from 1000 Pa to 70 Pa in N2-O2 or H2-N2 mixture), with a deposition temperature of 500°C or less, using a mixture of precursors such as organometallics (type |3-diacetonates, carboxylates) soluble in a common solvent (acetyl acetone, THF, etc.), or using several independent sources of precursors, in the presence of a reaction gas mainly comprising an oxidising reactant gas (for example O2, CO2, etc.) or a reducing reactant gas (H2).

To agree with the temperature behaviour properties of polymer compounds, low temperature precursors, such as organometallics, having COT or COD arene type groups (PtCOD, PtMe2Cp, etc.), are used at the average deposition temperatures ( As already mentioned, the fabrication method according to the invention serves to tend towards an ideal structure, in which the catalyst particles 2 are directly fixed on the electron conductor support which plays the role of a gas diffusion layer 1 (Figure 2). Thus, the catalysis zone effectively corresponds to the area called the "triple contact point", where the electron exchanges, the consumption of a gas reactant and the transfer of ionic species take place.
This method serves to obtain a very specific organisation of the catalyst layer. The electrode has dispersed catalyst particles in direct contact with the diffusion layer.
More precisely and as shown in Figure 3, nanometre sized metal islands are observed (diameter lower than 50 nm, preferably between 1 and 20 nm), uniformly dispersed with an inter-particle distance of 2 to 30 nm at the surface of the microporous support formed by the diffusion layer.
The distribution of the catalyst particles is especially more advantageous when the proton conductor can be brought into contact with them. Thus and advantageously, the formulation of the microporous support for the deposition of the particles incorporates a certain content of proton conductor, preferably having the same composition as the one constituting the electrolyte membrane. To facilitate the seeding properties of the deposited particles, a plasma gas surface pre-treatment may be carried out.
The method of deposition by DLI-MOCVD serves to ensure good infiltration (above 5 µm of the particles deposited on micro- and nanoporous structures. Thus penetration depths of about 100 µm can be obtained using the method according to the invention, whereas the prior art methods only allowed for penetrations of a few microns, see for example the publication of Brault et al. in the Journal of Physics D: Applied Physics (37 (2004) pp 3419-23).
The penetration into the microporous support is distributed in a decreasing concentration gradient from the surface of the said layer, thereby meeting the various power draw conditions of the electrochemical reactor.

Due to the chemical nature of the deposited particles (noble metals or metal oxides) and the morphology of the deposits (a large number are very well dispersed nanometre sized active sites), the active layers used in the present invention appear to be highly efficient for the electro catalysis of the reactions generated in fuel cells. This performance serves to obtain electrodes having catalyst loads, particularly of platinum, not exceeding 0.2 mg/cm2 .
The fuel cells and storage batteries comprising such electrodes are also part of the invention.
The invention and the advantages thereof will appear more clearly from the exemplary embodiments that follow, provided for information and non-limiting, in conjunction with the appended figures.
Figure 1: Schematic of the membrane/electrode assembly according to the prior art.
Figure 2: Schematic of a catalyst deposit according to the invention.
Figure 3: Micrograph of a catalyst deposit obtained according to the invention.
Figure 4: Bias curve obtained in the exemplary embodiment in H2-O2.
Figure 5: Bias curve obtained in the exemplary embodiment in H2 - air (T - 80°C; P
= 4 bar absolute).
Figure 6: Platinum penetration profile in a porous carbon diffusion layer.
Figure 7: Platinum infiltration into microporous carbon, measured by X-ray analysis.
The examples presented below were prepared using a vapour deposition device sold by JIPELEC under the name "Inject, Systeme d'injection et d'evaporation de precurseurs liquides purs ou sous forme de solutions", coupled with a chemical vapour deposition chamber.
The JIPELEC device comprises several parts: the storage tank for the chemical solution, an injector (petrol, diesel) connected to the liquid tank by a feed line and controlled by an electronic control device, a carrier gas feed line, and a vaporisation device (evaporator).
The deposition chamber, which contains the substrate to be coated, comprises a heating system, a gas feed and pumping and pressure control means. The deposition chamber and the substrate are heated to a temperature above that of the evaporator, in order to create a positive thermal gradient.

|The chemical solution is introduced into the pressurised tank (2 bar in the present case), and sent via the injector or injectors by pressure differential into the evaporator.
The injection flow rate is controlled for frequency and opening time by the injector.
This type of installation can easily be inserted in a continuous production line for electrode materials.
The method used is suitable for forming large electrode surfaces (> 2 500 cm2).
In the deposition conditions stated below, the platinum (Pt) nanoparticles are prepared on a commercial diffusion layer substrate of the ELAT type (product E-Tek, sold by De
The chemical deposition solution comprises the organometallic Pt precursor (acetylacetonate), dissolved in a solvent (acetylacetone).
The temperatures of the evaporator and the substrate are set respectively at 220 °C and 340°C.
The other operating conditions of the two examples are given in Table I below:

Concentration mol/1 Injector
(Hz) Injector
opening time
(ms) N2/O2 flow rates (cc) Pressure (Pa) Deposition time (min)
Test 1 0.03 2 2 40/160 800 30
Test 2 0.03 2 2 40/160 800 20
Table I: Operating condition supplied for tests 1 and 2.
The bias curves (Figures 4 and 5), obtained in a cell test with assembly, concern electrodes according to the invention. These curves reveal an improvement in mass transports at high current densities under air pressure (Fig. 5).
This behaviour is related to the more open structure of the electrode material having a thinner catalyst layer than the standard carbon-supported platinum deposits.
The electrode material according to the invention is suitable for operation in air.

(Performance in pure oxygen (Fig. 4) is similar to that of the commercial products using carbon-supported platinum catalysts. However, it is important to note that the platinum loads are 0.17 mg/cm2 for deposition of 30 minutes and 0.11 mg/cm2 for deposition of 20 minutes respectively.
In comparison with the commercial materials prepared with carbon-supported platinum (platinum load = 0.35 mg/cm2), the electroactive surface liberated with an electrode according to the invention is therefore 40% larger.
Figure 6 and 7 illustrate the platinum penetration profiles in a porous carbon diffusion layer.
More precisely, Figure 7 shows an X-ray mapping of the platinum on microtomy section (magnification: x 1500). This is an electrode loaded with 0.15 mg/cm2 of platinum. The deposition was carried out under the following conditions: 3.5 Hz; 30 minutes; Pt(COD) precursor = dimethyl 1-5 cyclooctadiene platinum (II) in xylene in a concentration of 0.025 mol/litre, with a substrate at 244°C and under 1000 Pa. The infiltration of the catalyst into the microporous carbon is observed to reach a depth of about 100 microns. This considerable depth illustrates the advantage of the DLI-MOCVD technique compared to the other methods which only allow penetration of a few microns.
The method according to the invention and the electrodes described in the context of this invention therefore have substantial advantages. Among them, mention can be made of the following:
■ the fabrication of electrodes for PEMFC (Proton Exchange Membrane Fuel Cell) fuel cells with low catalyst load is suitable for reducing costs and for high electrocatalytic activity allowing improved performance;
■ the possibility of industrialising a continuous fabrication method;
■ the possibility of having a rapid and controllable growth rate in the context of such a device;
■ elimination of the post-sintering or pressing steps, necessary in the prior art methods;
■ improved mass transfer properties;
■ formulation of the catalyst layer support incorporating the electron charge percolation network (carbon network) and the proton transport network;
■ improved catalyst behaviour thanks to deposition at relatively high temperatures.

1. Method for fabricating an electrode for electrochemical reactor, the said electrode comprising a diffusion layer and a catalyst layer, characterized in that the step of depositing the catalyst on the diffusion layer is carried out by the DLI-MOCVD process and in that the diffusion layer is made of porous carbon.
2. Method for fabricating an electrode for electrochemical reactor according to Claim 1, characterized in that the catalyst is deposited at a temperature lower than 500°C, preferably between 200 and 350°C.
3. Method for fabricating an electrode for electrochemical reactor according to one of the preceding claims, characterized in that the catalyst is deposited under atmospheric pressure or under vacuum.
4. Method for fabricating an electrode for electrochemical reactor according to one of the preceding claims, characterized in that the deposition of the catalyst by DLI-MOCVD is carried out using low temperature precursors, such as organometallics.
5. Method for fabricating an electrode for electrochemical reactor according to one of Claims 1 to 3, characterized in that the deposition of the catalyst by DLI-MOCVD is carried out using the plasma enhanced chemical vapour deposition (PECVD) process.
6. Method for fabricating an electrode for electrochemical reactor according to one of the preceding claims, characterized in that the catalyst consists of platinum (Pt).
7. Method for fabricating an electrode for electrochemical reactor according to one of the preceding claims, characterized in that the diffusion layer is made of porous carbon incorporating proton conductor.

Method for fabricating an electrode for electrochemical reactor according to one of the preceding claims, characterized in that the porous carbon consists of carbon nanotubes.
Dated this 28th day of July, 2008






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Patent Number 259291
Indian Patent Application Number 1600/MUMNP/2008
PG Journal Number 10/2014
Publication Date 07-Mar-2014
Grant Date 06-Mar-2014
Date of Filing 28-Jul-2008
Applicant Address 25, RUE LEBLANC, IMMEUBLE LE PONANT D, 75015 PARIS
# Inventor's Name Inventor's Address
PCT International Classification Number H01M4/88
PCT International Application Number PCT/FR2007/050651
PCT International Filing date 2007-01-15
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 0650399 2006-02-03 France