Localization of Electrochemical Reactions in Electrocatalytic Processes on Nanocomposite Electrodes

Electrochemical power sources and fuel cells, in which electrocatalytic processes take place, belong to alternative or minor energetics. At the present time, the power generated by all current sources in the world equals the power generated by all nuclear, thermal and water power stations. In view of the sharp deterioration of the environmental conditions and depletion of oil and gas resources, which give rise to energy crisis, the development of electrochemical generators becomes very topical. Electrocatalytic reactions and processes are the basis of any electrochemical energy generation system. Research in the field of developing highly efficient catalysts has been done for a long time and fairly successfully. But it is of semi empirical character. The review on electrocatalysis[1] shows that the main mechanism with the aid of which the laws governing it were explained was based on the activated-chemisorption model. At the present time, a number of papers[2-4] show an alternative mechanism, which is known as incipient hydrous oxide/adatom mediator (IHOAM) model[5]. The need for new approaches to catalysis became necessary after Haruta et al[6] had revealed an astonishing catalytic activity of gold nanoparticles deposited onto substrates. Describing IHOAM in their paper, Burke et al[5] laid special emphasis on the role of nonequilibrium surface states of metal, in which active atoms on the surface may undergo fast redox electron transitions at low potentials and serve as mediators in electrocatalytic processes. Surface atoms or oxide groups (active centers) are regarded not merely as “anchors” for adsorption; these particles with low surface coverage undergo chemical or electrochemical transformations as a part of electro-catalytic processes. References[7,8] propose two mechanisms for platinum: activated chemisorption and IHOAM, which act for different reactions at this catalyst. RefInstitute of General & Inorganic Chemistry of National Academy of Science, Kyiv, Ukraine


Introduction
Electrochemical power sources and fuel cells, in which electrocatalytic processes take place, belong to alternative or minor energetics. At the present time, the power generated by all current sources in the world equals the power generated by all nuclear, thermal and water power stations. In view of the sharp deterioration of the environmental conditions and depletion of oil and gas resources, which give rise to energy crisis, the development of electrochemical generators becomes very topical. Electrocatalytic reactions and processes are the basis of any electrochemical energy generation system. Research in the field of developing highly efficient catalysts has been done for a long time and fairly successfully. But it is of semi empirical character.
The review on electrocatalysis [1] shows that the main mechanism with the aid of which the laws governing it were explained was based on the activated-chemisorption model. At the present time, a number of papers [2][3][4] show an alternative mechanism, which is known as incipient hydrous oxide/adatom mediator (IHOAM) model [5] . The need for new approaches to catalysis became necessary after Haruta et al [6] had revealed an astonishing catalytic activity of gold nanoparticles deposited onto substrates. Describing IHOAM in their paper, Burke et al [5] laid special emphasis on the role of nonequilibrium surface states of metal, in which active atoms on the surface may undergo fast redox electron transitions at low potentials and serve as mediators in electrocatalytic processes. Surface atoms or oxide groups (active centers) are regarded not merely as "anchors" for adsorption; these particles with low surface coverage undergo chemical or electrochemical transformations as a part of electro-catalytic processes. References [7,8] propose two mechanisms for platinum: activated chemisorption and IHOAM, which act for different reactions at this catalyst. Ref-Institute of General & Inorganic Chemistry of National Academy of Science, Kyiv, Ukraine 2 erence [9] shows the role of intensive parameters, such as Tafel slope and zero-charge point for oxide electrodes, with the aid of which electron and geometric factors in electrocatalysis can be separated. As follows from these papers, however, there is no unified theory which makes it possible to describe electrocatalytic processes.
It is known that all electrocatalytic processes are based on the compromise potential of the electrochemical reactions proceeding at the electrode. The value of this compromise potential depends on the potentials of the electrochemical reactions that proceed simultaneously at this electrode. Therefore, by localizing electrochemical reactions or varying their route one can influence the electrocatalytic properties of the material.
The aim of our work was to study and substantiate the effect of change or localization of the route of electrochemical reactions on the electrocatalytic properties of nanocomposites materials.

Experimental
Multiwalled carbon nanotubes (MWCNT) were used as the catalyst support. They were prepared by catalytic ethylene pyrolysis on a catalyst [10] . The product was obtained as black powder with a bulk density of 25-30 g dm -3 . The outer diameter of nanotubes was about 10-30 nm, the specific surface was 230 m 2 g -1 , and the mineral impurity content of unpurified product was 15-20 wt%. The catalyst impurities were removed from MWCNTs by treatment with a hydrofluoric acid solution. The oxygen electrodes were prepared by pressing. The hydrophobic layer contained 0.07 g cm -2 acetylene black with 25% polytetrafluoroethylene, and the active layer contained 0.02 g cm -2 MWCNTs, modified by manganese dioxide, with 5% polytetrafluoroethylene. The hydrogen electrodes were prepared by pressing from various compositions based on MWCNTs and catalysts with addition of 25% polytetrafluoroehylene as binder. The investigations were carried out in a fuel cell mockup. The mockup for testing gas-diffusion electrodes is described in Ref [11] . The electrolyte was a solution of analytical grade 6M KOH. For the oxygen electrode, zinc was used as the auxiliary electrode. For the hydrogen electrode, the auxiliary electrode was a nickel oxide electrode. In all investigations, the reference electrode was a silver-chloride electrode connected through a salt bridge. All potentials are given with respect to silver-chloride reference electrode. The electrochemical curves were taken under galvanostatic conditions. The hydrogen and oxygen source was a U-shaped electrolyzer with alkaline electrolyte. Hydrogen and oxygen were supplied to the gas electrodes under an excess pressure of 0.01 mPa. Before operation, the gas electrodes were blown through with appropriate gas for an hour. In electrochemical tests, the electrolyzer current exceeded by a factor of three the current generated at the gas electrode. The study of the polarization curves were performed on potentiostat P-8S Elins (Russia) on a standard three-electrode scheme. As auxiliary electrode used cylindrical platinum electrode with area of 7 cm 2 . The linear polarization and chronopotentiometry technique were employed to determine the electrode process kinetics. The linear polarization was performed between the steady potential in 6M KOH solution to +0.5 V with scan rate of 1 mV/s. In all investigations, the reference electrode was a silver-chloride electrode connected through a salt bridge. The intermetallic compound La 0.84 Co 0.16 Ni 4.83 Fe 0.04 with a gravimetric composition of under 40 nm was investigated as a hydride electrode material for nickel-metal hydride batteries. Coatings were deposited on intermetallic compound particles by chemical reduction from aqueous solutions of metal salts with reductants. The electrodes made of these materials were tested in a nickel-metal hydride battery mockup under galvanostatic conditions. The charge and discharge current magnitude was the same (100 mA cm -2 ). A cermet nickel oxide electrode was prepared by pressing powders onto a nickel net. A PTFE emulsion was used as the binder. Before the beginning of investigations, five training charge-discharge cycles were performed. The tests were carried out in a 5M solution of potassium hydroxide with addition of 1M lithium hydroxide [12] .

Results and Discussion
During the electrocatalytic reaction at the electrode, the reagent supply stage, the electrochemical act of electron transfer, and reagent withdrawal take place. By using a heterogeneous catalyst-support composites with different energy barriers for different electrochemical reaction stages one can change the catalytic activity of this composites. The principle of reaction localization manifests itself to the greatest extent in nanostructured catalytic compositions, which is associated with rapid diffusion of reactant across the interface between catalyst and support particles. Carbon-base nanomaterials with deposited catalysts are best suited for such composites. Consider the following examples of the application of the principle of electrochemical reaction localization: 1. For oxygen reduction reaction, which proceeds in fuel cell oxygen electrodes; 2. For hydrogen oxidation reaction, which proceeds in fuel cells at hydrogen electrodes; 3. For hydride formation reaction, which proceeds at the hydride electrode of nickel-metal hydride battery.
Consider the principle of reaction localization for the oxygen electrode of a fuel cell. The use of a heterogeneous composites of carbon-base material and catalyst with high oxygen evolution overpotential makes it possible to localize electrochemical reactions. In this case, adsorption of molecular oxygen on the carbon support will take place, and at the catalyst with high oxygen evolution overpotential, electron attachment with bond rupture takes place, which accelerates the oxygen ionization process.
Therefore, the most active catalysts for oxygen reduction in an alkaline medium for oxygen electrode are materials with high molecular oxygen evolution overpotential in alkaline medium, i.e. materials with high value of the coefficient a in the Tafel equation: If a series of metals is made up in order of increasing oxygen evolution overpotential in alkaline medium, it will be as follows [13] : Co < Fe < Ni < Cd < Pb < Au < Pt [2] The catalytic activity of these metals will also increase for oxygen electrode in alkaline medium. The value of the coefficient a depends on the nature of material, specific surface, J Nanotech Mater Sci | volume 2: issue 2 Localization of Electrochemical Reactions www.ommegaonline.org orientation of the single-crystal faces, solution composition, the degree of surface oxidation [13] . Metals and oxides were used as catalyst for investigations. Platinum, nickel and lead were chosen from metals [14,15] . Manganese [16] , molybdenum [17] , chromium [18] , cobalt and niobium oxides were used as metal oxides. The catalysts were deposited by electrochemical and chemical methods developed by us [14][15][16][17][18] . As an example, we chose MWCNTs with deposited manganese dioxide (Figure 1) [16] , which has a high oxygen evolution overpotential and hence a high catalytic activity. From the above series of catalysts [2] we chose for comparison the cheapest material (lead). A nanocomposites of carbon nanotubes with 10% lead content was prepared by the method of reduction of metal compounds [16] . Figure 2 shows current-potential curves for oxygen electrodes based on a composites of MWCNT s with 10% manganese dioxide ( Figure 2, curve 1) and MWCNTs with 10% lead content ( Figure 2, curve 2). As is seen from Figure 2, the electrodes containing a 10% nanocomposites of lead and MWCNTs operate at current densities of over 150 mA cm -2 better than the composites based on manganese dioxide with MWCNTs. Thus, the fact that lead, which has a high oxygen evolution overpotential, has a better catalytic activity in the oxygen reduction reaction supports the principle of reaction localization. Figure 3 shows plots of potential against current density for oxygen electrodes with active mass based on composites of carbon nanotubes with different catalysts deposited on them: metallic platinum, lead, nickel (  Table 1 lists values of the coefficient a, obtained by us, for oxygen evolution at a Ni electrode with different materials deposited on the surface and electrical characteristics of oxygen electrodes fabricated from nanocomposites based on carbon nanotubes with the same catalysts deposited on them. As is seen from Fig. 3 and Table 1, there is a correlation between the value of the coefficient a for molecular oxygen evolution at the materials under investigation and the electrical characteristics of oxygen electrodes based on nanocomposites of the same materials deposited on carbon nanotubes. The larger value of the coefficient a for the reaction of molecular oxygen evolution at the catalyst under investigation, give the higher the electrochemical characteristics of oxygen electrodes based on nanocomposites consisting of these catalysts and carbon nanotubes.        Another support for this principle is the fact that the oxide compounds of Ni with variable valence, which also have a high oxygen evolution overpotential in alkaline solutions, possess catalytic properties. Iron, which is a catalytic poison, has, as we see, for manganese dioxide a lower oxygen evolution overpotential in the oxygen reduction reaction. This fact is an indirect support for the principle of reaction localization.
Consider the requirements to catalysts for the hydrogen electrode of a fuel cell with alkaline electrolyte. Here, in accordance with the principle of reaction localization, catalysts with low hydrogen evolution overpotential in alkaline medium must be used. In this case, adsorbed hydrogen atoms with bond rupture in the molecule are formed on the catalyst, and on carbon-base nanomaterials, electron detachment with desorption of hydrogen ions takes place. The series of metals in order of decreasing coefficient a for hydrogen evolution in an alkaline medium is as follows [13] : Metal Pb < Sn < Zn < Cd < Cu < Ti < Fe < Ag < Ni < Al < Co < Pd < Pt Materials consisting of nanocompositions of MWCNTs with 10% palladium content and mixtures of powders of the Ni 2 Al 3 and Mg 2 Ni alloys with 50% MWCNT content were chosen for investigations. From these materials, hydrogen electrodes for fuel cell were made by pressing. Figure 8 shows current-potential curves for these hydrogen electrodes, which were obtained in a KOH-based 6M electrolyte. As follows from the electrochemical characteristics of the electrodes, these materials are arranged according to activity for hydrogen electrode in the following series: Pd (curve 4, Figure 8), Ni 2 Al 3 (curve 3, Figure  8), Mg 2 Ni (curve 2, Figure 8), and pure carbon nanotubes (curve 1, Figure 8). This series fully coincides with the arrangement of metals in a series with decreasing hydrogen evolution overpotential in an alkaline medium. Let us now see how heterogeneous composition is affected by the introduction of a deliberately bad catalyst for hydrogen electrode. Following the principle of electrochemical reaction localization, lead is such a catalyst. Using the above method for the deposition of metals on carbon nanotubes, we have obtained composites containing: MWCNTs with 5% Pd (Figure 9, curve 2) and MWCNTs with 5% Pd and 10% Pb deposited on them (Figure 9, curve 1). As is seen from Figure 9 (curve 1), introduction of lead in MWCNT-Pd composites deteriorates the characteristics of the fuel cell hydrogen electrode. This confirms once move the possibility of predicting catalytic properties of materials with the aid of the principle of electrochemical reaction localization. Thus, the principle of reaction localization is also substantiated for catalysts of fuel cell hydrogen electrode.  Now consider the reaction of electrochemical hydrogen accumulation which proceeds at the metal-hydride (MH) elec-trode of nickel-metal hydride battery. The principle of reaction localization was studied for a LaNi 5 -type hydride-forming intermetallic compound and various metals-catalysts deposited on the surface of metallide particles.
Consider the processes occurring in a nickel-metal hydride battery. They are characterized by effective migration of hydroxyl ions from the positive to the negative electrode during charge and from the negative to the positive electrode during discharge without change in electrolyte volume. The discharge reaction equation is: The overall discharge reaction is: The same reactions proceed reversibly during charge. Besides, during charge an oxygen evolution reaction proceeds at nickel oxide electrode in addition to the conversion Ni(OH) 2 to the NiOOH. It starts at 80% conversion into NiOOH proceeds according to the scheme: In the case of overcharge of MH electrode, a reaction of evolution of gaseous hydrogen occurs, which is chemically absorbed by this electrode in the case of proper battery design. To avoid strong overcharge of nickel oxide electrode, an excess amount of it must be taken when designing the battery. The main problem of nickel-metal hydride batteries is MH corrosion reaction in the presence of dissolved oxygen. The rate of the corrosion process becomes especially high at a temperature above 40 o C: 2 МН + О 2 → 2М(ОН) To prevent this reaction, the authors propose microcapsulation [19,20] . Another way of reducing corrosion is the use of polymeric electrolyte or good separators. In addition to corrosion prevention, microcapsulation plays a big role in the metal hydride formation process. To coat intermetallic compounds, metals with high molecular hydrogen evolution overpotential in alkaline medium must be used. At such metals, the water adsorption reaction with electron attachment is localized, as a result of which adsorbed hydrogen is formed, which diffuses subsequently into intermetallic compound to form a metal hydride. The role of the catalyst with high hydrogen overpotential reduces to the formation of adsorbed hydrogen and prevention of its recombination on the charge of the electrode. Therefore, the series of catalysts for use in hydride electrode will be reverse to the series of catalysts [2] for fuel cell hydrogen electrode.
Here the characteristics of the catalysts improve from platinum to lead with increasing coefficient a from the Tafel equation.
Powders of the intermetallic compound La 0.

84
Co 0.16 Ni 4.83 Fe 0.04 with < 40 nm grain size with coatings of the following composition: nickel-phosphorus and cobalt-phosphorus alloys, copper, silver and palladium were obtained for investigation [12] .  Figure 10, curve 2). According to the value of discharge capacity, they may be arranged, depending on the type of coating, in the following order: Cu, Ag, Pd, Co-P, Ni-P. This series differs slightly from the series in which the coefficient a decreases: Cu (0.96), Ag (0.73), Ni (0.65), Co (0.60), Pd (0.53). This is most likely accounted for by the nonoptimal number and size of the clusters of the deposited metals. This assumption is substantiated by the nonlinear dependence of electrode discharge capacity on the percentage of copper ( Figure 11). It has been found that the discharge capacity of electrodes with 2.5% and 9% copper ( Figure 11, curves 1,2) is higher than that of electrodes with 5% copper (Figure 11, curve 3).  These experiments and literature data [19] showed that the use of materials with high hydrogen evolution overpotential and hence the coefficient a in the Tafel equation makes it possible to improve the characteristics of hydride electrode. Thus, the principle of reaction localization is applicable to hydride electrodes too.
When considering the above variants of using the principle of electrochemical reaction localization, it may be formulated as follows. For any electrocatalytic reaction proceeding in a particular electrolyte at an electrode consisting of an inhomo-geneous catalyst -support system, materials for the catalyst and support with diametrically opposite properties in this electrolyte with respect to the catalyzed reaction must be selected. For example, for oxygen reduction reaction in an alkaline electrolyte, if a carbonaceous material having relatively low oxygen evolution overpotential has been chosen as the catalyst support, then a material with high oxygen evolution overpotential in alkaline medium must be taken as the catalyst for this medium. The catalytic activity of different inhomogeneous composites can be estimated from the value of the difference in the evolution overpotential of the reagent under investigation at the catalyst and support in a particular medium. A limitation in selecting materials on the basis of the principle of electrochemical reaction localization is the corrosion stability of the chosen materials in a particular electrolyte.
Thus, the principle of reaction localization allows one to explain why some materials or others are catalysts for the chosen reaction; and the catalytic activity of the chosen inhomogeneous composition can be judged from the difference in the electrochemical evolution overpotential of the reagent under investigation between the catalyst and support. The larger this difference, the higher the catalytic activity of the composition obtained.
Making use of this principle, one can perform goal-directed synthesis or selection of catalytic materials for electrochemical power sources and for other electrochemical systems and reactions.

1.
A principle of electrochemical reaction localization has been proposed, which makes it possible to estimate the activity of electrodes, consisting of catalyst and support, for electrochemical power sources from the difference in the evolution overpotential of the reagent under investigation between the catalyst and support. 2. In accordance with the principle of electrochemical reaction localization, good catalysts for the fuel cell oxygen electrode in an alkaline medium with carbon support are materials with high molecular oxygen evolution overpotential in alkaline medium. The higher the a values from the Tafel equation, the more active the catalyst. 3. In accordance with the principle of electrochemical reaction localization, good catalysts for the fuel cell hydrogen electrode in alkaline medium with carbon support are materials with low hydrogen evolution overpotential in alkaline medium. The lower the a values from the Tafel equation, the more active the catalyst. 4. In accordance with the principle of electrochemical reaction localization, additions of catalysts with high hydrogen evolution overpotential in alkaline medium must be used for the hydride electrode of nickel-metal hydride battery for intermetallic compounds with low hydrogen evolution overpotential in alkaline medium. The higher the a value from the Tafel equation, the better the characteristics of hydride electrode. 5. The principle of electrochemical reaction localization allows one to synthesize or select novel organic or inorganic materials for electrochemical power sources and to assess them by the value of electrochemical overpotential, i.e. by the coefficient a from the Tafel equation. The larger the difference in the value between the catalyst and support, the higher activity of the electrode.