CA2499733A1

CA2499733A1 - Current collector structure and methods to improve the performance of a lead-acid battery

Info

Publication number: CA2499733A1
Application number: CA002499733A
Authority: CA
Inventors: Elod Gyenge; Joey Jung; Alvin A. Snaper
Original assignee: Individual
Current assignee: Individual
Priority date: 2001-09-26
Filing date: 2002-09-25
Publication date: 2003-04-03
Also published as: US20050100791A1; US7060391B2; EP1449269A4; CN1613159A; WO2003028130A1; JP2005505102A; EP1449269A1; CN100355131C

Abstract

A battery, a battery electrode structure, and methods to make the same. The product and method comprise applying a layer of lead-tin containing alloy to substrates for anodes or cathodes for lead-acid batteries, in which the substrates are porous or reticulated.

Description

CURRENT COLLECTOR STRUCTURE AND METHODS TO IMPROVE THE
PERFORMANCE OF A LEAD-ACID BATTERY
FIELD OF THE INVENTION
This invention relates generally to lead-acid battery electrodes and particularly to high surface area electrodes which improve the performance of lead-acid batteries in one or more ways alone or in combination such as:
specific discharge capacity, positive active mass utilization, and discharge/recharge cyclability.
BACKGROUND OF THE INVENTION
The lead-acid battery in its various configurations is a time-honoured power source for diverse applications such as starting-lighting-ignition (SLI), uninterrupted power supply (UPS) and motive power. Continuous developments on the application side, for instance in the area of electric vehicles and hybrid electric vehicles (EV and HEV), impose challenging performance demands on battery technologies in general and lead acid batteries in particular.
Pavlov summarized the relationship between battery specific energy in watt hours/kilogram (VVh/kg) and number of battery discharge/charge cycles for both flooded and valve-regulated type lead acid batteries.
For both battery types, the higher the battery specific energy the lower the number of discharge/charge cycles and hence, the battery cycle fife.
Typically, a flooded battery with a specific energy of 40 Whlkg can be used for about 500 discharge/charge cycles, white a battery producing only 30 Wh/kg can be employed for about 850 cycles. Thus, there is clearly a need to improve both the specific energy and cycle life of lead-acid batteries in order to make them more suitable for electric traction applications.
SUBSTITUTE SHEET (RULE 26) It is well known that the low utilization efficiency of the active mass, especially on the positive electrode, in conjunction with the heavy weight of the lead current collectors, limits the actual specific energy of the lead-acid battery. The structure of the current collector plays an important role in determining the utilization efficiency of the positive active mass (PAM). During discharge, on the positive electrode, the structure of the current collector must allow for significant volume increase (e.g. molar ratio of PbSOa to Pb02 is 1.88) while maintaining electrical contact with the active material and assuring ionic transport to the electroactive sites.
There are many examples in the prior art describing techniques to increase the specific energy output by improving the porosity and specific surface area of the lead compound based paste (active material) applied onto the battery current collector (or grid). For example, Stoilov et al in US patent 5,332,634 states that "there is a need for making lead electrodes with a porous active mass, which has a large active surface area and which strengthens the electrical connection between the active mass and the grid. Such a porous lead electrode would lead to electrochemical cells and accumulators which produce more power per unit of weight and also present very low electrical resistance."
Regarding improvements in the battery current collector structure, Czerwinski and Zelazowska have described the electrochemical behaviour of lead deposited on a non-metallic open pore substrate, namely reticulated vitreous carbon (RVC).
These authors prepared small, 1 cm2 geometric area, collectors by electrodeposition for 10 minutes of Pb from an alkaline solution containing 20 g/I
NaOH to produce the negative electrode and anodic oxidation to form lead dioxide (Pb02) on the positive electrode using a concentrated lead nitrate based solution (Pb(N03)2). The amount of generated active material, Pb and PbOz, was small at about 19.3 mg and 22.3 mg, respectively. Consequently, if a battery had been assembled with the above described electrodes, the corresponding capacity would have been extremely low, in the range of 4.5 mAh, insufficient for SUBSTITUTE SHEET (RULE 26) practical use. Furthermore, the battery structure described by Czerwiriski and Zelazowska is not rechargeable in sulfuric acid, which is the operational electrolyte of lead-acid batteries, since the recommended active material generation procedure required alkaline and nitrate based electrolyte.
Therefore, this prior art proposes a technique to manufacture a lead-acid battery with a cycle life of ooe (i.e. one time use). Clearly, it was not envisaged to paste active materials onto the reticulated substrate in order to create a high capacity, rechargeable battery.
Das and Mondal suggested developing lead acid current collectors with thin layers of active materials deposited on lightweight, electronically conducting substrates, such as a carbon rod. The rationale was only to reduce the 'dead weight' of the lead acid system, which would somewhat increase the specific energy.
Snaper, in United States patent 6,060,198 describes the use of reticulated metal structures for use as current collectors in batteries in which the reticulated structure consists of a plurality of pentagonally faced dodecahedrons.
This prior art does not teach methods for using such a structure to improve the cycle life and performance of a lead acid battery and does not envisage the use of non-metallic electrically conductive substrates such as reticulated carbon to reduce battery weight. None of the above mentioned prior art references regarding reticulated structure suggest any need for combining the reticulated structure with a lead containing paste to create a rechargeable battery suitable for use in multiple chargeldischarge cycles.
Additional cited art is referenced in the accompanying Appendix.
SUMMARY OF THE INVENTION
The present invention relates to methods of improving the performance, especially cycling performance, of lead-acid batteries by using current collector SUBSTITUTE SHEET (RULE 26) structures based on light-weight, porous, open pore, high specific surface area (e.g. > 500 m21m3) substrates coated with a lead-tin alloy. More specifically it relates to the use of lead-tin alloys deposited on lightweight, open pore substrates such as carbon or aluminum to dramatically enhance the cyclability of the subsequent high surface area electrode for use as an anode andlor cathode in lead acid batteries while achieving all of the prior art mentioned advantages of high surface area porous electrodes, for example reticulated electrodes.
The present invention provides an improved current collector structure for generating power in a lead-acid battery. The current collector is comprised of a reticulated, light-weight, electronically conductive three-dimensional substrate matrix characterized by high specific surface area (i.e., between 5x102 and 2x104 m2/m3) and void fraction.(i.e. between 70 and 98%). A number of materials could serve as the above-mentioned substrate such reticulated vitreous carbon, aluminum, copper and organic conductors, either alone or in combination.
Furthermore, an integral part of the structure consists of a layer of lead-tin deposited throughout the surface and depth of the three-dimensional reticulated matrix to cover as uniformly as possible all 'the ligaments of the substrate matrix.
The thickness of the deposited lead-alloy layer can range for example between 20 to 2000 um, depending on the intended application and battery cycle life.
The resulting composite structure composed of the light-weight matrix covered by a layer of lead-alloy, is used as the positive and/or negative current collector in lead-acid batteries. It is understood for those skilled in the art that in order to obtain a functional lead-acid battery the above-described collectors might be subjected to pasting with any variety of lead oxide and/or lead sulfate based pastes. The electrode formed by pasting the current collector is brought into contact with sulfuric acid of desired concentration and assembled in any type of flooded or valve-regulated lead-acid batteries. After forming (initial charging) the paste is converted into the active material (or active mass) which is lead dioxide on the positive electrode and lead on the negative electrode, SUBSTITUTE SHEET (RULE 26) respectively. When the lead-acid battery is subjected to discharge both the lead dioxide on the positive electrode and lead on the negative electrode are converted to lead sulfate and current is transferred via the cu«ent collector (or grid) to a consumption source (load). During charge, do current is supplied to lead sulfate by the current collector and the active materials are regenerated.
Thus, the interaction of current collector with the active mass is of crucial importance for the functioning of the lead-acid battery.
The present invention also provides methods for producing the high-performance current collectors, which includes the steps of lead or lead-alloy deposition and attachment of lugs, tabs and frames to the three-dimensional substrate.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG.1 A, is a front view schematic of the current collector according to one embodiment of this invention, FIG.1 B is a front view schematic of the current collector according to another embodiment of this invention, FIG 1 C is a front view schematic of the current collector according to an alternative embodiment of the present invention, FIG. 2 is a scanning electron microscopy image of the high-specific surface area, r ticulated part of the current collector structure according to one embodiment of this invention, FIG. 3 shows a cross-sectional view, obtained by backscattered electron microscopy of the current collector structure according to the present invention.
FIG. 4 compares the early stage cycling performance of pure lead and lead-tin (99:1 weight ratio of lead to tin) coated current collectors manufactured according to the present invention.
FIG. 5 compares the nominal specific capacity (Peukert diagram) for the limiting positive electrode for the lead-tin electroplated reticulated vitreous S
SUBSTITUTE SHEET (RULE 26) carbon manufactured according to the present invention and book-mould current collector designs.
FIG. 6 shows the cycling performance with respect to the positive limiting electrode for a flooded single cell 2 volt battery equipped with lead-tin electroplated vitreous carbon current collectors manufactured according to the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
FIG. 1 represents a front view of the current collector structure according to one embodiment of the present invention. Denoted by reference numeral 1 is the high specific surface area part manufactured by depositing lead or lead-alloys on an electrically conductive, reticulated substrate such as but not limited to reticulated vitreous carbon. The high specific surface area part is attached to a frame 2, which in turn is connected to lug 3. Both the frame and lug are made of lead or a lead-alloy.
In another embodiment, shown by FIG. 1 B, the lead or lead-tin alloy deposited reticulated part 1 is compartmentalized by intercalated stripes which are part of the overall frame structure 2. The compartmentalization improves the current and potential distribution characteristics across the high specific surface area component of the current collector structure, especially in case of larger plate designs.
A further design variation is presented by FIG 1 C. In this case the top connector 3 has a triangular design, gradually widening toward the edge of the collector, where lug 4 is situated. This design feature combines the need for weight reduction of the connector with good corrosion resistance in the area of highest current concentration, i.e. current entry and exit zone 4. The frame 2 around the reticulated structure can be of similar or different width. One might use a wider SUBSTITUTE SHEET (RULE 26) frame on the side that is in contact with the lug and a thinner one on the opposite side (FIG 1C) A scanning electron microscopy image of the reticulated part of the collector is shown by FIC-' 2. In this particular cUse reticulated vitreous carbon with 30 pores per inch (ppi) (ERG Materials and Aerospace Corporation, Oakland, CA, USA) served as substrate and it was plated with a lead alloy to give a functional collector for lead-acid batteries. FIG 2 shows the interconnected, open-cell network, which forms the physical basis for current transfer to and from the active mass. The latter covers the surface of the wires and also occupies the openings of the reticulated structure. The proximity of the current collector wires to the active mass (e.g. diameter of the openings about 2 mm for the case depicted by FIG 2) leads to enhancement of the active mass utilization efficiency and charge acceptance.
The invention is further described by the following examples.
EXAMPLE 1: MANUFACTURING OF THE RETICULATED CURRENT
COLLECTOR
In one embodiment of the present invention, reticulated vitreous carbon (RVC) slabs with 20 and 30 pores per inch (about 8 and 12 pores per centimeter, respectively) were used as substrates for grid manufacturing. The RVC slab having dimensions of: 15.2 cm x15.2 cm x 12.8 mm (height x width x thickness) was sliced to a preferred thickness of about 3.5 mm, using a steel cutter.
After slicing, the height and width of the carbon slab was adjusted to the size needed for the particular battery. One of the commonly employed current collector sizes is 12.7 cm x 12.7 cm (height x width).
Following size adjustment, the vitreous carbon substrate was uniformly coated with a layer of lead-tin alloy. A variety of methods can be used for the deposition SUBSTITUTE SHEET (RULE 26) of lead-tin alloys on carbon based substrates, such as electroplating and vacuum deposition. In the present invention electroplating (or electrodeposition) was chosen to apply the lead-alloy coating on the RVC substrate. However, it is understood to those skilled in the art that other methods might be used to coat RVC with lead-tin alloy.
1n the case of the electroplating method, in order to supply current to the vitreous carbon structure during electroplating, a 2.5 mm thick connector and 6 cm x 1.3 cm (height x width) lug, both made of 99.8% by weight purity lead, were attached to the reticulated vitreous carbon slab. This was accomplished by immersing the top part of the carbon piece in melted lead at 370 °C using aluminum molds, followed by rapid cooling by an air-jet.
To electroplate lead on reticulated vitreous carbon, there are several lead electroplating bath compositions, such as fluoborate, sulfamate, and fluosilicate.
In the present example the fluoborate bath was used. However, it is understood to those skilled in the art that other electroplating bath formulations could be considered. For the electroplating of a pure lead coating on the RVC
substrate the fluoborate bath per one liter of stock solution was composed of:
500 m1 of 50%- by weight lead tetrafluoroborate (Pb(BF4)2), 410 ml of deionized water, 27 g of boric acid (H3B03), 90 ml of fluoboric acid (HBF4), and 3 g of peptone. During preparation the plating solution was thoroughly mixed at room temperature.
To electroplate a lead-tin alloy on the RVC substrate, the lead electroplating bath composition described above, was modified by the addition of various concentrations of tin tetrafluoroborate. The concentration of tin in the plating bath determines to large extent the tin content of the lead alloy. The typically employed lead-tin alloy electroplating solutions had the following composition per one liter of stock solution: between 74 and 120 ml of 50% by weight tin tetrafluoroborate (Sn(BF4)2) solution, 510 ml of 50% by weight lead SUBSTITUTE SHEET (RULE 26) tetrafluoroborate (Pb(BFa)z) solution, between 330 and 376 ml of deionized water, 27 g of boric acid (H3B03), 40 ml of fluoboric acid (HBF4), and 1 g of gelatin. During electroplating the tin content of the plating bath was kept constant either by using a sacrificial lead-tin anode or by adding at certain time intervals, fresh tin tetrafluoroborate solution.
The RVC plate was placed in the electroplating bath and acted as the cathode, whilst two 80/20 (by weight of lead to tin) lead-tin plates of 3.2 mm thickness (Metal Distributors Inc., Vancouver, BC, Canada) acted as sacrificial anodes sandwiching the RVC cathode. The distance between the RVC cathode and the lead-tin anode was 3.8 cm. The cathode and anode had similar geometric areas.
Following immersion in the electroplating bath, the electrodes were connected to a DC power supply characterized by a maximum voltage and current output of 25 V and 100 A, respectively. The typical electroplating conditions for either lead or lead-tin electroplating on RVC were as follows: current density 570 A/m2, cell voltage 0.3-0.7 V, temperature 20-25 °C. The coating thickness was adjusted by varying the plating time (typically between 1 and 2 hours). The required lead or lead alloy coating thickness is a function of the intended battery type, application and electrode polarity. For the flooded lead acid battery the negative collector was produced with a 30-50 yin thick coating while the coating on the positive collector had a thickness of 200-500 Vim. By employing different coating thickness on the negative and positive electrodes, both the weight saving and long cycle 4ife objectives can be simultaneously achieved. Figure 3 shows the back scattered electron microscopy image of ~ the cross section for the plated reticulated vitreous carbon. The plated reticulated vitreous carbon has a lead-tin coating of 235 um thickness, i.e. the positive collector.
After the electroplating was completed, the plated RVC was subjected to a sequential washing procedure in the following order: distilled water rinse, alkaline wash (0.1 M NaOH), distilled water wash, acetone wash and acetone dipping.
Drying in a nitrogen atmosphere followed the last washing step. The described SUBSTITUTE SHEET (RULE 26) procedure assured complete removal of the electroplating bath components from the high surface area collector while minimizing the surface oxidation. In the case of lead alloy deposition the typical tin content of the collectors was between 0.5-2% by weight tin, ft is understood to those skilled in the art that other coating tin contents can be easily achieved by adjusting the plating time, current density andlor plating bath composition.
Following the electroplating, washing and drying steps the current collector was further processed by replacing the tab and lug, which served as current feeder during electroplating, with a wider top connecting element that in one embodiment of the present invention had a triangular shape as shown by FIG
1 C. Additionally, three frames were also attached on the sides of the electroplated RVC plate. The process of attaching the new connector and frames was identical to the one described before for attaching the electroplating connector. The material for the battery grid tab and frames was a lead ahoy containing 2% by weight of tin.
EXAMPLE 2: EFFECT OF COATING COMPOSITION ON THE BATTERY
CYCLING PERFORMANCE
fn order to compare the performance of the pure lead and lead-tin alloy reticulated collectors, two flooded, single cell, 2 V, batteries were assembled, equipped with pasted plates using pure lead and lead-tin (1% by weight of tin) coated collectors, respectively. The pure lead and lead-tin coated collectors were manufactured according to the procedure described in Example 1. The following table summarizes the plating recipes and plating conditions.
1 U.' SUBSTITUTE SHEET (RULE 26) Table 1 Electroplating conditions.
Lead Lead Lead-Tin Lead-Tin Coated Coated Coated Coated Positive Negative Positive Negative Recipe per one liter of 500 ml of 50% by 74 ml of 50% ~by electrolyte weight Pb(BFd)2; 410 weight Sn(BF4)2, 510 ml of deionized water, ml of 50% by weight 27 g of H3B03, 90 ml Pb(BF4)2, 376 ml of of HBF4, and 3 g of deionized water, 27 g peptone of H3B03, 40 ml of HBF4, and 1 g of gelatin Current Density (Alm 570 570 570 J 570 Plating Temperaturere (C 25 ~ 25 25 ~ 25 Plating Time (Hr) 2.5 1 2.5 1 Coating Thickness (txm) --235 -95 --235 -75 Size(cmxcmxmm) 12.7x12.7x3.5 12.7x12.7x3.5 Each battery was composed of two negative and one positive reticulated collector pasted with an . industry standard lead-acid battery paste obtained directly from a battery manufacturer and composed of lead sulfate, lead monoxides and lead dioxide. Two single-cell batteries were assembled using the respective battery plates (i.e. cured pasted collectors). First the battery plates were formed in dilute sulfuric acid (specific gravity 1.05) by applying a constant constant current charge in order to supply a Charge Of 520 Ah/kgdry~aste in 72 hours. The forming step is necessary to create the active materials on the plates, i.e. Pb on the negative and Pb02 on the positive.
The testing protocol was comprised of consecutive daily cycles at 5 hour discharge rate with cut-off voltage at 1.5 V followed by 19 hour recharge at a float voltage of 2.35 V/cell using sulfuric acid with an initial specific gravity of 1.26.
11?
SUBSTITUTE SHEET (RULE 26) The above protocol is relevant for deep cycling of stand-by batteries and it is considered an extreme level of cycling for the latter battery type. FIG 4 shows the comparison cycling characteristics of the two batteries. After first 4 days of cycling, the specific capacity of the pure lead plated RVC battery dropped, i.e.
the specific capacity of lead-tin alloy electroplated RVC battery was 2.6 times higher of the specific capacity of pure lead plated RVC battery.
The results presented in FIG 4 underline the beneficial effect of tin as an alloying element for stabilizing the capacity of deep-cycle lead-acid in the early stages of cycling.
EXAMPLE 3: PERFORMANCE COMPARISON BETWEEN BATTERIES
EMPLOYING BOOK-MOULD GRIDS AND ELECTROPLATED RETICULATED
VITREOUS CARBON CURRENT COLLECTORS
The comparative nominal capacities, Peukert diagram [12], for the performance limiting positive electrode in the case of two flooded single-cell 2 V
batteries employing book-mould and lead-tin ( 1 % by weight of tin) electrodeposited RVC
collectors, respectively, is shown by FIG 5. Both battery types were pasted, assembled and formed under identical conditions. The lead-tin electrodeposited reticulated grids were prepared according to the method described in Example 1 and Example 2. The employed discharge currents corresponded to discharge rates between 24 to 2 h for the positive limited electroplated RVC collector battery and 12 to 2 h for the book-mould grid battery, respectively (FIG 5).
Discharging the two batteries at a current of 27.5 A/kgPa,M the specific discharge capacity of the positive plate using the electrodeposited RVC collector was 105.7 Ah/kgPAM (utilization efficiency of 47.2%), whilst in the case of the book-mould collector only 59.3 Ah/KgPAM was obtained indicating a low utilization efficiency of the positive active mass, i.e. 26.2% (FIG. 5). Therefore, the specific capacity of 12' SUBSTITUTE SHEET (RULE 26) the positive plate with electroplated reticulated collector was 78% higher than the capacity of the plate that used an industry standard book-mould grid.
At a discharge current of 6 AIKgPAM the specific capacity of the electroplated RVC
positive plate was 66% higher than in the case of book-mould grid. The improvement of the positive active mass utilization efficiency and specific capacity of the limiting positive electrode is directly correlated with the enhancement of the specific energy of the battery. Based on the presented results the specific energy of a flooded lead-acid battery equipped with electroplated RVC collectors was 62.7 Wh/kg at a discharge rate of 20 hrs.
Under similar conditions a battery equipped with book-mould collectors would provide only 39.1 Wh/kg. This clearly shows the ~ significant performance improvement obtained by using lead-tin electroplated RVC current collectors in lead-acid batteries.
EXAMPLE 4: CYCLE LIFE OF A FLOODED LEAD-ACID BATTERY
EQUIPPED WITH ELECTROPLATED RVC CURRENT COLLECTORS
A test cell composed of one positive and two negative pasted electroplated lead-tin RVC electrodes was subjected to long-term cycling. The electrodes were prepared by the method described in Example 1 and Example 2. Each cycle comprised of a discharge at 63 A/KgPAM (nominal utilization efficiency 21 %
and 0.75 h rate) followed by a two-step constant current c; urge at 35 A/KgPnnn and 9.5 A/KgPAM, respectively, with a cut-off voltage at 2.6 V. The returning charge was 105-115 % of previous discharge.
FIG. 6 shows the cycling performance of the battery under the above conditions.
Using the specific capacity of cycle 10 as a reference, the lead-tin (1 % by weight tin) electrodeposited RVC battery completed 706 cycles above or at 80% of the reference specific capacity, corresponding to over 2100h of continuous SUBSTITUTE SHEET (RULE 26) operation. The above experiment indicates therefore, that lead-tin electrodeposited RVC electrodes are capable of providing long battery cycle life.
EXAMPLE 5: COMPARATIVE TESTING OF 2 V BATTERIES EQUIPPED WITH
RETICULATED ALUMINUM COLLECTORS PLATED WITH LEAD-TIN
ALLOYS OF VARIOUS COMPOSITION
In one embodiment of the present invention, metal reticulated foams such as aluminum with 20 pores per inch was used as substrate for grid manufacturing.
The aluminum reticulated foam having dimensions of: 12.2 cm x15.2 cm x 5.9 mm (height x width x thickness) was uniformly coated with a layer of lead-tin alloy using the method described in Example 1. It is understood to those skilled in the art that other lead coating methods can also be employed to produce lead deposited reticulated aluminum current collectors. Two negative and ohe positive lead electrodeposited aluminum collector was pasted and assembled to form a single cell flooded 2 V battery. For comparative testing purposes another single cell flooded battery was assembled and formed in an identical fashion but equipped with industry standard book-mould collectors. Table 2 compares the discharge current, the specific capacity of the positive limiting plate, and the utilization efficiency of the positive active mass (PAM utilization efficiency) in the case of the 20 h discharge rate.

SUBSTITUTE SHEET (RULE 26) Table 2: Comparison between book-mould and electroplated aluminum current collectors in flooded single cell 2 V batteries.
Book-mould Lead-tin collector efectrodeposited reticulated aluminum Discharge time (h) 20 20 Discharge current (A/kgpnM)2.7 5.8 Discharge capacity (Ah/kgPAM)55,1 116.1 PAM utilization efficiency24.G 51.8 (%) The PAM utilization efficiency and discharge capacity of the lead electrodeposited reticulated aluminum electrode was 42% higher than for the book-mould electrode. This example shows that high specific surface area reticulated metals can also serve as substrates for lead or lead-alloy deposited battery current collectors.
EXAMPLE 6: SINGLE OR MULTI-LAYER OPEN PORE SUBSTRATES
Other than reticulated substrates, which are open pore multi-layer substrates, the following non-limiting additional types of substrates can be considered. For example, single or multi-layer screens) coated with lead or lead-tin alloy could be considered. The difference in these two types of substrates is in the number of struts, which connect the pores, for example, typically three strut joints in reticulated versus typically four strut joints in screens. However, other number of strut joints can be anticipated by those skilled in the art for other geometries.
15;
SUBSTITUTE SHEET (RULE 26)

Claims

1. An electrode for use in batteries comprising an electrically conductive substrate, said substrate containing open pores which are bounded by surfaces, and a layer of a lead-tin containing alloy applied to said surfaces.

2. An electrode according to Claim 1, in which said layer is applied by electrodeposition.

3. An electrode to Claim 1, in which said layer is applied by vapor deposition.

4. An electrode according to anyone of Claims 1-3, in which said substrate contains carbon.

5. An electrode according to Claim 4, in which said carbon is reticulated vitreous carbon forming said pores.

6. An electrode according to anyone of Claims 1-5, in which said substrate contains aluminum.

7. An electrode according to Claim 1, in which said substrate is a conductive metal formed as a reticulated structure.

8. An electrode according to Claim 7, in which said conductive metal contains aluminum.

9. An electrode according to anyone of Claims 1-8, in which said electrode includes structure to mount and form a functional electrode in a battery.

10. An electrode according to anyone of Claims 1-9, in which the tin content of said alloy is between about 0.2% to about 3% by weight of said alloy.

11. An electrode according to anyone of Claims 1-10, in which the tin content of said alloy is between about 0.5% to about 2% by weight of said alloy.

12. An electrode according to anyone of Claims 1-11, in which the surface area of the pores in said substrate is between about 500 to 20,000 square meters per cubic meter of substrate.

13. An electrode according to anyone of Claims 1-12, in which the dimension of thickness of said alloy is between about 20 to 2,000 microns.

14. An electrode according to Claim 5, in which said vitreous carbon contains between about 20 to about 30 pores per inch of measured length.

15. An electrode according to anyone of Claims 1-14, in which at least a portion of said surfaces is coated with an electrically conductive lead-containing paste, whereby to form a lead-acid battery plate.

16. An electrode according to anyone of Claims 1-15, in which said paste includes lead sulfate, lead oxide, or a mixture of them.

17. An electrode for use in lead-acid batteries comprising a substrate formed as reticulated rigid structure having pores with substantial surface area, said substrate being electrically conductive, a layer of lead-tin alloy deposited on said structure in intimate conductive contact with the surfaces of said pores, and a layer of a lead-containing paste on said layer of alloy.

18. An electrode according to Claim 17, in which said substrate is aluminum or vitreous carbon.

19. An electrode according to Claim 17 or 18, in which said lead-tin alloy is a deposition product of electrodeposition or vapor deposition.

20. In combination:
a battery housing;
a pair of spaced-apart electrodes according to anyone of Claims 1-19;
an electrolyte contacting said electrodes and bridging the space between them; and terminal connections for connecting said electrodes into a circuit.

21. Method for producing an electrode according to anyone of Claims 1-19 comprising:
(a) adjusting the substrate to the needed rise;
(b) uniformly coating of the substrate with a layer of lead-tin alloy.
(c) washing of the coated substrate; and (d) drying of the coated substrate.

22. Method for producing an electrode according to Claim 21, wherein lead-tin alloy coating according to process step (b) is applied by electrodeposition on the substrate.

23. Method for producing an electrode according to Claim 21 or 22, wherein the electrodeposition solution according to process step (b) contains the following substances:
(Sn(BF4)2), (Pb(BF4)2), deionized water, (H3BO3), (HBF4) and gelatin.

24. Method for producing an electrode according to anyone of Claims 21-23, wherein the electrodeposition according to process step (b) is conducted at cell voltage 0.3-0.7 V and temperature 20°-25°C.

25. Method for producing an electrode according to anyone of Claims 21-24, wherein the washing according to process stage (c) is performed by distilled water rinse, alkaline wash, distilled water wash, acetone wash and acetone dipping.

26. Method for producing an electrode according to anyone of Claims 21-25, wherein the drying according to process steps (d) is performed in a nitrogen atmosphere.