Title of Invention

LOW ELECTRICAL RESISTANCE BIPOLAR PLATE-DIFFUSION MEDIA ASSEMBLY

Abstract A fuel cell assembly and method of forming the same is disclosed, the fuel cell assembly including a membrane electrode assembly, a plurality of diffusion media, and a plurality of bipolar plates, wherein the diffusion media are adhered to the bipolar plates with an adhesive layer adapted to minimize an electrical resistance within the fuel cell assembly.
Full Text LOW ELECTRICAL RESISTANCE BIPOLAR PLATE-
DIFFUSION MEDIA ASSEMBLY
FIELD OF THE INVENTION
[0001] The invention relates to a fuel cell stack system and more
particularly to a fuel cell assembly and a method of preparing the
same, adapted to minimize an electrical resistance within the fuel cell
system, the fuel cell assembly including a membrane electrode
assembly having a plurality of diffusion media adhered to a plurality of
bipolar plates with an electrically conductive adhesive layer.
BACKGROUND OF THE INVENTION
[0002] Fuel cell stack systems (hereinafter fuel cells) are increasingly
being used as a power source for electric vehicles and other
applications. Different fuel cell types can be provided such as
phosphoric acid, alkaline, molten carbonate, solid oxide, and proton
exchange membrane (PEM), for example.
[0003] In proton exchange membrane (PEM) fuel cells, a hydrogen gas
reactant is supplied as a fuel to an anode side of the fuel cell and an
oxygen gas reactant is supplied as an oxidant to a cathode side of the
fuel cell. The reaction that occurs between the reactant gases in the
fuel cell consumes the hydrogen at the anode side and produces
product water at the cathode side.
[0004] The basic components of a PEM-type fuel cell are two
electrodes separated by a polymer membrane electrolyte. Each
electrode is coated on one side with a thin catalyst layer. The
electrodes, catalyst, and membrane together form a membrane
electrode assembly (MEA). The MEA is typically sandwiched between
"anode" and "cathode" diffusion media or diffusion layers that are
formed from a resilient, conductive, and gas permeable material such
as carbon fabric or paper. The diffusion media serve as the primary
current collectors for the anode and cathode as well as providing

mechanical support for the MEA.
[0005] The diffusion media and MEA are pressed between a pair of
electronically conductive plates which serve as secondary current
collectors for collecting the current from the primary current collectors.
The plates conduct current between adjacent cells internally of the
fuel cell stack in the case of bipolar plates and conduct current
externally of the stack in the case of unipolar plates at the end of the
stack.
[0006] The bipolar plates typically include two thin, facing metal
sheets. One of the sheets defines a flow path on one outer surface
thereof for delivery of the fuel to the anode of the MEA. An outer
surface of the other sheet defines a flow path for the oxidant for
delivery to the cathode side of the MEA. When the sheets are joined,
a flow path for a dielectric cooling fluid is defined. The plates are
typically produced from a formable metal that provides suitable
strength, electrical conductivity, and corrosion resistance, such as 316
alloy stainless steel, for example.
[0007] The fuel cell stack, which may contain more than one hundred
plates, is compressed, and the elements held together by bolts
through corners of the stack and anchored to frames at the ends of
the stack. In order to militate against undesirable leakage of fluids
from between the pairs of plates, a seal or gasket is often used. The
seal is typically disposed along a peripheral edge of the pairs of
plates. Prior art seals have included the use of an elastomeric
material. Additional prior art seals have included the use of a metal
seal, such as disclosed in published Patent Cooperation Treaty (PCT)
Pat. Appl. No. PCT/EP2003/011347, hereby incorporated herein by
reference in its entirety.
[0008] Efficient operation of PEM fuel cells may depend on an amount
of electrical resistance present in the system, and more particularly to
the electrical resistance at an interface between the bipolar plates and
the diffusion media of the MEA.
[0009] It is desirable to produce a fuel cell adapted to minimize
electrical resistance between the bipolar plates and the MEA of a fuel

cell assembly to optimize system performance. In the fuel cell
described herein, efficient operation of the fuel cell is maximized by
adhering diffusion media adjacent a membrane electrode assembly to
adjacent bipolar plates with an electrically conductive adhesive layer.
SUMMARY OF THE INVENTION
[0010] Concordant and congruous with the present invention, a
diffusion media adapted to optimize water management while
maximizing the performance of the fuel cell has surprisingly been
discovered.
[0011] In one embodiment, a fuel cell assembly comprises a
membrane electrode assembly including a membrane disposed
between a plurality of catalyst layers; a plurality of diffusion media,
each having a microporous layer disposed on a side thereof, wherein
the side of said diffusion media having the microporous layer is
adhered to the catalyst layers of said membrane electrode assembly;
a first bipolar plate; a second bipolar plate; and an electrically
conductive adhesive layer disposed on at least a portion of said first
bipolar plate and said second bipolar plate, wherein said adhesive
layer adheres said first bipolar plate to one of said diffusion media
and said second bipolar plate to another of said diffusion media to
minimize an electrical contact resistance between said diffusion media
and said first and second bipolar plates.
[0012] In one embodiment, a fuel cell stack comprises a plurality of
membrane electrode assemblies, each including a membrane
disposed between a plurality of catalyst layers; a plurality of diffusion
media, wherein one of said plurality of diffusion media is adjacent
each side of said membrane electrode assemblies; a pluralrty of
bipolar plates, each of said bipolar plates having a perimeter portion,
wherein each of said bipolar plates is disposed between two of said
membrane electrode assemblies; a sealant disposed in a void formed
by the perimeter portions of said bipolar plates, wherein said sealant
forms a seal between said first bipolar plate, said second bipolar
plate, and said membrane electrode assembly; and an electrically

conductive adhesive layer disposed on at least a portion of a first
bipolar and a second bipolar plate, wherein said adhesive layer
adheres the first bipolar plate to one of said diffusion media and said
second bipolar plate to another of said diffusion media to minimize an
electrical contact resistance between said diffusion media and the first
and the second bipolar plates.
[0013] In another embodiment, a method for making a fuel cell assembly
for use in a PEM fuel cell, comprises the steps of providing a plurality of
bipolar plates, each plate having a first working face and a second
working face; providing an electrically conductive adhesive layer on
the first working face and the second working face of the bipolar
plates; providing a membrane electrode assembly having a membrane
disposed between catalyst layers; coating a diffusion media with a
paste to form a microporous layer thereon; sintering the diffusion
media and microporous layers together; adhering the microporous
layers of the diffusion media to the catalyst layers of the membrane
electrode assembly; adhering the catalyst layers and the proton
exchange membrane; adhering the diffusion media to the first working
face of one of the bipolar plates with the adhesive layer and adhering
another diffusion media to the first working face of another bipolar
plate with the adhesive layer.
DESCRIPTION OF THE DRAWINGS
[0014] The above, as well as other advantages of the present invention, will
become readily apparent to those skilled in the art from the following detailed
description of a preferred embodiment when considered in the light of the
accompanying drawings in which:
[0015] Fig. 1 is an exploded perspective view of a fuel cell stack including two
fuel cell assemblies according to an embodiment of the invention;
[0016] Fig. 2 is a fragmentary cross-sectional view of a fuel cell assembly as
shown in Fig. 1; and
[0017] Fig. 3 is a fragmentary cross-sectional view of a fuel cell assembly
according to another embodiment of the invention.

DESCRIPTION OF THE PREFERRED EMBODIMENT
[0018] The following detailed description and appended drawings describe
and illustrate various exemplary embodiments of the invention. The
description and drawings serve to enable one skilled in the art to make and
use the invention, and are not intended to limit the scope of the invention in
any manner. In respect of the methods disclosed, the steps presented are
exemplary in nature, and thus, the order of the steps is not necessary or
critical.
[0019] Fig. 1 illustrates a fuel cell stack 10 including two fuel cell assemblies
according to an embodiment of the invention, however, it is understood that
any number of fuel cell assemblies and bipolar plates may be used in a
typical fuel cell stack, as desired. The fuel cell stack 10 is a two cell PEM
fuel cell stack 10 having a pair of membrane-electrode-assemblies (MEAs)
56, 57 separated by an electrically conductive fluid distribution element 52,
hereinafter a bipolar plate 52. The MEAs 56, 57 and bipolar plate 52 are
stacked together between end plates 16, 18, and end contact elements 20,
22. The bipolar plate 52 and the end contact elements 20, 22 include
working faces 26, 28, 24, 30, respectively, for distributing fuel and oxidant
gases (e.g., H2 and O2) to the MEAs 56, 57. Nonconductive gaskets 32
provide seals and electrical insulation between the several components of
the fuel cell stack 10.
[0020] The MEAs 56, 57 are disposed adjacent gas permeable conductive
materials known as gas diffusion media. The gas diffusion media may
include carbon or graphite diffusion paper. As described herein, the gas
diffusion media are adhered to the MEAs 56, 57. The end contact units 20,
22 contact the diffusion media of the MEAs 56, 57. The bipolar plate 52
contacts the diffusion media on the anode face of the MEA 56, configured to
accept a hydrogen-bearing reactant, and also contacts gas diffusion media
on the cathode face of MEA 57, configured to accept an oxygen-bearing
reactant. Oxygen is supplied to the cathode side of the fuel cell stack 10
from an oxygen source 46, for example, via an appropriate supply conduit
42. Hydrogen is supplied to the anode side of the fuel cell from a hydrogen
source 48, for example, via an appropriate supply conduit 44. Alternatively,
ambient air may be supplied to the cathode side as an oxygen source and

hydrogen to the anode from a methanol or gasoline reformer, and the like.
Exhaust conduits (not shown) for both the anode and the cathode sides of
the MEAs 56, 57 are also provided. Additional conduits 36, 38, 40 are
provided for supplying liquid coolant to the bipolar plate 52 and the end
plates 16, 18. Appropriate conduits for exhausting coolant from the bipolar
plate 52 and end plates 16, 18 are also provided (not shown).
[0021] Referring next to Fig. 2, a fuel cell assembly 50 is shown including a
bipolar plate 52 illustrated in Fig. 1 and a second bipolar plate 54. The fuel
cell assembly 50 includes a membrane electrode assembly (MEA) 56
disposed between a plurality of diffusion media 55, one of the diffusion
media 55 disposed between the MEA 56 and the first bipolar plate 52 and
another of the diffusion media 55 disposed between the MEA 56, and the
second bipolar plate 54.
[0022] The MEA 56 is disposed intermediate the diffusion media 55 and
includes a proton exchange membrane (PEM) 78 disposed between two
catalyst layers 80. In the embodiment shown in Fig. 2, the PEM 78 is a thin,
solid polymer membrane-electrolyte but may be any conventional PEM, as
desired. The catalyst layers 80 are formed from platinum supported on high-
structure carbon in the illustrated embodiment, but may be any convention
catalyst such as a platinum-ruthenium catalyst, for example, as desired.
[0023] One of the diffusion media 55 is disposed between a side of the MEA
56 and the first bipolar plate 52 and another of the diffusion media 55 is
disposed between another side of the MEA 56 and the second bipolar plate
54. The MEA 56 includes a first side 72 and a second side 74. A
microporous layer 76 is disposed on the second side 74 of the diffusion
media 55 between the diffusion media 55 and the MEA 56. In the
embodiment shown, the diffusion media 55 are carbon fiber paper such as
the MRC U-105 paper produced by Mitsubishi Rayon Company. It is
understood that the diffusion media 55 may also be a carbon cloth or other
conventional material adapted to be electrically and thermally conductive.
Furthermore, the diffusion media 55 may be untreated or treated on the
second side 74 with a fluorocarbon polymer, as desired. The microporous
layers 76 are formed from a carbon powder and fluorocarbon polymer

mixture and may be formed from any conventional carbon ink or carbon
paste, as desired.
[0024] The first bipolar plate 52 and the second bipolar plate 54 are formed
from a first unipolar plate 60 and a second unipolar plate 62, and each plate
52, 54 includes the first working face 26 and the second working face 28.
Each of the working faces 26, 28 includes a plurality of flow channels 64
adapted to distribute the fuel and oxidant gases across the working faces
26, 28 of the bipolar plates 52, 54. The plurality of flow channels 64 defines
a plurality of lands 66 disposed therebetween.
[0025] Further, the unipolar plates 60, 62 cooperate to form a flow path 68
intermediate the lands 66 of the unipolar plates 60, 62. The flow path 68 is
adapted to facilitate a distribution of a dielectric cooling fluid through the
bipolar plates 52, 54. Any number of flow paths 68 may be formed by the
unipolar plates 60, 62, as desired. In the embodiment shown, the unipolar
plates 60, 62 of the bipolar plates 52, 54 are coupled together with fused tin
70. However, the unipolar plates 60, 62 may be coupled by any conventional
means such as with a b-stage adhesive or by weld-adhering, for example, or
the bipolar plates 52, 54 may be formed from a single piece of material, as
desired. In the embodiment shown, the bipolar plates 52, 54 are formed
from 316 stainless steel, but may be formed from any conventional material
such as graphite, for example. It is understood that the flow channels 64
may be linear, substantially undulated, serpentine, or may have any other
configuration, as desired.
[0026] An adhesive layer 58 is disposed on the flow channels 64 and lands
66 of each of the bipolar plates 52, 54. In the embodiment shown, the
adhesive layers 58 are adjacent the second sides 74 of the diffusion media
55 and are formed by an electrically conductive b-stage adhesive. The
adhesive layers 58 couple the lands 66 of the bipolar plates 52, 54 to the
first sides 72 of the diffusion media 55. The adhesive layers 58 may be
formed from any electrically conductive material, as desired. The adhesive
layers 58 may also be a conductive thermoplastic adhesive, or a combined
conductive primer and conductive adhesive.
[0027] To assemble the fuel cell assembly 50 shown in Fig. 2, the first
unipolar plate 60 is adhered to the second unipolar plate 62 to form the

bipolar plates 52, 54. The first unipolar plate 60 may be adhered to the
second unipolar plate 62 by any conventional adhering means such as spot
welding, laser welding, adhesive, or soldering, for example, as desired. The
first unipolar plate 60 is adhered to the second unipolar plate 62 to minimize
interfacial electrical resistance through the bipolar plates 52, 54. It is
understood that the bipolar plates 52, 54 may be formed from a single,
integrally formed plate, as desired. The working faces 26, 28 of the bipolar
plates 52, 54 are treated with a primer to facilitate improved adhering of the
adhesive layer 58 and unipolar plates 60, 62. The primer may be an acid
primer, an alkaline primer, or a self-etching adhesive layer, as desired. The
adhesive layer 58 is disposed on the flow channels 64 and the lands 66 of
the working faces 26, 28 of the bipolar plates 52, 54. The adhesive layer 58
may be disposed on the bipolar plates 52, 54 by any conventional method
such as pressed on or sprayed on, for example, as desired. Also, when the
unipolar plates 60, 62 are formed from a metal, the adhesive layer 58 may
be applied to the metal during a coil coating process and prior to a stamping
process that forms the unipolar plates 60, 62. It is understood that if the
bipolar plates 52, 54 are formed from a polymeric material, the adhesive
layer 58 may be applied directly to the bipolar plates 52, 54 without applying
a primer, or the polymeric bipolar plates 52, 54 may receive a corona
discharge treatment or radio frequency glow discharge treatment to facilitate
improved adhering of the adhesive layer 58 to the bipolar plates 52, 54.
[0028] The diffusion media 55, the microporous layers 76, the PEM 78, and
the catalyst layers 80 are assembled together. A paste (not shown) is
formed containing a mixture of a carbon powder and fluorocarbon polymers,
applied to the second side 74 of the diffusion media 55, and sintered at or
near 380°C to cause the diffusion media 55 and the microporous layer 76 to
adhere. Commonly owned U.S. Patent No. 7,063,913 is hereby
incorporated herein by reference to further describe methods for preparing
the paste and other materials and processes used in preparing the diffusion
media 55. The microporous layer 76 is adhered to a first face of the catalyst
layer 80 with a self-blocking mechanism by heating the diffusion media 55,
the microporous layer 76, and the catalyst layer 80 at or near 130°C. A
second face of the catalyst layer 80 is adhered to a first side of the PEM 78.

A second diffusion media 55, microporous layer 76, and catalyst layer 80
assembly is prepared as described above and adhered to a second side of
the PEM 78. One of the diffusion media 55 is pressed against the adhesive
layer 58 of the bipolar plate 52 and the other diffusion media 55 is pressed
against the adhesive layer 58 of the second bipolar plate 54. Once
assembled, the fuel cell assembly 50 may be heated to facilitate an
improved adhesion of the MEA 56 and bipolar plates 52, 54.
[0029] In use, hydrogen is supplied to the end contact element 22 and the
anode side of the bipolar plate 52 of the fuel cell stack 10 from the hydrogen
source 48. Oxygen is supplied as the oxidant to the end contact element 20
and the cathode side of the bipolar plate 52 from the oxygen source 46.
Alternatively, ambient air may be supplied to the cathode side as an oxidant
and hydrogen may be supplied to the anode from a methanol or gasoline
reformer. At the anode side, the hydrogen is catalytically split into protons
and electrons. The protons formed permeate through the PEM 78 to the
cathode side. The electrons travel along an external load circuit (not shown)
to the cathode side of the MEA 56, thus creating a current output of the fuel
cell stack 10. Meanwhile, a stream of oxygen is delivered to the cathode
side of the MEA 56. At the cathode side, oxygen molecules react with the
protons permeating through the PEM 78, and the electrons arriving through
the external circuit to form water molecules (not shown). To avoid flooding
the electrodes of the fuel cell assembly 50 and to maintain a degree of
hydration of the PEM 78, excess product water and water vapor is caused to
flow to the diffusion media 55 by the gas flow through the fuel cell assembly
50. The diffusion media 55 facilitate the removal of the excess product water
from the fuel cell stack 10 during wet operating conditions by absorbing the
water and wicking it away from the bipolar plates 52, 54. By wicking the
water away from the bipolar plates 52, 54 and toward the PEM 78, the PEM
78 maintain a degree of hydration to facilitate adequate conductivity in the
fuel cell stack during dry operating conditions. The water in the diffusion
media 55 is removed from the fuel cell stack 10 through manifolds (not
shown) by the flow of hydrogen and oxygen gas adjacent to and through the
diffusion media 55.

[0030] Because the adhesive layers 58 are electrically conductive, the
contact resistance between the diffusion media 55 and the bipolar plates 52,
54 is minimized. Furthermore, because the adhesive layers 58 provide
electrically conductive contact points between the diffusion media 55 and
the bipolar plates 52, 54, the amount of compressive force placed on the
fuel cell stack 10 to obtain adequate conductivity may be minimized. By
minimizing the compressive force, elastic and plastic deformation of the
bipolar plates 52, 54 and diffusion media 55 may be minimized, thereby
increasing a useful life of the bipolar plates 52, 54. Minimizing the
compressive force on the fuel cell stack 10 also militates against the
intrusion of the diffusion media 55 into the flow channels 64 of the bipolar
plates 52, 54 and fiber creep into the MEA 56.
[0031] Referring next to Fig. 3, a fuel cell assembly 50' is shown according
to another embodiment of the invention. The structure repeated from Fig. 2
includes the same reference numerals and a prime symbol ('). The fuel cell
assembly 50' includes a membrane electrode assembly (MEA) 56' disposed
between a plurality of diffusion media 55', one of the diffusion media 55'
disposed between the MEA 56' and a first bipolar plate 52' and another of
the diffusion media 55' disposed between the MEA 56' and a second
bipolar plate 54'.
[0032] The MEA 56' is disposed between the diffusion media 55' and
includes a proton exchange membrane (PEM) 78' disposed between two
catalyst layers 80'. In the embodiment shown in Fig. 3, the PEM 78' is a
thin, solid polymer membrane-electrolyte but may be any conventional PEM,
as desired. The catalyst layers 80' are typically formed from platinum, but
may be any convention catalyst such as a platinum-ruthenium catalyst, for
example.
[0033] One of the diffusion media 55' is disposed between a side of the
MEA 56' and the first bipolar plate 52' and another of the diffusion media
55' is disposed between another side of the MEA 56' and the second
bipolar plate 54'. The MEA 56' includes a first side 72' and a second side
74'. A microporous layer 76' is disposed on the second side 74' of the
diffusion media 55' between the diffusion media 55' and the MEA 56'. In the
embodiment shown, the diffusion media 55' are carbon fiber paper such as

the MRC U-105 paper produced by Mitsubishi Rayon Company. It is
understood that the porous diffusion media 55' may also be a carbon cloth
or other conventional material adapted to be electrically and thermally
conductive. Furthermore, the diffusion media 55' may be untreated or
treated on the second side 74', with a fluorocarbon polymer, as desired. The
microporous layers 76' are formed from a carbon powder and fluorocarbon
polymer mixture, and may be formed from any conventional carbon ink or
carbon paste.
[0034] The first bipolar plate 52' and the second bipolar plate 54' are formed
from a first unipolar plate 60' and a second unipolar plate 62'. Each of the
first bipolar plate 52' and the second bipolar plate 54' include a first working
face 26' and a second working face 28'. The working faces 26', 28' include
a plurality of flow channels 64' formed therein adapted to distribute a fuel
and an oxidant gas across the bipolar plates 52', 54'. The plurality of flow
channels 64' defines a plurality of lands 66' disposed therebetween.
[0035] Further, the unipolar plates 60', 62' cooperate to form a flow path 68'
intermediate the lands 66' of the unipolar plates 60, 62'. The flow path 68' is
adapted to facilitate a distribution of a dielectric cooling fluid through the
bipolar plates 52', 54'. Any number of flow paths 68' may be formed by the
unipolar plates 60', 62', as desired. Also, the unipolar plates 60', 62' each
form a perimeter portion 84 on an inner surface of an outer peripheral edge
of the unipolar plates 60', 62'. The perimeter portions 84 cooperate to form
a void adapted to receive a sealant 82. In the embodiment shown, the
unipolar plates 60', 62' of the bipolar plates 52', 54' are coupled together
with solder 70'. However, the unipolar plates 60', 62' may be coupled by
any conventional means such as with a b-stage adhesive or by weld-
adhering, for example, or the bipolar plates 52', 54' may be formed from a
single piece of material, as desired. In the embodiment shown, the bipolar
plates 52', 54' are formed from 316 stainless steel but may be formed from
any conventional material such as graphite or a polymer, for example, as
desired. It is understood that the flow channels 64' may be linear,
substantially undulated, serpentine, or may have any other configuration, as
desired.

[0036] An adhesive layer 58' is disposed on the flow channels 64' and lands
66' of each of the bipolar plates 52', 54'. In the embodiment shown, the
adhesive layers 58' are adjacent the second sides 74' of the diffusion media
55' and is formed by an electrically conductive b-stage adhesive. The
adhesive layers 58' couple the lands 66' of the bipolar plates 52', 54' to the
first sides 72' of the diffusion media 55'. The adhesive layers 58' may be
formed from any electrically conductive material, as desired. The adhesive
layers 58' may also be a conductive thermoplastic adhesive, a conductive
thermoplastic adhesive, or a combined conductive primer and conductive
adhesive.
[0037] The sealant 82 is disposed between the voids formed by the
perimeter portions 84 of each of the bipolar plates 52', 54', the MEA 56',
and an outer portion 85 of a fuel cell stack (not shown) to bond the
aforementioned components together and form a seal between the
components. In the embodiment shown, the sealants 82 are a hot melt
sealant such as an epoxy resin. The perimeter portions 84 may be formed in
the outer peripheral edge of the bipolar plates 52', 54' or the perimeter
portions 84 may be formed intermediate the outer peripheral edge and the
working faces 26', 28' of the bipolar plates 52', 54'. The outer portion 85
may be a gasket, a compression means, or other fuel cell stack component,
as desired. It is understood that the sealant 82 may be any conventional
material adapted to form a seal between the bipolar plates 52', 54'and the
MEA 56'. It is understood that the sealant 82 may be separately formed
using an injection molding procedure and disposed in the perimeter portions
84. The sealant 82 may also be applied directly to the perimeter portions 84
of the bipolar plate 52' using a conventional process such as hand coating
or spray coating the sealant 82 on the perimeter portions 84. Also, the
sealant 82 may be applied to the unipolar plates 60', 62' during a coil
coating process, or the sealant 82 may be a gasket separately formed and
disposed in the perimeter portions 84, as desired.
[0038] To assemble the fuel cell assembly 50' shown in Fig. 3, the first
unipolar plate 60' is adhered to the second unipolar plate 62' to form the
bipolar plates 52', 54'. The first unipolar plate 60' may be adhered to the
second unipolar plate 62' by any conventional adhering means such as spot

welding, laser welding, adhesive adhering, or soldering, for example, as
desired. The first unipolar plate 60' is adhered to the second unipolar plate
62' to minimize interfacial electrical resistance through the bipolar plates
52', 54'. It is understood that the bipolar plates 52', 54' may be formed from
a single, integrally formed plate, as desired. The working faces 26', 28' of
the bipolar plates 52', 54' are treated with a primer to facilitate improved
adhering of the adhesive layer 58' and unipolar plates 60', 62'. The primer
may be an acid primer, an alkaline primer, or a self-etching adhesive layer,
as desired. The adhesive layer 58' is disposed on the flow channels 64' and
the lands 66' of the working faces 26', 28' of the bipolar plates 52', 54'. The
adhesive layer 58' may be disposed on the bipolar plates 52', 54' by any
conventional method such as pressed on or sprayed on, for example, as
desired. Also, if the unipolar plates 60', 62' are formed from a metal, the
adhesive layer 58' may be applied to the metal during a coil coating process
and prior to a stamping process that forms the unipolar plates 60', 62'. It is
understood that if the bipolar plates 52', 54' are formed from a polymeric
material, the adhesive layer 58' may be applied directly to the bipolar plates
52', 54' without applying a primer, or the polymeric bipolar plates 52', 54'
may receive a corona discharge treatment or radio frequency glow
discharge treatment to facilitate improved adhering of the adhesive layer 58'
to the bipolar plates 52', 54'.
[0039] The diffusion media 55', the microporous layer 76', the PEM 78', and
the catalyst layer 80' are assembled together. A paste (not shown) is formed
containing a mixture of a carbon powder and fluorocarbon polymers, applied
to the second side 74' of the diffusion media 55', and sintered at or near
380°C to cause the diffusion media 55' and the microporous layer to adhere
together. The microporous layer 76' is adhered to a first face of the catalyst
layer 80' with a self-blocking mechanism by heating the diffusion media 55',
the microporous layer 76', and the catalyst layer 80' at or near 130°C. The
second face of the catalyst layer 80' is adhered to a first side of the PEM
78'. A second diffusion media 55', microporous layer 76', and catalyst layer
80' assembly prepared as described above is adhered to a second side of
the PEM 78'.

[0040] The sealant 82 is disposed in the perimeter portions 84 of the first
bipolar plate 52'. One of the diffusion media 55' is pressed against the
adhesive layer 58' of the bipolar plate 52', and the other diffusion media 55'
is pressed against the adhesive layer 58' of a second bipolar plate 54'.
Once assembled, the fuel cell assembly 50' may be heated to cause the
sealant 82 to bond to the bipolar plates 52', 54' and a perimeter of the MEA
56' and to facilitate an improved adhesion of the MEA 56' and the bipolar
plates 52', 54'. The sealant 82' may also form a fluid-tight seal between the
MEA 56' and the bipolar plates 52', 54', as desired.
[0041] Because the adhesive layers 58' are electrically conductive, the
contact resistance between the diffusion media 55' and the bipolar plates
52', 54' is minimized. Furthermore, because the adhesive layers 58' provide
electrically conductive contact points between the diffusion media 55' and
the bipolar plates 52', 54', the amount of compressive force placed on the
fuel cell stack to obtain adequate conductivity is minimized. By minimizing
the compressive force, elastic and plastic deformation of the bipolar plates
52', 54' and diffusion media 55' is minimized, thereby increasing a useful
life of the bipolar plates 52', 54'. Minimizing the compressive force on the
fuel cell stack also militates against the intrusion of the diffusion media 55'
into the flow channels 64' of the bipolar plates 52', 54' and fiber creep into
the MEA 56'.
[0042] From the foregoing description, one ordinarily skilled in the art can
easily ascertain the essential characteristics of this invention and, without
departing from the spirit and scope thereof, can make various changes and
modifications to the invention to adapt it to various usages and conditions.

WHAT IS CLAIMED IS:
1. A fuel cell assembly comprising:
a membrane electrode assembly including a membrane disposed
between a plurality of catalyst layers;
a plurality of diffusion media, each having a microporous layer
disposed on a side thereof, wherein the side of said diffusion
media having the microporous layer is adhered to the catalyst
layers of said membrane electrode assembly;
a first bipolar plate;
a second bipolar plate; and
an electrically conductive adhesive layer disposed on at least a
portion of said first bipolar plate and said second bipolar plate,
wherein said adhesive layer adheres said first bipolar plate to
one of said diffusion media and said second bipolar plate to
another of said diffusion media to minimize an electrical
contact resistance between said diffusion media and said first
and second bipolar plates.
2. The fuel assembly of Claim 1, wherein said first bipolar plate
and said second bipolar plate include a plurality of flow channels and a
plurality of lands formed therein.
3. The fuel assembly of Claim 2, wherein said adhesive layer
adheres said diffusion media to the lands of said first bipolar plate and said
second bipolar plate.
4. The fuel cell assembly of Claim 1, wherein said adhesive layer
is a b-stage adhesive.

5. The fuel assembly of Claim 1, wherein said first bipolar plate
and said second bipolar plate each include a first unipolar plate having an
inner surface and a second unipolar plate having an inner surface, wherein
the inner surface of the first unipolar plate is coupled to the inner surface of
the second unipolar plate.
6. The fuel cell assembly of Claim 5, wherein the inner surface of
the first unipolar plates and the inner surface of the second unipolar plates
are coupled by one of a b-stage adhesive, soldering, and weld-adhering.
7. The fuel cell assembly of Claim 1, further including a primer
layer disposed intermediate said first bipolar plate and said adhesive layer
and intermediate said second bipolar plate and said adhesive layer.
8. The fuel cell assembly of Claim 1, wherein said first bipolar
plate and said second bipolar plate each include a perimeter portion
adapted to receive a sealant therein.
9. The fuel cell assembly of Claim 8, wherein the sealant is
adapted to adhere said first bipolar plate, said second bipolar plate, and said
membrane electrode assembly and provide and a substantially fluid-tight
seal.

10. A fuel cell stack comprising:
a plurality of membrane electrode assemblies, each including a
membrane disposed between a plurality of catalyst layers;
a plurality of diffusion media, wherein one of said plurality of diffusion
media is adjacent each side of said membrane electrode
assemblies;
a plurality of bipolar plates, each of said bipolar plates having a
perimeter portion, wherein each of said bipolar plates is
disposed between two of said membrane electrode
assemblies;
a sealant disposed in a void formed by the perimeter portions of said
bipolar plates, wherein said sealant forms a seal between said
first bipolar plate, said second bipolar plate, and said
membrane electrode assembly; and
an electrically conductive adhesive layer disposed on at least a
portion of a first bipolar and a second bipolar plate, wherein
said adhesive layer adheres the first bipolar plate to one of
said diffusion media and said second bipolar plate to another
of said diffusion media to minimize an electrical contact
resistance between said diffusion media and the first and the
second bipolar plates.
11. The fuel cell stack of Claim 10, wherein said plurality of bipolar
plates include a plurality of flow channels and a plurality of lands formed
therein.
12. The fuel cell stack of Claim 11, wherein said adhesive layer
adheres said diffusion media to the lands of said plurality of bipolar plates.
13. The fuel cell stack of Claim 10, wherein said adhesive layer is
a b-stage adhesive.

14. The fuel cell stack of Claim 10, wherein said first bipolar plate
and said second bipolar plate each include a first unipolar plate having an
inner surface and a second unipolar plate having an inner surface, wherein
the inner surface of the first unipolar plate is coupled to the inner surface of
the second unipolar plate by one of a b-stage adhesive, soldering, and weld-
adhering.
15. The fuel cell stack of Claim 10, wherein the seal between said
first bipolar plate, said second bipolar plate, and said membrane electrode
assembly is a fluid-tight seal.
16. A method for making a fuel cell assembly for use in a PEM fuel
cell, comprising the steps of:
providing a plurality of bipolar plates, each plate having a first
working face and a second working face;
providing an electrically conductive adhesive layer on the first
working face and the second working face of the bipolar
plates;
providing a membrane electrode assembly having a
membrane disposed between catalyst layers;
coating a diffusion media with a paste to form a microporous
layer thereon;
sintering the diffusion media and microporous layers together;
adhering the microporous layers of the diffusion media to the
catalyst layers of the membrane electrode assembly;
adhering the catalyst layers and the proton exchange
membrane;
adhering the diffusion media to the first working face of
one of the bipolar plates with the adhesive layer and
adhering another diffusion media to the first working
face of another bipolar plate with the adhesive layer.

17. The method of Claim 16, wherein the adhesive layers is a b-
stage adhesive.
18. The method of Claim 16, further including the step of forming
the plurality of bipolar plates from a material coil coated with the adhesive
layer.
19. The method of Claim 16, wherein each of the plurality of
bipolar plates include a perimeter portion.
20. The method of Claim 19, further including the step of providing
a sealant disposed on the perimeter portion of said bipolar plates adapted to
seal a first bipolar plate, a second bipolar plate, and the membrane
electrode assembly together.

A fuel cell assembly and method of forming the same is
disclosed, the fuel cell assembly including a membrane electrode
assembly, a plurality of diffusion media, and a plurality of bipolar
plates, wherein the diffusion media are adhered to the bipolar plates
with an adhesive layer adapted to minimize an electrical resistance
within the fuel cell assembly.

Documents:

01053-kol-2008-abstract.pdf

01053-kol-2008-claims.pdf

01053-kol-2008-correspondence others.pdf

01053-kol-2008-description complete.pdf

01053-kol-2008-drawings.pdf

01053-kol-2008-form 1.pdf

01053-kol-2008-form 2.pdf

01053-kol-2008-form 3.pdf

01053-kol-2008-form 5.pdf

01053-kol-2008-gpa.pdf

1053-KOL-2008-(11-03-2014)-ABSTRACT.pdf

1053-KOL-2008-(11-03-2014)-ANNEXURE TO FORM 3.pdf

1053-KOL-2008-(11-03-2014)-CLAIMS.pdf

1053-KOL-2008-(11-03-2014)-CORRESPONDENCE.pdf

1053-KOL-2008-(11-03-2014)-DESCRIPTION (COMPLETE).pdf

1053-KOL-2008-(11-03-2014)-DRAWINGS.pdf

1053-KOL-2008-(11-03-2014)-FORM-1.pdf

1053-KOL-2008-(11-03-2014)-FORM-2.pdf

1053-KOL-2008-(11-03-2014)-OTHERS.pdf

1053-KOL-2008-ASSIGNMENT.pdf

1053-KOL-2008-CORRESPONDENCE OTHERS 1.1.pdf

1053-KOL-2008-CORRESPONDENCE OTHERS 1.2.pdf

1053-KOL-2008-CORRESPONDENCE-1.3.pdf

1053-KOL-2008-OTHERS.pdf

1053-KOL-2008-TRANSLATED COPY OF PRIORITY DOCUMENT.pdf

abstract-01053-kol-2008.jpg


Patent Number 264014
Indian Patent Application Number 1053/KOL/2008
PG Journal Number 49/2014
Publication Date 05-Dec-2014
Grant Date 28-Nov-2014
Date of Filing 17-Jun-2008
Name of Patentee GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Applicant Address 300 GM RENAISSANCE CENTER DETROIT, MICHIGAN 48265-3000
Inventors:
# Inventor's Name Inventor's Address
1 MICHAEL K. BUDINSKI 10 CARRIAGE STREET HONEOYE FALLS, NEW YORK 14472
PCT International Classification Number H01M8/02; H01M4/86; H01M8/10
PCT International Application Number N/A
PCT International Filing date
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 11/768,471 2007-06-26 U.S.A.