CN201741756U - Fuel cell comprising pluralities of independent battery sub-units - Google Patents

Fuel cell comprising pluralities of independent battery sub-units Download PDF

Info

Publication number
CN201741756U
CN201741756U CN2010201656937U CN201020165693U CN201741756U CN 201741756 U CN201741756 U CN 201741756U CN 2010201656937 U CN2010201656937 U CN 2010201656937U CN 201020165693 U CN201020165693 U CN 201020165693U CN 201741756 U CN201741756 U CN 201741756U
Authority
CN
China
Prior art keywords
fuel cell
catalyst layer
cell
proton exchange
independent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CN2010201656937U
Other languages
Chinese (zh)
Inventor
高勇
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shanghai Everpower Technologies Ltd.
Original Assignee
SHANGHAI EVERPOWER TECHNOLOGIES Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SHANGHAI EVERPOWER TECHNOLOGIES Ltd filed Critical SHANGHAI EVERPOWER TECHNOLOGIES Ltd
Priority to CN2010201656937U priority Critical patent/CN201741756U/en
Application granted granted Critical
Publication of CN201741756U publication Critical patent/CN201741756U/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Landscapes

  • Fuel Cell (AREA)

Abstract

The utility model provides a fuel cell comprising pluralities of independent battery sub-units, comprising a plurality of fuel cell units, wherein each fuel cell unit comprises a bipolar plate and a membrane electrode component; the membrane electrode component comprises a proton exchange membrane and catalyst layers arranged at two sides of the proton exchange membrane; two sides of the proton exchange membrane are provided with mutually independent catalyst layers symmetrically; the proton exchange membrane, the catalyst layer, the air-breathing layer and the bipolar plate at the position of the same catalyst layer form a fuel cell sub-unit; the fuel cell sub-units at the same positions of a plurality of fuel cell units are connected in series to form fuel cell sub-unit groups; and all fuel cell sub-unit groups are connected in series with a diode and are connected with one another in parallel. In the utility model, the whole fuel cell is divided into a plurality of independent fuel cell sub-unit groups, the association among the reaction regions is eliminated, the amplitude of the voltage difference which possibly occurs is segmented and reduced, and the occurrence of the electro-chemical corrosion phenomenon is reduced.

Description

The fuel cell that comprises a plurality of independent cell subunit groups
Technical field
The utility model belongs to the fuel cell technology field, particularly the fuel cell of independent reaction areas.
Background technology
Fuel cell is made of a plurality of battery units usually, and each battery unit comprises two electrodes (bipolar plates), and these two electrodes are separated by electrolyte element, and assembling with being one another in series, forms fuel cell pack.By supplying with suitable reactant for each electrode, promptly give an electrode fueling and another supply oxidant, the realization electrochemical reaction, thus between electrode, form potential difference, and therefore produce electric energy.
For improving the needs that satisfy more high-power output, adopt the mode of conversion zone (catalyst layer) area in the membrane electrode assembly (MEA) that increases each battery unit to realize usually.As shown in Figure 1, the two sides of proton exchange mould 1 among Fig. 1 (front of a side only is shown among Fig. 1) is equipped with catalyst layer 2, reactant enters the runner of bipolar plates from passage 4, the release reaction thing on the catalyst layer 2 of membrane electrode assembly (MEA) electrochemical reaction takes place in the runner.
Compare with technology before, though the runner of bipolar plates design has at present had suitable progress, but along with the increase of conversion zone area in the membrane electrode assembly (MEA), in electrochemical reaction process, the runner on the bipolar plates can not guarantee also that it can carry reactant equably.In the membrane electrode assembly as shown in Figure 1 (MEA), at the runner zone that entire cell is set, from the import to the outlet, in other words, in different regional areas, distribution of air flow is uneven.In these overall or local zones, the concentration of fuel and oxidant also is uneven in addition, in working order down, the electric transient effect that fluctuation produced of the supply of reactant, the relation of its voltage V and same flow channel length L longitudinally is as shown in Figure 2.In the same runner that length L is, may produce bigger voltage difference delta V at the runner two ends; In like manner, phenomenon in this big voltage difference of transversely also may producing of membrane electrode assembly (MEA) conversion zone, and between runner, also may there be the phenomenon that produces voltage difference because of the inhomogeneous release of reactant, cause bigger horizontal (Inplane) electric current of the inner generation of each battery unit, cause the electrochemical corrosion of membrane electrode, this will greatly reduce the useful life of fuel cell.And the zone that the reactant quantity delivered is big is subject to the little zone of reactant quantity delivered, and this associated effect also can cause the big regional output voltage of reactant quantity delivered to be dragged down, and influences the power output of fuel cell.
The utility model content
The purpose of this utility model is to provide a kind of fuel cell that comprises a plurality of independent cell subunit groups, easily produces the technical problem that transverse current causes the corrosion of fuel cell with each battery unit that solves existing fuel cell.
For achieving the above object, the utility model adopts following technical scheme:
A kind of fuel cell that comprises a plurality of independent cell subunit groups, comprise a plurality of cell of fuel cell, each described cell of fuel cell comprises bipolar plates and the membrane electrode assembly between described bipolar plates, described membrane electrode assembly comprises the proton exchange mould and is positioned at the catalyst layer of these proton exchange mould both sides that described proton exchange mould both sides all are arranged with separate catalyst layer;
Position corresponding to each described catalyst layer is provided with an air-permeable layer;
Described bipolar plates comprises non-electrochemical conversion zone and a plurality of electrochemical reactions zone, described electrochemical reaction zone is corresponding with the position of described catalyst layer, splicing is connected with the non-electrochemical conversion zone in described electrochemical reaction zone, and the material of described non-electrochemical conversion zone is a non-conducting material;
The position of the catalyst layer of each described cell of fuel cell is identical, proton exchange mould, catalyst layer, air-permeable layer and the bipolar plates of same catalyst layer position becomes a fuel cell subelement, the fuel cell subelement at a plurality of described cell of fuel cell same positions place is connected in series and constitutes fuel cell subelement group, and is in parallel after each described fuel cell subelement group is connected with a diode.With existing make as far as possible reactant the design concept of the uniform single fuel cell pack of entire reaction region allocation different be, the utility model adopts overall fuel cell is divided into a plurality of individual fuel cell subelement groups, eliminated the relevance between the conversion zone, the amplitude of the voltage difference of cutting apart and having reduced to occur, reduced the generation of electrochemical corrosion phenomenon, brought into play usefulness to greatest extent from an individual fuel cell subelement and even whole fuel cell.
Further, the both sides lateral symmetry of described proton exchange mould is provided with the catalyst layer of a plurality of mutual separations.
Further, the both sides of described proton exchange mould vertically are arranged with the catalyst layer of a plurality of mutual separations.
Further, gap between the described catalyst layer in the same described cell of fuel cell and the gap location between the air-permeable layer filler that is provided with insulation.
Further, described filler and described non-electrochemical conversion zone are structure as a whole.
The utility model is designed to a plurality of distinct area with the catalyst layer in the membrane electrode assembly of fuel cell, and further with correspondingly separately design of air-permeable layer, two plates or the like, can avoid on catalyst layer, air-permeable layer and bipolar plates, producing respectively bigger transverse current so effectively, delay the corrosion phenomenon of fuel cell greatly, improved the life-span of fuel cell.And by the diode that increases, effectively avoided generation because of voltage difference deleterious current between fuel cell subelement group, further improved the life-span of fuel cell, brought into play usefulness to greatest extent from an individual fuel cell subelement and even whole fuel cell.
Further specify the utility model below in conjunction with drawings and Examples.
Description of drawings
Fig. 1 is the structural representation of the membrane electrode assembly of existing fuel cell;
Fig. 2 is the voltage V graph of a relation of membrane electrode assembly on same flow channel length L of existing fuel cell;
Fig. 3 is the structural representation of the membrane electrode assembly among the fuel cell embodiment of the utility model comprises a plurality of independent cell subunit groups;
Fig. 4 is the structural representation that the utility model comprises the bipolar plates among the fuel cell embodiment of a plurality of independent cell subunit groups;
Fig. 5 among the fuel cell embodiment of the utility model comprises a plurality of independent cell subunit groups at the cutaway view at Fig. 3 membrane electrode assembly A-A place;
Fig. 6 is the voltage V graph of a relation of membrane electrode assembly on same flow channel length L among the fuel cell embodiment of the utility model comprises a plurality of independent cell subunit groups;
The fuel cell example structure schematic diagram of Fig. 7 a plurality of independent cell subunit groups for the utility model comprises.
Embodiment
As shown in Figure 5, a kind of fuel cell that comprises a plurality of independent cell subunit groups, comprise a plurality of cell of fuel cell, described cell of fuel cell comprises bipolar plates 10 and the membrane electrode assembly 20 between described bipolar plates 10, described membrane electrode assembly 20 comprises proton exchange mould 22 and is positioned at the catalyst layer 21 of these proton exchange mould both sides, wherein, the catalyst layer 21 of described proton exchange mould 22 both sides is a plurality of separate catalyst layers 21.Being that catalyst layer 21 is separated from each other design, is that one whole design is distinguished mutually with existing catalyst layer 2, avoids producing on catalyst layer 21 bigger transverse current.
Wherein, the catalyst layer 21 of described proton exchange mould 22 both sides is symmetrical arranged.
Wherein, the position corresponding to each described catalyst layer 21 is provided with an air-permeable layer 24.It is this separately mode of design that air-permeable layer 24 also adopts catalyst layer 21.Can avoid on air-permeable layer 24 producing bigger transverse current equally like this.
Wherein, described bipolar plates 10 comprises non-electrochemical conversion zone 12 and a plurality of electrochemical reactions zone 11, described electrochemical reaction zone 11 is corresponding with the position of described catalyst layer 21, and 12 splicings are connected with the non-electrochemical conversion zone in described electrochemical reaction zone 11.Wherein, the material of described non-electrochemical conversion zone 12 is a non-conducting material.
Wherein, as shown in Figure 5, the position of the catalyst layer 21 of each described cell of fuel cell is identical, the proton exchange mould 22 of same catalyst layer 21 positions, catalyst layer 21, air-permeable layer 24 and bipolar plates 10 constitute a fuel cell subelement, the fuel cell subelement at a plurality of described cell of fuel cell same positions place is connected in series and constitutes fuel cell subelement group, in parallel after each described fuel cell subelement group is connected with a diode, as shown in Figure 7.Each fuel cell subelement is separate in the same cell of fuel cell, can not produce transverse current between each subelement, and can not produce electric current between each fuel cell subelement group unit, therefore the useful life that can improve fuel cell effectively because of the difference of voltage yet.
Like this,, and produce transient effect on same described cell of fuel cell, also can not produce bigger voltage difference even the reactant flow that provides owing to runner is inhomogeneous.As shown in Figure 6, in the same longitudinally runner of membrane electrode assembly 20,, and produce transient effect, its voltage V and the relation of same flow channel length L longitudinally because that reactant flow distributes is inhomogeneous.In the same runner that length L is, by catalyst layer 21 is designed to a plurality of distinct area, under the constant situation of flow field condition, it may produce the part that voltage difference delta V has only existing membrane electrode assembly (concrete numerical value depends on the number of catalyst layer 21 on vertical same runner) at the runner two ends, this has reduced the amplitude of variation of voltage in the flow field or electric current greatly.In like manner, the voltage difference that transversely produces at conversion zone 21 also has only the part of existing MEA (concrete numerical value depends on the number of catalyst layer 21 on the horizontal same runner), this has also reduced the inner transverse current that produces of each cell of fuel cell greatly, and the slight lateral electric current that produces is limited in the single fuel cell subelement of branch, avoid the corrosion of whole fuel cell, greatly improved the useful life of fuel cell.Among Fig. 3, the passage 14 (shown in Figure 4) on channel interface 14 and the corresponding bipolar plates 10 is communicated with.
Wherein, the quantity of described catalyst layer 21 can the demand flexible design, and as from 2 to 200, its arrangement mode also can have multiple.Design is as far as possible evenly to distribute preferably, under the prerequisite that does not influence performance, improves the utilance of membrane electrode assembly as far as possible.As, be provided with the catalyst layer 21 of a plurality of mutual separations in the both sides of described proton exchange mould 22 lateral symmetry, and/or vertically be arranged with the catalyst layer 21 of a plurality of mutual separations in the both sides of described proton exchange mould 22.
Describe with four catalyst layers 21 in the present embodiment, should be understood that, this embodiment does not constitute restriction of the present utility model.
Fig. 5 is assembled into the cutaway view of fuel cell at membrane electrode assembly A-A place shown in Figure 3.Wherein, gap between the described catalyst layer 21 in the described same cell of fuel cell and the gap location between the air-permeable layer 24 filler 120 that is provided with insulation.This filler 120 is used to fill this part space and makes the insulation between interchange and the air-permeable layer 24 of insulating between the catalyst layer 21.This filler 120 also can be the part of the non-electrochemical conversion zone 12 of described bipolar plates 10, and promptly this filler 120 is structure as a whole with described non-electrochemical conversion zone 12.Can simplify the processing and the assembling of fuel cell like this.
Wherein, the electrochemical reaction zone 1 of described bipolar plates 10 is meant the zone that fueling and oxidant react, but not electrochemical reaction zone 12 is meant the zone that electrochemical reaction does not take place.This non-electrochemical conversion zone 12 is used to support described electrochemical reaction zone 11, bears extraneous active force.Electrochemical reaction zone 11 and separately design of non-electrochemical conversion zone 12 by with bipolar plates can effectively reduce design difficulty.For example, the bipolar plate material in described electrochemical reaction zone 11 can adopt the material that satisfies fuel battery double plates to make, as adopting carbon plate, metallic plate etc.And the material that the bipolar plate material of described non-electrochemical conversion zone 12 can adopt the cheapness with certain intensity and heat resistance to be easy to machine-shaping is made, and 1 splicing of electrochemical reaction zone is connected in this non-electrochemical conversion zone 12 and gets final product during assembling.
Wherein, the material of described non-electrochemical conversion zone 12 is an insulating material.For example ABS (by styrene-butadiene-acrylonitrile is the base terpolymers), PVC materials such as (pvc materials).This non-electrochemical conversion zone 12 can integrative-structure, also can be to be spliced by polylith.Conversion zone and its peripheral non-reaction zone territory are with a kind of electric conducting material in the bipolar plates of existing fuel cell, this part electric current that makes reaction produce passes through from its peripheral non-reaction zone territory, form eddy current, cause the gradient deviation of electric current, cause the generation of current loss phenomenon, this harmful current phenomenon causes the fuel cell pack reduction in useful life easily.The utility model is by electrochemical reaction zone 11 and separately design of non-electrochemical conversion zone 12 with bipolar plates, and adopt insulating material to make described non-electrochemical conversion zone 12, electric current is passed through from electrochemical reaction zone 12 equably, avoid the generation of eddy current, improved the useful life of fuel cell.And because described non-electrochemical conversion zone 12 is made for insulating material, this connected mode can further be avoided the generation of transverse current.
Wherein, described electrochemical reaction zone 11 is positioned at the middle part, and described non-electrochemical conversion zone 12 is positioned at described electrochemical reaction zone 11 peripheries.
Wherein, the reactant transfer passage 14 that the runner in described non-electrochemical conversion zone 12 electrochemical reaction that be provided with and described zones 12 communicates can adopt the multiple correlation technique of existing bipolar plates to realize, in the detailed description of this omission to this part.
Wherein, described electrochemical reaction zone 1 can adopt multiple mode to realize with the splicing of described non-electrochemical conversion zone 2, as splicing after bonding, hot pressing, the extruding, perhaps the part that will splice mutually is made as definite shape, as step, zigzag, groove, projection and realize by multiple modes such as annular seal bar sealing splicings.
Above-described embodiment only is used to illustrate technological thought of the present utility model and characteristics, its purpose is to make those skilled in the art can understand content of the present utility model and implements according to this, can not only limit claim of the present utility model with present embodiment, be all equal variation or modifications of doing according to the spirit that the utility model disclosed, still drop in the claim of the present utility model.

Claims (5)

1. fuel cell that comprises a plurality of independent cell subunit groups, comprise a plurality of cell of fuel cell, each described cell of fuel cell comprises bipolar plates and the membrane electrode assembly between described bipolar plates, described membrane electrode assembly comprises the proton exchange mould and is positioned at the catalyst layer of these proton exchange mould both sides, it is characterized in that:
Described proton exchange mould both sides all are arranged with separate catalyst layer;
Position corresponding to each described catalyst layer is provided with an air-permeable layer;
Described bipolar plates comprises non-electrochemical conversion zone and a plurality of electrochemical reactions zone, described electrochemical reaction zone is corresponding with the position of described catalyst layer, splicing is connected with the non-electrochemical conversion zone in described electrochemical reaction zone, and the material of described non-electrochemical conversion zone is a non-conducting material;
The position of the catalyst layer of each described cell of fuel cell is identical, proton exchange mould, catalyst layer, air-permeable layer and the bipolar plates of same catalyst layer position becomes a fuel cell subelement, the fuel cell subelement at a plurality of described cell of fuel cell same positions place is connected in series and constitutes fuel cell subelement group, and is in parallel after each described fuel cell subelement group is connected with a diode.
2. the fuel cell that comprises a plurality of independent cell subunit groups according to claim 1 is characterized in that:
The both sides lateral symmetry of described proton exchange mould is provided with the catalyst layer of a plurality of mutual separations.
3. the fuel cell that comprises a plurality of independent cell subunit groups according to claim 1 and 2 is characterized in that:
The both sides of described proton exchange mould vertically are arranged with the catalyst layer of a plurality of mutual separations.
4. the fuel cell that comprises a plurality of independent cell subunit groups according to claim 3 is characterized in that:
The filler that gap between the described catalyst layer in the same described cell of fuel cell and the gap location between the air-permeable layer are provided with insulation.
5. the fuel cell that comprises a plurality of independent cell subunit groups according to claim 4 is characterized in that:
Described filler and described non-electrochemical conversion zone are structure as a whole.
CN2010201656937U 2010-03-30 2010-03-30 Fuel cell comprising pluralities of independent battery sub-units Expired - Lifetime CN201741756U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010201656937U CN201741756U (en) 2010-03-30 2010-03-30 Fuel cell comprising pluralities of independent battery sub-units

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010201656937U CN201741756U (en) 2010-03-30 2010-03-30 Fuel cell comprising pluralities of independent battery sub-units

Publications (1)

Publication Number Publication Date
CN201741756U true CN201741756U (en) 2011-02-09

Family

ID=43557033

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010201656937U Expired - Lifetime CN201741756U (en) 2010-03-30 2010-03-30 Fuel cell comprising pluralities of independent battery sub-units

Country Status (1)

Country Link
CN (1) CN201741756U (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011120425A1 (en) * 2010-03-30 2011-10-06 上海恒劲动力科技有限公司 Fuel cell with multiple independent reaction regions
WO2011120426A1 (en) * 2010-03-30 2011-10-06 上海恒劲动力科技有限公司 Bipolar plate for fuel cell

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011120425A1 (en) * 2010-03-30 2011-10-06 上海恒劲动力科技有限公司 Fuel cell with multiple independent reaction regions
WO2011120426A1 (en) * 2010-03-30 2011-10-06 上海恒劲动力科技有限公司 Bipolar plate for fuel cell

Similar Documents

Publication Publication Date Title
CN101540401B (en) Interlockable bead seal
CN102148387B (en) Conductive porous spacers for nested stamped plate fuel cell
CN207558943U (en) A kind of fuel battery double plates
CN101253645A (en) Gas separator for fuel cell and fuel cell
CN106575776A (en) Flow fields for use with an electrochemical cell
US20120258377A1 (en) Fuel cell
CN105529478B (en) A kind of pile of fuel battery double plates and its composition
US8722276B2 (en) Multiple transition flow field and method
WO2002069426A9 (en) Fluid flow field plates for electrochemical devices
Baroutaji et al. Design and development of proton exchange membrane fuel cell using open pore cellular foam as flow plate material
CN108172857A (en) A kind of fuel cell pile flow-field plate for supporting Dicharged at High Current Desity
CN101807708B (en) Fuel cell containing multiple independent cell subunit groups
CN101826628B (en) Fuel cell with a plurality of independent reaction areas
CN101826621A (en) Bipolar plate for fuel cells
CN104617324A (en) Fuel battery pack with testing function
CN105336967B (en) A kind of fuel cell bipolar plate structure
CN201741756U (en) Fuel cell comprising pluralities of independent battery sub-units
US10141595B2 (en) Fuel cell stack
Li et al. Novel gas distributors and optimization for high power density in fuel cells
Pandiyan et al. Design and analysis of a proton exchange membrane fuel cells (PEMFC)
CN201741755U (en) Fuel cell with independent reaction areas
CN111313049A (en) Gas distribution structure of flow field transition region of graphite bipolar plate
CN215644582U (en) Proton exchange membrane fuel cell cathode plate
CN211743309U (en) Bipolar plate for testing power generation performance of membrane electrode of hydrogen fuel cell
US7097931B2 (en) Fluid flow-fields for electrochemical devices

Legal Events

Date Code Title Description
C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: SHANGHAI EVERPOWER POWER TECHNOLOGY (CANADA) CO.,

Free format text: FORMER OWNER: SHANGHAI EVERPOWER POWER TECHNOLOGY CO., LTD.

Effective date: 20121023

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20121023

Address after: Ben City, British Columbia, Canada

Patentee after: Shanghai Heng Heng Power Technology (Canada) Co., Ltd.

Address before: 201203 Shanghai Zhangjiang hi tech park, No. 1388 East Cheung Road, building 1

Patentee before: Shanghai Everpower Technologies Ltd.

TR01 Transfer of patent right

Effective date of registration: 20180709

Address after: Pudong New Area, Shanghai, China (Shanghai) free trade trial area, 1000 Jinsui Road, 2 Building 1, E area, 2 floor, E area

Patentee after: Shanghai Everpower Technologies Ltd.

Address before: Ben City, British Columbia, Canada

Patentee before: Shanghai Heng Heng Power Technology (Canada) Co., Ltd.

CX01 Expiry of patent term

Granted publication date: 20110209

CX01 Expiry of patent term