IP Library Granted Patent US 8,709,677
Granted Patent B2
US 8,709,677 · App. 13/039,432 · Granted Apr 29, 2014

Proton conducting electrolytes with cross-linked copolymer additives for use in fuel cells

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Quick Facts
Patent No.
US 8,709,677
App. No.
13/039,432
Granted
Apr 29, 2014
Kind
B2
Abstract

A proton conducting polymer electrolyte comprising a proton conducting ionomer cross-linked with an amount of a copolymer additive comprising cross-linking functional groups and other functional groups (e.g. proton carriers, chelating agents, radical scavengers) shows improved durability over the ionomer alone and provides for more stable inclusion of these other functional groups. The copolymer additive comprises at least two types of metal oxide monomers, one having cross-linking functional groups and the other having the other functional groups.

Claims (31)

1. A proton conducting polymer electrolyte comprising a proton conducting ionomer and a polymetaloxane copolymer additive, wherein the polymetaloxane copolymer additive, prior to addition, comprises (i) cross-linking functional groups and (ii) other functional groups, and wherein, in the proton conducting polymer electrolyte, the ionomer and copolymer additive are covalently bonded or acid-base complexed together at the cross-linking functional groups of the polymetaloxane copolymer, wherein: the polymetaloxane copolymer prior to addition comprises a polymerized network of

a plurality of metal oxide monomers with the cross-linking functional groups and

a plurality of metal oxide monomers with the other functional groups, in random or block sequence, wherein:

the metal oxide monomers with the cross-linking functional groups comprise:

a first metal bonded to at least two oxygen atoms and selected from the group consisting of Si, Ti, Zr, Ce, Ta, and Cr; and

the cross-linking functional groups bonded to the first metal and comprising a functional end group containing nitrogen or oxygen and characterized by a chemical structure selected from the group consisting of —NH 2 , ═NH, -(aliphatic) —OH, -(aryl)-OH,

wherein R is a hydrocarbon group; and

the metal oxide monomers with other functional groups comprise:

a second metal bonded to at least two oxygen atoms and selected from the group consisting of Si, Ti, Zr, Ce, Ta, and Cr; and

the other functional groups bonded to the second metal and selected from the group consisting of:

i) proton carrier functional groups comprising a functional end group selected from the group consisting of —PO 3 H 2 , —COOH, —SO 3 H, and —SO 2 NHSO 2 CF 3 ,

ii) metal chelating functional groups comprising a functional end group selected from the group consisting of phosphonic acid, bipyridine, phenanthroline, and derivatives thereof, and

iii) free radical scavenger functional groups comprising a functional end group selected from the group consisting of aminophenyl, hydroxyphenyl and derivatives thereof.

2. The electrolyte of claim 1 , wherein the first and second metals are the same.

3. The electrolyte of claim 2 , wherein the first and second metals are Si.

4. The electrolyte of claim 1 , wherein the cross-linking functional groups have a chemical structure of the form —X-(end group) wherein X is a linear chain comprising a number of CH 2 , O, NH, or aryl groups in random sequence.

5. The electrolyte of claim 4 , wherein the cross-linking functional groups are —(CH 2 ) 3 —NH 2 , -phenyl-NH2, or —(CH 2 ) 3 -(1H-benzimidazol-2-yl).

6. The electrolyte of claim 1 wherein the other functional groups are proton carrier functional groups comprising an end group selected from the group consisting of —PO 3 H 2 , —COOH, —SO 3 H and —SO 2 NHSO 2 CF 3 .

7. The electrolyte of claim 6 , wherein the proton carrier functional groups have a chemical structure of the form —Y-(end group) wherein Y is a linear chain comprising a number of CH 2 , CF 2 , or aryl groups in random sequence.

8. The electrolyte of claim 7 , wherein the proton carrier functional groups are —(CH 2 ) 2 —PO 3 H 2 .

9. The electrolyte of claim 7 , wherein the cross-linking functional groups are —(CH 2 ) 3 —NH 2 , -phenyl-NH 2 , or —(CH 2 ) 3 -(1H-benzimidazol-2-yl) and the proton carrier functional groups are —(CH 2 ) 2 —PO 3 H 2 .

10. The electrolyte of claim 9 wherein the ratio of cross linking functional groups to proton carrier functional groups in the copolymer is from about 1:9 to 3:7.

11. The electrolyte of claim 1 , wherein the polymerized network comprises at least two different metal oxide monomers with other functional groups.

12. The electrolyte of claim 11 , wherein the polymerized network comprises a plurality of metal oxide monomers with proton carrier functional groups and a plurality of metal oxide monomers with free radical scavenger functional groups.

13. The electrolyte of claim 12 , wherein the free radical scavenger functional groups are -3-nitro-4-amino-phenyl.

14. The electrolyte of claim 1 , wherein the proton conducting ionomer comprises sulfonic acid groups.

15. The electrolyte of claim 14 , wherein the proton conducting ionomer is perfluorosulfonic acid ionomer.

16. The electrolyte of claim 15 , wherein the amount of copolymer is from about 5% to 10% by weight of the electrolyte.

17. The electrolyte of claim 1 comprising the proton conducting ionomer and the amount of a copolymer comprising cross-linking functional groups and other functional groups and excluding a basic ionomer.

18. A polymer electrolyte fuel cell comprising the electrolyte of claim 1 .

19. The polymer electrolyte fuel cell of claim 18 , wherein the fuel cell is for operation at temperatures greater than 95° C. and relative humidity less than 50% RH.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2021
From: DAIMLER AG
To: CELLCENTRIC GMBH & CO. KG
Reel/Frame 058386/0706 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2011
From: WANG, KEPING; LI, JING; YANG, YUNSONG
To: DAIMLER AG; FORD MOTOR COMPANY
Reel/Frame 025892/0955 →