IONIC POLYMERS CONTAINING SPIRO STRUCTURE AND PREPARATION METHOD AND APPLICATION THEREOF

Abstract

The present invention introduces ionic polymers featuring with a spiro structure, which enhances the solubility and gas permeability of the ionic polymer while maintaining excellent conductivity, mechanical properties, and dimensional stability. This is achieved by incorporating a spiro fragment with a large free volume into the polymer backbone. As a result, the gas permeability of the catalyst layer prepared from this ionic polymer is improved, making it suitable as a catalyst binder for proton exchange membrane fuel cells (PEMFCs) or anion exchange membrane fuel cells (AEMFCs). Furthermore, the electrochemical performance of the fuel cell is enhanced. Additionally, the proton exchange membrane and anion exchange membrane derived from this ionic polymer containing a spiro structure effectively improve the conductivity of both types of membranes by increasing the space volume due to the presence of the large free volume spiro fragment.

Claims

1. Ionic polymers containing a spiro structure, having a structure as shown in Formula I: ##STR00089## wherein m in Formula I determines the size of the spiro, and m is independently an integer between 2 and 4; x in Formula I is any number between 0.01 and 1.00, y and z are each independently any number between 0 and 0.99, x+y+z=1, and when z is 0, R.sup.2 contains at least one anionic group or cationic group; n in Formula I represents a degree of polymerization, and n is an integer between 10 and 1,000,000; each R.sup.1 in Formula I is independently selected from one or more of the following structures: ##STR00090## p being an integer between 1 and 15; each R.sup.2 in Formula I is independently selected from a hydrogen atom or a cationic group, i.e. the polymer of the structure shown in Formula I is a cationic polymer containing a spiro structure, and a counter ion is an anion; R.sup.2 is selected from one or more of the following structures: ##STR00091## and when z=0, R.sup.2 in x and y units cannot simultaneously be a hydrogen atom; R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 are each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter anion A.sup. is selected from a halide ion, a hydroxide ion, or a bicarbonate ion; when the polymer of the structure shown in Formula I is the cationic polymer containing the spiro structure, R.sup.4 in Ar.sub.2 fragment is a quaternary ammonium cationic group if z is not 0; or each R.sup.2 in Formula I is independently selected from a hydrogen atom or a sulfonate ion, i.e. ##STR00092## then the polymer of the structure shown in Formula I is an anionic polymer containing a spiro structure, and the counter ion is a cation; and when z=0, R.sup.2 in the x and y units cannot simultaneously be a hydrogen atom; a counter ion B.sup.+ is selected from a hydrogen ion, a sodium ion, or a potassium ion; when the polymer of the structure shown in Formula I is the anionic polymer containing the spiro structure, R.sup.4 in the Ar.sub.2 fragment is a sulfonate ion if z is not 0; each R.sup.3 in Formula I is independently selected from one or more of the following structures: ##STR00093## each Ar.sub.1 fragment in Formula I is independently selected from one or more of the following structures: ##STR00094## ##STR00095## each Ar.sub.2 fragment in Formula I is independently selected from one or more of the following structures with ionic groups: ##STR00096## each R being independently selected from the alkylene or arylene groups with the carbon atom number of 1 to 15; R.sup.4 being a quaternary ammonium cation or sulfonate group, wherein if R.sup.4 is the quaternary ammonium cation, R.sup.4 has one or more of the following structures: ##STR00097## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter ion A being selected from a halide ion, a hydroxide ion, or a bicarbonate ion; and the counter ion B.sup.+ being selected from a hydrogen ion, a sodium ion, or a potassium ion if R.sup.4 is the sulfonate ion, that is, ##STR00098##

2. The ionic polymer containing a spiro structure according to claim 1, wherein each R.sup.1 in Formula I is independently selected from one or more of the following structures: ##STR00099## R.sup.2 in Formula I is independently selected from the hydrogen atom or the cationic group, i.e. the cationic polymer containing the spiro structure, and the counter ion is the anion; R.sup.2 is independently selected from ##STR00100## or R.sup.2 is independently selected from the hydrogen atom or the sulfonate ion, ##STR00101## i.e. the anionic polymer containing the spiro structure, and the counter ion is the cation; each Ar.sub.1 fragment in Formula I is independently selected from one or more of the following structures: ##STR00102## each Ar.sub.2 fragment in Formula I is independently selected from one or more of the following structures: ##STR00103## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15; R.sup.4 being an anionic group or a cationic group.

3. A preparation method of the ionic polymer containing a spiro structure according to claim 1, wherein when each R.sup.2 in Formula I is independently selected from one or more of ##STR00104## R.sup.4 in Formula I is the quaternary ammonium cation, having one or more of the following structures: ##STR00105## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter ion A.sup. being selected from a halide ion, a hydroxide ion, or a bicarbonate ion; the polymer of the structure shown in Formula I is a cationic polymer containing a spiro structure, and a preparation method of the cationic polymer containing the spiro structure comprises the following steps: mixing a halogen-terminated polymer precursor with the structure shown in Formula II, a first organic solvent, and a tertiary amine compound, and then carrying out a first substitution reaction to obtain the cationic polymer containing the spiro structure, ##STR00106## in Formula II, X.sup.1, X.sup.2, and X.sup.3 being each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 being not hydrogen atoms at the same time; in Formula II, Ar.sub.2 is an arylene unit tethering with halogen atoms, having one or more of the following structures: ##STR00107## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; and the tertiary amine compound being selected from one or more of ##STR00108## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10.

4. A preparation method of the ionic polymer containing a spiro structure according to claim 1, wherein when each R.sup.2 in Formula I is independently selected from one or more of ##STR00109## and R.sup.4 is a sulfonate group, i.e. ##STR00110## then the polymer of the structure shown in Formula I is an anionic polymer containing a spiro structure; the counter ion B.sup.+ being selected from the hydrogen ion, the sodium ion, or the potassium ion; a preparation method of the anionic polymer containing the spiro structure comprises the following steps: (1) combining a halogen-terminated polymer precursor with the structure shown in Formula II with a second organic solvent and a thioacetate before carrying out a second substitution reaction to obtain a polymer precursor with a structure shown in Formula IV; the second substitution reaction is shown in Formula V: ##STR00111## in Formula II, X.sup.1, X.sup.2, and X.sup.3 being each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 being not hydrogen atoms at the same time; in Formula II, Ar.sub.2 is an arylene unit tethering with halogen atoms, having one or more of the following structures ##STR00112## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; ##STR00113## in Formula IV and V, X.sup.5, X.sup.6, and X.sup.7 being each independently selected from an acetylthio group or a hydrogen atom, and when z=0, X.sup.5 and X.sup.6 being not hydrogen atoms at the same time; in Formulas IV and V, Ar.sub.2 being an arylene unit tethering with the acetylthio group, having one or more of the following structures: ##STR00114## a structural formula of the thioacetate being ##STR00115## and the thioacetate being selected from one or more of ##STR00116## (2) performing an oxidation reaction after mixing the polymer precursor IV obtained in the step (1) with an oxidizing reagent, to obtain the anionic polymer containing the spiro structure, the oxidizing reagent being selected from one or more of a carboxylic acid solution containing hydrogen peroxide or a peroxyacid oxidant, and the peroxyacid oxidant being one or more of ##STR00117##

5. The preparation method of the ionic polymer containing a spiro structure according to claim 3, wherein a preparation method of the halogen-terminated polymer precursor with the structure shown in Formula II comprises the following steps: performing a polycondensation reaction after mixing a spiro-containing aromatic compound, Ar.sub.1, Ar.sub.2, a ketone monomer, and a third organic solvent and an organic strong acid, to obtain the halogen-terminated polymer precursor with the structure shown in Formula II, wherein the polycondensation reaction is shown in Formula III, ##STR00118## wherein in Formula III, when the amount of Ar.sub.1 as a raw material is zero, y=0; in Formula III, when the amount of Ar.sub.2 as a raw material is zero, z=0; in Formula III, X is independently selected from a halogen atom or a hydrogen atom, X.sup.1, X.sup.2, and X.sup.3 are each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 are not hydrogen atoms at the same time; the spiro-containing aromatic compound has one or more of the following structures: ##STR00119## a structure of the ketone monomer is ##STR00120## Ar.sub.1 is an aromatic compound having one or more of the following structures: ##STR00121## Ar.sub.2 is an aromatic compound tethering with halogen group, having one or more of the following structures: ##STR00122## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; and the strong organic acid is at least one of methanesulfonic acid, trifluoromethanesulfonic acid, and trifluoroacetic acid.

6. Application of the ionic polymer containing a spiro structure according to claim 1 as a catalyst binder for a proton exchange membrane fuel cell (PEMFC) or an anion exchange membrane fuel cell (AEMFC).

7. The application according to claim 6, wherein counter ions in the ionic polymer containing a spiro structure are converted into other kinds of counter ions as needed before the ionic polymer containing a spiro structure is used as the catalyst binder for the PEMFC or the AEMFC.

8. Application of the ionic polymer containing a spiro structure according to claim 1 in preparation of a proton exchange membrane or an anion exchange membrane.

9. The application according to claim 8, wherein a method for preparing the proton exchange membrane or the anion exchange membrane using the ionic polymer containing a spiro structure comprises the following steps: dissolving or dispersing the ionic polymer containing a spiro structure in an organic solvent to acquire a solution or dispersion of the polymer; coating the solution or dispersion of the polymer on a substrate and then removing the solvent to obtain the proton exchange membrane or the anion exchange membrane; and converting counter ions in the proton exchange membrane or the anion exchange membrane into other kinds of counter ions as needed.

10. A preparation method of the ionic polymer containing a spiro structure according to claim 2, wherein when each R.sup.2 in Formula I is independently selected from one or more of ##STR00123## R.sup.4 in Formula I is the quaternary ammonium cation, having one or more of the following structures: ##STR00124## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter ion A.sup. being selected from a halide ion, a hydroxide ion, or a bicarbonate ion; the polymer of the structure shown in Formula I is a cationic polymer containing a spiro structure, and a preparation method of the cationic polymer containing the spiro structure comprises the following steps: mixing a halogen-terminated polymer precursor with the structure shown in Formula II, a first organic solvent, and a tertiary amine compound, and then carrying out a first substitution reaction to obtain the cationic polymer containing the spiro structure, ##STR00125## in Formula II, X.sup.1, X.sup.2, and X.sup.3 being each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 being not hydrogen atoms at the same time; in Formula II, Ar.sub.2 is an arylene unit tethering with halogen atoms, having one or more of the following structures: ##STR00126## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; and the tertiary amine compound being selected from one or more of ##STR00127## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10.

11. A preparation method of the ionic polymer containing a spiro structure according to claim 2, wherein when each R.sup.2 in Formula I is independently selected from one or more of ##STR00128## and R.sup.4 is a sulfonate group, i.e. ##STR00129## then the polymer of the structure shown in Formula I is an anionic polymer containing a spiro structure; the counter ion B.sup.+ being selected from the hydrogen ion, the sodium ion, or the potassium ion; a preparation method of the anionic polymer containing the spiro structure comprises the following steps: (1) combining a halogen-terminated polymer precursor with the structure shown in Formula II with a second organic solvent and a thioacetate before carrying out a second substitution reaction to obtain a polymer precursor with a structure shown in Formula IV; the second substitution reaction is shown in Formula V: ##STR00130## Formula II, in Formula II, X.sup.1, X.sup.2, and X.sup.3 being each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 being not hydrogen atoms at the same time; in Formula II, Ar.sub.2 is an arylene unit tethering with halogen atoms, having one or more of the following-structures: ##STR00131## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; ##STR00132## in Formulas IV and V, X.sup.5, X.sup.6, and X.sup.7 being each independently selected from an acetylthio group or a hydrogen atom, and when z=0, X.sup.5 and X.sup.6 being not hydrogen atoms at the same time; in Formulas IV and V, Ar.sub.2 being an arylene unit tethering with the acetylthio group, having one or more of the following structures: ##STR00133## a structural formula of the thioacetate being ##STR00134## and the thioacetate being selected from one or more of ##STR00135## (2) performing an oxidation reaction after mixing the polymer precursor IV obtained in the step (1) with an oxidizing reagent, to obtain the anionic polymer containing the spiro structure, the oxidizing reagent being selected from one or more of a carboxylic acid solution containing hydrogen peroxide or a peroxyacid oxidant, and the peroxyacid oxidant being one or more of ##STR00136##

12. The preparation method of the ionic polymer containing a spiro structure according to claim 4, wherein a preparation method of the halogen-terminated polymer precursor with the structure shown in Formula II comprises the following steps: performing a polycondensation reaction after mixing a spiro-containing aromatic compound, Ar.sub.1, Ar.sub.2, a ketone monomer, and a third organic solvent and an organic strong acid, to obtain the halogen-terminated polymer precursor with the structure shown in Formula II, wherein the polycondensation reaction is shown in Formula III, ##STR00137## wherein in Formula III, when the amount of Ar.sub.1 as a raw material is zero, y=0; in Formula III, when the amount of Ar.sub.2 as a raw material is zero, z=0; in Formula III, X is independently selected from a halogen atom or a hydrogen atom, X.sup.1, X.sup.2, and X.sup.3 are each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 are not hydrogen atoms at the same time; the spiro-containing aromatic compound has one or more of the following structures: ##STR00138## a structure of the ketone monomer is ##STR00139## Ar.sub.1 is an aromatic compound having one or more of the following structures: ##STR00140## Ar.sub.2 is an aromatic compound tethering with halogen group, having one or more of the following ##STR00141## each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; and the strong organic acid is at least one of methanesulfonic acid, trifluoromethanesulfonic acid, and trifluoroacetic acid.

13. Application of the ionic polymer containing a spiro structure according to claim 2 as a catalyst binder for a proton exchange membrane fuel cell (PEMFC) or an anion exchange membrane fuel cell (AEMFC).

14. Application of the ionic polymer containing a spiro structure according to claim 2 in preparation of a proton exchange membrane or an anion exchange membrane.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0062] FIG. 1 is a graph of water uptake as a function of temperature for PCPTPA membrane of Application example 2 of the present invention and the PTPA membrane of Comparative example 1;

[0063] FIG. 2 is a graph of a swelling ratio of the PCPTPA membrane of Application example 2 of the present invention and a PTPA membrane of Comparative example 1 as a function of temperature;

[0064] FIG. 3 is a graph of chloride ion conductivity as a function of temperature for the PCPTPA membrane of Application example 2 of the present invention and the PTPA membrane of Comparative example 1;

[0065] FIG. 4 is a graph of changes before and after alkaline treatment of PCPTPA membrane in Application example 2 according to the present invention;

[0066] FIG. 5 is a graph of electrochemical performances of PCPTPA membrane in Application example 2 of the present invention and PTPA membrane in Comparative example 1, respectively;

[0067] FIG. 6 is a graph of hydrogen ion conductivity as a function of temperature for SPFL membrane in Application example 6 of the present invention and commercial Nafion 212 membrane;

[0068] FIG. 7 is a graph of an oxidative stability test of a proton exchange membrane with hydrogen ion as counter ion in Application example 7 of the present invention at 80 C. in a 3 ppm Fe.sup.2+, 3% H.sub.2O.sub.2 solution;

[0069] FIG. 8 is an electrochemical performance diagram of a proton exchange membrane with a counter ion of a hydrogen ion in Application example 8 according to the present invention;

[0070] FIG. 9 is a graph showing the gas permeation current density of the ion exchange membrane with a spiro structure prepared in Application example 6 according to the present invention and Nafion 212.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0071] The present invention provides ionic polymers containing a spiro structure, having a structure as shown in Formula I:

##STR00038## [0072] where m in Formula I determines the size of the spiro, and m is independently an integer between 2 and 4; [0073] where x in Formula I is any number between 0.01 and 1.00, y and z are each independently any number between 0 and 0.99, x+y+z=1, and when z is 0, R.sup.2 contains at least one anionic group or cationic group; [0074] where n in Formula I represents the degree of polymerization, and n is an integer between 10 and 1,000,000; [0075] where each R.sup.1 in Formula I is independently selected from one or more of the following structures:

##STR00039## [0076] p being an integer between 1 and 15; [0077] where each R.sup.2 in Formula I is independently selected from a hydrogen atom or a cationic group, i.e. if a polymer of the structure shown in Formula I is a cationic polymer containing a spiro structure, and a counter ion is an anion; R.sup.2 is selected from one or more of the following structures:

##STR00040## and when z=0, R.sup.2 in x and y units cannot simultaneously be a hydrogen atom; R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 are each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter anion A.sup. is selected from a halide ion, a hydroxide ion, or a bicarbonate ion; [0078] or where each R.sup.2 in Formula I is independently selected from a hydrogen atom or a sulfonate ion, i.e.

##STR00041## then the polymer of the structure shown in Formula I is an anionic polymer containing a spiro structure, and the counter ion is a cation; and when z=0, R.sup.2 in the x and y units cannot simultaneously be a hydrogen atom; a counter ion B.sup.+ is independently selected from a hydrogen ion, a sodium ion, or a potassium ion; [0079] where each R.sup.3 in Formula I is independently selected from one or more of the following structures:

##STR00042## [0080] where each Ar.sub.1 fragment in Formula I is independently selected from one or more of the following structures:

##STR00043## ##STR00044## [0081] where each Ar.sub.2 fragment in Formula I is independently selected from one or more of the following structures:

##STR00045## [0082] each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15; R.sup.4 being a quaternary ammonium cation or sulfonate group, where if R.sup.4 is the quaternary ammonium cation, R.sup.4 has one or more of the following structures:

##STR00046## [0083] R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter ion A.sup. being selected from a halide ion, a hydroxide ion, or a bicarbonate ion; [0084] the counter ion B.sup.+ being selected from a hydrogen ion, a sodium ion, or a potassium ion if R.sup.4 is the sulfonate ion, that is,

##STR00047##

[0085] In the present invention, each Ar.sub.1 fragment in Formula I is preferably independently selected from one or more of the following structures,

##STR00048##

[0086] In the present invention, each Ar.sub.2 fragment in Formula I is preferably independently selected from one or more of the following structures:

##STR00049## [0087] each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15; R.sup.4 being an anionic group or a cationic group.

[0088] In the present invention, each R.sup.1 in Formula I is preferably independently selected from one or more of the following structures:

##STR00050##

[0089] In the present invention, R.sup.2 in Formula I is independently selected from the hydrogen atom or a cationic group, i.e. the cationic polymer containing the spiro structure, and the counter ion is the anion; R.sup.2 is independently selected from

##STR00051## [0090] R.sup.2 is independently selected from the hydrogen atom or the sulfonate ion,

##STR00052## i.e. the anionic polymer containing the spiro structure, and the counter ion is the cation.

[0091] In the present invention, each R.sup.3 in Formula I is preferably independently selected from one or more of the following structures:

##STR00053##

[0092] In the present invention, the ionic polymer containing a spiro structure preferably has one or more of the following structures:

##STR00054## ##STR00055## ##STR00056##

[0093] The present invention also provides a preparation method of the ionic polymer containing a spiro structure according to the above technical solution, when each R.sup.2 in Formula I is independently selected from one or more of

##STR00057##

R.sup.4 in Formula I is the quaternary ammonium cation, having one or more of the following structures:

##STR00058## [0094] R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10; a counter ion A.sup. being selected from a halide ion, a hydroxide ion, or a bicarbonate ion; [0095] the polymer of the structure shown in Formula I is a cationic polymer containing a spiro structure, and a preparation method of the cationic polymer containing the spiro structure includes the following steps: [0096] mixing a halogen-terminated polymer precursor with the structure shown in Formula II, a first organic solvent, and a tertiary amine compound, and then carrying out a first substitution reaction to obtain the cationic polymer containing the spiro structure,

##STR00059## [0097] in Formula II, X.sup.1, X.sup.2, and X.sup.3 being each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 being not hydrogen atoms at the same time; [0098] in Formula II, Ar.sub.2 is an arylene unit tethering with halogen atoms, having one or more of the following structures:

##STR00060## [0099] each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; and [0100] the tertiary amine compound being selected from one or more of

##STR00061## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10.

[0101] In the present invention, the tertiary amine compound being selected from one or more of

##STR00062## R.sup.01, R.sup.02, R.sup.03, R.sup.04, and R.sup.05 being each independently selected from a hydrocarbyl with the carbon atom number of 1 to 10. In the present invention, the molar ratio of the amount of halogen end group in halogen-terminated polymer precursor to the amount of tertiary amine compound is between 1:1 and 1:10.

[0102] In the present invention, the first organic solvent is preferably a polar aprotic solvent, more preferably at least one of dimethylsulfoxide, N-methylpyrrolidone, N, N-dimethylformamide, and N, N-dimethylacetamide.

[0103] In the present invention, the temperature of the first substitution reaction is preferably 0 to 100 C., more preferably 20 to 80 C.; the time for the first substitution reaction is from 0.1 to 200 h, more preferably from 2 to 48 h.

[0104] After the first substitution reaction is completed, the present invention preferably combines the product of the first substitution reaction and a first precipitant, and then sequentially performs solid-liquid separation, washing and drying to obtain a cationic polymer containing a spiro structure.

[0105] In the present invention, the first precipitant is preferably at least one of water, acetone, diethyl ether, ethyl acetate, toluene, and petroleum ether. The operation of the solid-liquid separation, washing, and drying according to the present invention is not particularly limited and can be performed using techniques that are well known in the related field.

[0106] The present invention also provides a preparation method of the ionic polymer containing a spiro structure according to the above technical solution, when each R.sup.2 in Formula I is independently selected from one or more of

##STR00063##

and R.sup.4 is a sulfonate group,

##STR00064##

then the polymer of the structure shown in Formula I is an anionic polymer containing a spiro structure; the counter ion B.sup.+ being selected from the hydrogen ion, the sodium ion, or the potassium ion; a preparation method of the anionic polymer containing the spiro structure includes the following steps: [0107] (1) combining a halogen-terminated polymer precursor with the structure shown in Formula II with a second organic solvent and a thioacetate before carrying out a second substitution reaction to obtain a polymer precursor with a structure shown in Formula IV; the second substitution reaction is shown in Formula V:

##STR00065## [0108] in Formula II, X.sup.1, X.sup.2, and X.sup.3 being each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 being not hydrogen atoms at the same time; [0109] in Formula II, Ar.sub.2 is an arylene unit tethering with halogen atoms, having one or more of the following structures:

##STR00066## [0110] each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I; and

##STR00067## [0111] in Formulas IV and V, X.sup.5, X.sup.6, and X.sup.7 being each independently selected from the acetylthio group or hydrogen atom, and when z=0, X.sup.5 and X.sup.6 being not hydrogen atoms at the same time; [0112] in Formulas IV and V, Ar.sub.2 being an arylene unit tethering with the acetylthio group, having one or more of the following structures:

##STR00068## [0113] a structural formula of the thioacetate being

##STR00069## and [0114] the thioacetate is selected from one or more

##STR00070## [0115] (2) performing an oxidation reaction after mixing the polymer precursor IV obtained in the step (1) with an oxidizing reagent, to obtain the anionic polymer containing the spiro structure, [0116] the oxidizing reagent being selected from one or more of a carboxylic acid solution containing hydrogen peroxide or a peroxyacid oxidant, and the peroxyacid oxidant being one or more of

##STR00071##

[0117] In the present invention, the molar ratio of the amount of halogen end group in halogen-terminated polymer precursor to the amount of thioacetate compounds is between 1:1 and 1:10.

[0118] In the present invention, the second organic solvent is preferably a polar aprotic solvent, more preferably at least one of dimethylsulfoxide, N-methylpyrrolidone, N, N-dimethylformamide, and N, N-dimethylacetamide.

[0119] In the present invention, the temperature of the second substitution reaction is preferably 0 to 100 C., more preferably 0 to 60 C.; the time for the second substitution reaction is preferably from 1 to 100 h, more preferably from 4 to 24 h, further preferably from 5 to 16 h.

[0120] In the present invention, the molar ratio of the amount of acetylthio group in the precursor represented by Formula IV to the amount of oxidizing reagent is between 1:1 and 1:10.

[0121] In the present invention, the temperature of the oxidation reaction is preferably 0 to 100 C., more preferably 0 to 50 C.; the time of the oxidation reaction is preferably 0 to 100 h, more preferably 5 to 48 h, further preferably 8 to 20 h.

[0122] After the oxidation reaction is completed, the present invention preferably combines the product of the oxidation reaction with a second precipitant, and then sequentially performs solid-liquid separation, washing, and drying to obtain an anionic polymer containing a spiro structure.

[0123] In the present invention, the second precipitant is preferably at least one of water, acetone, diethyl ether, ethyl acetate, toluene, and petroleum ether. The operation of the solid-liquid separation, washing, and drying according to the present invention is not particularly limited and can be performed using techniques that are well known in the related field.

[0124] In the present invention, the halogen-terminated polymer precursor with the structure shown in Formula II in the present invention preferably includes the following steps:

[0125] performing a polycondensation reaction after mixing spiro-containing aromatic compound, Ar.sub.1, Ar.sub.2, ketone monomer, and third organic solvent and organic strong acid, to obtain the halogen-terminated polymer precursor with the structure shown in Formula II, where the polycondensation reaction is shown in Formula III,

##STR00072## [0126] in Formula III, when the amount of Ar.sub.1 as a raw material is zero, y=0; when the amount of Ar.sub.2 as a raw material is zero, z=0; [0127] in Formula III, X is independently selected from a halogen atom or a hydrogen atom, X.sup.1, X.sup.2, and X.sup.3 are each independently selected from a halogen atom or a hydrogen atom, and when z=0, X.sup.1 and X.sup.2 are not hydrogen atoms at the same time; [0128] the spiro-containing aromatic compound has one or more of the following structures:

##STR00073## [0129] a structure of the ketone monomer is

##STR00074## [0130] Ar.sub.1 is an aromatic compound having one or more of the following structures:

##STR00075## [0131] Ar.sub.2 is an aromatic compound tethering with halogen group, having one or more of the following structures:

##STR00076## [0132] each R being independently selected from an alkylene or an arylene group with the carbon atom number of 1 to 15, and X.sup.4 being a halogen atom selected from one or more of Cl, Br, and I.

[0133] The strong organic acid is at least one of methanesulfonic acid, trifluoromethanesulfonic acid, and trifluoroacetic acid.

[0134] In the present invention, the molar ratio of the ketone monomer to the strong organic acid is preferably between 1:1 and 1:20.

[0135] In the present invention, the third organic solvent is preferably at least one of dichloromethane, chloroform, carbon tetrachloride, dichloroethane, nitromethane, and nitrobenzene.

[0136] In the present invention, the temperature of the polycondensation reaction is preferably 20 to 100 C., more preferably 0 to 30 C.; the polycondensation reaction time is preferably 0.1 to 100 h, more preferably 0.5 to 48 h.

[0137] After the polycondensation reaction is completed, the present invention preferably combines the product of the polycondensation reaction with a third precipitant, and then sequentially performs solid-liquid separation, washing and drying to obtain a halogen-terminated polymer precursor with the structure shown in Formula II.

[0138] In the present invention, the third precipitant is preferably at least one of water, methanol, ethanol, acetone, diethyl ether, and ethyl acetate. The operation of the solid-liquid separation, washing, and drying according to the present invention is not particularly limited and can be performed using techniques that are well known in the related field.

[0139] The preparation method of the ionic polymer containing a spiro structure provided by the present invention is simple and easy process, and suitable for large-scale production.

[0140] The present invention also provides the application of the ionic polymer containing a spiro structure according to the above technical solution as a binder for the catalyst layer of a PEMFC or an AEMFC.

[0141] In the present invention, before using the ionic polymer containing a spiro structure as a catalyst binder for a PEMFC or an AEMFC, it is preferable to convert the counter ion of the ionic polymer containing a spiro structure into another kind of counter ion as needed.

[0142] In the present invention, the method of converting the counter ion of the ionic polymer containing a spiro structure into another kind of counter ion according to necessity, preferably includes the following steps: the ionic polymer containing a spiro structure is soaked into a solution containing other kinds of counter ions and then washed with deionized water thoroughly to obtain an ionic polymer containing a spiro structure with other kinds of counter ions.

[0143] In the present invention, when the counter ion in the ionic polymer containing a spiro structure is an anion, the counter ion of the other kind is preferably at least one of hydroxide ion, carbonate ion, bicarbonate ion, sulfate ion, other halide ion different from A.sup.; the solution containing other kinds of counter ions is preferably one of Na.sub.2SO.sub.4 solution, NaOH solution, NaCl solution, Na.sub.2CO.sub.3 solution, K.sub.2CO.sub.3 solution, NaHCO.sub.3 solution, and KHCO.sub.3 solution.

[0144] In the present invention, when the counter ion in the ionic polymer containing a spiro structure is a cation, the counter ion of the other kind is preferably at least one of hydrogen ion, sodium ion, potassium ion; the solution containing other kinds of counter ions is preferably one of H.sub.2SO.sub.4 solution, HCl solution, Na.sub.2CO.sub.3 solution, K.sub.2CO.sub.3 solution, NaHCO.sub.3 solution, and KHCO.sub.3 solution.

[0145] In the present invention, the concentration of the solution containing other kinds of counter ions is preferably 0.01 to 10 mol/L.

[0146] In the present invention, the soaking time is preferably 12 to 48 h; the temperature of the soaking is preferably from 30 to 50 C.

[0147] In the present invention, the application of the ionic polymer containing a spiro structure as a catalyst binder for a PEMFC or an AEMFC for preparing a slurry of a catalyst binder containing a spiro structure, preferably includes the following steps: dissolving or dispersing the ionic polymer containing a spiro structure in an organic solvent to obtain a solution or dispersion of a catalyst binder; the catalyst binder solution or dispersion is then mixed uniformly with the catalyst to obtain a slurry containing the catalyst binder.

[0148] In the present invention, the organic solvent is preferably a low boiling point organic solvent, more preferably at least one of methanol, isopropanol, and ethanol. In the present invention, the concentration of the ionic polymer containing a spiro structure in the slurry of the catalyst binder having a spiro structure is 0.5 to 80 wt. %.

[0149] The present invention also provides the application of the ionic polymer containing a spiro structure according to the above technical solution for preparing a proton exchange membrane or an anion exchange membrane.

[0150] In the present invention, the preparation method of a proton exchange membrane or an anion exchange membrane using the ionic polymer containing a spiro structure preferably includes the following steps: [0151] dissolving or dispersing the ionic polymer containing a spiro structure in a fifth organic solvent to acquire a solution or dispersion of the polymer; [0152] coating the solution or dispersion of the polymer on a substrate and then removing the solvent to obtain the proton exchange membrane or the anion exchange membrane; and

[0153] In the present invention, the fifth organic solvent is preferably a polar aprotic solvent, more preferably at least one of dimethylsulfoxide, N-methylpyrrolidone, N, N-dimethylformamide, and N, N-dimethylacetamide. In the present invention, the substrate is selected from a glass plate, a Teflon plate, or a reinforcing fabric. In the present invention, the method of coating membrane is preferably solution casting membrane, spin coating membrane, wiped membrane, casting, or dipping membrane. In the present invention, the method for removing the solvent is preferably evaporation at room temperature or drying by heating at 30 to 100 C.

[0154] In the present invention, the method of converting the counter ion in the proton exchange membrane or anion exchange membrane into other kinds of counter ion according to need preferably includes the following steps: the proton exchange membrane or anion exchange membrane is soaked in a solution containing other kinds of counter ions, and then washed with deionized water thoroughly to obtain a proton exchange membrane or anion exchange membrane containing other kinds of counter ions.

[0155] In the present invention, when the counter ion in the anion exchange membrane is an anion, the counter ion is preferably at least one of hydroxide ion, carbonate ion, bicarbonate ion, sulfate ion, other halide ion different from A.sup.; the solution containing other kinds of counter ions is preferably one of Na.sub.2SO.sub.4 solution, NaCl solution, Na.sub.2CO.sub.3 solution, K.sub.2CO.sub.3 solution, NaHCO.sub.3 solution, and KHCO.sub.3 solution.

[0156] In the present invention, when the counter ion in the proton exchange membrane is a cation, the counter ion is preferably at least one of the hydrogen ion, sodium ion, or potassium ion; the solution containing other kinds of counter ions is preferably one of H.sub.2SO.sub.4 solution, HCl solution, Na.sub.2CO.sub.3 solution, K.sub.2CO.sub.3 solution, NaHCO.sub.3 solution, and KHCO.sub.3 solution.

[0157] In the present invention, the solution containing other kinds of counter ions is preferably 0.01 to 10 mol/L.

[0158] In the present invention, the soaking time is preferably 12 to 48 h; the temperature of the soaking is preferably from 30 to 60 C.

[0159] The present invention will now be described more detailed hereinafter concerning examples thereof. It is to be understood that the described embodiments are only a few, but not all embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by a person of ordinary skill in the art without inventive effort fall within the scope of the present invention.

Example 1

[0160] An ionic polymer containing a spiro structure has a structure represented by Formula (1-1):

##STR00077##

[0161] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro (cyclohexane-1,9-fluorene) (0.50 g, 2.135 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (0.53 g, 2.135 mmol), dichloromethane (2.0 mL), and trifluoromethanesulfonic acid (2.0 mL) were subjected to a polycondensation reaction at room temperature for 12 h to obtain a viscous polymer solution. After the polycondensation reaction was complete, the product was slowly added dropwise to a mixed solvent of ethanol and water (1:1) to obtain a white fibrous polymer, which was then filtered, thoroughly washed, and dried. 0.86 g of a white fibrous bromo-terminated polymer was obtained.

[0162] Then, the above bromo-terminated polymer was dissolved in 15 mL of N-methylpyrrolidone, 2.6 mL of trimethylamine in ethanol (4.2 mol/L) was added, and after the first substitution reaction was carried out at room temperature for 48 hours, the product of the first substitution reaction was slowly added to anhydrous diethyl ether, filtered, and dried to obtain 0.82 g of an off-white fibrous (at which time the counter ion is bromide ion) cationic polymer containing a spiro structure.

Application Example 1

[0163] The counter ions of the ionic polymer containing a spiro structure prepared in Example 1 were exchanged into HCO.sub.3.sup. by ion exchange as the following procedure: soaking the ionic polymer containing a spiro structure in a 2 mol/L NaHCO.sub.3 solution for 48 h, and then washing with deionized water thoroughly to obtain an ionic polymer containing a spiro structure with a counter ion of HCO.sub.3.sup. as a catalyst binder.

[0164] The ionic polymer containing a spiro structure prepared in Example 1 was dissolved in 10 mL of dimethyl sulfoxide to obtain a polymer solution. After filtration, the solution was coated on a clean glass plate by a solution casting method, and the glass plate was placed in a thermoventilated oven at 80 C. to dry for 24 h to evaporate the solvent. Once the temperature was cooled to room temperature, the glass plate was taken out, and the membrane was removed after soaking in deionized water. After thorough washing with deionized water, an anion exchange membrane with a counter ion of Br.sup. was obtained.

[0165] The anion exchange membrane in which the counter ion prepared above is Br.sup. can be exchanged into Cl.sup. by ion exchange as needed, and the steps are as follows: immersing the anion exchange membrane with the counter ion of Br.sup. in a 2 mol/L NaCl solution for 48 h, and then thoroughly washing with deionized water to obtain an anion exchange membrane in Cl.sup. form.

Example 2

[0166] An ionic polymer containing a spiro structure has a structure represented by Formula (1-2):

##STR00078##

[0167] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro (cyclopentane-1,9-fluorene) (0.22 g, 0.924 mmol), p-terphenyl (0.26 g, 1.129 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (0.61 g, 2.460 mmol), dichloromethane (1.0 mL) and trifluoromethanesulfonic acid (2.2 mL) were subjected to a polycondensation reaction at room temperature for 10 h to produce a viscous polymer solution. Once the polycondensation reaction was complete, the product was slowly added dropwise to a mixed solvent of ethanol and water (1:1). A white fibrous polymer was filtered, and dried to obtain 0.98 g of bromo-terminated polymer.

[0168] Then, the aforementioned bromo-terminated polymer was dissolved in 15 mL of N-methylpyrrolidone, 2.7 mL of trimethylamine in ethanol (4.2 mol/L) was added. After the first substitution reaction was carried out at room temperature for 48 hours, the reaction solution was added to anhydrous diethyl ether, filtered, and dried to obtain 1.02 g of an off-white fibrous cationic polymer containing a spiro structure.

Application Example 2

[0169] The ionic polymer containing a spiro structure prepared in Example 2 was dissolved in 11 mL of dimethyl sulfoxide to produce a polymer solution. After filtration, the solution was coated on a clean glass plate by a solution casting method. The glass plate was placed in a thermoventilated oven at 80 C. for 24 h to evaporate the solvent. After the temperature was cooled to room temperature, the glass plate was taken out and placed in deionized water to remove a membrane, and after thorough washing with deionized water, an anion exchange membrane with a counter ion of Br.sup. was obtained.

[0170] The anion exchange membrane in which the counter ion prepared above is Br.sup. can be exchanged into Cl.sup. by ion exchange as needed, and the steps are as follows: immersing the anion exchange membrane with the counter ion of Br.sup. in a 2 mol/L NaCl solution for 48 h, and then thoroughly washing with deionized water to obtain an anion exchange membrane with the counter ion of Cl.sup..

Example 3

[0171] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-3):

##STR00079##

[0172] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro (cyclopentane-1,9-fluorene) (0.16 g, 0.677 mmol), 9,9-bis (6-bromohexyl)-9H-fluorene (0.22 g, 0.4514 mmol), trifluoroacetone (0.21 g, 1.862 mmol), dichloromethane (5.0 mL) and trifluoromethanesulfonic acid (5.0 mL) were subjected to a polycondensation reaction at room temperature for 48 h to obtain a viscous polymer solution. After the reaction was complete, the product was slowly added dropwise to a mixed solvent of methanol and water (1:1) to obtain a white fibrous polymer. The white fibrous polymer was filtered and dried to obtain 0.51 g of bromo-terminated polymer.

[0173] Then, the above bromo-terminated polymer was dissolved in 13 mL of N-methylpyrrolidone, 1.8 mL of trimethylamine in ethanol (4.2 mol/L) was added, and after the first substitution reaction was carried out at room temperature for 48 hours, the reaction solution was added to ethyl acetate, filtered, and dried to obtain 0.52 g of an off-white fibrous cationic polymer containing a spiro structure.

Application Example 3

[0174] According to the method of Application example 1, the counter ion of the ionic polymer containing a spiro structure prepared in Example 3 is subjected to ion exchange as needed to obtain an ionic polymer containing a spiro structure having a counter ion Cl.sup. as a catalyst binder.

[0175] According to the method of Application example 2, using the ionic polymer containing a spiro structure prepared in Example 3 to prepare an anion exchange membrane with a counter ion of Br.sup.; the difference from Application example 2 was the application of 8 mL of dimethyl sulfoxide.

[0176] According to the method of Application example 2, the anions in the above-prepared anion exchange membrane with the counter ion of Br.sup. are subjected to ion exchange as needed to obtain an anion exchange membrane with the counter ion of Cl.sup..

Example 4

[0177] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-4):

##STR00080##

[0178] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro (cyclopentane-1,9-fluorene) (0.16 g, 0.677 mmol), 7,7,7-trifluoro-6,6-diphenyl-1-bromoheptane (1.34 g, 4.062 mmol), biphenyl (0.28 g, 2.031 mmol), 2,2,2-trifluoroacetophenone (1.29 g, 7.448 mmol), dichloromethane (10.0 mL) and trifluoromethanesulfonic acid (10.0 mL) were reacted at room temperature for 48 h to obtain a viscous polymer solution. The product of the polycondensation reaction was added dropwise to a mixed solvent (1:1) of methanol and water to obtain a white fibrous polymer. The white fibrous polymer was filtered and dried to obtain 2.06 g of a bromo-terminated polymer.

[0179] Then, the above bromo-terminated polymer was dissolved in 50 mL of N-methylpyrrolidone, 10.4 mL of trimethylamine in ethanol (4.2 mol/L) was added, and after the first substitution reaction at room temperature for 48 hours, the reaction solution was added to ethyl acetate, filtered, and dried to obtain 2.04 g of an off-white fibrous cationic polymer containing a spiro structure.

Application Example 4

[0180] According to the method of Application example 2, using the ionic polymer containing a spiro structure prepared in Example 4 to prepare an anion exchange membrane with a counter ion of Br.sup.; the difference from Application example 2 was the application of 27 mL of dimethyl sulfoxide.

[0181] According to the method of Application example 2, the anions in the above-prepared anion exchange membrane with the counter ion of Br.sup. are subjected to ion exchange as needed to obtain an anion exchange membrane with the counter ion of Cl.sup..

Example 5

[0182] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-5):

##STR00081##

[0183] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro (cyclohexane-1,9-fluorene) (0.36 g, 1.544 mmol), bibenzyl (0.42 g, 2.316 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (1.94 g, 7.864 mmol), dichloromethane (7.0 mL) and trifluoromethanesulfonic acid (7.0 mL) were reacted at room temperature for 48 h to obtain a viscous polymer solution. After the reaction was complete, it was added dropwise to water to obtain a white fibrous polymer, which was filtered and dried to obtain 1.57 g of a white fibrous bromo-terminated polymer.

[0184] Then, the above bromo-terminated polymer was dissolved in 31 mL of N-methyl pyrrolidone, 3.27 g of quinuclidine was added, and after 5 days of the first substitution reaction at 60 C., the product of the first substitution reaction was slowly added to anhydrous diethyl ether, filtered, and dried to obtain 2.1 g of an off-white fibrous cationic polymer containing a spiro structure.

Application Example 5

[0185] According to the method of Application example 1, the counter ion of the ionic polymer containing a spiro structure prepared in Example 5 is subjected to ion exchange as needed to obtain an ionic polymer containing a spiro structure with a counter ion of HCO.sub.3.sup. as a catalyst binder.

Comparative Example 1

[0186] Ionic polymer backbone without a spiro unit: terphenyl backbone structural formula:

##STR00082##

[0187] The ionic polymer backbone without the spiro unit terphenyl backbone is prepared by: performing a polycondensation reaction on terphenyl (0.60 g, 2.608 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (0.71 g, 2.869 mmol), dichloromethane (6.9 mL) and trifluoromethanesulfonic acid (2.4 mL) at room temperature for 20 h to obtain a viscous polymer solution, and after the reaction was complete, dropwise adding the product of the polycondensation reaction to a mixed solvent of methanol and water (1:1) to obtain a white fibrous polymer. The white fibrous polymer was filtered and dried to obtain 1.12 g of a white fibrous bromo-terminated polymer.

[0188] Then, the above bromo-terminated polymer was dissolved in 20 mL of N-methylpyrrolidone, 3.9 mL of trimethylamine in ethanol (4.2 mol/L) was added, and after the first substitution reaction at 30 C. for 72 hours, the reaction solution was added to anhydrous diethyl ether, filtered, and dried to obtain 1.10 g of a cationic polymer having a backbone without spiro unit.

[0189] Using the above ionic polymer having a backbone free of the spiro unit terphenyl backbone as a starting material, a PTPA membrane is prepared by:

[0190] According to the method of Application example 2, an anion exchange membrane with a counter ion of Br.sup. was prepared by using the ionic polymer with the backbone prepared in comparative example 1 without the spiro cyclic element terphenyl backbone; the difference from Application example 2 is the application of 15 mL of dimethyl sulfoxide.

[0191] According to the method of Application example 2, the anions in the above-prepared anion-exchange membrane with the counter ion of Br.sup. are subjected to ion exchange as needed to obtain an anion-exchange membrane with the counter ion of Cl.sup. (abbreviated as PTPA membrane).

[0192] Anion exchange membrane (abbreviated as PCPTPA membrane) with the counter ion of Cl.sup. in Application example 2 and catalyst binder with the counter ion of HCO.sub.3.sup. in Application example 1 prepared from the ionic polymer containing a spiro structure prepared in Example 2 and PTPA membrane in Comparative example 1 were respectively tested to characterize their basic properties.

(1) Water Uptake, Swelling Ratio, and Conductivity

[0193] The water uptake and swelling ratio were measured by the soaking method, and graphs showing the water uptake and swelling ratio of the PCPTPA membrane in Application example 2 and the PTPA membrane in Comparative example 1 as a function of temperature are shown in FIGS. 1 and 2. It can be seen from FIGS. 1 and 2 that PCPTPA membranes exhibited higher water uptake and swelling ratios than PTPA membranes without the spiro unit in the backbone. This is due to the loose packing of the polymer backbone in PCPTPA membranes, which is a result of the incorporated spiro structure.

[0194] The four-electrode AC impedance method was used to measure the conductivity, and the graphs of the chloride ion conductivity of the PCPTPA membrane in Application example 2 and the PTPA membrane in Comparative example 1 as a function of temperature are shown in FIG. 3, and it can be seen from FIG. 3 that: at 80 C., the chloride ion conductivity of PCPTPA membrane reaches 38 mS/cm, which is 19% higher than that of PTPA membrane (32 mS/cm).

Alkali Stability

[0195] After the PCPTPA membrane in Application example 2 was subjected to alkaline treatment at 80 C. in an aqueous solution of 1 mol/L NaOH for 1000 hours, the change before and after the nuclear magnetic resonance was observed and the alkaline stability was examined to obtain a plot of the change before and after the alkaline treatment (solvent: DMSO-d.sub.6) is shown in FIG. 4. As can be seen from FIG. 4, the content of trimethylammonium groups (3.00 ppm) remains essentially unchanged relative to the integral of chemically inert aromatic protons (7.10 to 8.00 ppm) after 1000 hours of aging of the PCPTPA membrane, demonstrating the strong base durability of the PCPTPA membrane.

(3) Cell Performance

[0196] Using the PCPTPA membrane (namely, the anion exchange membrane with the counter ion of Cl.sup.) in Application example 2 and the catalyst binder with the counter ion of HCO.sub.3.sup. in Application example 1, and the PTPA membrane in comparative example 1 and the catalyst binder with the counter ion of HCO.sub.3.sup. in Application example 1, Pt/C was employed as both cathode and anode catalysts, with the loading amount of Pt in both the anode and cathode was set at 0.5 mg/cm.sup.2. A MEA was fabricated by ultrasonic spraying, and an H.sub.2O.sub.2 fuel cell test was conducted at 80 C. with a gas flow rate of 300 mL min.sup.1. As shown in FIG. 5, the maximum power density of the MEA composed of the PCPTPA membrane reached 1.05 W/cm.sup.2, whereas the maximum power density of the MEA composed of the PTPA membrane reached 0.76 W/cm.sup.2. The PCPTPA membrane in Application example 2 and the PTPA membrane in Comparative example 1 were tested as part of an MEA, respectively.

Example 6

[0197] An ionic polymer containing a spiro structure has a structure represented by Formula (1-6):

##STR00083##

[0198] The preparation method of the ionic polymer containing a spiro structure is as follows: [0199] spiro [cyclopentane-1,9-[9H] fluorene] (0.52 g, 2.3603 mmol), 8-bromo-1,1,1-trifluorooctan-2-one (1.6848 g, 6.4532 mmol), dichloromethane (5.1 mL) and trifluoromethanesulfonic acid (5.1 mL) were subjected to a polycondensation reaction at room temperature for 48 h to obtain a viscous polymer solution. After the polycondensation reaction was complete, the product was slowly added dropwise to a mixed solvent of methanol and water (1:1) to obtain a white fibrous polymer. This polymer was then filtered and washed thoroughly to obtain 1.00 g of a white fibrous bromo-terminated polymer after vacuum drying.

[0200] (1) The above-mentioned bromo-terminated polymer was dissolved in 12 mL of N, N-dimethylacetamide, adding potassium thioacetate (2.42 g, 21.2 mmol), heating to 50 C. for a second substitution reaction for 22 h, and cooling to room temperature to obtain a polymer precursor.

[0201] (2) To the polymer precursor obtained in the step (1), meta-chloroperoxybenzoic acid (3.65 g, 21.2 mmol) was added for an oxidation reaction for 18 h, and the product of the oxidation reaction was slowly added to 120 mL of a 2 mol/L NaCl solution to obtain 1.01 g of an anionic polymer containing a spiro structure as an off-white fiber.

Application Example 6

[0202] The counter ion of the ionic polymer containing a spiro structure prepared in Example 6 was exchanged into a cation H.sup.+ by ion exchange as needed, the procedure was: soaking the ionic polymer containing a spiro structure in a 2 mol/L H.sub.2SO.sub.4 solution for 24 h, and washing with deionized water to obtain an ionic polymer containing a spiro structure with a counter ion of H.sup.+ as a catalyst binder.

[0203] The ionic polymer containing a spiro structure prepared in Example 6 was dissolved in 10.4 mL of dimethyl sulfoxide to obtain a polymer solution, and after filtration, the solution was coated on a clean glass plate by a solution casting method, and the glass plate was placed in a thermoventilated oven at 80 C. for 24 h to evaporate the solvent; after the temperature was cooled to room temperature, the glass plate was taken out, and it was subjected to de-membrane in deionized water, and after thorough washing with deionized water, a proton exchange membrane with a counter ion of Na.sup.+ was obtained.

[0204] The counter ion in the above-mentioned prepared proton exchange membrane of which the counter ion is Na.sup.+ is exchanged into a cation H.sup.+ by ion exchange as needed, the steps being: the prepared proton exchange membrane with a counter ion of Na.sup.+ was immersed in a 2 mol/L H.sub.2SO.sub.4 solution for 24 h, and then washed with deionized water thoroughly to obtain a proton exchange membrane with a counter ion of H.sup.+.

Example 7

[0205] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-7):

##STR00084##

[0206] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro [cyclopentane-1,9-[9H] fluorene] (0.12 g, 0.5447 mmol), 7,7,7-trifluoro-6,6-diphenyl-1-bromoheptane (0.72 g, 2.1788 mmol), 2,2,2-trifluoroacetophenone (1.67 g, 9.5675 mmol), dichloromethane (5.6 mL) and trifluoromethanesulfonic acid (5.6 mL) were subjected to a polycondensation reaction at room temperature for 24 h to obtain a viscous polymer solution. After the polycondensation reaction was complete, the product of the polycondensation reaction was slowly added dropwise to a mixed solvent of methanol and water (1:1) to obtain a white fibrous polymer. Then, it was filtered and washed thoroughly, and after vacuum drying, 1.17 g of a white fibrous bromo-terminated polymer was obtained.

[0207] (1) The above-mentioned bromo-terminated polymer was dissolved in 13.7 mL of N, N-dimethylacetamide, adding potassium thioacetate (2.13 g, 18.6 mmol), heating to 50 C. for a second substitution reaction for 10 h, and cooling to room temperature to obtain a polymer precursor.

[0208] (2) To the polymer precursor obtained in the step (1), meta-chloroperoxybenzoic acid (3.22 g, 18.6 mmol) was added for an oxidation reaction for 10 h, and the product of the oxidation reaction was slowly added to 137 mL of a 2 mol/L NaCl solution to obtain 1.15 g of an anionic polymer containing a spiro structure as an off-white fiber.

Application Example 7

[0209] Proton exchange membranes with Na.sup.+ counter ions were prepared according to the method of Application example 6 using the ionic polymer containing a spiro structure prepared in Example 7, which is different from Example 6 by using 12.1 mL of dimethyl sulfoxide.

[0210] According to the method of Application example 6, the counter ion in the above-prepared proton exchange membrane with the counter ion of Na.sup.+ is subjected to ion exchange as needed to obtain a proton exchange membrane with the counter ion of Na.sup.+.

Example 8

[0211] In this example, the ionic polymer containing a spiro structure has a structural formula represented by formula (1-8):

##STR00085##

[0212] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro [cyclopentane-1,9-[9H] fluorene] (0.20 g, 0.9078 mmol), para-quaterphenyl (0.42 g, 1.3617 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (1.1337 g, 4.5892 mmol), dichloromethane (5.7 mL) and trifluoromethanesulfonic acid (5.7 mL) were subjected to a polycondensation reaction at room temperature for 36 h to obtain a viscous polymer solution. The product was slowly dropped into a mixed solvent (1:1) of methanol and water to obtain a white fibrous polymer. The white fibrous polymer was filtered and dried to obtain 1.05 g of bromo-terminated polymer.

[0213] (1) The above-mentioned bromo-terminated polymer precursor was dissolved in 12.5 mL of N, N-dimethylacetamide, adding potassium thioacetate (2.81 g, 24.5 mmol), heating to 50 C. for a second substitution reaction for 15 h, and cooling to room temperature to obtain a polymer precursor.

[0214] (2) To the polymer precursor obtained in the step (1), meta-chloroperoxybenzoic acid (4.24 g, 24.5 mmol) was added for an oxidation reaction for 20 h, and the product of the oxidation reaction was slowly added to 125 mL of a 2 mol/L NaCl solution to obtain 1.05 g of an anionic polymer containing a spiro structure as an off-white fiber.

Application Example 8

[0215] Proton exchange membranes with Na.sup.+ counter ions were prepared according to the method of Application example 6 using the ionic polymer containing a spiro structure prepared in Example 8, which is different from Example 6 by using 10.8 mL of dimethyl sulfoxide.

[0216] According to the method of Application example 6, the counter ion in the above-prepared proton exchange membrane with the counter ion of Na.sup.+ is subjected to ion exchange as needed to obtain a proton exchange membrane with the counter ion of H.sup.+.

Example 9

[0217] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-9):

##STR00086##

[0218] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro [cyclohexane-1,9-[9H] fluorene] (0.66 g, 2.8 mmol), hexafluoro-2,2-diphenylpropane (0.21 g, 0.7 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (1.81 g, 7.3 mmol), dichloromethane (3.6 mL) and trifluoromethanesulfonic acid (3.6 mL) were reacted at room temperature for 36 h to obtain a viscous polymer solution. After the reaction was complete, it was slowly added dropwise to a mixed solvent (1:1) of methanol and water to obtain a white fibrous polymer. The white fibrous polymer was filtered and dried to obtain 1.58 g of bromo-terminated polymer.

[0219] (1) The above-mentioned bromo-terminated polymer was dissolved in 19 mL of N, N-dimethylacetamide, adding potassium thioacetate (3.08 g, 27.0 mmol), heating to 50 C. for a second substitution reaction for 14 h, and cooling to room temperature to obtain a polymer precursor.

[0220] (2) To the polymer precursor obtained in the step (1), meta-chloroperoxybenzoic acid (4.66 g, 27.0 mmol) was added for an oxidation reaction for 19 h, and the product of the oxidation reaction was slowly added to 190 mL of a 2 mol/L NaCl solution to obtain 1.51 g of an anionic polymer containing a spiro structure as an off-white fiber.

Application Example 9

[0221] According to the method of Application example 6, the counter ion of the ionic polymer containing a spiro structure prepared in Example 9 is subjected to ion exchange as needed to obtain an ionic polymer containing a spiro structure with a counter ion of H.sup.+ as a catalyst binder.

Example 10

[0222] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-10):

##STR00087##

[0223] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro [cyclohexane-1,9-[9H] fluorene] (0.32 g, 1.3 mmol), 7,7,7-trifluoro-6,6-diphenyl-1-bromoheptane (0.45 g, 1.3 mmol), 1,1,1-trifluoroacetone (1.06 g, 9.3 mmol), dichloromethane (5.6 mL) and trifluoromethanesulfonic acid (5.6 mL) were reacted at room temperature for 11 h to obtain a viscous polymer solution. After the reaction was complete, it was slowly added dropwise to a mixed solvent (1:1) of methanol and water to obtain a white fibrous polymer, which was filtered and dried to obtain 1.10 g of a bromo-terminated polymer.

[0224] (1) The above-mentioned bromo-terminated polymer precursor was dissolved in 11 mL of N, N-dimethylacetamide before adding potassium thioacetate (1.38 g, 12.1 mmol), and carrying out a second substitution reaction at room temperature for 24 h to obtain a polymer precursor.

[0225] (2) To the polymer precursor obtained in the step (1), m-chloroperoxybenzoic acid (2.09 g, 12.1 mmol) was added and oxidized for 22 h, and the product of the oxidation was added to 110 mL of a 2 mol/L NaCl solution to obtain 1.05 g of an anionic polymer containing a spiro structure in the form of an off-white fiber.

Application Example 10

[0226] Proton exchange membranes with Na.sup.+ counter ions were prepared according to the method of Application example 6 using the ionic polymer containing a spiro structure prepared in Example 10, which is different from Example 6 by using 9 mL of dimethyl sulfoxide.

[0227] According to the method of Application example 6, the counter ion in the above-prepared proton exchange membrane with the counter ion of Na.sup.+ is subjected to ion exchange as needed to obtain a proton exchange membrane with the counter ion of Na.sup.+.

Example 11

[0228] An ionic polymer containing a spiro structure has a structural formula represented by Formula (1-11):

##STR00088##

[0229] The preparation method of the ionic polymer containing a spiro structure is as follows: spiro [cyclohexane-1,9-[9H] fluorene] (0.20 g, 0.8 mmol), 9,9-bis (6-bromohexyl)-9H-fluorene (0.07 g, 0.1 mmol), p-terphenyl (0.09 g, 0.4 mmol), 7-bromo-1,1,1-trifluoroheptan-2-one (2.68 g, 10.9 mmol), dichloromethane (12.4 mL) and trifluoromethanesulfonic acid (12.4 mL) were subjected to a polycondensation reaction at room temperature for 16 h to obtain a viscous polymer solution. After the polycondensation reaction was complete, the product of the polycondensation reaction was slowly dropped into a mixed solvent (1:1) of methanol and water to obtain a white fibrous polymer. It was then filtered and washed thoroughly. After vacuum drying, 0.31 g of a white fibrous bromo-terminated polymer was obtained.

[0230] (1) The above-mentioned bromo-terminated polymer was dissolved in 8 mL of N, N-dimethylacetamide, adding potassium thioacetate (2.03 g, 17.8 mmol), heating to 50 C. for 22 h, and cooling to room temperature to obtain a polymer precursor.

[0231] (2) To the polymer precursor obtained in the step (1), m-chloroperoxybenzoic acid (3.07 g, 17.8 mmol) was added and oxidized for 19 h, and the product of the oxidation was slowly added to 160 mL of a 2 mol/L NaCl solution to obtain 0.30 g of an anionic polymer containing a spiro structure as an off-white fiber.

Application Example 11

[0232] According to the method of Application example 6, the counter ion of the ionic polymer containing a spiro structure prepared in Example 11 is subjected to ion exchange as needed to obtain an ionic polymer containing a spiro structure with a counter ion of H.sup.+ as a catalyst binder.

[0233] The proton exchange membrane and the catalyst binder in Application examples 6 to 11 prepared from the ionic polymer containing a spiro structure prepared in Examples 6 to 11 were respectively tested to evaluate their basic properties.

[0234] FIG. 6 is a graph showing the variation of the hydrogen ion conductivity with the temperature of the proton exchange membrane SPFL membrane and the Nafion 212 membrane. The counter ion prepared from the ionic polymer containing a spiro structure in Example 6 is a hydrogen ion, and it can be seen from FIG. 6 that: the hydrogen ion conductivity of the SPFL membrane reaches 289 mS/cm, which is 38% higher than that of the Nafion 212 membrane (209 mS/cm).

[0235] The oxidative stability is important for the practical application of ionic polymers. FIG. 7 is a graph showing changes in conductivity and weight of a proton exchange membrane of Application example 7 in which a counter ion is a hydrogen ion, prepared from an ionic polymer containing a spiro structure of Example 7, after oxidative stability testing in a 3 ppm Fe.sup.2+, 3% H.sub.2O.sub.2 solution at 80 C. for 4 hours and 8 hours. It can be seen from FIG. 7 that the weight and conductivity of the proton exchange membrane with the counter ion of hydrogen ion in Application example 7 do not significantly decrease after soaking for 4 hours, indicating that the polymer with a spiro structure in Application example 7 has excellent oxidative stability, and the conductivity and weight of the proton exchange membrane decrease by 0.9% and 1.7% after soaking for 8 hours in Fenton reagent, respectively.

[0236] A proton exchange membrane with a hydrogen ion as a counter ion in Application example 8, which was prepared using the ionic polymer containing a spiro structure in Example 8, the ionic polymer containing a spiro structure in Example 6 as a binder for a catalyst layer, Pt/C as a catalyst for a cathode and an anode, the Pt loading amount in the anode and cathode is 0.2 mg/cm.sup.2, are used, and the assembled MEA is subjected to H.sub.2O.sub.2 fuel cell test at 80 C., with a gas flow rate of 100 mL/min, a back pressure of 100 kPa, and a relative humidity (RH) of 30%. The electrochemical performance of the membrane electrode of the proton exchange membrane whose counter ion is hydrogen ion in Example 8 is shown in FIG. 8, it can be seen from FIG. 8 that the maximum power density of the MEA of the proton exchange membrane in which the counter ion is hydrogen ion in Application example 8 reaches 1.09 W/cm.sup.2.

[0237] FIG. 9 is a graph showing the gas permeation current density of the ion exchange membrane having a spiro structure prepared in Application example 6 and the commercial Nafion212 membrane, and it can be seen from FIG. 9 that the ionic membrane having a spiro structure prepared in Application example 6 has a higher gas permeation current density than Nafion212, indicating that the ionic membrane with a spiro structure prepared in Application example 6 has better gas permeability.

[0238] In light of the above, the present invention provides an ionic polymer containing a spiro structure. By incorporating a spiro fragment with a medium-large free volume into the polymer main chain, the ionic polymer exhibits improved solubility, gas permeability, and ion conductivity while maintaining good adhesiveness, mechanical properties, and dimensional stability. This contributes to enhanced gas permeability in the catalyst layer prepared from the ionic polymer, serving as either a catalyst binder for a PEMFC or an AEMFC. Moreover, the reactant gas can more easily reach the surface of the catalyst, facilitating the electrochemical reaction within the fuel cell and improving its overall electrochemical performance. Proton exchange membranes and anion exchange membranes derived from ionic polymers containing spiro structures benefit from the increased space volume provided by the large free volume spiro fragments, leading to enhanced conductivity of both types of membranes.

[0239] While the foregoing is directed to the preferred embodiment of the present invention, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the spirit and scope of the invention.