Atomically dispersed platinum-group metal-free catalysts and method for synthesis of the same
Atomically dispersed platinum-group metal-free catalyst and method for synthesizing the same. According to one embodiment, the catalyst is made by a method in which, in a first step, an Mn-doped ZIF-8 catalyst precursor is prepared by reacting a first solution comprising zinc nitrate hexahydrate and manganese chloride dissolved in an acid/water solution with a second solution comprising 2-methylimidazole dissolved in water. Then, in a second step, the Mn-doped ZIF-8 catalyst precursor is thermally activated, i.e., carbonized, to form an Mn—N—C catalyst. Preferably, the thermal activation is performed in a multistep fashion, first at a lower temperature of about 800° C. and then at a higher temperature of about 1100° C. After carbonization, the catalyst material may optionally be subjected to an absorption process, followed by a second thermal activation. The absorption process may involve dispersing the catalyst material in a solution of manganese chloride and urea in hydrochloric acid and isopropanol.
1. A method of preparing a catalyst, the method comprising the steps of:
(a) preparing an M-doped ZIF-8 catalyst precursor in an aqueous synthesis reaction, wherein M is selected from the group consisting of Mn, Fe, Ni, Cu, and Co, wherein ZIF-8 is a 2-methylimidazole zinc salt, and wherein the aqueous synthesis reaction takes place in the presence of an acid and in the absence of an organic solvent; and
(b) then, carbonizing the M-doped ZIF-8 catalyst precursor in a first thermal activating step to form an M—N—C catalyst, wherein M is said metal, N is nitrogen, and C is carbon.
2. A method of preparing a catalyst, the method comprising the steps of:
(a) preparing an M-doped ZIF-8 catalyst precursor in an aqueous synthesis reaction, wherein M is selected from the group consisting of Mn, Fe, Ni, Cu, and Co, wherein ZIF-8 is a 2-methylimidazole zinc salt, and wherein the M-doped ZIF-8 catalyst precursor is prepared by reacting a first solution comprising zinc nitrate hexahydrate and manganese chloride dissolved in a solution of hydrochloric acid dissolved in water with a second solution comprising 2-methylimidazole dissolved in water; and
(b) then, carbonizing the M-doped ZIF-8 catalyst precursor in a first thermal activating step to form an M—N—C catalyst, wherein M is said metal, N is nitrogen, and C is carbon.
3. The method as claimed in claim 2 wherein the molar ratio of Mn 2+ to Zn 2+ used for the aqueous synthesis reaction ranges from greater than 0 up to about 10%.
4. The method as claimed in claim 2 wherein the molar ratio among MnCl 2 , Zn(NO 3 ) 2 ·6H 2 O, and 2-methylimidazole is about 0.015:1:47, respectively.
5. The method as claimed in claim 1 wherein M is Mn.
6. The method as claimed in claim 1 wherein the first thermal activating step comprises heating the Mn-doped ZIF-8 catalyst precursor at an elevated temperature of at least 600° C.
7. A method of preparing a catalyst, the method comprising the steps of:
(a) preparing an M-doped ZIF-8 catalyst precursor in an aqueous synthesis reaction, wherein M is selected from the group consisting of Mn, Fe, Ni, Cu, and Co, and wherein ZIF-8 is a 2-methylimidazole zinc salt; and
(b) then, carbonizing the M-doped ZIF-8 catalyst precursor in a first thermal activating step to form an M—N—C catalyst, wherein M is said metal, N is nitrogen, and C is carbon, wherein the first thermal activating step comprises heating the Mn-doped ZIF-8 catalyst precursor in a first step at a first temperature of about 600° C.-1000° C. and then in a second step at a second temperature of about 900° C.-1100° C., and wherein the second temperature is higher than the first temperature.
8. The method as claimed in claim 7 wherein the first thermal activating step comprises heating the Mn-doped ZIF-8 catalyst precursor in a first step at a first temperature of about 800° C. and then in a second step at a second temperature of about 1100° C.
9. The method as claimed in claim 6 wherein the first thermal activating step comprises heating the Mn-doped ZIF-8 catalyst precursor at a temperature of about 1100° C.
10. A method of preparing a catalyst, the method comprising the steps of:
(a) preparing an M-doped ZIF-8 catalyst precursor in an aqueous synthesis reaction, wherein M is selected from the group consisting of Mn, Fe, Ni, Cu, and Co, and wherein ZIF-8 is a 2-methylimidazole zinc salt;
(b) then, carbonizing the M-doped ZIF-8 catalyst precursor in a first thermal activating step to form an M—N—C catalyst, wherein M is said metal, N is nitrogen, and C is carbon, and wherein the M—N—C catalyst is an Mn—N—C catalyst;
(c) adsorbing additional Mn ions into the Mn—N—C catalyst; and
(d) then, performing a second thermal activating step on the catalyst of step (c).
11. The method as claimed in claim 10 wherein the aqueous synthesis reaction of step (a) takes place in the presence of an acid, wherein the first thermal activating step comprises a first temperature of about 800° C. and a second temperature of about 1100° C., and wherein the second thermal activating step comprises heating at about 1100° C.
12. The method as claimed in claim 1 wherein the M—N—C catalyst has a particle size of about 30 nm to about 200 nm.
13. A method of preparing a catalyst, the method comprising the steps of:
(a) preparing an M-doped ZIF-8 catalyst precursor in an aqueous synthesis reaction, wherein M is selected from the group consisting of Mn, Fe, Ni, Cu, and Co, and wherein ZIF-8 is a 2-methylimidazole zinc salt; and
(b) then, carbonizing the M-doped ZIF-8 catalyst precursor in a first thermal activating step to form an M—N—C catalyst, wherein M is said metal, N is nitrogen, and C is carbon, and wherein the M—N—C catalyst has a particle size of about 85 nm.
14. A catalyst prepared by the method of claim 1 .
15. A catalyst prepared by the method of claim 2 .
16. A catalyst prepared by the method of claim 3 .
17. A catalyst prepared by the method of claim 4 .
18. A catalyst prepared by the method of claim 5 .
19. A catalyst prepared by the method of claim 6 .
20. A catalyst prepared by the method of claim 7 .
21. A catalyst prepared by the method of claim 8 .
22. A catalyst prepared by the method of claim 9 .
23. A catalyst prepared by the method of claim 10 .
24. A catalyst prepared by the method of claim 11 .
25. A catalyst prepared by the method of claim 12 .
26. A catalyst prepared by the method of claim 13 .
27. A membrane electrode assembly suitable for use in a proton-exchange membrane fuel cell, the membrane electrode assembly comprising:
(a) a proton-exchange membrane, the proton-exchange membrane having opposing first and second faces;
(b) an anode coupled to the first face of the proton-exchange membrane, the anode comprising an anode catalyst; and
(c) a cathode coupled to the second face of the proton-exchange membrane, the cathode comprising a cathode catalyst, the cathode catalyst comprising the catalyst of claim 14 .
28. A membrane electrode assembly suitable for use in a proton-exchange membrane fuel cell, the membrane electrode assembly comprising:
(a) a proton-exchange membrane, the proton-exchange membrane having opposing first and second faces;
(b) an anode coupled to the first face of the proton-exchange membrane, the anode comprising an anode catalyst; and
(c) a cathode coupled to the second face of the proton-exchange membrane, the cathode comprising a cathode catalyst, the cathode catalyst comprising the catalyst of claim 24 .
29. The method as claimed in claim 1 wherein the M-doped ZIF-8 catalyst precursor is prepared by reacting a first solution comprising zinc nitrate hexahydrate and manganese chloride dissolved in water with a second solution comprising 2-methylimidazole dissolved in water.
30. The method as claimed in claim 1 wherein the aqueous synthesis reaction of step (a) takes place in a solvent of water.
31. The method as claimed in claim 1 wherein the aqueous synthesis reaction of step (a) takes place at room temperature.