Dipyridyl ketone coordination complexes for reduction of carbon dioxide

Abstract

A series of 2,2′-dipyridyl ketone (DPK) containing metal complexes have been synthesized with metals including Mn, Fe, Co, Ni, Cu, Ru, Pd, and Pt. These complexes have one, two or three DPK ligands chelated to the metal center. In addition to the DPK ligands the complexes can comprise halogen ligands that can easily exchange with carbon dioxide to allow for reduction to small molecules such as methanol or oxalate. Initial electrochemical measurements show a reversible binding of carbon dioxide to the metal catalyst.

Claims

1. A catalytic, solar fuel production method comprises reducing gaseous carbon dioxide from a gas source comprising exposing a carbon dioxide reduction catalyst to said source of gaseous carbon dioxide; said carbon dioxide reduction catalyst comprising a dipyridyl ketone coordination complex comprised of a transition metal and dipyridyl ketone.

2. The catalytic method of claim 1 wherein said solar fuel produced comprises fuel feedstocks, triazines, and various combinations thereof.

3. The catalytic method of claim 1 wherein said solar fuel produced comprises CO, HCO.sub.2H, HCHO, CH.sub.3OH, CH.sub.4, 2,4,6-trimethyl-1,3,5-triazine, and various combinations thereof.

4. The catalytic method of claim 1 wherein said solar fuel produced comprises 2,4,6-trimethyl-1,3,5-triazine.

5. The method of claim 1 wherein said source of gaseous carbon dioxide is the atmosphere.

6. The method of claim 1 wherein said coordination complex comprises a discrete complex with a single transition metal center.

7. The method of claim 1 wherein the catalyst having the formula: ##STR00003## where M is a transition metal and X is a halogen.

8. The method of claim 1 wherein the catalyst having the formula: ##STR00004## where M is a transition metal and X is a halogen.

9. The method of claim 1 wherein the catalyst having the formula: ##STR00005## where M is a transition metal and X is a halogen; and, where R is a heteroatom containing group.

10. The method of claim 1 wherein the catalyst having the formula: ##STR00006## where M is a transition metal and X is a halogen; and, where R is a heteroatom containing group.

11. The method of claim 1 wherein the wherein said transition metal is selected from the group consisting of Mn, Fe, Go, Ni, Gu, Ru, Pd, and Pt.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is an illustration of a donor-acceptor complex system for carbon dioxide reduction using dipyridyl ketone coordination complexes according to embodiments of the invention.

(2) FIG. 2 is a schematic of the reactions of the carbon reduction process using dipyridyl ketone coordination complexes according to embodiments of the invention.

(3) FIG. 3 is an X-Ray crystallography of the carbon reducing dipyridyl ketone coordination complex Co(DPK).sub.2(PF.sub.6) according to embodiments of the invention.

(4) FIG. 4 is an X-Ray crystallography of the carbon reducing dipyridyl ketone coordination complex Cu(DPK).sub.2(PF.sub.6)(Cl) according to embodiments of the invention.

DETAILED DESCRIPTION OF THE EMBODIMENTS OF THE INVENTION

(5) In an effort toward production of solar fuels the present invention provides catalysts for the process of carbon dioxide (CO.sub.2) reduction to a fuel feedstock such as methanol. A series of carbon dioxide reduction catalysts have been synthesized and characterized. These catalysts possess activity toward carbon dioxide and the products generated from the reduction. Such products include, but are not limited to, fuel feedstocks and triazine compounds. Examples of such products include, but are not limited to, CO, HCO.sub.2H, HCHO, CH.sub.3OH, CH.sub.4, 2,4,6-trimethyl-1,3,5-triazine, and various combinations thereof.

(6) Preferred embodiments of the catalysts can be synthetically modified to attach to an electron donor that can donate multiple electrons. For example, photosensitized Reduced Graphene Oxide (RGO) is used as the electron donor in these systems. The donor-acceptor catalyst synthesized is characterized using Raman, IR, XRD, TGA-IR, and multi-nuclear NMR as well as high-resolution magic angle spinning (HRMAS) NMR in an effort to ensure covalent bonding between the catalyst and the RGO donor. The donor-acceptor composite catalyst has a high efficiency for CO.sub.2 reduction. Preferred donor-acceptor complexes can be used in larger systems that can produce renewable fuel feedstocks from CO.sub.2 using solar energy.

(7) Preferred CO.sub.2 reduction catalysts have high efficiencies and long lifetimes and can be produced from inexpensive materials. The CO.sub.2 reduction catalysts can be used alone or used in conjunction with electron donors (FIG. 1) that provide the transport medium for a comprehensive self-contained solar fuel production system. (FIG. 2).

(8) Preferred CO.sub.2 reduction catalysts of the present invention include, but are not limited to, species made from transitions metals; preferably species made from Mn, Fe, Co, Ni, Cu, Ru, Pd, and Pt; more preferably species made from cobalt, nickel, manganese, iron and 2 different oxidation states of copper. Complexes of the present invention have been characterized using X-Ray crystallography, examples are shown in FIGS. 3 and 4. These complexes are distinguishable from other art in that other metal complexes reported in the literature with the DPK ligand tend to form clusters rather than discrete complexes with a single metal center. This could be a factor in the ability of the present complexes to bind CO.sub.2.

(9) Preferred embodiments of the catalysts have the formula:

(10) ##STR00001## or
where M is a transition metal; and,
X is halogen

(11) The process segment for the carbon dioxide sequestration is illustrated in FIG. 2 and by the formula:

(12) ##STR00002##

(13) Major advantages of the invention include, but are not limited to, the current CO.sub.2 reduction catalysts have high efficiencies and long lifetimes and can be produced from inexpensive materials. Also, the DPK ligands form discrete complexes with a single metal center.

EXAMPLES

(14) A series of catalysts were synthesized using Manganese, Cobalt, Copper and Nickel. The catalysts were characterized by IR and NMR. Crystal structures were obtained for cobalt and copper catalysts showing both metals as distinct complexes with two ligands.

(15) Initial cyclic voltammetry measurements were made for both copper complexes and the cobalt complex.

Example 1

(16) Catalysts with the molecular formula M(DPK).sub.2(PF.sub.6).sub.2 were made where M is Cu and Co.

(17) A 2:1 mole ratio of dipyridyl ketone ligand to the selected metal salt were added to water and stirred at room temperature overnight. The metal salts used were the chlorides.

(18) A solution consisting of 0.5 mmol of DPK and 0.25 mmol of metal ion were reacted in 15 mL of distilled water with stirring at room temperature overnight. The catalyst was then isolated as the PF.sub.6 salt by adding excess ammonium hexafluorophosphate to the same solution and then filtering. The powder was then rinsed with water and dried in a vacuum oven overnight.

(19) X-ray quality crystals were obtained for Cu and Co catalysts through slow diffusion with DMSO and ether OR acetonitrile and hexanes.

(20) Preferred metal salts are the metal halide salts; more preferably, CuCl.sub.2, CoCl.sub.2, NiCl.sub.2, MnCl.sub.2, CuI.sub.2, FeCl.sub.2, and FeCl.sub.3.

Example 2

(21) A series of 2,2′-dipyridyl ketone (DPK) containing metal complexes were synthesized with metals including Mn, Fe, Co, Ni, Cu, Ru, Pd, and Pt following the method from Example 1.

Example 3

(22) In another embodiment, the mole ratio of the ligand and metal was changed to specifically make more clustered catalysts. One preferred catalyst comprises a 1:1 ligand to metal ratio.

(23) The Copper(I) complex that was synthesized appears to be some alternate type of cluster based on solubility and crystallinity, this could not be confirmed with x-ray quality crystals.

Example 4

(24) Another preferred embodiment accommodates the binding of 3 DPK ligands to the metal centers.

(25) In other preferred embodiments the DPK ligands are modified. Preferred modifications are at the 4, 4′-positions or 3, 3′ positions on the pyridine rings. These modifications are preferably a heteroatom containing group; such groups would enhance adherence or even possible chemical bonding to a donor substrate when used in a device. Examples of such modifications include, but are not limited to, a carboxylic acid, an amine, or a thiol; preferably with an intermediate carbon chain of C from 1 to 10.

Example 5

(26) Bulk electrolysis was done with a catalyst from Example [Cu(II)DPK.sub.2](PF.sub.6)(Cl), in a solution of 0.1M TBAPF.sub.6 in acetonitrile using a carbon foam working electrode, platinum counter electrode and Ag/AgNO.sub.3 reference. The auxiliary electrode was isolated in a fitted glass chamber and a small amount of ferrocene was added to the solution in the chamber as a sacrificial donor to minimize side reactions. The samples were bubbled with CO.sub.2 for 2 hours before the potential was applied and another CV run. At this point the −2V potential was applied for 3 hours. Over the course of the reaction the solution went from light blue to yellow.

(27) GC-MS data was collected for the bulk material at the end of the run. Products of this electrolysis include both CO and triazine (2,4,6-trimethyl-1,3,5-triazine) and were, confirmed.

Example 6

(28) The experiment from Example 5 was also run under the same conditions but with N.sub.2 instead of CO.sub.2 and no color change was observed, as well as an absence of any triazine. There were also other tests run as controls, without catalyst with CO.sub.2 and N.sub.2, and no color change or triazine was observed.

(29) While the invention has been described, disclosed, illustrated and shown in various terms of certain embodiments or modifications which it has presumed in practice, the scope of the invention is not intended to be, nor should it be deemed to be, limited thereby and such other modifications or embodiments as may be suggested by the teachings herein are particularly reserved.

(30) Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limits of that range is also specifically disclosed. Each smaller range between any stated value or intervening value in a stated range and any other stated or intervening value in that stated range is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included or excluded in the range, and each range where either, neither or both limits are included in the smaller ranges is also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the invention.