Electrode material for electrolytic hydrogen generation

Abstract

Some examples of a method for manufacturing an electrode material for electrolytic hydrogen generation are described. Tungsten salt and nickel salt are mixed in a determined molar ratio on a carbon support by effectively controlling synthesis temperature and composition. Water and adsorbed oxygen, produced by mixing the tungsten salt and nickel salt are removed. Then, methane gas is flowed over the mixture resulting in the electrode material. The electrode material is suitable for use as a catalyst in electrolytic hydrogen generation processes, for example, at an industrial scale, to produce large quantities of hydrogen.

Claims

1. A method comprising: mixing a first quantity of tungsten (W) salt and a second quantity of nickel (Ni) salt in the presence of a carbon support; and flowing methane gas over the mixture of the first quantity and the second quantity to form tungsten-nickel carbides (WNiC) on said carbon support, wherein the molar ratio of tungsten to nickel is about 4:1.

2. The method of claim 1, wherein the tungsten salt is dissolved in isopropanol.

3. The method of claim 1, wherein the nickel salt is on the carbon support.

4. The method of claim 1, further comprising removing water and oxygen, flowing the methane gas over the mixture after removing the water and the oxygen.

5. The method of claim 4, wherein, after removing the water and the oxygen, flowing methane gas over the mixture of the first quantity and the second quantity comprises increasing a temperature of the mixture to about 1000 C.

6. The method of claim 5, further comprising increasing the temperature at a rate of 5 C/min.

7. The method of claim 5, further comprising holding the temperature of the mixture for a respective duration at each of about 700 C., about 800 C., about 900 C. and about 1000 C.

8. The method of claim 5, further comprising, after removing the water and the oxygen and flowing the methane gas over the mixture of the first quantity and the second quantity, using the mixture as an electrode material for hydrogen generation from brine by electrolysis.

9. The method of claim 1, further comprising pre-treating the carbon support before mixing the first quantity and the second quantity.

10. The method of claim 9, wherein pre-treating the carbon support comprises removing impurities from the carbon support.

11. The method of claim 9, wherein pre-treating the carbon support comprises mixing a third quantity of the carbon support with a first volume of hydrochloric acid.

12. The method of claim 11, wherein the third quantity comprises about 0.2 g of the carbon support.

13. The method of claim 11, wherein the first volume comprises about 40 mL.

14. The method of claim 11, wherein the hydrochloric acid has a molarity of about 0.5M.

15. The method of claim 11, further comprising mixing the third quantity with the first volume for a duration at a rotational speed.

16. The method of claim 15, wherein the duration is about 15 hours.

17. The method of claim 15, wherein the rotational speed is about 400 rpm.

18. The method claim 1, wherein the first quantity of tungsten consists of WCl.sub.6 and the second quantity of nickel consists of Ni(NO.sub.3).sub.2.6H.sub.2O.

19. The method of claim 1, wherein mixing the first quantity of tungsten (W) salt and the second quantity of nickel (Ni) salt on the carbon support comprises: dispersing a fourth quantity of the carbon support in a second volume of de-ionized water to form a carbon slurry; dissolving the first quantity of tungsten salt in a third volume of isopropanol; adding the dissolved first quantity of tungsten salt in the third volume of isopropanol to the carbon slurry; adding a fourth volume of de-ionized water to the mixture of the tungsten salt in the carbon slurry; stirring a mixture of the fourth volume of de-ionized water and the mixture of the tungsten in the carbon slurry for a duration; and vacuum drying the mixture of the fourth volume of de-ionized water and the mixture of the tungsten salt in the carbon slurry after the duration.

20. The method of claim 1, wherein the carbon support is conductive and hydrophobic.

21. The method of claim 1, wherein flowing methane through the mixture produces a nickel-tungsten carbide alloy.

22. The method of claim 21, wherein the tungsten-nickel carbides on the carbon supports have a particle size ranging between about 10 nanometers (nm) and 100 nm.

23. The method of claim 1, wherein a surface area of the carbon support ranges between about 50 m.sup.2/g to about 3000 m.sup.2/g.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a flowchart of an example process for producing electrode materials.

(2) FIG. 2 shows a schematic diagram of an example system for producing electrode materials.

(3) FIG. 3A shows Hydrogen Evolution Reaction (HER) Polarization curves in WNiC/Vu (1:1) at different heat treatment temperature.

(4) FIG. 3B shows HER Polarization curves in Vulcan carbon (Vu), Ni/Vu, W/Vu, WNiC/Vu (1:1) and Pt/C respectively.

(5) FIG. 3C shows HER Polarization curves in WNiC/Vu at different mole ratio of Ni:W.

(6) FIG. 4A shows polarization curves of WNiC/Vu (4:1) in N.sub.2 saturated 0.5 M NaBr, pH7.04 with consecutive cyclic volt-ammograms recorded, potential scan rate of 50 mV/s.

(7) FIG. 4B shows polarization curves of WNiC/Vu (4:1) in N.sub.2 saturated 0.5 M NaBr, pH7.04 before and after 1000 potential sweeps (0.45 to +0.75 V/RHE), potential scan rate of 20 mV/S.

(8) FIG. 4C shows chrono-amperometry curves of WNiC/Vu (4:1) in N.sub.2 saturated 0.5 M NaBr, pH7.04 at 0.37 V/RHE.

(9) FIGS. 5A-5D show Scanning Electron Microscope (SEM) images of electrode materials of different Ni:W molar ratios.

(10) FIGS. 6A-6D show X-Ray diffraction patterns of synthesized catalysts at different mole ratios atomic of Ni to W.

(11) Like reference numbers and designations in the various drawings indicate like elements.

DETAILED DESCRIPTION

(12) Electrolytic or photo-catalytic hydrogen production (or both) from brine water can be an improvement relative to other industrial hydrogen production techniques, for example, in terms of cost and environmental impact. Such hydrogen production techniques use energy that is high enough to dissociate water molecules and release hydrogen. The type of surface on which the dissociation occurs affects significantly the quantity of energy used. Also, energy cost can be affected by using a catalyst that can lower the over voltage of the electrolytic process to produce hydrogen from brine.

(13) Precious metals, for example, platinum (Pt), which are used as catalysts in electrolysis, offer low over potential and faster reaction kinetics for hydrogen evolution reaction (HER). However, such metals, particularly Pt, can be expensive and, consequently, prohibitive for application for hydrogen production from brine on an industrial scale. For example, it is known that coating Pt on Tungsten Carbide (WC), for example, by atomic layer deposition or physical vapor deposition, can reduce Pt loading, but is a complicated process that is difficult to be scaled up to industrial levels.

(14) This disclosure describes electrolytic hydrogen generation and an electrode material for electrolytic hydrogen generation. The electrode material described here can be implemented as an efficient electro-catalyst for hydrogen generation from brine, for example, at industrial levels. As described later, the electrode material is prepared from materials that are abundantly available on earth. The electrode material described here shows significant reduction in over-potential for HER in brine electrolysis. The resulting electrode material can be based on a nano-structured electro-active material and can be implemented as a catalyst in brine electrolysis and can serve as a cost-effective, stable and active alternative to expensive, precious metals, for example, Pt.

(15) In some implementations, the electrode material can include tungsten-nickel based carbides, for example, W.sub.xNi.sub.yC, WC, W.sub.2C, or other tungsten-nickel based carbides, prepared by effectively controlling the synthesis temperature and composition. As described later, such mixtures have shown excellent electro-activeness toward hydrogen evolution reaction from brine with an electrode performance close to that of Pt-based catalysts.

(16) FIG. 1 is a flowchart of an example process 200 for producing electrode materials. In some implementations, the process 100 can be implemented using the system 100. At 102, tungsten (W) salt is mixed with nickel (Ni) salt on a carbon support. For example, WCl.sub.6, is mixed with Ni(NO.sub.3).sub.2.6H.sub.2O on a carbon support, for example, a conductive and hydrophobic carbon support, such as Vulcan XC-72R in a container 102. In some implementations, a surface area of the carbon support can range between about 50 m.sup.2/g to about 3000 m.sup.2/g. At 104, water and adsorbed oxygen are removed from the mixture prior to heating at different temperatures, for example, 700 C., 800 C., 900 C., 1000 C. or other temperatures. For example, the mixture resulting by implementing step 102 can be kept in a container 104 having an inert atmosphere, for example, N.sub.2 atmosphere. Then, at 106, low flow of CH4 gas, for example, from a CH4 gas source 106, can be passed over the mixture to form the carbides at higher temperature, >700 C. For example, the methane gas can be flowed at a low flow rate, for example, 100 milliliters per minute (mL/min) for a reactor of about 5 centimeter ( )m diameter. At 108, a carbide composite having a specified mole ratio can be synthesized. For example, the mole ratios of Ni to W can be about 1:1, 1:3, 1:4, 1:5 or other mole ratios. In general, the tungsten-nickel carbides can be represented as W.sub.xNi.sub.y in carbide form with x being about 50% to 75% atomic and y being about 50% to 25% atomic. In some examples, x can range between 75% and 80%, and y can range between 20% and 25%. In some implementations, the carbide composites can be characterized and also prepared in the form of electrodes, and tested for HER in brine medium using a two or three-electrode electrolytic cell implementation. Experiments described later are performed on a laboratory-scale, but can be scaled up to industrial levels to produce large quantities of the electrode materials.

EXPERIMENT I

Pre-treatment of Carbon Support

(17) FIG. 2 shows a schematic diagram of an example system for producing electrode materials. Initially, Vulcan XC-72R carbon support was pre-treated to remove traces of any impurities, such as metals. In a container 202, a quantity of 0.2 g of the Vulcan XC-72R was mixed in 40 mL of 0.5 M hydrochloric acid (HCl) for a duration of approximately 15 hrs at moderate temperature (20 C.-40 C.), while stirring at 400 rpm, for example, using a magnetic stirrer. The quantity of carbon support, for example, Vulcan XC-72R, ranged from 0.3 g to 0.4 g during pre-treatment in acid. In general, a quantity of carbon support used can depend on an amount of electrode material, for example, catalyst, to be produced. After carbon cleaning, for example, by the pre-treatment described here, in acid to remove traces of impurities, for example, metals or other impurities, 0.2 g of treated carbon was used to develop the carbide materials on the carbon surface. The amount of carbon used can be more than the amount of carbon needed to account for carbon loss. The carbon support was then filtered, washed and dried in an oven 204 at 80 C. for 6-7 hrs.

EXPERIMENT II

Preparation of Electrode Material Having Ni:W in a 1:1 Ratio

(18) To prepare the electrode material, 0.2 g of Vulcan carbon, pre-treated as described earlier, was dispersed in a container 206 containing 40 mL de-ionized water by sonication for 20-30 minutes, and then transferred to a glass beaker 208 with magnetic stirrer 210 (rotated by a stir plate 212) to form a carbon slurry. Thereafter, 0.4 g of WCl.sub.6 dissolved in a container 212 containing 30 mL isopropanol (IPA) was slowly added to the carbon slurry. To maintain an atomic ratio of Ni:W or 1:1, 0.29 g of Ni(NO.sub.3).sub.2.6H.sub.2O was dissolved in a container 214 containing 20 mL of de-ionized H.sub.2O and added, drop-wise, to the mixture in the container 208, followed by a final rinse with 10 mL of de-ionized H.sub.2O to make-up 100 mL of reaction volume. The mixture was left under stirring at 500 rpm for 2-3 days for proper impregnation of metal salts onto the carbon matrix. The mixture was then vacuum-dried at 80 C. between 6 and 7 hrs in an oven 216.

(19) The resulting sample was heat-treated as follows. The powdered sample was placed in a crucible boat and transferred into a quartz tube MTI furnace 218 (OTF-1200X-S). Gas cylinders were connected to the gas inlet of the furnace and the exhaust/outlet was directed to an oil bath. Nitrogen (N.sub.2) gas was first passed into the furnace while the temperature was first increased from room temperature to 100 C. for 30 minutes and held at this temperature for 10 minutes to purge out adsorbed oxygen and water. Methane (CH.sub.4) gas flow was then passed while ramping temperature of the furnace at a rate of 5 C./min to the desired temperatures of 700 C., 800 C., 900 C. or 1000 C., and held for 1 hr. In general, a quality of the sample is affected by a ramping period, that is, the time to reach a set temperature value at which catalyst formation begins and a temperature hold period, that is, the time for which the temperature is held for catalyst active sites formation.

(20) Subsequently, some of the samples synthesized at Ni:W ratio of 1:1 were cooled and used to study the effect of temperature on HER performance, as described later. In some implementations, the samples can be cooled at any rate. For example, the cooling can be done under ambient conditions without an external cooling system. In some implementations, external cooling systems can be used to cool the samples at cooling rates ranging between about 5 C./min and 10 C./min. In some implementations, the cooling can be implemented by simply turning off the heating chamber in which the samples are heated. Cooling can be done under the flow of methane or an inert gas to avoid leak of oxygen into reactor.

EXPERIMENT III-V

Preparation of Electrode Material Having Ni:W in a 1:3, 1:4 and 1:5 Ratio, Respectively

(21) To prepare the electrode material having Ni:W in ratios of 1:3, 1:4 and 1:5, 1.2 g, 1.6 g and 2.0 g of WCl.sub.6, respectively, was mixed with 0.29 g of Vulcan carbon, pre-treated as described earlier. The electrode material in each of these ratios was prepared by processing each mixture in a manner similar to that described earlier. Each obtained sample was characterized using a thin film electrode in a three-electrode geometric cell and also by spectroscopic techniques to investigate the morphological structure and composition of each sample.

(22) For each sample prepared as described later, HER activity in brine were studied, as described later.

EXPERIMENT VI

Studying HER Activity in Brine

(23) For each sample prepared as described earlier, approximately 5 mg of the sample was dispersed in a mixture of water and isopropanol (30% V/V) and 37 L of 1.66% wt Nafion (prepared from 5% wt). The mixture was sonicated to obtain a uniform ink. The working electrode used during electrolysis was prepared by depositing 16 L of the ink suspension on the pre-cleaned glassy carbon substrate and allowed to dry under air flow at room temperature. The loading operation was repeated until the desired catalyst loading, 0.4 mg/cm.sup.2 was achieved and the geometric area of the glassy carbon rotating disk electrode (RDE) was about 0.196 cm.sup.2. A Pt mesh was used as a counter electrode during activity measurements in brine (0.5 M NaBr, pH7.04, specific gravity1.54). A Calomel electrode (calibrated against reversible hydrogen electrode every day prior to activity measurement of HER) was used as a reference electrode. All potential measurements during these studies were converted to reversible hydrogen electrode (RHE).

RESULTS

HER Activity in Brine

(24) FIG. 3A shows HER polarization curves for Ni:W in a mole ratio of 1:1 at different heat treatment temperatures in the presence of methane gas flow. The polarization curves show that sample treated at 800 C. shows better HER activity than the other samples with an over-voltage of 300 millivolt (mV) as compared to Pt/C catalyst. This can indicate that formation of more active sites for HER for the specific composite is more favorable at this temperature.

(25) FIG. 3B shows HER polarization curves obtained for individual metal carbides. Vulcan carbon shows the highest over potential for HER. WC/Vu behaves better than its homologue, NiC/C. A significant improvement in HER activity is observed when both metals are incorporated at 1:1 mole ratio of Ni:W.

(26) FIG. 3C shows HER polarization curves in brine for the carbide composites including two metals. The polarization curves were generated to study if the electro-catalytic synergistic effect of the two metals increased the HER performance of the carbide composite. An increase in current density and a reduction in over-potential were observed with HER activity close to that of bulk Pt/C. When the mole ratio of Ni:W was optimized from 1:1 to 1:4, a corresponding reduction in over potential was significant. However, when the ratio is 1:5, a drastic reduction in activity of the catalyst toward HER in brine was noticed suggesting that the best molar ratio of Ni:W to lead to metal carbide alloys as potential Pt-free electro-catalyst for HER is 1:4. Such enhancement in HER activity may be due to effective utilization of the synergistic effect of the two metals that favor faster HER kinetics.

EXPERIMENT AND RESULTS

Catalyst Stability

(27) For stability studies, the catalyst that demonstrated highest HER activity, that is, Ni:W in a molar ratio of 1:4 (for example, WNiC/Vu in a 4:1 ratio), was used. To investigate the long term performance for the catalyst in brine, potential sweeps were conducted from 0.45 to +0.75 V/RHE for 1000 cycles as shown in FIG. 4A. FIG. 4B shows the polarization curve recorded before and after the stability test. The catalyst demonstrated good stability by maintaining almost its initial polarization behavior in brine medium. To further establish the catalyst stability, chrono-amperometry (CA) studies was also conducted at a potential hold of 0.37 V/RHE (corresponding to j=1 mA cm.sup.2) for 1 hr as shown in FIG. 4C.

(28) Scanning Electron Microscope (SEM) Images and X-Ray Diffraction

(29) FIGS. 5A-5D are Scanning Electron Microscope (SEM) images of electrode materials of different Ni:W molar ratios. FIG. 5A is the SEM image of the composition having W:Ni in a 1:1 ratio. FIG. 5B is the SEM image of the composition having W:Ni in a 3:1 ratio. FIG. 5C is the SEM image of the composition having W:Ni in a 4:1 ratio. FIG. 5D is the SEM image of the composition having W:Ni in a 5:1 ratio. The composite with molar ratio of W:Ni of 5 to 1 (FIG. 5D) appears to be more dense than those corresponding to ratios, 4:1, 3:1, and 1:1. The difference in density maybe the reason that HER activity was decreased significantly for this composition relative to the other compositions.

(30) FIGS. 6A-6D show X-Ray diffraction patterns of synthesized catalysts at different mole ratios atomic of Ni to W. FIG. 6A is an XRD pattern of catalyst having W:Ni in a 1:1 ratio. FIG. 6B is an XRD pattern of catalyst having W:Ni in a 3:1 ratio. FIG. 6C is an XRD pattern of catalyst having W:Ni in a 4:1 ratio. FIG. 6A is an XRD pattern of catalyst having W:Ni in a 5:1 ratio. The XRD patterns of the synthesized catalysts show formations of mixture of metal carbides of tungsten metal (WC and W.sub.2C) and WNi carbides alloys at different diffraction angles. The unassigned peak in the XRD figure corresponds to Carbon (002) plane.

(31) In summary, the electrode material described here can serve as a cost effective and cheaper alloy material that can be used for hydrogen formation from brine through electrolysis. The alloy composition described here can allow hydrogen formation at high rates. The alloy composition can replace relatively more expensive, precious metals, for example, Pt.

(32) Thus, particular implementations of the subject matter have been described. Other implementations are within the scope of the following claims.