Palladium and palladium alloy nanoparticles can be used as catalysts, particularly in fuel cells used to produce electrical energy. For example, in a hydrogen fuel cell, a palladium catalyst can be used to oxidize hydrogen gas into protons and electrons at the anode of the fuel cell. At the cathode of the fuel cell, the palladium catalyst triggers the oxygen reduction reaction (ORR), leading to formation of water.
Fuel cell performance depends in part on the available surface area of the palladium nanoparticles. Fuel cell performance generally increases when the surface area of the palladium nanoparticles is increased. In addition to size, the shape of the palladium nanoparticles can also be selected in order to further increase the oxygen reduction reaction (ORR) activity. Surfactants are commonly used during nanoparticle formation to control the particle size and shape. The surfactants bind to the nanoparticles as they are shaped and sized.
Once the nanoparticles have been formed, the surfactants used for shaping and sizing the particles need to be removed. Some surfactants can be removed by washing and low temperature heat treatment. Other surfactants, however, require long washing times (as long as weeks in special solvents) or high temperature treatment at temperatures above 300° C. For some catalyst nanoparticles, high temperature treatment presents problems. For example, at 300° C., cubic palladium nanoparticles may lose their shape and increase in particle size. As a result, using high temperature treatment to remove surfactants from the nanoparticles removes benefits the surfactants were intended to provide.
A method for removing a surfactant from a palladium nanoparticle includes exposing the palladium nanoparticle to hydrogen and removing the surfactant from the palladium nanoparticle.
A method includes synthesizing the palladium nanoparticle using a surfactant. The surfactant influences a geometric property of the palladium nanoparticle and bonds to the palladium nanoparticle. The method also includes exposing the palladium nanoparticle to hydrogen to remove the surfactant from the palladium nanoparticle.
The present invention provides a simple and efficient method for removing surfactants from palladium nanoparticles. Electrochemical and chemical processes use hydrogen to weaken the adsorption of surfactant on a palladium nanoparticle. The method provides a simple and efficient way to remove surfactants from palladium nanoparticles without using high temperatures.
Surfactants are often used to modify the size and shape of palladium nanoparticles that serve as fuel cell catalysts. Surfactant micelles present during the formation of palladium nanoparticles affect the geometry of the nanoparticles. Particular surfactants and surfactant concentrations can be used to form palladium nanoparticles having the specific sizes and shapes needed to meet fuel cell performance requirements. Suitable surfactants for sizing and shaping palladium nanoparticles include polyvinylpyrrolidone (PVP), and chlorine- and bromine-based salts. The surfactants bind to the palladium nanoparticles as they shape the nanoparticles. These surfactants must be removed from the palladium nanoparticles before they are used as catalysts in order for the nanoparticles to be fully accessible by reactants.
As noted above, surfactants are typically removed by washing the nanoparticles (with or without low temperature heat treatment) or high temperature treatment. Each of these surfactant removal methods has drawbacks. Some surfactants can be removed only after extremely long washing times. Long periods of time spent washing the nanoparticles increases the time and costs required for production of the final nanoparticle catalyst. High temperature treatments typically require temperatures above 300° C. and can have deleterious effects on palladium nanoparticles. As noted above, at 300° C., palladium nanoparticles may lose their shape and increase in size. High temperature treatment to remove surfactants from the nanoparticles can eliminate the size and shape modifications the surfactants were used to provide.
Instead of using a lengthy washing method or a harmful high temperature method, the present invention uses molecular hydrogen to weaken bonds between a nanoparticle and the surfactant used to shape and/or size the nanoparticle.
In step 20, the electric potential is maintained for a time sufficient to allow hydrogen to penetrate into the nanoparticle. The nanoparticle acts as an electrode and hydrogen forms as a result of a multistep reaction. First, adsorbed hydrogen atoms form at the surface of the nanoparticle
H3O++e−H·ads+H2O (1)
where H·ads is an adsorbed hydrogen atom at the nanoparticle surface. The adsorbed hydrogen atoms combine to form molecular hydrogen
H·ads+H·ads→H2 (2)
or a further electrochemical reaction produces molecular hydrogen
H·ads+H3O++e−→H2+H2O (3)
depending on the electrode potential. The formed hydrogen penetrates into the palladium nanoparticle forming palladium hydrides and expanding the palladium nanoparticle lattice. Palladium hydride is metallic palladium that contains a substantial quantity of hydrogen within its crystal lattice. At room temperature and atmospheric pressure, palladium can absorb up to 900 times its own volume of hydrogen. The adsorption of surfactants becomes weaker and the surfactants easily desorb from the palladium surface due to the lattice expansion. In some cases, molecular hydrogen is not necessary. Atomic hydrogen formed in reaction (1) can also be absorbed by palladium and cause lattice expansion.
In exemplary embodiments, the electric potential is maintained for less than about five minutes. In one particular embodiment, the electric potential is maintained for no more than about one minute. Steps 18 and 20 are typically performed at room temperature (between about 15° C. and about 30° C.). Electrolytes are used during steps 18 and 20. Suitable electrolytes include dilute aqueous acids such as 0.1 M perchloric acid (HClO4).
Once a sufficient amount of hydrogen has been absorbed by the palladium nanoparticle, the bonds between the surfactant and the palladium nanoparticle will have weakened enough so that the surfactant merely desorbs from the nanoparticle (i.e. the surfactant “falls off” the nanoparticle). The hydrogen present at the surface of the palladium nanoparticle or within the palladium crystal lattice also requires no further treatment. Any hydrogen present will leave on its own prior to or during use as a fuel cell catalyst.
To summarize, hydrogen is used to weaken a bond between a palladium nanoparticle and the surfactant used to shape and size the nanoparticle. Hydrogen can be formed at the surface of the palladium nanoparticle using an electrochemical method so that it is absorbed by the nanoparticle. Hydrogen can also be added to the nanoparticle environment so that it is absorbed by the nanoparticle. The exposure of the nanoparticle to hydrogen expands the nanoparticle's lattice structure and weakens the bond between the surfactant and the nanoparticle, allowing the surfactant to be easily removed. The method described herein allows for simple, quick and efficient surfactant removal without using deleterious high temperatures or requiring long processing times.
Although the present invention has been described with reference to preferred embodiments, workers skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the invention.
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/US2011/001030 | 6/8/2011 | WO | 00 | 11/26/2013 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2012/169992 | 12/13/2012 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
5712062 | Yamana | Jan 1998 | A |
7879153 | Seo et al. | Feb 2011 | B1 |
20020034675 | Starz et al. | Mar 2002 | A1 |
20020194958 | Lee | Dec 2002 | A1 |
20060134505 | Wang et al. | Jun 2006 | A1 |
20080096986 | Thomazeau et al. | Apr 2008 | A1 |
20100261028 | Kondoh | Oct 2010 | A1 |
Number | Date | Country |
---|---|---|
10111337 | Jan 2008 | CN |
101198407 | Jun 2008 | CN |
101690884 | Apr 2010 | CN |
2 177 257 | Mar 2016 | EP |
2000-351603 | Dec 2000 | JP |
2010-103512 | May 2010 | JP |
20100024169 | Mar 2010 | KR |
20100038069 | Apr 2010 | KR |
10-0959245 | May 2010 | KR |
Entry |
---|
The International Search Report mailed Jan. 2, 2012 for International Application No. PCT/US2011/001030. |
Extended European Search Report dated Dec. 9, 2015, for corresponding EP Application No. 11867235.1-1353/2718046, 7 pages. |
Number | Date | Country | |
---|---|---|---|
20140096645 A1 | Apr 2014 | US |