University of Michigan

T/j Technologies, Inc.

Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V.

Inmatech, Inc.

Levi T Thompson

Michael R Wixom

Paul G Rasmussen

Saemin Choi

Jeremy J Patt

Shyamal K Bej

Chang Hwan Kim

Gunnar Walther

Cory Bernard Phillips

Binay Prasad

Daryl Clerc

Matthew Fay

Jeffery M Parker

Lynne Owens

Dong Ju Moon

Abdoulaye Djire

Burghardt Kloeden

Cong Pu

David Tarnowski

Disclosed are systems and methods for a supercapacitor. One form of the supercapacitor has a first electrode comprising a first active material, a second electrode comprising a second active material, and an electrolyte comprising a protic ionic liquid. The protic ionic liquid may be capable of undergoing a faradaic charge transfer with an electrode of a supercapacitor.

Systems and methods for improved supercapacitors with ionic liquid electrolytes

In accordance with an embodiment of the disclosure, an asymmetric supercapacitor includes a first active material with a high hydrogen over-potential and a second active material with a high oxygen over-potential. The first active material is based on a nitride, an oxynitride, a carbide, an oxycarbide, a boride, or an oxyboride of a metal selected from Groups III, IV, V, VI, and VII of the Periodic Table.

High performance transition metal carbide and nitride and boride based asymmetric supercapacitors

This invention discloses an electrochemical device having a multilayer structure and methods for making such a device. Specifically, this invention discloses a multilayer electrochemical device having nano-sized cobalt oxyhydroxide conductive agents and/or active materials within the polymer layers.

Electrochemical device electrode including cobalt oxyhydroxide

In accordance with an embodiment of the disclosure, a method of making a supercapacitor includes impregnating a foam electrode substrate with an active material precursor, wherein the foam electrode substrate includes a plurality of pores and the active material precursor is dispersed into the pores. The method further includes reacting the active material precursor infiltrated foam substrate with a reductant under conditions sufficient to convert the active material precursor to an active material, wherein the active material is based on a nitride, an oxynitride, a carbide, or an oxycarbide of a metal selected from Groups III, IV, V, VI, or VII of the Periodic Table.

Transition metal carbide or nitride or boride based supercapacitors with metal foam electrode substrate

A catalyst is disclosed herein. The catalyst includes a reducible oxide support and at least one noble metal fixed on the reducible oxide support. The noble metal(s) is loaded on the support at a substantially constant temperature and pH.

Reducible oxide based catalysts

Catalysts for the water gas shift reaction contain a variety of late transition metals. The catalytic compositions contain a late transition metal carried on a support which is a carbide, nitride, or mixed carbide nitride of a group 6 metal such as molybdenum, tungsten, and mixtures thereof. The late transition metal includes ruthenium, cobalt, nickel, palladium, platinum, copper, silver, or gold. The water gas shift reaction may be catalyzed by contacting a gaseous stream containing carbon monoxide and water with such a solid catalyst composition. In some embodiments, the catalysts are several times more active than known commercial catalysts for the water gas shift reaction.

Carbide/nitride based fuel processing catalysts

Mono- and bimetallic transition metal carbides, nitrides and borides, and their oxygen containing analogs (e.g. oxycarbides) for use as water gas shift catalysts are described. In a preferred embodiment, the catalysts have the general formula of M1 M2 Z O , wherein M1 is selected from the group consisting of Mo, W, and combinations thereof; M2 is selected from the group consisting of Fe, Ni, Cu, Co, and combinations thereof; Z is selected from the group consisting of carbon, nitrogen, boron, and combinations thereof; A is an integer; B is 0 or an integer greater than 0; C is an integer; O is oxygen; and D is 0 or an integer greater than 0. The catalysts exhibit good reactivity, stability, and sulfur tolerance, as compared to conventional water shift gas catalysts. These catalysts hold promise for use in conjunction with proton exchange membrane fuel cell powered systems.

Transition metal carbides, nitrides and borides, and their oxygen containing analogs useful as water gas shift catalysts

A catalyst comprises an electrically conductive ceramic substrate having at least one noble metal supported thereupon. The substrate may be a transition metal based ceramic such as a carbide, nitride, boride, or silicide of a transition metal, and the noble metal may comprise a mixture of noble metals. The substrate may comprise a high surface area ceramic. Also disclosed are fuel cells incorporating the catalysts.

Catalyst

A transition metal based ceramic material having the general formula Li,M,T,N,O,, wherein M is a transition metal, T is a dopant metal, and wherein x is greater than 0 and less than or equal to l, &dgr; is 0, or less than or equal to 4; &agr; is less than or equal to 3&minus;x, and &bgr; is less than 1 is disclosed. The ceramic material has utility as a cathode material for rechargeable lithium batteries.

Transition metal based ceramic material and electrodes fabricated therefrom

A non-oxide, transition metal based ceramic material has the general formula A.sub.y M.sub.2 Z.sub.x, wherein A is a group IA element, M is a transition metal and Z is selected from the group consisting of N, C, B, Si, and combinations thereof, and wherein x.ltoreq.2 and y.ltoreq.6-x. In these materials, the group IA element occupies interstitial sites in the metallic lattice, and may be readily inserted into or released therefrom. The materials may be used as catalysts and as electrodes. Also disclosed herein are methods for the fabrication of the materials.

Transition metal-based ceramic material and articles fabrication

Mesoporous desigels are fabricated as nitrides, carbides, borides, and silicides of metals, particularly transition metals, and most particularly early transition metals. The desigels are prepared by forming a gel of a metallic compound, and removing solvent from the gel. In some instances, the thus produced desigel may be further reacted to change its composition, while preserving its mesoporous structure. The materials are particularly suited as electrodes for capacitors, including ultracapacitors, and for batteries.

High surface area mesopourous desigel materials and methods for their

High surface area electrodes for use in electrical and electrochemical energy storage and conversion devices comprise conductive transition metal nitrides, carbides, borides or combinations thereof where the metal is molybdenum or tungsten. Disclosed is a method of manufacturing such electrodes by forming or depositing a layer of metal oxide, then exposing the metal oxide layer at elevated temperature to a source of nitrogen, carbon or boron in a chemically reducing environment to form the desired metal nitride, carbide or boride film. Also disclosed is an ultracapacitor comprised of the new high surface area electrodes having a specific capacitance of 100 mF/cm.sup.2 and an energy density of 100 mJ/cm.sup.3 with improved conductivity and chemical stability when compared to currently available electrodes.

Growing community of inventors

Northville, MI, United States of America

Levi T Thompson