M
Matthew M. Seabaugh
Researcher at Pennsylvania State University
Publications - 35
Citations - 966
Matthew M. Seabaugh is an academic researcher from Pennsylvania State University. The author has contributed to research in topics: Ceramic & Electrochemical cell. The author has an hindex of 15, co-authored 35 publications receiving 909 citations.
Papers
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Journal ArticleDOI
Templated Grain Growth of Textured Piezoelectric Ceramics
Gary L. Messing,Susan Trolier-McKinstry,Edward M. Sabolsky,Cihangir Duran,Seongtae Kwon,Bhaskar Brahmaroutu,P. Park,Huseyin Yilmaz,Paul W. Rehrig,K. B. Eitel,Ender Suvaci,Matthew M. Seabaugh,K. S. Oh +12 more
TL;DR: In this article, a reactive TGG (RTGGG) was used to obtain highly oriented Pb(Mg1/3Nb2/3)O3-PbTiO3, Sr0.53Ba0.47Nb 2O6, and (N...
Patent
Nano-composite electrodes and method of making the same
TL;DR: In this paper, a method of making ceramic electrode materials comprising intimate mixtures of two or more components, including at least one nanoscale ionically conducting ceramic electrolyte material (e.g., yttrium-stabilized zirconia, gadolinium-doped ceria, samarium-ceria, etc.).
Journal ArticleDOI
Fuel processing catalysts based on nanoscale ceria
TL;DR: The water-gas shift (WGS) reactor is a key component in fuel processors, but existing WGS catalysts are unsuitable for transportation applications, since the iron-chrome catalysts used at high temperatures are relatively inactive, and the copper-based catalysts tend to degrade under the severe conditions encountered in an automotive system.
Journal ArticleDOI
Textured-Ba(Zr,Ti)O3 piezoelectric ceramics fabricated by templated grain growth (TGG)
TL;DR: In this article, the authors showed that grain-oriented BZT ceramics display piezoelectric coefficients (d33-coefficients) that are similar to currently used lead-based materials.
Patent
Supported ceramic membranes and electrochemical cells and cell stacks including the same
TL;DR: In this article, a dense ceramic electrolyte membrane supported by symmetrical porous porosity layers is proposed, where the thin (t < 100 microns) electrolyte layer is sandwiched between two fugitive-containing electrolyte support layers that become highly porous after firing.