Bulk and Surface Compositions of PtRu Catalysts and Their Methanol Oxidation Activity and Durability

2019 ◽  
Vol 33 (1) ◽  
pp. 275-286
Author(s):  
Taigo Onodera ◽  
Shuichi Suzuki ◽  
Yoshiyuki Takamori ◽  
Hideo Daimon
2010 ◽  
Vol 5 (2) ◽  
pp. 120-124 ◽  
Author(s):  
H. Daimon ◽  
T. Onodera ◽  
T. Nakagawa ◽  
H. Nitani ◽  
T. A. Yayamoto

2001 ◽  
Vol 7 (S2) ◽  
pp. 1112-1113
Author(s):  
Rhonda M. Stroud ◽  
Jeffrey W. Long ◽  
Karen E. Swider-Lyons ◽  
Debra R. Rolison

To address how the chemical and structural heterogeneity of Pt50Ru50 nanoparticles affects methanol oxidation activity, we have employed an arsenal of transmission electron microscopy techniques (conventional bright field-imaging, selected area diffraction, atomic-resolution lattice imaging, electron-energy loss spectroscopy, and energy-dispersive x-ray spectroscopy) to characterize 2.5-nm particles in differing oxidation and hydration states. Our studies demonstrate that electrocatalysts containing a high fraction of Ru-rich hydrous oxide, as apposed to the anhydrous PtRu bimetallic alloy, have as much as 250x higher methanol oxidation activityThe nominally 2.5-nm Pt50Ru50 particles were studied in as-received, reduced and reoxidized forms. The reducing treatment consisted of 2 h at 100 °C in flowing 10% PL/argon mixture. For re-oxidation, the reduced particles were heated for 20 h at 100 °C in an H2O-saturated oxygen atmosphere. The particles were suspended in methanol, and pipetted onto holey-carboncoated Cu grids for TEM studies.


Author(s):  
Archana Sekar ◽  
Nathaniel Metzger ◽  
Sabari Rajendran ◽  
Ayyappan Elangovan ◽  
Yonghai Cao ◽  
...  

2011 ◽  
Vol 13 (10) ◽  
pp. 5275-5287 ◽  
Author(s):  
Satoru Kageyama ◽  
Satoshi Seino ◽  
Takashi Nakagawa ◽  
Hiroaki Nitani ◽  
Koji Ueno ◽  
...  

2000 ◽  
Vol 6 (S2) ◽  
pp. 24-25
Author(s):  
R.M. Stroud ◽  
J.W. Long ◽  
K.E. Swider ◽  
D.R. Rolison

Direct methanol fuel cells (DMFCs) offer a simpler, safer technology for point-of-use power sources compared to other hydrogen fuel cells, by avoiding the need to store hydrogen fuel or to carry out the reformation of hydrocarbons. The direct methanol oxidation electrocatalyst of choice is a nanoscale black consisting of a 50:50 atom % mixture of Pt and Ru. It has recently become known that these presumed bimetallic alloys in fact contain an array of metal, oxide and hydrous phases, which are easily misidentified in routine x-ray diffraction measurements due to particle size-broadening and poor crystallinity. By combining transmission electron microscopy, electrochemistry and thermogravimetric studies, we demonstrate here that the route to improved catalytic activity is not by phase purification of the bimetallic alloys, but instead phase engineering of hydrous ruthenium oxide and Pt mixtures.


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