scholarly journals Effect of Pt Oxidation State on Methanol Oxidation Activity

2011 ◽  
Vol 32 (1-2) ◽  
pp. 86-92 ◽  
Author(s):  
Jianhuang ZENG ◽  
Ting SHU ◽  
Shijun LIAO ◽  
Zhenxing LIANG
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.


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.


2011 ◽  
Vol 287-290 ◽  
pp. 1369-1374 ◽  
Author(s):  
Jian Feng Ju ◽  
Dong Hui Wu ◽  
Yu Jun Shi

The PtRu-SiO2-TiO2/C anode electrocatalyst ( loading 10wt% PtRu ) of direct methanol fuel cell is prepared by the surface reductive deposition method, using Vulcan XC-72 carbon black coated with nanometer SiO2-TiO2 (SiO2-TiO2/C) as the isotopic carrier. The surface characteristics of nanometer SiO2-TiO2 is studied through nitrogen adsorption, which shows that it is of porous structure together with large surface area, that is benefit to enhance the activity of SiO2-TiO2 and the dispersion of PtRu nanoparticle on the carrier of SiO2-TiO2/C. X-ray diffraction( XRD ) and transmission electron microscopy( TEM ) are used to characterize the catalyst. The PtRu nanoparticle homodisperse in SiO2-TiO2/C carrier with diameter around 2.4 nm. Cyclic voltammograms and chronoamperograms are conducted to compare the electrochemical methanol oxidation activity of the PtRu-SiO2-TiO2/C catalyst with the commercial PuRu/C catalyst ( 20 wt% of PtRu ). The results show that PtRu-SiO2-TiO2/C has higher catalytic activity and anti-poisoning ability for methanol oxidation, the addition of porous SiO2-TiO2 can replace the PtRu to some extent, comparing with the commercial PuRu/C catalyst, not only the loading of PtRu has been cut down 50%, but also the electro-oxidizing activity of methanol improved. The electro-oxidizing mechanism is basically analyzed.


2019 ◽  
Vol 33 (1) ◽  
pp. 275-286
Author(s):  
Taigo Onodera ◽  
Shuichi Suzuki ◽  
Yoshiyuki Takamori ◽  
Hideo Daimon

2004 ◽  
Vol 108 (2) ◽  
pp. 689-695 ◽  
Author(s):  
Aislinn H. C. Sirk ◽  
Josephine M. Hill ◽  
Sherman K. Y. Kung ◽  
Viola I. Birss

2021 ◽  
Vol 03 (03) ◽  
pp. 1-1
Author(s):  
Dan Fang ◽  
◽  
Sri Narayan ◽  

Direct methanol oxidation catalysts Pt1-x-Tax (0<x<1) were prepared using co-sputter deposition. Characterization of these thin film catalysts was performed using scanning electron microscopy (SEM), energy dispersive X-ray (EDX), X-ray Diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Assessment of the methanol oxidation activity of Pt1-x-Tax catalysts were achieved through half-cell experiments. Among all the Pt1-x-Tax catalysts, Pt0.77-Ta0.23 catalyst showed the best electrochemical area specific activity which was comparable to platinum-ruthenium alloy on carbon (PtRu/C) catalysts. Pt1-x-Tax catalysts worked as bi-functional methanol oxidation catalysts. The surface oxides species activated water molecules and hence facilitated the process of removing carbon monoxide from the platinum sites. The membrane electrode assembly (MEA) of Pt0.77-Ta0.23 catalyst was tested at 60, 80 and 90 °C. The power density achieved at 90 °C was 82 mW/cm2/mg Pt, which was 1.82 times of PtRu/C catalyst with similar platinum loading.


2019 ◽  
Vol 1 (2) ◽  
pp. 1-4
Author(s):  
Ayşe Bayrakçeken Yurtcan

The oxidation of small organic molecules on the catalyst under electrocatalytic conditions is important for the operation of liquid feed fuel cells. The basic reaction mechanisms toward the oxidation of methanol and formic acid continue to be a matter of debate under real operational conditions of electrochemical systems. The electrocatalytic activity of the commercial Pt/C catalyst was investigated in sulfuric acid/methanol and sulfuric acid/formic acid mixtures using electrochemical measurements. This work presents the variation of formic acid and methanol oxidation on the catalyst depending on hydrodynamic conditions using the rotating disk electrode. Cyclic voltammograms were obtained at different scan rates, rotating speeds and concentrations. As the rotating speed increases, the oxidation activity of formic acid and methanol decrease under voltammetric measurements. The peak currents of formic acid and methanol oxidation increased with the increase in the scan rate and concentration.


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