A mesoporous PtCu catalyst modified with a Ru submonolayer is successfully synthesized by a facile electrochemical process of electrodeposition, dealloying and Ru underpotential deposition. The material has a large specific surface area comparable to nanoparticles (11 m(2) g(-1)) and exhibits a promising catalyst activity for the methanol oxidation reaction.

Low-cost and high-performance advanced electrocatalysts for direct methanol fuel cells are of key significance for the improvement of environmentally-pleasant energy technologies. Herein, we report the facile synthesis of cobalt phosphate (Co3(PO4)2) nanospheres by a microwave-assisted process and utilized as an electrocatalyst for methanol oxidation. The phase formation, morphological surface ...

Introduction Direct methanol fuel cells are very important as a clean, low cost and portable power source because of several environmental problems in traditional energy producing systems. Compared to the hydrogen fueled PEMFCs, direct methanol PEMFCs are more compact and can be used in power portable electric devices. Platinum is the most active electro-catalyst for the electro-oxidation of me...

steam reforming integrated with oxidation of methanol was considered with numerical simulation. the parallel micro-channels with circular cross sections were used. because when the catalytic deposited inside the rectangular micro-channels, it fills up the edges. hence, the approximation of a cylindrical channel is appropriate. effect of this changing in cross section was considered and results ...

The electrocatalytic reactivity of Pt nanoparticles supported on high-pressure-high-temperature diamond particles towards adsorbed CO, methanol and formic acid oxidation is investigated employing differential electrochemical mass spectrometry (DEMS). Surface treatment of diamond particles, employed as dimensionally stable electrocatalyst supports, leads to materials with surfaces featuring main...

Previous to 1950, when Bonnichsenl isolated crystalline alcohol dehydrogenase (ADH) and showed that it did not react with methanol,$ it was believed that the ADH system was responsible for the oxidation of all primary aliphatic alcohols, including methanol (FIGURE 1 ) . This observation redirected attention to the peroxidative system as a means of oxidizing methanol. As early as 1936, Keilin an...

The catalytic activities of an equal amount of 3 different carbon supported catalysts containing 10% Pt, 20% Pt + 10% Ru, and 30% Pt were evaluated in neutral and basic media for methanol oxidation by cyclic voltammetry. The prominent oxidation peak for methanol appeared in the forward anodic sweep at around 1.0 V in neutral medium, while in basic medium it appeared at significantly lower poten...

The oxidation of methanol over highly dispersed vanadia supported on TiO2 (anatase) has been investigated using in situ Fourier transform infrared spectroscopy (FTIR), near ambient pressure X-ray photoelectron spectroscopy (NAP XPS), X-ray absorption near-edge structure (XANES), and a temperature-programmed reaction technique. The data were complemented by kinetic measurements collected in a fl...

Active and durable electrocatalysts for methanol oxidation reaction are of critical importance to the commercial viability of direct methanol fuel cell technology. Unfortunately, current methanol oxidation electrocatalysts fall far short of expectations and suffer from rapid activity degradation. Here we report platinum-nickel hydroxide-graphene ternary hybrids as a possible solution to this lo...