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Same selectivity hides different pathways: The same apparent 4-electron process for the oxygen-reduction-reaction hides different pathways over carbon-supported cobalt oxide catalysts depending on the potential. At low overpotentials, the ORR intermediate HO(2) (-) preferably disproportionates to oxygen, whereas at high overpotentials the disproportionation and reduction reaction occur in parallel., (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Iron‐nitrogen‐doped carbon (Fe‐NC) is an ideal candidate to replace Pt‐based oxygen reduction reaction (ORR) electrocatalysts due to its low cost and comparably high intrinsic activity. To further enhance the ORR performance of Fe‐NC electrocatalysts, efforts have been focused on two main methods. One is to enhance the intrinsic activity of FeNx sites through electronic and geometric regulation, and the other is to increase the density of active sites by introducing high‐nitrogen‐containing precursors or co‐doping methods. Herein, we report a strategy to further increase the Fe loading through the introduction of a trace amount of Cu atoms. Significant enhancement of the electrocatalytic ORR property is observed in the as‐prepared Fe and Cu co‐doped electrocatalyst with superior half‐wave potential (E1/2) in both alkaline and acid electrolyte. Experimental and theoretical study reveals that the introduction of a trace amount of Cu atoms is beneficial for the formation of FeN4 sites, owing to the reduced formation energy. This work opens up a wide avenue to further increase the Fe loading in Fe‐NC electrocatalysts through bimetal co‐doping method. [ABSTRACT FROM AUTHOR]

Abstract: A graphitic mesoporous carbon (denoted as GMC) was synthesized using resorcinol and formaldehyde as carbon precursors and iron nitrate as a graphitization catalyst. The GMC was characterized by X-ray diffraction, Raman spectroscopy, transmission electron microscopy (TEM), and nitrogen adsorption. The results show that the GMC has a mesoporous structure and a high surface area of 403 m2 g−1, and particularly, a well-defined graphitic framework. Using the GMC as the support, a PtRu/GMC was synthesized to act as an electrocatalyst for the methanol oxidation reaction (MOR). A counterpart with Vulcan® XC-72 (denoted as XC) as the support was prepared for comparison. TEM images show that PtRu nanoparticles are distributed uniformly on the carbon supports for both electrocatalysts. The electrochemical activity of the PtRu/GMC toward the MOR is slightly higher than that of the PtRu/XC in both half cell and single cell measurements. The 1500h stability test of a single cell suggests that the PtRu/GMC is excellent stable. [Copyright &y& Elsevier]

Abstract: Using resorcinol and formaldehyde as carbon precursors, graphitic mesoporous carbons (GMC) with different surface areas were synthesized by adjusting the amount of iron nitrate used as a graphitization catalyst. The BET surface area of the GMC decreases with increasing pore diameter and the material becomes more graphitic with increasing amount of catalyst. Using the GMC as the support, a series of PtRu electrocatalysts (PtRu-GMC) were synthesized. The electrocatalytic activities of the PtRu-GMC toward the methanol oxidation reaction were investigated in both half cells and single cells. The results indicate that the pore size of the GMC is especially important in determining the performance of direct methanol fuel cells. [Copyright &y& Elsevier]

Abstract: Carbon-supported bimetallic PdAg catalysts with Pd/Ag atomic ratios varying from 4/1 to 1/2 were prepared by an impregnation–reduction method. The impregnated black mixture was treated in H2/N2 atmosphere at a temperature varying from 180 to 500°C. The obtained Pd x Ag y /C catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), cyclic voltammetry (CV) and chronoamperometry (CA). XRD results show that the lattice constant of Pd is dilated, suggesting the formation of PdAg alloy. The lattice constant of Pd for the Pd x Ag y /C-500 (reduced at 500°C by H2) increases linearly and the average metal particle size decreases slightly from 6.8 to 5.1nm with increasing Ag fractions from 20% to 67% in the PdAg composition. For Pd x Ag y /C catalysts with a certain specific Pd/Ag atomic ratio, e.g., Pd2Ag1/C, the dilated lattice constant of Pd is independent of the reducing temperature, indicating the alloy degree for the Pd2Ag1/C-t catalysts is comparable. The average metal particle size for the Pd2Ag1/C-t catalysts increases from 3.4 to 5.2nm with H2 reduction temperature increasing from 180 to 500°C. The potentiodynamic measurements on ethanol electrooxidation reaction (EOR) show that the catalytic activities for the Pd x Ag y /C-t catalysts toward the EOR are improved by alloying Pd with Ag. At typical potential of a working fuel cell, e.g., −0.4V vs. Hg/HgO, the EOR current density presents a volcano shape as a function of the Ag fractions in PdAg with the maximum occurs at the Pd/Ag atomic ratios between 2/1 and 3/1. The CA tests show that the Pd x Ag y /C-500 catalysts perform high stability than that of Pd/C-500. The improved EOR activity for the Pd x Ag y /C-t catalysts, compared with whether Pd/C or Ag/C catalyst, may possibly be attributed to the formation of PdAg alloy and the fitted particle size. [Copyright &y& Elsevier]

Abstract: Vulcan XC-72R, Ketjen Black EC 300J and Black Pearls 2000 carbon blacks were used as the additive in Pt black cathode catalyst layer to investigate the effect on direct methanol fuel cell (DMFC) performance. The carbon blacks, Pt black catalyst and catalyst inks were characterized by N2 adsorption and scanning transmission electron microscopy (STEM) with Energy dispersive X-ray (EDX) spectroscopy. The cathode catalyst layers without and with carbon black additive were characterized by scanning electron microscopy, EDX, cyclic voltammetry and current-voltage curve measurements. Compared with Vulcan XC-72R and Black Pearls 2000, Ketjen Black EC 300J was more beneficial to increase the electrochemical surface area and DMFC performance of the cathode catalyst layer. The cathode catalyst layer with Ketjen Black EC 300J additive was kept intimately binding with the Nafion membrane after 360 h stability test of air-breathing DMFC. [ABSTRACT FROM AUTHOR]