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Oxygen Evolution Reaction at Electrodes of Single Phase Ruthenium Oxides with Perovskite and Pyrochlore Structures

机译:具有钙钛矿和烧绿石结构的单相氧化钌电极上的析氧反应

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Single phase ruthenium oxides with perovskite (ATi1-xRuxO3 (A=Ca, Sr)) and pyrochlore structure (Bi2Ru2O7, Pb2Ru2O6.5) have been prepared reproducibly by solid state reaction methods and their electrocatalytic activities for oxygen evolution have been examined by Tafel plots. Tafel slopes vary from a low value of 42 mV/decade up to 222 mV/decade at room temperature. The high exchange current densities and high Tafel slopes compared with those obtained from the RuO2 DSA electrode at the crystalline single phase metal oxide electrodes suggest that they are better electrocatalysts at low overpotentials. A favorable change in the Tafel slope for the oxygen evolution reaction occurs as the ruthenium content increases. Substitution of Ti for Ru in the perovskite solid solutions enhanced their chemical stability by losing marginal electrochemical activity.
机译:通过固相反应法可重现制备具有钙钛矿型(ATi1-xRuxO3(A = Ca,Sr)和烧绿石结构(Bi2Ru2O7,Pb2Ru2O6.5)的单相氧化钌,并通过Tafel曲线研究了其对氧释放的电催化活性。 Tafel斜率在室温下从42 mV /十倍的低值到222 mV /十倍的低值不等。与在结晶单相金属氧化物电极上从RuO2 DSA电极获得的相比,高交换电流密度和高Tafel斜率表明它们在低过电势下是更好的电催化剂。随着钌含量的增加,发生放氧反应的塔菲尔斜率发生有利变化。钛在钙钛矿固溶体中取代Ru会失去边缘的电化学活性,从而增强了其化学稳定性。

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