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Surface Structures and Electrochemical Stabilities for Pt/Pd(111) Model Electrocatalysts

机译:Pt / Pd(111)模型电催化剂的表面结构和电化学稳定性

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We investigated surface structures and electrochemical stabilities for Pt/Pd(111) bimetallic surfaces fabricated using molecular beam epitaxy. The Pt/Pd(111) surfaces were prepared by depositing four monolayer (ML)-thick Pt onto Pd(111) at substrate temperatures of 300°C. The oxygen reduction reaction (ORR) activity of the pristine 4ML-Pt/Pd(111) surface was ca. 4.5 times higher than that of clean Pt(111). Electrochemical stabilities were evaluated by applying square-wave potential cycles (PCs) between 0.6 and x V (x = 0.8, 0.85, 0.9 and 1.0; xV-PCs) in O_2-saturated 0.1 M HClO_4 at 80°C. Although the 0.9V- and 1.0V-PCs cause ORR deactivation, the pristine ORR activities remained nearly unchanged by the 0.8V- and 0.85V-PCs even after 5000 PCs. The results suggest that the electrochemical structural stability of Pt/Pd core-shell type catalysts depends on the cell voltages used under the practical operating conditions of polymer electrolyte fuel cells.
机译:我们研究了使用分子束外延制造的Pt / Pd(111)双金属表面的表面结构和电化学稳定性。通过在300℃的衬底温度下沉积四个单层(ML) - 染色Pt到Pd(111)上,制备Pt / Pd(111)表面。原始4ml-Pt / Pd(111)表面的氧还原反应(ORR)活性是Ca.比清洁Pt(111)高4.5倍。通过在80℃下在O_2饱和0.1M HClO_4中施加0.6和X = 0.8,0.85,0.9和1.0; XV-PC之间的方波电位循环(PC)在0.6和x = 0.8,0.5,0.9和1.0; XV-PC之间进行评估电化学稳定性。虽然0.9V-和1.0V-PC引起ORR停用,但即使在5000个PC之后,原始ORR活动也仍然在0.8V-和0.85V-PC上几乎不变。结果表明,Pt / Pd核 - 壳型催化剂的电化学结构稳定性取决于聚合物电解质燃料电池的实际操作条件下使用的电池电压。

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