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Optimization of Pt-Ni Alloy Catalysts Synthesized by Potentiostatic Electrodeposition for Cathode in PEMFC

机译:PEMFC阴极静电沉积合成Pt-Ni合金催化剂的优化

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摘要

The development of highly active and low-cost catalysts is a challenge for the application and large-scale commercialization of proton exchange membrane fuel cell (PEMFC). In this study, a series of Pt-Ni alloy catalysts is synthesized by potentiostatic electrodeposition, and the optimum deposition parameters are determined by an orthogonal array experiment. The effect of electrodeposition parameters on the morphology, composition, and electrocatalytic activity for oxygen reduction reaction (ORR) is investigated. The Pt-Ni alloy catalyst prepared with the optimum deposition parameters of -0.35 V versus saturated calomel electrode (SCE), 50℃ for 20 min exhibits the higher ORR activity. Rapid potential cycling dealloying is also employed to modify the morphology of Pt-Ni catalysts, which results in the increase of the electrochemical surface area (ECSA) and the improvement of the ORR electrocatalytic activity. The electrochemical active surface area (ECSA) for the dealloying Pt-Ni catalyst (D-OP-sample) with the grain size of 6.2 nm is 87.0 m~2 g~(-1). The current density and the mass activity for the electrode with D-OP-sample catalyst are 281.5 mA·cm~(-2) at 0.4V and 587.9 mA·mg_(Pt)~(-1) at 0.6V, respectively.
机译:高活性和低成本催化剂的开发对于质子交换膜燃料电池(PEMFC)的应用和大规模商业化是一个挑战。本研究通过恒电位电沉积合成了一系列的Pt-Ni合金催化剂,并通过正交实验确定了最佳的沉积参数。研究了电沉积参数对氧还原反应(ORR)的形态,组成和电催化活性的影响。相对于饱和甘汞电极(SCE),最佳沉积参数为-0.35 V制备的Pt-Ni合金催化剂,在50℃下保持20 min表现出较高的ORR活性。快速电势循环脱合金还用于修饰Pt-Ni催化剂的形态,这导致电化学表面积(ECSA)的增加和ORR电催化活性的提高。粒径为6.2 nm的脱金属Pt-Ni催化剂(D-OP-sample)的电化学活性表面积(ECSA)为87.0 m〜2 g〜(-1)。 D-OP样品催化剂的电极在0.4V时的电流密度和质量活度分别为281.5 mA·cm〜(-2)和0.6V时为587.9 mA·mg_(Pt)〜(-1)。

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