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Performance and characterization of a Pt-Sn(oxidized)/C cathode catalyst with a SnO2-decorated Pt3Sn nanostructure for oxygen reduction reaction in a polymer electrolyte fuel cell

机译:具有SnO2-修饰的Pt3Sn纳米结构的Pt-Sn(氧化)/ C阴极催化剂的性能和表征,用于聚合物电解质燃料电池中的氧还原反应

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We have prepared and characterized a SnO2-decorated Pt-Sn(oxidized)/C cathode catalyst in a polymer electrolyte fuel cell (PEFC). Oxygen reduction reaction (ORR) performance of Pt/C (TEC10E50E) remained almost unchanged or even tended to reduce in repeated l-V load cycles, whereas the l-V load performance of the Pt-Sn(oxidized)/C prepared by controlled oxidation of a Pt-Sn alloy/C sample with the Pt3Sn phase revealed a significant increase with increasing l-V load cycles. The unique increase in the ORR performance of the Pt-Sn(oxidized)/C catalyst was ascribed to a promoting effect of SnO2 nano-islands formed on the surface of Pt3Sn core nanoparticles. Also in a rotating disk electrode (RDE) setup, the mass activity of an oxidized Pt3Sn/C catalyst was initially much lower than that of a Pt/C catalyst, but it increased remarkably after 5000 rectangular durability cycles and became higher than that of the fresh Pt/C. The maximum power density per electrochemical surface area for the Pt-Sn(oxidized)/C catalyst in a PEFC was about 5 times higher than that for the Pt/C catalyst at 0.1-0.8 A cm~(-2) of the current density. In situ X-ray absorption near-edge structure (XANES) analysis at the Pt Lm-edge in increasing/decreasing potential operations and at the Sn /(-edge in the l-V load cycles revealed a remarkable suppression of Pt oxidation compared with the Pt/C catalyst at higher potentials and no change in the Sn oxidation state, respectively, resulting in higher performance and stability of the Pt-Sn(oxidized)/C catalyst due to the SnO2 nano-islands under the PEFC operation conditions. The SnO2 nano-island decorated Pt-Sn(oxidized)/C catalyst with a Pt3Sn alloy nanostructure is regarded as a promising candidate for a PEFC cathode catalyst.
机译:我们已经在聚合物电解质燃料电池(PEFC)中制备并表征了SnO2修饰的Pt-Sn(氧化)/ C阴极催化剂。 Pt / C(TEC10E50E)的氧还原反应(ORR)性能在重复的lV负载循环中几乎保持不变甚至趋于降低,而通过控制Pt氧化制备的Pt-Sn(氧化)/ C的lV负载性能具有Pt3Sn相的-Sn合金/ C样品显示随着lV负载循环的增加而显着增加。 Pt-Sn(氧化)/ C催化剂的ORR性能的独特提高归因于在Pt3Sn核纳米颗粒表面形成的SnO2纳米岛的促进作用。同样在旋转圆盘电极(RDE)设置中,氧化的Pt3Sn / C催化剂的质量活性最初比Pt / C催化剂的质量活性低得多,但在经过5000个矩形的耐久性循环后,其质量活性显着提高,并高于Pt / C催化剂的质量活性。新鲜的Pt / C。在电流密度为0.1-0.8 A cm〜(-2)的情况下,PEFC中Pt-Sn(氧化)/ C催化剂的每个电化学表面积的最大功率密度约为Pt / C催化剂的最大功率密度的5倍。在Lt负载循环中增加/减少电位操作和在Sn /(-边缘)时,在Pt Lm边缘进行的原位X射线吸收近边缘结构(XANES)分析显示,与Pt相比,Pt氧化受到显着抑制/ C催化剂在较高的电势下且Sn的氧化态没有变化,分别由于PEFC操作条件下的SnO2纳米岛,导致Pt-Sn(氧化)/ C催化剂具有更高的性能和稳定性。具有Pt3Sn合金纳米结构的岛状装饰的Pt-Sn(氧化)/ C催化剂被认为是PEFC阴极催化剂的有希望的候选者。

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