Enhanced oxygen reduction electrocatalysis on PtCoSn alloy nanocatalyst mediated by Ta-doped SnO2 support for polymer electrolyte fuel cells

催化作用 电解质 活化能 电催化剂 阿累尼乌斯方程 化学 合金 铂金 无机化学 离解(化学) 吸附 化学工程 材料科学 电化学 物理化学 电极 有机化学 工程类
作者
Guoyu Shi,Takuma Hashimoto,Donald A. Tryk,Tetsuro Tano,Akihiro Iiyama,Makoto Uchida,Katsuyoshi Kakinuma
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:390: 138894-138894 被引量:15
标识
DOI:10.1016/j.electacta.2021.138894
摘要

• The PtCoSn/Ta-SnO 2 catalyst exhibits remarkably improved ORR kinetics and specific ORR activity. • The incorporation of Sn favors O 2 adsorption and dissociation. • The PtCoSn/Ta-SnO 2 catalyst shows exceptional load cycle durability. For polymer electrolyte fuel cells (PEFCs), platinum-based catalysts for the air cathode supported on metal oxides such as SnO 2 exhibit highly promising durability. Yet, the activity for the oxygen reduction reaction (ORR) has still not been sufficiently high toward widespread application. Here, we report a new type of catalyst with significantly boosted ORR activity, based on PtCoSn alloy nanostructures formed on Ta-doped SnO 2 support (PtCoSn/Ta-SnO 2 ). The ORR activity of the PtCoSn/Ta-SnO 2 catalyst is evaluated in acidic media (0.1 M HClO 4 ) from 20 to 80 °C. The apparent rate constants ( k app ) for the ORR on PtCoSn/Ta-SnO 2 are found to be about 4.5 and 1.5 times greater than those of commercial Pt and Pt 3 Co alloy catalysts supported on carbon black (c-Pt/C and c-Pt 3 Co/C), respectively, and increase with temperature, in accordance with an Arrhenius-type relation from 20 to 60 °C. The enhanced ORR rates of the PtCoSn/Ta-SnO 2 catalyst can be correlated with an increase in the preexponential factor of the Arrhenius equation, together with a lowered activation energy. Experimental and density functional theory results reveal that the incorporation of Sn facilitates O 2 adsorption and dissociation, which is beneficial to overcome the kinetic limitation of ORR. Moreover, the durability of PtCoSn/Ta-SnO 2 examined by potential-step cycling between 0.6 and 1.0 V at 80 °C has been found to be much higher as compared with c-Pt/C and c-Pt 3 Co/C.
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