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Depositing the PtNi nanoparticles on Niobium Oxide to Enhance the Activity and CO-tolerance for Alkaline Methanol Electrooxidation

化学 催化作用 甲醇 塔菲尔方程 电化学 氧化物 阳极 乙二醇 甲醇燃料 过渡金属 氧化铌 无机化学 化学工程 有机化学 电极 物理化学 工程类
作者
X. Joan Hu,Riguang Zhang,Zhao Jiang
出处
期刊:Chinese Journal of Structural Chemistry [Elsevier BV]
卷期号:: 100157-100157
标识
DOI:10.1016/j.cjsc.2023.100157
摘要

Direct methanol fuel cells have the advantages of simple system, convenient operation, high conversion rate and low carbon emission,which are considered as the environmental and friendly energy conversion devices. However, the low activity, CO-tolerance and high cost of anode catalysts restrict the large-scale commercial applications. Therefore, it is of great practical significance to design and construct the anodic catalysts with high activity, stability and low cost for methanol oxidation reaction. In this work, the PtM/Nb2O5-C (M=Co, Sn, Ni) catalysts are synthesized by the ethylene glycol solvothermal method using transition metal oxide Nb2O5 as the support. The catalytic performance of differentcatalysts is further evaluated for alkaline MOR. The results show that the introduction of Ni (existence in Ni2+ and Ni3+) has the most obvious improvement for alkaline MOR performance. By adjusting the doped ratio of Pt:Ni, it is shown that PtNi/Nb2O5-C has the highest mass activity (3877.9 mA·mgPt-1), 12 times that of the commercial Pt/C catalyst. CV, LSV, Tafel and EIS analysis show that PtNi/Nb2O5-C has the lowest onset potential and charge transfer resistance, and the fastest electrocatalytic oxidation rate of methanol. CA tests show that the electrochemical stability is also significantly improved with the introduction of Nb2O5 and Ni. Combined with the structural characterization and electrochemical tests, it was found that the evident electronic effect among Pt and Ni, Nb2O5 and the hydroxyl brought from Ni species were mainly ascribed for enhancing the activity, CO resistance and stability of PtNi/Nb2O5-C.

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