铂金
催化作用
X射线光电子能谱
铂纳米粒子
氧化态
色散(光学)
材料科学
甲苯
锡
化学
核化学
分析化学(期刊)
无机化学
化学工程
冶金
有机化学
物理
光学
工程类
作者
Ivan Marić,Goran Dražić,Edi Radin,Robert Peter,M. Škrabić,Tanja Jurkin,Anđela Pustak,Nikola Baran,Lara Mikac,Mile Ivanda,M. Petravić,Goran Štefanić,Marijan Gotić
标识
DOI:10.1016/j.apsusc.2022.155073
摘要
The Pt/SnO2 (SP-samples) and Pt/α-Fe2O3 (FP-samples) with platinum loadings between 1 and 10 mol% were synthesized mechanochemically starting from platinum(II) acetylacetonate dissolved in toluene and from SnO2 and α-Fe2O3 powders obtained from tin(II) and iron(II) acetates. The STEM results show that the ultrasmall platinum nanoparticles (PtNPs) are well dispersed on the SnO2 and α-Fe2O3 supports. The PtNPs size distributions calculated with lognormal functions ranged from 1.0 to 1.3 nm. The results of temperature programmed reduction in hydrogen showed maxima at 120–160 °C due to the reduction of PtOx to Pt0. The Pt-4f-XPS results showed that the dispersed platinum on the SnO2 and α-Fe2O3 supports consisted of all three oxidation states of platinum: Pt4+, Pt2+ and Pt0. The average oxidation state of platinum as a function of molar fraction of Pt loading in the SP samples varies from 1.69 to 2.11, whereas the oxidation state of Pt in the FP samples varies more linearly and steeply from 1.42 to 2.58. The synthesized samples showed high catalytic activity for the reduction of 4-nitropenol (4-NP) to 4-aminophenol (4-AP), which can be explained by the high dispersion of non-aggregated ultrasmall PtNPs with a size of about 1 nm on the SnOx and FeOx supports.
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