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首页> 外文期刊>Applied Surface Science >Insight into the effect of promoter Pb in Pb-Pd catalyst on methyl methacrylate formation via direct oxidative esterification: A DFT study
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Insight into the effect of promoter Pb in Pb-Pd catalyst on methyl methacrylate formation via direct oxidative esterification: A DFT study

机译:通过直接氧化酯化深入了解助催化剂Pb在Pb-Pd催化剂中对甲基丙烯酸甲酯形成的影响:DFT研究

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The effect of promoter Pb in Pb-Pd alloy on the direct oxidative esterification of methacrolein (MAL) and CH3OH to methyl Methacrylate (MMA) reaction has been systematically investigated using density functional theory for the first time. Formation energies results showed Pb-4-Pd(1 1 1) was the easiest formation surface in Pb-Pd alloy. Adsorption and co-adsorption energies results revealed the addition of Pb weakened CH3OH adsorption, but enhanced adsorption capacity of CH3O, MAL and MMA, and greatly increased co-adsorption energies of CH3O with H, MAL and carbonyl species, which were further demonstrated by charge density difference, PDOS and HOMO/LUMO orbitals analysis. Activation energies results indicated that MMA formation via MAL dehydrogenation following carbonyl coupling with CH3O was the favorable path on the Pb-4-Pd(1 1 1) surface. The effect of promoter Pb on adsorption, co-adsorption, and activation energies were attributed to strong electronic interactions between Pb and Pd atoms. Promoter Pb played an electronic donor role realizing bimetallic synergetic effect, and its introduction unchanged actual catalytic active site of Pd, which was confirmed by comparative results of combined electronic structure analysis and reaction mechanism on the pure Pd and Pb-4-Pd(1 1 1) surfaces. These results are beneficial for the design of Pb-Pd bimetallic catalyst implied in direct oxidative esterification reactions.
机译:首次使用密度泛函理论系统地研究了促进剂Pb在Pb-Pd合金中对甲基丙烯醛(MAL)和CH3OH直接氧化酯化为甲基丙烯酸甲酯(MMA)反应的影响。形成能结果表明,Pb-4-Pd(1 1 1)是Pb-Pd合金中最容易形成的表面。吸附和共吸附能结果表明,Pb的添加减弱了CH3OH的吸附,但增加了CH3O,MAL和MMA的吸附能力,并大大增加了CH3O与H,MAL和羰基物质的共吸附能,这进一步由电荷证明。密度差,PDOS和HOMO / LUMO轨道分析。活化能结果表明,羰基与CH3O偶联后,通过MAL脱氢形成MMA是Pb-4-Pd(1 1 1)表面上的有利路径。促进剂Pb对吸附,共吸附和活化能的影响归因于Pb和Pd原子之间的强电子相互作用。促进剂Pb发挥电子给体作用,实现了双金属协同作用,并引入了不变的Pd实际催化活性位点,这通过结合电子结构分析和对纯Pd和Pb-4-Pd的反应机理的比较结果得以证实(1 1 1)表面。这些结果对于直接氧化酯化反应中隐含的Pb-Pd双金属催化剂的设计是有益的。

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