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Epitaxial growth of Pd nanoparticles on molybdenum disulfide by sonochemistry and its effects on electrocatalysis

机译:Sonochemisty钼钼酰纳米粒子的外延生长及其对电寄生分析的影响

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In this work, we have synthesized Pd/MoS _(2) samples in which about 7 nm sized Pd NPs are formed on a MoS _(2) surface with the Pd content varied from 14.4 wt% to 33.6 wt% and studied their electrocatalytic activity for oxygen reduction reaction (ORR) in an alkaline medium. The syntheses were achieved by single-step sonochemical reactions between palladium acetylacetonate and 2H-MoS _(2) in ethylene glycol. Based on the structural characterization data, the Pd NPs are firstly grown epitaxially on the MoS _(2) surface in the [1?10] _(Pd) ||[100] _(MoS _(2) ) and (111) _(Pd) ||(001) _(MoS _(2) ) relationship. As the Pd-content increases, Pd NPs are formed on top of the first layer of Pd NPs as well as on the available MoS _(2) surface. The epitaxially grown Pd NPs experience a tensile strain and charge-transfer to MoS _(2) , which raises the d-band center of Pd, lowering the on-set potential in ORR. On the other hand, the enhanced adsorption of O _(2) on MoS _(2) can facilitate the ORR kinetics of Pd NPs. The observed ORR data on Pd/MoS _(2) can be explained as the net result of these two opposing effects of the MoS _(2) support.
机译:在这项工作中,我们具有合成的PD / MOS _(2)样品,其中在MOS _(2)表面上形成约7nm大小的Pd NP,PD含量从14.4wt%变化至33.6wt%,并研究了它们的电催化碱性介质中氧还原反应(ORR)的活性。通过在乙二醇中的乙酰丙酮酸钯和2H-MOS _(2)之间的单步交学化学反应来实现合成。基于结构表征数据,PD NPS首先在[1?10] _(PD)|| [100] _(MOS _(2))和(111)中在MOS _(2)表面上延伸在MOS _(2)表面上。(MOS _(2))和(111) _(pd)||(001)_(mos _(2))关系。随着PD含量的增加,PD NP形成在PD NP的第一层顶部以及可用的MOS _(2)表面上。外延生长的PD NPS体验拉伸应变和电荷转移到MOS _(2),其升高了PD的D波段中心,降低了ORR中的开启电位。另一方面,O _(2)对MOS _(2)的增强吸附可以促进PD NPS的ORR动力学。 PD / MOS _(2)上的观察到的ORR数据可以解释为MOS _(2)支持的这两个相反效果的净结果。

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