Ferrando Riccardo, Rossi Giulia, Nita Florin, Barcaro Giovanni, Fortunelli Alessandro
dagger Dipartimento di Fisica and INFM/CNR, Via Dodecaneso 33, Genova, I16146, Italy.
ACS Nano. 2008 Sep 23;2(9):1849-56. doi: 10.1021/nn800315x.
The control of the structure of oxide-supported metal nanoparticles is crucial in determining their properties and possible applications. Here, building principles are derived for predicting the epitaxies of metal nanoparticles on square-symmetry oxide surfaces. Unusual phases are found for an appropriate choice of the metal-oxide pair, where nanoparticles with hcp structure are stabilized for fcc metals such as Ni, Pd, and Pt, or for Co in a size range in which Co has typically nonhcp arrangements. These predictions are supported by a comparison with available experimental data on Ni/MgO(100) nanodots, and generalized to a whole class of metal-oxide systems of great potential interest, such as Pd and Pt on CaO, Ni on CoO, and Co on MgO. The atomistic features of the nanoparticles in turn suggest that these materials should possess peculiar properties; in particular, the facets exposed by the nanodots reveal adsorption sites with unusual geometry of possible effect on their catalytic properties, while the destabilization of stacking faults and the structural deformations observed for these particles are expected to influence their magnetic behavior.
控制氧化物负载金属纳米颗粒的结构对于确定其性质和可能的应用至关重要。在此,推导了用于预测金属纳米颗粒在方形对称氧化物表面上的外延关系的构建原则。对于适当选择的金属 - 氧化物对,发现了不寻常的相,其中对于面心立方(fcc)金属如Ni、Pd和Pt,或者对于Co在通常具有非六方密堆积(hcp)排列的尺寸范围内,具有hcp结构的纳米颗粒得以稳定。这些预测通过与Ni/MgO(100)纳米点的现有实验数据进行比较得到支持,并推广到一类具有极大潜在兴趣的整个金属 - 氧化物体系中,例如CaO上的Pd和Pt、CoO上的Ni以及MgO上的Co。纳米颗粒的原子特征进而表明这些材料应具有特殊性质;特别是,纳米点暴露的晶面揭示了具有可能影响其催化性质的不寻常几何形状的吸附位点,而这些颗粒中观察到的堆垛层错的失稳和结构变形预计会影响它们的磁行为。