Kaw Kevin A, Louwerse Rick J, Bakker Joost M, Lievens Peter, Janssens Ewald, Ferrari Piero
Quantum Solid-State Physics, Department of Physics and Astronomy, KU Leuven, Celestijnenlaan 200d, 3001, Leuven, Belgium.
Radboud University, Institute for Molecules and Materials, HFML-FELIX, 6525, Nijmegen, ED, Netherlands.
Commun Chem. 2024 Jun 4;7(1):124. doi: 10.1038/s42004-024-01206-2.
The interplay between constituent localized and itinerant electrons of metal clusters defines their physical and chemical properties. In turn, the electronic and geometrical structures are strongly entwined and exhibit strong size-dependent variations. Current understanding of low-energy excited states of metal clusters relies on stand-alone theoretical investigations and few comparisons with measured properties, since direct identification of low-lying states is lacking hitherto. Here, we report on the measurement of low-lying electronic transitions in cationic cobalt clusters using infrared photofragmentation spectroscopy. Broad and size-dependent absorption features were observed within 0.056 - 0.446 eV, well above the energies of the sharp absorption bands caused by cluster vibrations. Complementary time-dependent density functional theory calculations reproduce the main observed absorption features, providing direct evidence that they correspond to transitions between electronic states of mainly d-character, arising from the open d-shells of the Co atoms and the high spin multiplicity of the clusters.
金属团簇中局域电子和巡游电子之间的相互作用决定了它们的物理和化学性质。反过来,电子结构和几何结构紧密相连,并呈现出强烈的尺寸依赖性变化。目前对金属团簇低能激发态的理解依赖于独立的理论研究,与测量性质的比较很少,因为迄今为止缺乏对低能态的直接识别。在这里,我们报告了使用红外光解离光谱对阳离子钴团簇中低能电子跃迁的测量。在0.056 - 0.446 eV范围内观察到宽的且与尺寸相关的吸收特征,远高于团簇振动引起的尖锐吸收带的能量。互补的含时密度泛函理论计算重现了主要观察到的吸收特征,提供了直接证据,表明它们对应于主要具有d特征的电子态之间的跃迁,这些跃迁源于Co原子的开放d壳层和团簇的高自旋多重性。