Cao Wenjin, Zhang Yuchen, Wu Lu, Yang Dong-Sheng
Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, United States.
J Phys Chem A. 2021 Mar 11;125(9):1941-1948. doi: 10.1021/acs.jpca.1c00533. Epub 2021 Mar 2.
Mass-analyzed threshold ionization (MATI) spectroscopy was used to measure the vibronic spectra of LnO (Ln = La and Ce). Single-reference coupled cluster and relativistic multireference configuration calculations were carried out to compare with the measured vibronic energies. The spectrum of LaO displays a single vibronic band system, while that of CeO shows multiple ones. The ionization energies of LaO and CeO are measured as 5.2446(6) and 5.3332(6) eV, respectively, which are a 100-fold improvement over the literature values. The vibrational energies of the neutral molecule and corresponding ion reveal the charge effect on the metal-oxygen bond of both species. The single band system in the spectrum of LaO arises from the transition of the ground state of the neutral molecule with the La(6s)O(2p) valence configuration to the ground state of the singly charged ion with the La(6s)O(2p) configuration. The multiple band systems in the spectrum of CeO are attributed to the spin-orbit coupling for the Ce(4f6s)O(2p) configuration of the neutral molecule and an excited state for the Ce(4f)O(2p) configuration of the ion.
采用质量分析阈值电离(MATI)光谱法测量了LnO(Ln = La和Ce)的振转光谱。进行了单参考耦合簇和相对论多参考组态计算,以与测量的振转能量进行比较。LaO的光谱显示出单一的振转带系,而CeO的光谱则显示出多个振转带系。测得LaO和CeO的电离能分别为5.2446(6)和5.3332(6) eV,比文献值提高了100倍。中性分子和相应离子的振动能量揭示了电荷对这两种物质金属-氧键的影响。LaO光谱中的单带系源于具有La(6s)O(2p)价组态的中性分子基态到具有La(6s)O(2p)组态的单电荷离子基态的跃迁。CeO光谱中的多个带系归因于中性分子的Ce(4f6s)O(2p)组态的自旋轨道耦合以及离子的Ce(4f)O(2p)组态的一个激发态。