Gao Yang, Xie Weiyu, Wang Bo, Schreckenbach Georg, Govorov Alexander O, Li Xiaoan, Wang Zhiming M
Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, Sichuan 611731, China.
School of Physics and Optoelectronic Engineering, Hainan University, Haikou 570228, China.
Langmuir. 2024 Jul 23;40(29):15023-15030. doi: 10.1021/acs.langmuir.4c01345. Epub 2024 Jul 15.
Since delocalization of electronic states is a prerequisite for exerting unique electron transport properties, early actinides (An) with highly delocalized 5/6d orbitals are natural candidates. However, given the experimental difficulties of such radioactive compounds and the complex relativistic effects in theoretical studies, understanding the electronic structure and bonding of actinides is underdeveloped on the periodic table. A further challenge is the very complicated electronic structures encountered in the confinement of actinides, as vividly illustrated by the weakly radioactive Th(Thorium)-encapsulated metal chalcogenide clusters, Th@CoTeL (L = PH, PMe, PEt). Here we report the electronic structure and the electron transport properties of the Th@CoTeL clusters and compare them with those of the hollow CoTeL clusters using the nonequilibrium Green's function combined with relativistic density functional theory (NEGF-DFT). We found that the equilibrium conductance in Th@CoTe(PH) (0.76 ) has been greatly improved over that in CoTe(PH) (0.03 ), which has also been verified under an applied different bias voltage. The covalent bonding character between 6 (Th) and 3 (Co) atomic orbitals resulting from steric confinement is the source of the performance enhancement and a most important factor governing the accessibility of such 5/6d orbitals. The results are of significance to the rapidly developing field of molecular nanoelectronics.
