The reactivity of O2 with copper cluster anions Cun− (n = 7−20): Leveling effect of spin accommodation

• Published in: Chinese chemical letters Vol. 33; no. 2; pp. 995 - 1000
• Main Authors: Du, Qiuying, Yin, Baoqi, Zhou, Si, Luo, Zhixun, Zhao, Jijun
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.02.2022; Key laboratory of Material Modification by Laser,Ion and Electron Beams(Dalian University of Technology),Ministry of Education,Dalian 116024,China%Beijing National Laboratory for Molecular Sciences(BNLMS),State Key Laboratory for Structural Chemistry of Unstable and Stable Species,Institute of Chemistry,Chinese Academy of Sciences,Beijing 100190,China
• Subjects: Ab initio; Copper cluster; Leveling effect; Mass spectrometry; O2 adsorption; O2 dissociation; Spin accommodation; Ab initio; O2 adsorption; Copper cluster; Spin accommodation; O2 dissociation; Leveling effect; Mass spectrometry
• ISSN: 1001-8417; 1878-5964
• DOI: 10.1016/j.cclet.2021.08.127

The activation of molecular oxygen is an important step in metal-catalyzed oxidation reactions and a hot subject for the research of gas-phase metal clusters. It is known that the Ag and Au clusters readily react with O2 when they have open shell electronic structures. Distinct from this, here we observed Cun− (n = 7−20) clusters of both open and closed shells possess high reactivity with O2 with few exceptions. In a combination with ab initio calculations, we demonstrate that the activation of O2 on the even- and odd-sized Cun− clusters follows the single and double electron transfer models, respectively. Such phenomenon of metal clusters with different basicity to activate oxygen is enabled by the leveling effect of spin accommodation. The activity of Cun− clusters is correlated to the HOMO level, and for the close-shell clusters is also governed by the vertical spin excitation energy (VSE). In encountering the attack of dioxygen, the activity of the copper cluster anions not only depends on their basicity to donate electrons, but also closely associated with the cluster sizes. Small copper clusters Cun− (n = 7−13) can dissociate O2 spontaneously, while large clusters require extra energies and display close relationship between the reaction rates and electronic vertical detachment energies (VDE). Our work illuminates a novel reaction mechanism between Cun− clusters and O2, which sheds light in manipulating the activity and stability of coinage clusters by controlling the spin and charge states. Systematic study on the gas-phase adsorption and dissociation of O2 on Cun− (n = 7−20) cluster anions. We illustrate the chemisorption of O2 on even- and odd-sized clusters follows single and double electron transfer models, respectively, which is enabled by the leveling effect of spin accommodation. [Display omitted] .