摘要
The thermal gas-phase reactions of Nb2BN2- cluster anions with carbon dioxide have been explored by using the art of time-of-flight mass spectrometry and density functional theory calculations. Four CO2 molecules can be consecutively reduced by Nb2BN2-, resulting in the formation of Nb2BN2O1-4- anions and the release of one CO molecule each time. To illustrate the role of ligands in Nb2BN2-, the reactivities of Nb2N2- and Nb2B- toward CO2 were also investigated; two and three CO2 molecules are activated, respectively, and the rate constants are slower than that of Nb2BN2-/CO2 systems. This comparison indicates that metal-metal multiple bonds and appropriate ligands, such as B, are important factors for CO2 reduction. The synergy between a transition metal atom (Nb) and a main-group atom (B) in CO2 reduction mediated by gas-phase clusters is revealed for the first time. To the best of our knowledge, Nb2BN2- anions are gas-phase clusters that reduce the largest number of CO2 molecules. A fundamental understanding of the efficient reduction of carbon dioxide molecules may shed light on the rational design of active sites on supported transition metal/boron nitride catalysts.
源语言 | 英语 |
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页(从-至) | 14081-14087 |
页数 | 7 |
期刊 | Dalton Transactions |
卷 | 49 |
期 | 40 |
DOI | |
出版状态 | 已出版 - 28 10月 2020 |