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铌硼氮簇阴离子还原四个二氧化碳分子:配体对反应活性的增强作用

NbBN cluster anions reduce four carbon dioxide molecules: reactivity enhancement by ligands.

作者信息

Zhou Hai-Yan, Wang Ming, Ding Yong-Qi, Ma Jia-Bi

机构信息

Key Laboratory of Cluster Science of Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, 100081, Beijing, People's Republic of China.

出版信息

Dalton Trans. 2020 Oct 20;49(40):14081-14087. doi: 10.1039/d0dt02680h.

Abstract

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.

摘要

通过飞行时间质谱技术和密度泛函理论计算,对Nb2BN2-团簇阴离子与二氧化碳的热气相反应进行了研究。Nb2BN2-可连续还原四个二氧化碳分子,生成Nb2BN2O1-4-阴离子,每次释放一个一氧化碳分子。为了阐明配体在Nb2BN2-中的作用,还研究了Nb2N2-和Nb2B-与二氧化碳的反应活性;分别有两个和三个二氧化碳分子被活化,其反应速率常数比Nb2BN2-/二氧化碳体系的慢。这种比较表明,金属-金属多重键和合适的配体(如B)是二氧化碳还原的重要因素。首次揭示了气相团簇介导的二氧化碳还原过程中过渡金属原子(Nb)和主族原子(B)之间的协同作用。据我们所知,Nb2BN2-阴离子是能还原最多二氧化碳分子的气相团簇。对二氧化碳分子高效还原的基本理解可能有助于合理设计负载型过渡金属/氮化硼催化剂的活性位点。

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