Experimental and Theoretical Study of N2 Adsorption on Hydrogenated Y2C4H− and Dehydrogenated Y2C4− Cluster Anions at Room Temperature |
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| Authors: | Min Gao Yong-Qi Ding Jia-Bi Ma |
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| Affiliation: | 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, Beijing 102488, China; (M.G.); (Y.-Q.D.) |
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| Abstract: | The adsorption of atmospheric dinitrogen (N2) on transition metal sites is an important topic in chemistry, which is regarded as the prerequisite for the activation of robust N≡N bonds in biological and industrial fields. Metal hydride bonds play an important part in the adsorption of N2, while the role of hydrogen has not been comprehensively studied. Herein, we report the N2 adsorption on the well-defined Y2C4H0,1− cluster anions under mild conditions by using mass spectrometry and density functional theory calculations. The mass spectrometry results reveal that the reactivity of N2 adsorption on Y2C4H− is 50 times higher than that on Y2C4− clusters. Further analysis reveals the important role of the H atom: (1) the presence of the H atom modifies the charge distribution of the Y2C4H− anion; (2) the approach of N2 to Y2C4H− is more favorable kinetically compared to that to Y2C4−; and (3) a natural charge analysis shows that two Y atoms and one Y atom are the major electron donors in the Y2C4− and Y2C4H− anion clusters, respectively. This work provides new clues to the rational design of TM-based catalysts by efficiently doping hydrogen atoms to modulate the reactivity towards N2. |
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| Keywords: | N2 adsorption mass spectrometry density functional theory calculations |
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