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- W4286221662 abstract "Abstract The design of efficient non‐noble metal catalysts for CO 2 hydrogenation to fuels and chemicals is desired yet remains a challenge. Herein, we report that single Mo atoms with a MoN 3 (pyrrolic) moiety enable remarkable CO 2 adsorption and hydrogenation to CO, as predicted by density functional theory studies and evidenced by a high and stable conversion of CO 2 reaching about 30.4 % with a CO selectivity of almost 100 % at 500 °C and very low H 2 partial pressure. Atomically dispersed MoN 3 is calculated to facilitate CO 2 activation and reduces CO 2 to CO* via the direct dissociation path. Furthermore, the highest transition state energy in CO formation is 0.82 eV, which is substantially lower than that of CH 4 formation (2.16 eV) and accounts for the dominant yield of CO. The enhanced catalytic performances of Mo/NC originate from facile CO desorption with the help of dispersed Mo on nitrogen‐doped carbon (Mo/NC), and in the absence of Mo nanoparticles. The resulting catalyst preserves good stability without degradation of CO 2 conversion rate even after 68 hours of continuous reaction. This finding provides a promising route for the construction of highly active, selective, and robust single‐atom non‐precious metal catalysts for reverse water–gas shift reaction." @default.
- W4286221662 created "2022-07-21" @default.
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- W4286221662 date "2022-08-03" @default.
- W4286221662 modified "2023-10-05" @default.
- W4286221662 title "Single‐Atom Molybdenum‐N <sub>3</sub> Sites for Selective Hydrogenation of CO <sub>2</sub> to CO" @default.
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- W4286221662 doi "https://doi.org/10.1002/ange.202203836" @default.
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