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• W4285405264 endingPage "154239" @default.
• W4285405264 startingPage "154239" @default.
• W4285405264 abstract "The ever-increasing concentration of carbon dioxide (CO2) in atmosphere has been resulting in disastrous effect on the nature and environment. Among the various methods for the CO2 reduction, the electrochemical reduction of CO2 (e-CO2RR) into fuels is considered to be much more effective. In this work, we find that the single atom catalysts (SACs) (SACs = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn) can be firmly anchored on the N-terminated TiN(1 1 1) surface because of high binding energies on the basis of density-functional theory calculations. We show that the SACs on the N-terminate of TiN(1 1 1) can greatly reduce the energy barrier for e-CO2RR and improve the selectivity of products. SACs, including Sc, Ti, and V, show a high catalytic performance to produce CH4 with a low limiting potential of 0.68, 0.22, and 0.48 eV, respectively. Both CH4 and CH2O can be obtained on SAC-Ni with the potential-determining step (PDS) of 0.77 eV. SAC-Cu can produce CH4 and CH3OH. Our findings demonstrate that N-terminated surface is suitable for anchoring SACs and the catalytic performance for e-CO2RR, such as overpotential and selectivity, can be optimized by using different transition metals, which provides a great way for the convertion CO2 into fuels." @default.
• W4285405264 created "2022-07-14" @default.
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• W4285405264 date "2022-11-01" @default.
• W4285405264 modified "2023-10-13" @default.
• W4285405264 title "Electrochemical reduction of CO2 on single-atom catalysts anchored on N-terminated TiN (1 1 1): Low overpotential and high selectivity" @default.
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• W4285405264 doi "https://doi.org/10.1016/j.apsusc.2022.154239" @default.
• W4285405264 hasPublicationYear "2022" @default.
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