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As a high-active metal-free electrocatalyst for NH 3 production via NO reduction reaction, honeycomb carbon nanofiber achieves an NH 3 yield of 22.35 μmol h−1 cm−2 with a high Faradaic efficiency of 88.33%. [Display omitted] Electrocatalytic NO reduction is a promising technology for ambient NO removal with simultaneous production of highly value-added NH 3. Herein, we report that honeycomb carbon nanofiber coated on carbon paper acts as an efficient metal-free catalyst for ambient electroreduction of NO to NH 3. In 0.2 M Na 2 SO 4 solution, such catalyst achieves an NH 3 yield of 22.35 μmol h−1 cm−2 with a high Faradaic efficiency of up to 88.33%. Impressively, it also shows excellent stability for 10-h continuous electrolysis. Theoretical calculations reveal that the most active center of functional groups is –OH group for NO reduction with a low energy barrier (ΔG of 0.29 eV) for the potential-determining step (*NO + H → *HNO). [ABSTRACT FROM AUTHOR]

[Display omitted] • The adsorption energies of CO 2 on the surface oxygen vacancies of different crystalline In 2 O 3 were calculated using DFT. • The effect of the spatial distributions of two active components on the CO 2 hydrogenation to aromatics was studied. • The acidity of catalyst under different spatial distributions was studied through NH 3 -TPD. In tandem catalysts, not only good synergy between the two active components is required, but also the precise control of the spatial distribution between the two active components of metal oxides and zeolite is crucial for the migration and conversion of reaction intermediates in the direct conversion of CO 2 to hydrocarbons. The correlation between the metal and the acidic site of zeolite has traditionally been simplified as "the closer, the better". However, it should be noted that this principle only holds true for a portion of tandem catalysts. Therefore, this paper studied the effect of different crystalline In 2 O 3 (cubic phase, hexagonal phase, and mixed cubic/hexagonal phase) and sheet HZSM-5 zeolite tandem catalysts on the activity of CO 2 hydrogenation reaction under different spatial distribution. The generalized gradient approximation (GGA) of density functional theory (DFT) were used to simulate the adsorption energy of CO 2 by oxygen vacancy on c-In 2 O 3 (1 1 1) and h-In 2 O 3 (1 0 4) planes, it was found that O v1 on c-In 2 O 3 (1 1 1) and O v4 on h-In 2 O 3 (1 0 4) had the strongest adsorption energy for CO 2. In addition, it has been observed that the proximity of the two active components (e.g., during mortar mixing) results in decreased catalytic performance. This is due to the migration of metal In, which neutralizes the acid sites of zeolites and leads to inefficient conversion of methanol reaction intermediates to aromatics. As a result, CO 2 conversion and aromatic selectivity are decreased. [ABSTRACT FROM AUTHOR]