Chinese Journal of Catalysis ›› 2026, Vol. 87: 269-281.DOI: 10.1016/S1872-2067(26)65080-2
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Fengjuan Guoa, Chunyao Maa, Yue Huanga, Sitong Hanga, Junwei Maa,*(
), Hongtao Gaoa,b,*(
)
Received:2025-11-22
Accepted:2026-01-16
Online:2026-08-18
Published:2026-06-24
Supported by:Fengjuan Guo, Chunyao Ma, Yue Huang, Sitong Hang, Junwei Ma, Hongtao Gao. Unveiling the dominant distal-alternating hybrid mechanism in B-modulated Mo2TiC2Tx/MoO2 MXene for highly selective ambient NRR[J]. Chinese Journal of Catalysis, 2026, 87: 269-281.
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URL: https://www.cjcatal.com/EN/10.1016/S1872-2067(26)65080-2
Fig. 1. (a) Schematic depiction of the mechanism for N2 reduction to NH3. (b) Schematic diagram of the synthesis process for B@Mo2TiC2Tx/MoO2 MXene. (c) XRD patterns of the Mo2TiC2Tx/MoO2 and B@Mo2TiC2Tx/MoO2. The SEM (d) and HRTEM (e) images of B@Mo2TiC2Tx/MoO2 MXene. (f) Elemental mapping images of Mo, Ti, C, B, and O in B@Mo2TiC2Tx/MoO2 MXene composites.
Fig. 2. Mo 3d (a), Ti 2p (b), and O 1s (c) XPS spectra of B@Mo2TiC2Tx/MoO2 and Mo2TiC2Tx MXene. (d) The B 1s XPS spectrum of B@Mo2TiC2Tx/MoO2 MXene composites.
Fig. 3. (a) Ammonia yield and Faradaic efficiency of B@Mo2TiC2Tx/MoO2 at different potentials. (b) Cyclic stability and (c) Time-dependent current density of B@Mo2TiC2Tx/MoO2 at -0.2 V vs. Ag/AgCl. The ECSA (d), Nyquist plot (e) of B@Mo2TiC2Tx/MoO2 and Mo2TiC2Tx/MoO2 catalysts, and UV-Vis absorbance spectra (f) of B@Mo2TiC2Tx/MoO2 under various control conditions. (g) 1H NMR spectra of the electrolyte after NRR at -0.2 V using 15N2- and 14N2-saturated aliquots of 0.1 mol L?1 H2SO4 as the nitrogen sources. (h) Comparison of the results of this work with state-of-the-art electrocatalytic NRR catalysts in terms of yield rate and FE.
Fig. 4. The charge density difference of the B@Mo2TiC2Tx/MoO2 heterojunction (a) and the N2 molecule adsorbed on B@Mo2TiC2Tx/MoO2 MXene catalyst (b). (c) The PDOS of B@Mo2TiC2Tx/MoO2 MXene. The charge accumulation and depletion were depicted by yellow and green, respectively, and the isosurface value is 0.004 e Å?3.
Fig. 5. (a) Orbital compositions of the N2. (b) The electron “donation/back-donation” mechanism between N2 and the B atom. (c) The PDOS of free N2 and its adsorption on B@Mo2TiC2Tx/MoO2 MXene. (d) The COHP of free N2 and N2 adsorbed on B@Mo2TiC2Tx/MoO2 MXene.
Fig. 6. (a) In-situ FTIR spectra of B@Mo2TiC2Tx/MoO2 MXene. (b) Free energy profiles for NRR on B@Mo2TiC2Tx/MoO2. (c) Atomic configurations along the distal-alternating mechanism. (d) Free energy profiles for NRR on Mo2TiC2Tx/MoO2.
Fig. 7. (a) The Gibbs free energy profiles for HER on Mo2TiC2Tx/MoO2 and B@Mo2TiC2Tx/MoO2. (b) The adsorption Gibbs free energy of *H and *N2 on Mo2TiC2Tx/MoO2 and B@Mo2TiC2Tx/MoO2. (c) The plot of UL(NH3) versus UL(NH3) - UL(HER) for Mo2TiC2Tx/MoO2 and B@Mo2TiC2Tx/MoO2.
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