Electrocatalytic N2 reduction reaction (NRR) to synthesize ammonia is a sustainable reaction that is expected to replace Haber Bosch process. Laminated Bi2 WO6 has great potential as an NRR electrocatalyst, however, the effective activity requires that the inert substrate is fully activated. Here, for the first time, success is achieved in activating the Bi2 WO6 basal planes with NRR activity through Ti doping. The introduction of Ti successfully tunes the surface potential distribution and enhances the N2 adsorption. The subsequently strong hybrid coupling of d(Ti)-p(N) orbitals fills the electronic state of N2 antibonding molecular orbital, which greatly weakens the bonding strength of N≡N bonds. Further, in situ synchrotron radiation-based Fourier transform infrared (SR-FTIR) spectrum and theoretical calculations show that surface potential polarization enhances the adsorption of HNN* by Bi-Ti dual-metal sites, which is beneficial for the subsequent activation hydrogenation process. The Ti-Bi2 WO6 nanosheets achieve 11.44% Faradaic efficiency (-0.2 V vs. RHE), a NH3 yield rate of 23.14 µg mg-1 h-1 (15 N calibration), and satisfactory stability in 0.1 M HCl environment. The mutual assistance of theory and experiment can help understand and develop of excellent two-dimensional (2D) materials for the NRR.
Keywords: N2 adsorption; electrocatalytic nitrogen fixation; elemental doping; surface potential.
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