Activating Single-Atom Ni Site via First-Shell Si Modulation Boosts Oxygen Reduction Reaction

Atomically dispersed nitrogen-coordinated 3d transition-metal site on carbon support (M-NC) are promising alternatives to Pt group metal-based catalysts toward oxygen reduction reaction (ORR). However, despite the excellent activities of most of M-NC catalysts, such as Fe-NC, Co-NC et al., their durability is far from satisfactory due to Fenton reaction. Herein, this work reports a novel Si-doped Ni-NC catalyst (Ni-SiNC) that possesses high activity and excellent stability. X-ray absorption fine structure and aberration-corrected transmission electron microscopy uncover that the single-atom Ni site is coordinated with one Si atom and three N atoms, constructing Ni-Si1N3 moiety. The Ni-SiNC catalyst exhibits a half-wave potential (E-1/2) of 0.866 V versus RHE, with a distinguished long-term durability in alkaline media of only 10 mV negative shift in E-1/2 after 35 000 cycles, which is also validated in Zn-air battery. Density functional theory calculations reveal that the Ni-Si1N3 moiety facilitates ORR kinetics through optimizing the adsorption of intermediates.

Automated summary

A Si-doped Ni-NC catalyst (Ni-SiNC) with high activity and excellent stability was reported in this work. The single-atom Ni site in Ni-SiNC is coordinated with one Si atom and three N atoms, forming a Ni-Si1N3 moiety. The Ni-SiNC catalyst exhibits a half-wave potential of 0.866 V versus RHE and only a 10 mV negative shift in E-1/2 after 35,000 cycles, demonstrating its remarkable durability and stability.