Size- and crystallinity-dependent oxygen vacancy engineering to modulate Fe active sites for enhanced reversible nitrogen fixation in Lithium-nitrogen batteries
Abstact Lithium-nitrogen (Li-N 2 ) battery is not only an electrochemical energy storage platform, but also an environmentally friendly nitrogen fixation technology. However, a great challenge remains in regulating catalyst activity to accelerate cathode reaction kinetics. Herein, we proposed an oxygen vacancy-mediated modulation of Fe active sites in FeO x nano-particle catalysts and Fe single-atom catalysts to enhance nitrogen reduction reaction in Li-N 2 batteries. High-concentration oxygen vacancy is generated through a size- and crystallinity-dependent oxygen vacancy engineering based on the precise atomic layer deposition of reducible oxides. The oxygen vacancy on FeO x drives the electron redistribution of Fe 3+ d-orbitals to provide electron-donating Fe active sites for N 2 fixation. Meanwhile, oxygen vacancy-rich MoO y is used as a support to anchor Fe single atoms. Adjacent oxygen vacancy drives the stable coordination between Fe single atoms and O atoms to facilitate the directional electron transfer from MoO y to Fe to N 2 . Therefore, the Li-N 2 batteries exhibit large discharge capacity, excellent rate performance, and reliable cycle stability. In addition, the formation and decomposition of the discharge product Li 3 N indicate a reversible N 2 fixation. This work provides a precise regulation mechanism of catalytic active sites based on oxygen vacancy engineering, which is expected to promote the development of high-performance Li-N 2 batteries.
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