Chlorine Axial Coordination Activated Lanthanum Single Atoms for Efficient Oxygen Electroreduction with Maximum Utilization

Currently, there are still obstacles to rationally designing the ligand fields to activate rare-earth (RE) elements with satisfactory intrinsic electrocatalytic reactivity. Herein, axial coordination strategies and nanostructure design are applied for the construction of La single atoms (La-Cl SAs/NHPC) with satisfactory oxygen reduction reaction (ORR) activity. The nontrivial LaN 4 Cl 2 motifs configuration and the hierarchical porous carbon substrate that facilitates maximized metal atom utilization ensure high half-wave potential (0.91 V) and significant robustness in alkaline media. The aqueous and flexible Zinc-air battery (ZAB) integrating La-Cl SAs/NHPC as the cathode catalyst exhibits a maximum power density of 260.7 and 68.5 mW cm −2 , representing one of the most impressive RE-based ORR electrocatalysts to date. Theoretical calculations have demonstrated that the Cl coordination evidently modulate the electronic structures of La sites, which promoted electron transfer efficiency by d-p orbital couplings. With enhanced electroactivity of La sites, the adsorptions of key intermediates are optimized to alleviate the energy barriers of the potential-determining step. Importantly, this preparation strategy is also successfully applied to other REs. This work provides perspectives for near-range electronic structure modulation of RE-SAs based on a nonplanar coordination micro-environment for efficient electrocatalysis.