Bioinspired Surface Layer for the Cathode Material of High-Energy-Density Sodium-Ion Batteries

Cathode materials are usually active in the range of 2-4.3 V, but the decomposition of the electrolytic salt above 4 V versus Na+/Na is common. Arguably, the greatest concern is the formation of HF after the reaction of the salts with water molecules, which are present as an impurity in the electrolyte. This HF ceaselessly attacks the active materials and gradually causes the failure of the electrode via electric isolation of the active materials. In this study, a bioinspired -NaCaPO4 nanolayer is reported on a P2-type layered Na-2/3[Ni1/3Mn2/3]O2 cathode material. The coating layers successfully scavenge HF and H2O, and excellent capacity retention is achieved with the -NaCaPO4-coated Na-2/3[Ni1/3Mn2/3]O-2 electrode. This retention is possible because a less acidic environment is produced in the Na cells during prolonged cycling. The intrinsic stability of the coating layer also assists in delaying the exothermic decomposition reaction of the desodiated electrodes. Formation and reaction mechanisms are suggested for the coating layers responsible for the excellent electrode performance. The suggested technology is promising for use with cathode materials in rechargeable sodium batteries to mitigate the effects of acidic conditions in Na cells.