Tuning a compatible interface with LLZTO integrated on cathode material for improving NCM811/LLZTO solid-state battery

Poor interfacial contact and severe polarization of nickel-rich cathode materials are crucial problems that must be solved in the development of nickel-rich cathode/garnet-type electrolyte solid-state batteries. Herein, a binder-like Li3PO4 is introduced via an in-situ calcination process to build a compatible and Li+-conductive self-integrated layer of Li6.4La3Zr1.4Ta0.6O12-Li3PO4 on LiNi0.8Co0.1Mn0.1O2 cathode material, with a newly calculation method for estimating the interface compatibility theoretically. In addition, the routine helps weaken the space charge layer of active material commonly inevitable in the case, as demonstrated by calculation of Density Functional Theory and Atomic force microscopy analysis. With the interface engineering, the in-situ generated Li3PO4 tightly fix Li6.4La3Zr1.4Ta0.6O12 on LiNi0.8Co0.1Mn0.1O2, improving the compatibility between LiNi0.8Co0.1Mn0.1O2 cathode material and the solid electrolyte Li6.4La3Zr1.4Ta0.6O12. As a result, the interface-engineered LiNi0.8Co0.1Mn0.1O2/Li6.4La3Zr1.4Ta0.6O12 solid state battery exhibits an initial discharge capacity of 188.8 mAh g(-1) at 0.2C (40 mA g(-1)). Even at 1C, its retention still remained 91.6% (initial value of 130 mAh g(-1)) after 100 cycles. The SSBs could also work well under high temperature, delivering high initial discharge capacities of 153.4 mAh g(-1) (55 degrees C) and 149.6 mAh g(-1) (80 degrees C) at 1C, respectively. The work provides an effective strategy to improve NCM811-LP-LLZTO SSBs.

Automated summary

This research introduces a binder-like Li3PO4 through an in-situ calcination process to build a compatible and Li+-conductive self-integrated layer with LiNi0.8Co0.1Mn0.1O2 cathode material, improving the performance of LiNi0.8Co0.1Mn0.1O2/Li6.4La3Zr1.4Ta0.6O12 solid state batteries. Through interface engineering, the in-situ generated Li3PO4 tightly fixes Li6.4La3Zr1.4Ta0.6O12 on LiNi0.8Co0.1Mn0.1O2, demonstrating high initial discharge capacities and good retention rates under different conditions.