Cobalt-free, nickel-rich positive electrode materials are attracting attention because of their high energy density and low cost, and the ultimate material is LiNiO 2 (LNO). One of the issues of LNO is its poor cycling performance, which needs to be improved. Referring to a current study to show the improved stability of single-crystal-like high-nickelate materials, we fabricated single-crystal-like (SC-) LNO and the counterpart polycrystalline (PC-) LNO samples and examined their electrochemical properties. SC-LNO was nearly single-crystal-like, as proved by electron backscattering diffraction, and had more cation mixing than PC-LNO. Cycle tests under 2.5−4.2 V, a 2C rate, and 45 °C conditions showed that the capacity retention of SC-LNO after 500 cycles (63.5%) was significantly better than that of PC-LNO (36.1%) under the same conditions and even better than that of PC-LNO cycled between 2.5 and 4.15 V (50.7%) with the same initial capacity as SC-LNO. The derivative dQ/dV profile of PC-LNO became featureless during a long cycling time, suggesting the progress of cation mixing in PC-LNO, whereas that of SC-LNO was better maintained, in accordance with the serious particle cracking in PC-LNO and no particle cracking found in SC-LNO as the result of post-mortem analysis after 500 cycles. The electrode impedance increase of PC-LNO was considerably larger than that of SC-LNO, corresponding to the formation of rock-salt phases at the surface and the cracked interface of the PC-LNO and the formation of scattered spinel-like phases with a thick cathode electrolyte interphase at the surface of SC-LNO. Accordingly, SC-LNO is shown to be less degraded in both the bulk nature (stable dQ/dV profile and no cracking) and the surface characteristics (high rate capacity maintenance and less impedance increase), suggesting the importance of single-crystal-like particles as durable electrode materials.