Abstract The pursuit of high‐capacity Na‐ion batteries (NIBs) has propelled great forward the O3‐type Ni‐rich NaNi 0.5 Co 0.2 Mn 0.3 O 2 (NCM) cathodes. However, the inborn chemo‐mechanical instabilities caused by complex phase transitions and anisotropic lattice stress have severely delayed its widespread application. In the contribution, a cooperative surface‐to‐bulk modification strategy, i.e., in situ surface NaTi 2 (PO 4 ) 3 (NTP) coating and bulk Ti/F co‐doping, is first proposed to engineer an advanced NCM cathode (denoted as TF‐NCM@NTP). The NTP protective layer with high thermodynamic stability and ionic conductivity endows TF‐NCM@NTP with a highly stable interface and expedited de‐/sodiated kinetics. The robust Ni/Co/Mn─F bond and concurrent Ti─O bond greatly strengthen the bulk lattice oxygen and mitigate the internal strain self‐reproduction. Benefiting from these synergistic merits, the designed TF‐NCM@NTP cathode demonstrates exceptional sodium‐storage performance in terms of high‐rate capacities and long‐duration cycle life in both half and full cells. Particularly, the TF‐NCM@NTP‐based quasi‐solid‐state NIBs deliver an applicable material‐level energy density of 285 Wh kg −1 at 25 °C, and exhibit wide‐temperature‐tolerant Na‐storage behaviors ranging from −20 to 50 °C. More essentially, the multi‐level engineering strategy from surface to bulk developed here definitely makes enormous progress for rationally designing advanced cathode materials toward multi‐scenario applicable NIBs.