successfully accommodated by a poly mer network binder without signifi cantly scarifying the high capacity of the Sb electrode as reported in our previous work. [ 10 ] As a cathode material, the NASICONframework structure of Na 3 V 2 (PO 4 ) 3 is a host to the three sodium-ions per formula unit. [ 11 ] A single interstitial site per formula is occupied by a less-mobile sodiumion and three equivalent sites are occupied by two mobile sodium-ions. Na 3 V 2 (PO 4 ) 3 has an acceptable room-temperature sodium-ion conductivity, a high voltage of the V 4+ /V 3+ redox couple, and an excellent cycle life. [ 12 ] As an anode free of metallic sodium, alloy-type anodes can provide large capacities with a good reversibility of sodiation and desodiation provided the anode architecture can accommodate the large volume change that occurs during charge and discharge. [ 13 ] The electrochemical potential of the sodium-antimony alloy is about 0.7-0.8 eV below the Fermi energy of metallic sodium; this energy difference is large enough to allow a fast charge without plating of elemental sodium, thereby eliminating safety problems associated with sodium dendrite formation and growth. However, with an organic-liquid electrolyte, a sodium-ion permeable passivating solid-electrolyte interphase (SEI) forms on the alloy surface on the initial charge of a full-cell with its sodium-ions taken irreversibly from the cathode and trapped into the SEI. The loss of cathode capacity in a full-cell can be dramatically reduced either by performing a pre-sodiated anode [14][15][16] or by adding a sacrifi cial sodium-ion source of Na 2 NiO 2 to the cathode. [ 17 ] Since almost 10 wt% of Na 2 NiO 2 needs to be added to the cathode, we have chosen to prefer the pre-sodiation strategy to form the SEI on the Sb anode prior to the assembly of the full-cell.The tests of sodium-ion full-cells reported previously have concentrated on the application of organic-liquid electrolytes. [5][6][7][8][9] However, the utilization of fl ammable liquid electrolytes in sodium-ion batteries may raise safety concerns as in the case of lithium-ion batteries, especially in large-scale energy storage systems. The hard and brittle ceramic or glass electrolytes have been proposed to address the safety issues, but the solid-solid electrode-electrolyte interfaces may not sustain a long cycle life. [ 18,19 ] The solid-polymer electrolytes, typically based on poly(ethylene oxide) (PEO), have also been extensively explored, but they exhibit too low an ionic conductivity at room temperature (≈10 −5 S cm −1 ) and poor resistance to oxidation at relatively high voltage. [20][21][22][23] On the other hand, the gel-polymer electrolytes, taking advantages of the polymer fl exibility and the high ionic conductivity of the liquid electrolytes,The design of a sodium-ion rechargeable battery with an antimony anode, a Na 3 V 2 (PO 4 ) 3 cathode, and a low-cost composite gel-polymer electrolyte based on cross-linked poly(methyl methacrylate) is reported. The application of an antimony anode, on ...