Sodium-ion batteries offer a promising alternative to lithium-ion batteries due to their low cost, environmental friendliness, high abundance of sodium, and established electrochemical process. However, problems, such as low capacity, low storage voltage and capacity fade of electrode materials, must be resolved for the applications of sodium ion batteries. Many Ti-containing compounds were reported as cathode and anode materials, but very few studies focus on the role of Ti in electrodes used in sodium-ion batteries. This paper systemically reviews the roles of Ti in electrodes of sodium ion batteries. The Ti 4+ /Ti 3+ redox couple is a good choice for anodes due to its low potential and it exhibits different storage voltages in different structures. Although Ti 4+ does not participate in charge transfer in cathodes, it can indirectly enhance the capacity, cycling life and rate performance via structure change, cation order-disorder transition, and its interaction with the crystal lattice structure. This review will provide a new insight in designing and understanding novel high-performance electrodes. Keywords: sodium ion batteries, cathode, anode, titanium-based composite, order-disorder phase transition possibility of releasing fluorine gas becomes an environmental issue in large-scale production (Gover et al., 2006). Unlike LiFePO 4 , the olivine NaFePO 4 is thermally unstable in ambient environment and has to be produced (Kim et al., 2015) by the ion exchange of Li + in olivine LiFePO 4 with Na + , which complicates the production and increases cost (Oh et al., 2012). The commercial success of layered-LiCoO 2 in lithiumion batteries (Mizushima et al., 1980) has prompted extensive investigation of its sodium counterpart Na x TMO 2 (TM: Ni, Mn, Co, Ti) which crystallize into layered or tunneled structures depending on sodium content. The layered-structure consists of TM-O and Na-O layers. Compared to Li + , Na + has a larger radius and stronger interaction with O 2−. The sodiumlayered structure is further divided into O3, P3, P2, and O2. The O and P represent the octahedral and trigonal prismatic coordination environment of alkali ions, respectively; 3 and 2 describe the number of TM layers of repeated stacking (Delmas et al., 1980). The oxides P2/O3-Na x CoO 2 , Na x MnO 2 Na x VO 2 and Na x NiMnO 2 etc. are also investigated (Delmas et al.