LixMn2O4 spinel normally undergoes a transformation from its cubic to tetragonal phase when x exceeds 1 due to a collective Jahn-Teller distortion, resulting in poor cyclability when both the 4 and 3 V intercalation plateaus are utilized. In this study, we show that this transformation is suppressed in spinels of composition up to x approximate to 2 obtained through the electrochemical cyclings of orthorhombic LiMnO2. X-ray diffraction, transmission electron microscopy, and high-resolution electron microscopy studies together show that cycling produces a cubic spinel containing partial tetrahedral cation site occupancy and a nanodomain structure (20 to 50 nm size) within parent single-crystalline oxide particles. This structure is responsible for the cycling stability of electrochemically produced spinel. The reversible capacity (272 mAh/g) and energy density (853 Wh/kg) achieved at a low charge-discharge rate (3;33 mA/g) in the present samples are the highest among crystalline LiMnO2 materials reported to dare.