Manganese oxide with high theoretical specific capacity and intermediate reaction plateau is a promising anode candidate for lithium-ion hybrid capacitors (LIHCs). However, the sluggish kinetics and severe volume expansion have seriously hindered its practical progress. Herein, a mixedvalence manganese oxide confined by a dual-carbon skeleton network (MnO x @ C-R) was successfully prepared. Owing to the synergistic effect of the introduction of the dual-carbon skeleton-network structure in a reducing atmosphere, the reasonable pore size distribution, crystallinity, and phase composition have been optimized. The material exhibits excellent lithium storage performance (778.2 mA h g −1 after 10 cycles at 0.1 A g −1 ), along with excellent rate performance (141.7 mA h g −1 at 5 A g −1 ) and stable cycling ability (402.4 m Ah g −1 for 1000 cycles at 1 A g −1 ). Moreover, further characterization displayed the change of the valence state of manganese during the charging/discharging, revealing the source of the excellent electrochemical performance of MnO