The energy storage behavior of amorphous carbon is mostly dependent on the electrostatic interaction between the surface of the conducting electrode and the electrolytic ions. Therefore, the energy densities of commercial SCs are relatively low. [9] This essential defect seriously hinders the application of SCs in energy transformation system, so improving the energy density of them is an urgent problem. For this reason, a lot of pseudocapacitor materials with battery characteristics have been developed with the purpose of enhancing the energy density of SCs, including such as conjugated polymers [10,11] and transition metal compounds. [12,13] Transition-metal hydroxides are ideal pseudocapacitive materials for pseudocapacitors because of their large theoretical capacity. [14,15] Thus, intensive research work has been carried out to develop hydroxides with high pseudocapacitance performance. To date, a variety of low-cost hydroxides such as Ni(OH) 2 , [16,17] Co(OH) 2 , [18] CoAl-LDH, [19] CoFe-LDH, [20] NiMn-LDH, [21] NiCo-LDH, [22] and NiCu-LDH [23] have been widely investigated. However, these battery-type hydroxides usually possess poor electrical conductivity and relatively large volume changes during fast charge-discharge tests, thus leading to low cycling stability and poor rate capability. [24,25] The electronic conductivity and structural stability of layered double hydroxide (LDH) can be improved by heteroatomic doping. The heteroatom-doped LDH possesses large amounts of electronholes resulting from lattice distortion, thus increasing the electronic conductivity of LDH. Recently, Niu et al. [26] synthesized a N, C double-doped NiCo-LDH by hydrothermal reaction. The resultant sample exhibited an outstanding discharge capacitance of 606.9 C g −1 at 2 mV s −1 . In addition, N-C doping can greatly improve the rate capability and cycling stability.The logical microstructure design of transition-metal hydroxides at the nanoscale is another effective method to enhance the pseudocapacitance performance. [27] Among a variety of nanostructures, multi-dimensional nanostructures with welldefined inner void spaces and hierarchical nanocages can effectively avoid the self-aggregation of transition-metal hydroxides. The porous nanostructure is also appropriate for the infiltration of electrolyte ions and fast faraday reaction of active species. In addition, the nanocages are composed of interlaced ultrathin nanosheets, which possess rich electrochemically active sites and high superficial areas. Thus, the construction of