Pseudocapacitance is generally associated with either surface redox reactions or ion intercalation processes without a phase transition. Typically, these two mechanisms have been independently studied, and most works have focused on optimizing one or the other in different material systems. Here we have developed a strategy based on solubility contrast, in which the contribution from the two capacitive mechanisms is simultaneously optimized. Taking layered birnessite MnO2 as a model, controllable nanostructures and oxygen vacancies are achieved through a simple coprecipitation process. Simultaneously controlling crystallite size and defect concentration is shown to enhance the charging-discharging kinetics together with both redox and intercalation capacitances. This synergistic effect results from enhanced ionic diffusion, electronic conductivity, and large surface-to-volume ratio. In addition, considerable cycling durability is achieved, resulting from improved framework strength by defect creation and the absence of proton (de)intercalation during discharge/charge. This work underscores the importance of synergistically regulating nanostructure and defects in redox-active materials to improve pseudocapative charge storage.