Despite the remarkable ion-hosting capability of MXenes, their electrochemical performance is restricted to the ion shuttle barrier stemming from the capacious surface and the sluggish chemical activity of intrinsic transition metal layers. Herein, we construct a vertically aligned array of V₂CT_X flakes utilizing a carbon sphere template (V₂CT_X@CS), with the interlayer galleries outward facing the external electrolyte, to shorten the diffusion length and mitigate the ion shuttle barrier. Moreover, we leverage the high sensitivity of V₂CT_X flakes to the water–oxygen environment, fully activating the masked active sites of transition metal layers in an aqueous environment via continuous electrochemical scanning. Aqueous V₂CT_X@CS/Zn battery delivers a novel capacity enhancement over 42,000 cycles at 10 A g⁻¹. After activation, the capacity reaches up to 409 mAh g_V2CTX⁻¹ at 0.5 A g⁻¹ and remains at 122 mAh g_V2CTX⁻¹ at 18 A g⁻¹. With a 0.95-V voltage plateau, the energy density of 330.4 Wh kg_V2CTX⁻¹ surpasses previous records of aqueous MXene electrodes.

Obtaining stable aqueous K-ion capacitors is still challenging due to the cathode materials tended to structurally collapse after long-term cycling during large-radius K-ion insertion/extraction. In this work, three different typical MXene electrodes, i.e., Nb₂C, Ti₂C, and Ti₃C₂ were individually investigated upon their electrochemical behaviors for potassium-ion (K-ion) storage. All these MXene materials exhibited pseudocapacitive-dominated behaviors, fast kinetics, and durable K-ion storage, delivering superior performance compared with other K-ion host materials. According to the experimental results, it could be ascribed to the intrinsically large interlayer distance for K-ion transport and the superb structural stability of MXene even subjected to long-term potassiation/depotassiation process.