High-Capacitance Mechanism for TiCT MXene by in Situ Electrochemical Raman Spectroscopy Investigation.

MXenes represent an emerging family of conductive two-dimensional materials. Their representative, TiCT, has been recognized as an outstanding member in the field of electrochemical energy storage. However, an in-depth understanding of fundamental processes responsible for the superior capacitance of TiCT MXene in acidic electrolytes is lacking. Here, to understand the mechanism of capacitance in TiCT MXene, we studied electrochemically the charge/discharge processes of TiCT electrodes in sulfate ion-containing aqueous electrolytes with three different cations, coupled with in situ Raman spectroscopy. It is demonstrated that hydronium in the HSO electrolyte bonds with the terminal O in the negative electrode upon discharging while debonding occurs upon charging. Correspondingly, the reversible bonding/debonding changes the valence state of Ti element in the MXene, giving rise to the pseudocapacitance in the acidic electrolyte. In stark contrast, only electric double layer capacitance is recognized in the other electrolytes of (NH)SO or MgSO. The charge storage ways also differ: ion exchange dominates in HSO, while counterion adsorption in the rest. Hydronium that is characterized by smaller hydration radius and less charge is the most mobile among the three cations, facilitating it more kinetically accommodated on the deep adsorption sites between the MXene layers. The two key factors, i.e., surface functional group-involved bonding/debonding-induced pseudocapacitance, and ion exchange-featured charge storage, simultaneously contribute to the superior capacitance of TiCT MXene in acidic electrolytes.