Electronic Structure Engineering in MXene SACs: Unveiling the Role of Mixed Termination for ORR/OER Bifunctionality

Based on a pristine Ti 2 CCl 2 substrate with single functionalization, this study implemented precise electronic structure modulation to construct a series of Ti 2 CO X Cl Y models, aiming to elucidate the origin of catalytic activity in MXenes with mixed functional groups of varying ratios. It was discovered that precisely tuning the relative content of O/Cl terminal groups on the Ti 2 C substrate significantly optimizes the adsorption energy of the key intermediate OH * in both the oxygen reduction reaction and oxygen evolution reaction, thereby enabling superior bifunctional catalytic performance at the same active site. This work establishes a clear descriptor that clarifies the structure‐activity relationship in catalytic reactions from the unique perspective of mixed functional groups, providing new theoretical insights for designing high‐performance single‐atom catalysts.