Doping‐Engineered Piezoelectric Ultrathin Nanosheets for Synergistically Piezo‐Chemocatalytic Antitumor and Antibacterial Therapies Against Cutaneous Melanoma

Abstract The post‐surgical melanoma recurrence and wound infections have persistently troubled clinical management. Piezocatalytic therapy features high efficiency in generating reactive oxygen species (ROS) for tumor therapy, but it faces limitations in piezoelectricity and redox‐active site availability. Herein, Fe‐doped ultrathin Bi 4 Ti 3 O 12 nanosheets (designated as Fe‐UBTO NSs) with synergistically piezo‐chemocatalytic activity are engineered for antitumor and antibacterial treatment against cutaneous melanoma. The doping‐engineered strategy induces oxygen vacancies and lattice distortions in Fe‐UBTO NSs, which narrows bandgap to enhance piezocatalytic 1 O 2 and H 2 O 2 generation by improving the electron‐hole pairs separation, hindering their recombination, and increasing oxygen adsorption. Moreover, Fe doping establishes a piezo‐chemocatalytic system, in which the piezocatalysis enables the self‐supply of H 2 O 2 and expedites electron transfer in Fenton reactions, inducing increased ·OH production. Besides, the atomic‐level thickness and expanded surface area enhance the sensitivity to ultrasound stimuli and expose more redox‐active sites, augmenting the piezo‐chemocatalytic efficiency, and ultimately leading to abundant ROS generation. The Fe‐UBTO‐mediated piezo‐chemocatalytic therapy causes intracellular oxidative stress, triggering apoptosis and excessive autophagy of tumor cells. Moreover, this strategy accelerates wound healing by facilitating sterilization, angiogenesis, and collagen deposition. This work provides distinct options to develop doping‐engineered ultrathin nanosheets with augmented piezo‐chemocatalytic activity for postoperative management of cutaneous melanoma.