The insufficient exposure sites and active site competition of multienzyme are the two main factors to hinder its therapeutic effect. Here, we design and prepare a phase‐junction nanomaterial (amorphous‐crystalline CuxS−Ag2S) through a simple room temperature ion‐exchange process. A small amount of Ag+ is added into Cu7S4 nanocrystals, which transforms Cu7S4 into amorphous phased CuxS and produces crystalline Ag2S simultaneously. In this structure, the overhanging bonds on the amorphous CuxS surface provide abundant active sites for optimizing the therapeutic activity. Meanwhile, the amorphous state enhances the photothermal effect through non‐radiative relaxation, and due to its low thermal resistance, phase‐junction CuxS−Ag2S forms a significant temperature gradient to unlock the optimized thermo‐electrodynamic therapy. Furthermore, benefiting from the high asymmetry of the amorphous state, the material forms a spin‐polarized state that can effectively inhibit electron‐hole recombination. In this way, the thermoelectric effect can facilitate the enzyme‐catalyzed cycle by providing electrons and holes, enabling an enhanced coupling of thermoelectric therapy with multienzyme activity, which induces excellent anti‐tumor performance. More importantly, the catalytic process simulated by density‐functional theory proves that Ag+ alleviates the burden on the Cu sites through favorable adsorption of O2 and prevents active site competition.amorphous materials; enzyme catalysis; phase‐junction; photothermoelectric therapy; site competitionThis article is protected by copyright. All rights reserved