<p>Oxygen-dependent electrodynamic therapy is hindered by electron–hole recombination and hypoxia. This study provides a heterojunction-induced Jahn–Teller distortion-enhanced spin-engineering Fe<sub>3</sub>O<sub>4</sub>–Ag<sub>2</sub>S nanoplatform to address these limitations. The large interfacial lattice mismatch induces previously unrecognized Jahn–Teller distortions on high-spin Fe sites, modifying d-orbital splitting and enhancing spin-polarized catalytic activity. This lattice–spin–carrier coupling synergistically amplifies catalase-, peroxidase-, and glutathioneox-like pathways. Under near-infrared irradiation, the photothermal effect of Fe<sub>3</sub>O<sub>4</sub> activates the thermoelectric response of Ag<sub>2</sub>S and drives continuous hot-carrier injection. Thermoelectric fields drive hot holes to boost catalase activity through Jahn–Teller effect-enhanced spin catalysis sites and drive hot electrons to convert O<sub>2&#xa0;</sub> to cytotoxic O<sub>2</sub><sup>.</sup><sup>−</sup> and <sup>1</sup>O<sub>2</sub> under the Jahn–Teller distortion, promoting and forming a self-amplifying catalytic loop. Fine structure characterization and density functional theory calculations collectively verify strain-driven Fe–O bond differentiation and spin-state reconfiguration. The heterojunction achieves potent thermoelectric–enzyme co-catalysis with 95% tumor inhibition under near-infrared irradiation and supports dual-mode imaging. This work establishes a framework for designing high-performance photothermal–thermoelectric catalysts through crystal field/spin-state modulation in p–n heterojunctions, synergistically boosting multi-enzyme activity and catalytic efficiency for hypoxia-resistant therapy</p><p><MediaObject ID="MO101"> <ImageObject Color="Color" FileRef="MediaObjects/40820_2026_2175_Figa_HTML.png" Format="PNG" Height="591" Rendition="HTML" Resolution="300" Type="LinedrawHalftone" Width="1180" /> </MediaObject></p>

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Enhanced Spin-Engineering Photothermoelectric–Enzymatic Catalysis System via Lattice Mismatch-Induced Jahn–Teller Distortion for Tumor Therapy

  • Pengyu Zang,
  • Meiqi Yang,
  • Chenghao Yu,
  • Rui Zhang,
  • Avez Sharipov,
  • Ruifang Shen,
  • Dan Yang,
  • Shili Gai,
  • Piaoping Yang

摘要

Oxygen-dependent electrodynamic therapy is hindered by electron–hole recombination and hypoxia. This study provides a heterojunction-induced Jahn–Teller distortion-enhanced spin-engineering Fe3O4–Ag2S nanoplatform to address these limitations. The large interfacial lattice mismatch induces previously unrecognized Jahn–Teller distortions on high-spin Fe sites, modifying d-orbital splitting and enhancing spin-polarized catalytic activity. This lattice–spin–carrier coupling synergistically amplifies catalase-, peroxidase-, and glutathioneox-like pathways. Under near-infrared irradiation, the photothermal effect of Fe3O4 activates the thermoelectric response of Ag2S and drives continuous hot-carrier injection. Thermoelectric fields drive hot holes to boost catalase activity through Jahn–Teller effect-enhanced spin catalysis sites and drive hot electrons to convert O to cytotoxic O2. and 1O2 under the Jahn–Teller distortion, promoting and forming a self-amplifying catalytic loop. Fine structure characterization and density functional theory calculations collectively verify strain-driven Fe–O bond differentiation and spin-state reconfiguration. The heterojunction achieves potent thermoelectric–enzyme co-catalysis with 95% tumor inhibition under near-infrared irradiation and supports dual-mode imaging. This work establishes a framework for designing high-performance photothermal–thermoelectric catalysts through crystal field/spin-state modulation in p–n heterojunctions, synergistically boosting multi-enzyme activity and catalytic efficiency for hypoxia-resistant therapy