摘要
Piezoelectric materials for uranium extraction have attracted increasing attention, as they offer a self-powered, light-independent strategy to harness ambient mechanical energy. However, natural mechanical energies are typically weak and low-frequency, necessitating materials with high flexibility, facile deformation, and large surface area. Herein, we demonstrate that the ABCABC stacking sequence along the c-axis in two-dimensional (2D) 3R- zinc indium sulfide (3R-ZnIn2S4) nanosheets induces intrinsic non-centrosymmetry, enabling robust piezocatalysis for on-site hydrogen peroxide (H2O2) generation and simultaneous uranium extraction. Density functional theory (DFT) calculations confirm that solvation effects enhance the lattice flexibility and intrinsic dipole moment of 3R- ZnIn2S4, resulting in the formation of an electron-rich surface that thermodynamically favors the two-electron oxygen reduction reaction (2e− ORR) for H2O2 generation. Under mild ultrasonic agitation (35 kHz, 50 W), the 3R-ZnIn2S4 nanosheets achieved a H2O2 yield of 276.7 µmol g−1 h−1 and a uranium extraction capacity of 763.2 mg g−1. Mechanistic investigations elucidate that the uranium extraction process proceeds through a dual-coordination pathway, integrating direct piezoelectric reduction and in situ H2O2-mediated complexation of uranium species. Notably, 3R-ZnIn2S4 demonstrates excellent cycling stability over five cycles, high selectivity toward uranium, and effective anti-biofouling performance under ultrasonic conditions (35 kHz, 50 W). Collectively, our findings establish stacking-induced piezoelectricity as a light-independent strategy for sustainable uranium extraction to support nuclear energy development.
| 源语言 | 英语 |
|---|---|
| 期刊 | Advanced Science |
| DOI | |
| 出版状态 | 已接受/待刊 - 2026 |
| 已对外发布 | 是 |
学术指纹
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