Guardado en:
| Autores principales: | , , , , , |
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| Formato: | Preprint |
| Publicado: |
2026
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| Materias: | |
| Acceso en línea: | https://arxiv.org/abs/2602.04280 |
| Etiquetas: |
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- Zinc-based electrochromic devices offer a sustainable route for dynamic optical management but are plagued by poor cycling stability due to irreversible zinc plating/stripping and side reactions. Herein, we report a robust, high-contrast, and recyclable zinc-based dynamic window enabled by a synergistic electrolyte and interfacial engineering strategy. Molecular dynamics simulations and electrochemical analyses reveal a dual-ion cooperative mechanism that governs the reversibility: anions with the strongest binding affinity guide uniform Zn deposition by stabilizing the inner solvation shell, while formate anions co-enriched at the interface facilitate smooth stripping via protonation during the oxidation process. This orchestrated interplay effectively eliminates "dead Zn" accumulation and dendrite growth. Consequently, the device demonstrates a record-high lifespan of 15,000 cycles with negligible degradation and maintains a large optical modulation of >50%, along with multiple optical states (transparent, gray, black, and mirror). Furthermore, it achieves a large reflectance modulation (>50%) stable for over 2,000 cycles. This work establishes the recyclable zinc-based dynamic window as a scalable, high-performance alternative to conventional electrochromic systems, advancing the feasibility of solution-processed energy-saving windows in sustainable buildings.