摘要
A dual-site functional orchestration strategy is proposed using 2-imidazolidone to simultaneously reconfigure the anodic solvation structure and suppress the cathodic polyiodide shuttle. The carbonyl (C=O) group modulates Zn 2+ solvation to induce preferred (002) deposition, while the imino (N-H) group chemically moors polyiodides via hydrogen bonding, achieving decoupled synergistic regulation. This molecular engineering enables a record-breaking lifespan exceeding 5500 h at 8 mA cm -2 for Zn anodes and durable full-cell cycling with 79.4% capacity retention over 2500 cycles.
危险品化学品经营许可证(带存储)