Wang Yueyang, Jin Xiangrong, Xiong Jiawei, Zhu Qingyi, Li Qi, Wang Runze, Li Jiazhan, Fan Yanchen, Zhao Yi, Sun Xiaoming
State Key Laboratory of Chemical Engineering, College of Chemistry, Beijing University of Chemical Technology, Beijing, 100029, China.
Mary Frances Early College of Education, The University of Georgia, Athens, GA, 30602, USA.
Adv Mater. 2024 Jul;36(30):e2404093. doi: 10.1002/adma.202404093. Epub 2024 May 16.
Aqueous Zn-iodine (Zn-I) conversion batteries with iodine redox chemistry suffers the severe polyiodide shuttling and sluggish redox kinetics, which impede the battery lifespan and rate capability. Herein, an ultrastable Zn-I battery is introduced based on single-atom Fe-N-C encapsulated high-surface-area carbon (HC@FeNC) as the core-shell cathode materials, which accelerate the I/I /I° conversion significantly. The robust chemical-physical interaction between polyiodides and Fe-N sites tightly binds the polyiodide ions and suppresses the polyiodide shuttling, thereby significantly enhancing the coulombic efficiency. As a result, the core-shell HC@FeNC cathode endows the electrolytic Zn-I battery with an excellent capacity, remarkable rate capability, and an ultralong lifespan over 60 000 cycles. More importantly, a practical 253 Wh kg pouch cell shows good capacity retention of 84% after 100 cycles, underscoring its considerable potential for commercial Zn-I batteries.
具有碘氧化还原化学性质的水系锌碘(Zn-I)转换电池存在严重的多碘化物穿梭和迟缓的氧化还原动力学问题,这阻碍了电池的使用寿命和倍率性能。在此,基于单原子Fe-N-C封装的高比表面积碳(HC@FeNC)作为核壳阴极材料,引入了一种超稳定的Zn-I电池,该材料显著加速了I⁻/I₃⁻/I₂的转换。多碘化物与Fe-N位点之间强大的化学-物理相互作用紧密结合多碘化物离子,抑制了多碘化物穿梭,从而显著提高了库仑效率。结果,核壳结构的HC@FeNC阴极赋予了水系Zn-I电池优异的容量、出色的倍率性能以及超过60000次循环的超长寿命。更重要的是,一个实际的253 Wh kg软包电池在100次循环后显示出84%的良好容量保持率,突出了其在商用Zn-I电池方面的巨大潜力。