Qu Wentao, Zhu Jian, Cao Guozhong, Chen Shulin, Tan Yongwen, Chen Baohui, Zhang Ming
Hunan Provincial Key Laboratory of Low-Dimensional Structural Physics & Devices, School of Physics and Electronics, Hunan University, Changsha, 410082, China.
Engineering Research Center of Advanced Semiconductor Technology and Application of Ministry of Education & Key Laboratory for Micro-/Nano-Optoelectronic Devices of Ministry of Education, College of Semiconductors (College of Integrated Circuits), Hunan University, Changsha, 410082, China.
Small. 2024 Jun;20(26):e2310475. doi: 10.1002/smll.202310475. Epub 2024 Jan 17.
Zinc-iodine batteries (Zn-I2) are extremely attractive as the safe and cost-effective scalable energy storage system in the stationary applications. However, the inefficient redox kinetics and "shuttling effect" of iodine species result in unsatisfactory energy efficiency and short cycle life, hindering their commercialization. In this work, Ni single atoms highly dispersed on carbon fibers is designed and synthesized as iodine anchoring sites and dual catalysts for Zn-I2 batteries, and successfully inhibit the iodine species shuttling and boost dual reaction kinetics. Theoretical calculations indicate that the reinforced d-p orbital hybridization and charge interaction between Ni single-atoms and iodine species effectively enhance the confinement of iodine species. Ni single-atoms also accelerate the iodine conversion reactions with tailored bonding structure of I─I bonds and reduced energy barrier for the dual conversion of iodine species. Consequently, the high-rate performance (180 mAh g at 3 A g), cycling stability (capacity retention of 74% after 5900 cycles) and high energy efficiency (90% at 3 A g) are achieved. The work provides an effective strategy for the development of iodine hosts with high catalytic activity for Zn-I2 batteries.
锌碘电池(Zn-I₂)作为固定式应用中安全且具有成本效益的可扩展储能系统极具吸引力。然而,碘物种低效的氧化还原动力学和“穿梭效应”导致能量效率不理想以及循环寿命短,阻碍了它们的商业化。在这项工作中,设计并合成了高度分散在碳纤维上的镍单原子,作为锌碘电池的碘锚定位点和双功能催化剂,并成功抑制了碘物种的穿梭并促进了双反应动力学。理论计算表明,镍单原子与碘物种之间增强的d-p轨道杂化和电荷相互作用有效地增强了对碘物种的限制。镍单原子还通过调整I─I键的键合结构和降低碘物种双转化的能垒来加速碘转化反应。因此,实现了高倍率性能(3 A g时为180 mAh g)、循环稳定性(5900次循环后容量保持率为74%)和高能量效率(3 A g时为90%)。这项工作为开发具有高催化活性的锌碘电池碘宿主提供了一种有效策略。