Zhang Haoran, Yu Yue, Yang Dongyue, Fan Yingqi, Chen Hao, Zhang Ning, Wang Zhi, Huang Gang, Zhang Xinbo
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, China.
School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, 230026, China.
Adv Mater. 2025 Feb;37(7):e2413948. doi: 10.1002/adma.202413948. Epub 2024 Dec 29.
Li-O batteries have been considered as a kind of prospective next-generation batteries due to their ultrahigh energy densities. However, limited capacities, high charge overpotentials, and short lifetime are troubling obstacles for realizing their real-world implementation. Common strategies, including introducing solid-state catalysts (SSCs) and redox mediators (RMs), are insufficient to solve these issues. Herein, Ru-loaded amino-phenanthroline-based carbonized polymer dots (RuApCPDs) integrating the catalytic activity of SSCs with the mobility of RMs have been designed to behave as quasi-homogeneous catalysts in the electrolyte. Their mobile nature can ensure the avoidance of complete coverage of active sites, and the catalytic ability decreases the charge overpotential through co-deposition with the discharge products. Additionally, the RuApCPDs can also adjust the Li solvation structure and well protect the Li metal anodes with high stability. As a result, the introduction of RuApCPDs leads to a fivefold increase in discharge capacity, a low charge voltage of 3.75 V, and a running life of 168 cycles (79 cycles without RuApCPDs). The multifunctional quasi-homogeneous catalyst developed here demonstrates its advantageous potential as a new catalytic strategy for bringing Li-O batteries to become a viable technology.
锂氧电池因其超高的能量密度而被视为一种有前景的下一代电池。然而,容量有限、充电过电位高和寿命短是实现其实际应用的棘手障碍。包括引入固态催化剂(SSCs)和氧化还原介质(RMs)在内的常见策略不足以解决这些问题。在此,负载钌的氨基菲咯啉基碳化聚合物点(RuApCPDs)将SSCs的催化活性与RMs的迁移率相结合,被设计成在电解质中作为准均相催化剂。它们的可移动性可以确保避免活性位点被完全覆盖,并且催化能力通过与放电产物共沉积来降低充电过电位。此外,RuApCPDs还可以调整锂的溶剂化结构,并以高稳定性很好地保护锂金属负极。结果,RuApCPDs的引入使放电容量增加了五倍,充电电压低至3.75 V,运行寿命达到168个循环(没有RuApCPDs时为79个循环)。这里开发的多功能准均相催化剂展示了其作为一种新的催化策略的优势潜力,可使锂氧电池成为一种可行的技术。