Liu Xi, Zhang Minglu, Wang Xinying, Peng Yi, Liu Yang, Ullah Shafi, Duan Zhihua, Gao Wanjie, Song Bingyan, Wei Mingxuan, He Jiarui, Li Zhenghui, Wu Yuping
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing, 211189, P. R. China.
School of Materials and Energy, Guangdong University of Technology, Guangzhou, 510006, P. R. China.
Adv Mater. 2025 Jan;37(1):e2410673. doi: 10.1002/adma.202410673. Epub 2024 Nov 6.
Carbonaceous materials have been considered the most promising anode in sodium-ion batteries (SIBs) due to their low cost, good electrical conductivity, and structural stability. The main challenge of carbonaceous anodes prior to their commercialization is low initial coulomb efficiencies, derived from a lack of an efficient technique to reveal a fundamental comprehension of sodium storage mechanisms. Here, the direct observation of quasi-Na metallic clusters in carbonaceous anodes during cycling through in situ XRD is reported. By means of such a technique, a strong self-adsorption behavior forming quasi-Na metallic clusters is detected within a rationally designed highly defective ultrathin carbon nanosheets (HDCS) anode. Such a self-adsorption and crystalline system transformation mechanism in HDCS brings capacity retention about 100% after 1000 cycles at 1 A g. This work provides a new principle for designing high-performance carbon anodes for SIBs.
由于成本低、导电性好和结构稳定性强,碳质材料被认为是钠离子电池(SIBs)中最具潜力的负极材料。在碳质负极商业化之前,其主要挑战在于初始库仑效率较低,这是由于缺乏一种有效的技术来深入理解钠存储机制。在此,报道了通过原位XRD直接观察碳质负极在循环过程中的准钠金属簇。借助这种技术,在合理设计的高度缺陷超薄碳纳米片(HDCS)负极中检测到形成准钠金属簇的强烈自吸附行为。HDCS中的这种自吸附和晶体系统转变机制使得在1 A g的电流下循环1000次后容量保持率约为100%。这项工作为设计用于SIBs的高性能碳负极提供了新的原理。