Sharma Madhav, Dhaka Rajendra S
Department of Physics, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110016, India.
Small. 2025 Sep;21(35):e2505200. doi: 10.1002/smll.202505200. Epub 2025 Jul 14.
The electrochemical performance and diffusion kinetics of a newly designed NASICON-type NaMnTiMo(PO)/C composite material is reported as a cathode for cost-effective sodium-ion batteries. A novel strategy of small Mo doping successfully stabilizes the sample having high Mn content in single-phase rhombohedral symmetry. The high-resolution microscopy analysis reveals nanocrystallites of around ∼18 nm, uniformly embedded within the semi-graphitic carbon matrix, which enhances the surface electronic conductivity and effectively shortens the sodium-ion diffusion path. More importantly, a stable electrochemical behavior is demonstrated, with enhanced discharge capacity of 124 mAh/g at 0.1 C, having good reversibility and retaining 77% of its capacity after 300 cycles, and 70% even after 400 cycles at 2 C. The sodium-ion diffusion coefficients, estimated using both galvanostatic intermittent titration technique (GITT) and cyclic voltammetry, are found to lie within the range of 10 to 10 cm/s. Additionally, the bond-valence site energy mapping predicted a sodium-ion migration energy barrier of 0.76 eV. A detailed distribution of relaxation times (DRT) analysis is used to deconvolute the electrochemical impedance spectra into distinct processes based on their characteristic relaxation times. Notably, the solid-state diffusion of sodium ions within the bulk electrode, with a relaxation time of ∼50 s, shows a consistent trend with the diffusion coefficients obtained from GITT and Warburg-based evaluations across the state of charge.
报道了一种新设计的NASICON型NaMnTiMo(PO)/C复合材料作为经济高效的钠离子电池阴极的电化学性能和扩散动力学。一种小剂量Mo掺杂的新策略成功地稳定了具有高Mn含量的单相菱面体对称样品。高分辨率显微镜分析揭示了约18nm的纳米微晶,均匀地嵌入在半石墨碳基质中,这提高了表面电子导电性并有效地缩短了钠离子扩散路径。更重要的是,展示了稳定的电化学行为,在0.1C下放电容量增强至124mAh/g,具有良好的可逆性,在300次循环后保留其容量的77%,在2C下400次循环后甚至保留70%。使用恒电流间歇滴定技术(GITT)和循环伏安法估计的钠离子扩散系数在10至10cm/s范围内。此外,键价位点能量映射预测钠离子迁移能垒为0.76eV。基于详细的弛豫时间分布(DRT)分析,根据其特征弛豫时间将电化学阻抗谱解卷积为不同的过程。值得注意的是,钠离子在本体电极内的固态扩散,弛豫时间约为50s,与从GITT和基于Warburg的评估在整个充电状态下获得的扩散系数显示出一致的趋势。