Yan Haotian, Chai Dandan, Li Xiang, Fu Yongzhu
College of Chemistry, Zhengzhou University, Zhengzhou, 450001, P. R. China.
Small. 2024 Nov;20(46):e2404039. doi: 10.1002/smll.202404039. Epub 2024 Aug 11.
O3-type cathodes with sufficient Na content are considered as promising candidates for sodium-ion batteries (SIBs). However, these cathodes suffer from insufficient utilization of the active elements, restraining the delivered capacity. In this work, a high entropy strategy is applied to a typical O3 cathode NaLiNiMnO (NLNM), forming a high entropy oxide NaLiNiCuMgTiMnO (Na-HE). Results show that the active elements are fully exploited in Na-HE, with a two-electron reaction by Ni (further extended to Cu redox and even oxygen redox), vastly different from a one-electron reaction of Ni in NLNM. The full utilization of the active elements dramatically improves the output capacity of the cathode (122.6 mAh g of Na-HE versus 81 mAh g of NLNM). Moreover, the detrimental phase transition is well suppressed in Na-HE. The cathode exhibits high capacity retention of 88.7% after 100 cycles at 130 mA g, compared to only 36.4% for NLNM. These findings provide new insight for the design of new cathode materials for SIBs with high energy density and robust stability.
具有足够钠含量的O3型阴极被认为是钠离子电池(SIBs)的有前途的候选材料。然而,这些阴极存在活性元素利用率不足的问题,限制了其放电容量。在这项工作中,一种高熵策略被应用于典型的O3阴极NaLiNiMnO(NLNM),形成了一种高熵氧化物NaLiNiCuMgTiMnO(Na-HE)。结果表明,在Na-HE中活性元素得到了充分利用,镍发生两电子反应(进一步扩展到铜的氧化还原甚至氧的氧化还原),这与NLNM中镍的单电子反应有很大不同。活性元素的充分利用显著提高了阴极的输出容量(Na-HE为122.6 mAh g,而NLNM为81 mAh g)。此外,在Na-HE中有害的相变得到了很好的抑制。该阴极在130 mA g下循环100次后容量保持率高达88.7%,而NLNM仅为36.4%。这些发现为设计具有高能量密度和强稳定性的新型SIBs阴极材料提供了新的见解。