Xie Huixian, Liu Lingwen, Chen Hongyi, Hui Kwan San, Kuang Zhuoheng, Zhou Guangmin, Sun Yuanmiao, Cheng Hui-Ming, Hui Kwun Nam
Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau SAR, 999078, P. R. China.
Shenzhen Key Laboratory of Energy Materials for Carbon Neutrality, Institute of Technology for Carbon Neutrality, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, P. R. China.
Adv Mater. 2025 Jul;37(29):e2504248. doi: 10.1002/adma.202504248. Epub 2025 May 7.
Phosphorus-based anodes hold promise for energy storage due to their high theoretical capacity and favorable lithiation potential. However, their practical application is hindered by sluggish reaction kinetics and irreversible capacity loss, primarily attributed to multiphase lithiation/delithiation reactions and the dissolution of lithium polyphosphide intermediates. Herein, a universal design principle of weakly solvated electrolytes (WSEs) tailored for phosphorus-based anodes is proposed. Combined with a high dielectric constant, and significant dipole moment, a fluorinated cosolvent is incorporated into a WSE to effectively suppress the dissolutions of lithium polyphosphides, enhance interfacial stability, and accelerate reaction kinetics. With this electrolyte, a phosphorus-based anode achieves a remarkable capacity of 2615.2 mAh g⁻¹ at 1C, maintaining 91.7% capacity retention over 1000 cycles. Even at a high rate of 4 C, it delivers 2210.7 mAh g⁻¹ with an exceptional retention of 96.7% after 1500 cycles. Furthermore, at 0 °C, the anode sustains a capacity of 2016.7 mAh g⁻¹, with 97% retention after 300 cycles at 1C. This study provides a novel electrolyte design strategy to regulate the solvation sheath, paving the way for high-rate, long-cycle phosphorus-based anodes suitable for fast-charging applications.
基于磷的阳极由于其高理论容量和良好的锂化电位而在能量存储方面具有潜力。然而,其实际应用受到缓慢的反应动力学和不可逆容量损失的阻碍,这主要归因于多相锂化/脱锂反应以及多聚磷酸锂中间体的溶解。在此,提出了一种为基于磷的阳极量身定制的弱溶剂化电解质(WSEs)的通用设计原则。结合高介电常数和显著的偶极矩,将一种氟化共溶剂引入到WSE中,以有效抑制多聚磷酸锂的溶解,增强界面稳定性,并加速反应动力学。使用这种电解质,基于磷的阳极在1C下实现了2615.2 mAh g⁻¹的显著容量,在1000次循环中保持91.7%的容量保持率。即使在4C的高倍率下,它在1500次循环后仍能提供2210.7 mAh g⁻¹的容量,且具有96.7%的优异保持率。此外,在0°C时,阳极在1C下300次循环后保持2016.7 mAh g⁻¹的容量,保持率为97%。这项研究提供了一种调节溶剂化鞘层的新型电解质设计策略,为适用于快速充电应用的高倍率、长循环基于磷的阳极铺平了道路。