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亲钠性底物诱导富含NaF的固体电解质界面用于无枝晶钠金属负极。

Sodiophilic Substrate Induces NaF-Rich Solid Electrolyte Interface for Dendrite-Free Sodium Metal Anode.

作者信息

Liu Pei, Miao Licheng, Sun Zhiqin, Chen Xuchun, Jiao Lifang

机构信息

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), College of Chemistry, Nankai University, Tianjin, 300071, China.

出版信息

Adv Mater. 2024 Sep;36(39):e2406058. doi: 10.1002/adma.202406058. Epub 2024 Aug 4.

DOI:10.1002/adma.202406058
PMID:39097944
Abstract

3D substrate with abundant sodiophilic active sites holds promise for implementing dendrite-free sodium metal anodes and high-performance sodium batteries. However, the heightened electrode/electrolyte side reactions stemming from high specific surface area still hinder electrode structure stability and cycling reversibility, particularly under high current densities. Herein, the solid electrolyte interface (SEI) component is regulated and detrimental side reactions are restrained through the uniform loading of Na-Sn alloy onto a porous 3D nanofiber framework (NaSn-PCNF). The strong interaction between Na-Sn alloy and PF anions facilitates the dissociation of sodium salts and releases more free sodium ions for effective charge transfer. Simultaneously, the modulations of the interfacial electrolyte solvation structure and the construction of a high NaF content SEI layer stabilize the electrode/electrolyte interface. NaSn-PCNF symmetrical battery demonstrates stable cycling for over 600 h with an ultralow overpotential of 24.5 mV under harsh condition of 10 mA cm and 10 mAh cm. Moreover, the full cells and pouch cells exhibit accelerated reaction kinetics and splendid capacity retention, providing valuable insights into the development of advanced Na substrates for high-energy sodium metal batteries.

摘要

具有丰富亲钠活性位点的3D基底有望实现无枝晶钠金属负极和高性能钠电池。然而,高比表面积导致的电极/电解质副反应加剧,仍然阻碍了电极结构的稳定性和循环可逆性,尤其是在高电流密度下。在此,通过将Na-Sn合金均匀负载到多孔3D纳米纤维框架(NaSn-PCNF)上,调节了固体电解质界面(SEI)成分并抑制了有害的副反应。Na-Sn合金与PF阴离子之间的强相互作用促进了钠盐的解离,并释放出更多的游离钠离子以实现有效的电荷转移。同时,界面电解质溶剂化结构的调节和高NaF含量SEI层的构建稳定了电极/电解质界面。NaSn-PCNF对称电池在10 mA cm和10 mAh cm的苛刻条件下,以24.5 mV的超低过电位稳定循环超过600小时。此外,全电池和软包电池表现出加速的反应动力学和出色的容量保持率,为开发用于高能钠金属电池的先进钠基底提供了有价值的见解。

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