Yi Qiu, Wuliang Feng, Jiaming Hu, Xuan Yu, Xue Fan, Qinhao Shi, Peiyao Wang, Shuang Wu, Chenyao Ma, Xingbao Zhu, Ying Zhang, Mohd Ubaidullah, Reinaldo F. Teófilo, Yang Liu, Yufeng Zhao
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引用次数: 0
摘要
高界面热力学和接触稳定性是抑制固态金属钠电池枝晶生长的两个关键因素。然而,一个热力学稳定的界面往往具有疏钠特性,从而加剧了界面的接触亲和,从而使这两个关键因素相互矛盾。本文提出了一种解决高疏钠性与界面接触之间内在矛盾的新策略——“动力学驱动合金下沉”工艺。具体来说,亲钠导电合金(如KNa2)自发地“沉入”到体Na金属中,从而保留了一个疏钠/离子导电但密切接触的界面(如NaF)。与传统的亲钠界面概念不同,这项工作证明了用原位形成的离子导电界面进行疏钠改性的优势,这与先前的文献建立了根本性的区别。因此,实现了4.0 mA cm−2的超高时间常数模式临界电流密度(CCD),超过了现有文献中最先进的值。对界面憎钠性和介相传导类型的基本认识将为设计高性能SSSBs提供新的思路。
Interfacial Sodiopobicity Regulating for Dendrite-Free Solid-State Sodium Metal Batteries
High interfacial thermodynamic and contact stabilities are two key factors to suppress dendrite growth in solid-state sodium metal batteries (SSSBs). However, a thermodynamical stable interface often features with sodiophobic character to aggravate interfacial contact affinity, thus making the two key factors paradox with each other. Herein, a new strategy is reported to resolve the intrinsic contradictions between high sodiophobicity and interfacial contacts with a “kinetic-driven alloy sinking” process. Specifically, the sodiophilic and electronic conductive alloy (e.g., KNa2) is spontaneously “sunk” into bulk Na metal, thus remaining a sodiophobic/ionic conductive but intimately contacted interface (e.g., NaF). Unlike conventional concept of sodiophilic interface, this work demonstrates the advantage of sodiophobic modification with an in situ formed ionic conductive interphase, which establishes a foundational distinction from prior literatures. Consequently, an ultrahigh time-constant mode critical current density (CCD) of 4.0 mA cm−2 is achieved, surpassing the state-of-the-art values in existing literature. The fundamental understanding on interfacial sodiophobicity and conduction types of interphases will provide new insight for designing high-performance SSSBs.
期刊介绍:
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