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与液态钠钾相关的用于无枝晶碱金属阳极的自由基共价有机框架

Radical Covalent Organic Frameworks Associated with Liquid Na-K toward Dendrite-Free Alkali Metal Anodes.

作者信息

Wang Jianyi, Chen Menghui, Lu Zicong, Chen Zhida, Si Liping

机构信息

School of Materials Science and Hydrogen Energy, Foshan University, Foshan, 528000, P. R. China.

Institute for Sustainable Energy/College of Sciences, Shanghai University, Shanghai, 200444, P. R. China.

出版信息

Adv Sci (Weinh). 2022 Sep;9(26):e2203058. doi: 10.1002/advs.202203058. Epub 2022 Jul 21.

Abstract

Liquid sodium-potassium (Na-K) alloy has the characteristics of high abundance, low redox potential, high capacity, and no dendrites, which has become an ideal alternative material for potassium/sodium metal anodes. However, the high surface tension of liquid sodium potassium alloy at room temperature makes it inconvenient in practical use. Here, the Na-K as reducing agent treats with hydrazone linkages of covalent organic frameworks (COFs) and obtain the carbon-oxygen radical COFs (COR-Tf-DHzDM-COFs). The preparation method solves the problems that the preparation process of the traditional Na-K composite anode is complex and has high cost. The structures of the COR-Tf-DHzDM-COFs are characterized by X-ray diffraction (XRD), fourier transform infrared (FT-IR), electron paramagnetic resonance (EPR), and solid-state NMR measurements. It is the first time that carbon-oxygen radical COFs from bulk COFs are constructed by one-step method and the operation is flexible, convenient, and high rate of quality, which is suitable for big production and widely used. The cycle stability of the composite Na-K anode is improved, which provides a new idea for the design of high-performance liquid metal anode.

摘要

液态钠钾(Na-K)合金具有丰度高、氧化还原电位低、容量高且无枝晶的特点,已成为钾/钠金属负极的理想替代材料。然而,液态钠钾合金在室温下的高表面张力使其在实际应用中不便。在此,以Na-K作为还原剂处理共价有机骨架(COF)的腙键,得到碳氧自由基COF(COR-Tf-DHzDM-COF)。该制备方法解决了传统Na-K复合负极制备过程复杂且成本高的问题。通过X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、电子顺磁共振(EPR)和固体核磁共振测量对COR-Tf-DHzDM-COF的结构进行了表征。首次通过一步法从本体COF构建碳氧自由基COF,操作灵活、方便且质量产率高,适用于大规模生产并得到广泛应用。复合Na-K负极的循环稳定性得到提高,为高性能液态金属负极的设计提供了新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e898/9475504/5e609ebd162f/ADVS-9-2203058-g002.jpg

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