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Functionality of Dual-Phase Lithium Storage in a Porous Carbon Host for Lithium-Metal Anode

机译:锂金属阳极多孔碳基质中双相锂存储的功能

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Lithium (Li) metal is regarded as the most attractive anode material for high-energy Li batteries, but it faces unavoidable challenges-uncontrollable dendritic growth of Li and severe volume changes during Li plating and stripping. Herein, a porous carbon framework (PCF) derived from a metal-organic framework (MOF) is proposed as a dual-phase Li storage material that enables efficient and reversible Li storage via lithiation and metallization processes. Li is electrochemically stored in the PCF upon charging to 0 V versus Li/Li+ (lithiation), making the PCF surface more lithiophilic, and then the formation of metallic Li phase can be induced spontaneously in the internal nanopores during further charging below 0 V versus Li/Li+ (metallization). Based on thermodynamic calculations and experimental studies, it is shown that atomically dispersed zinc plays an important role in facilitating Li plating and that the reversibility of Li storage is significantly improved by controlled nanostructural engineering of 3D porous nanoarchitectures to promote the uniform formation of Li. Moreover, the MOF-derived PCF does not suffer from macroscopic volume changes during cycling. This work demonstrates that the nanostructural engineering of porous carbon structures combined with lithiophilic element coordination would be an effective approach for realizing high-capacity, reversible Li-metal anodes.
机译:锂(Li)金属被认为是高能锂电池最吸引人的负极材料,但它面临不可避免的挑战-锂的不可控制的树枝状生长以及在锂电镀和剥离过程中体积的剧烈变化。本文中,提出了源自金属-有机骨架(MOF)的多孔碳骨架(PCF)作为双相Li存储材料,其能够通过锂化和金属化工艺进行有效且可逆的Li存储。相对于Li / Li +(锂化)充电至0 V时,Li被电化学存储在PCF中,使PCF表面更具亲脂性,然后在低于0 V相对于0 V充电时可以自发地在内部纳米孔中诱导金属Li相的形成Li / Li +(金属化)。基于热力学计算和实验研究,表明原子分散的锌在促进Li电镀中起着重要作用,并且通过3D多孔纳米结构的纳米结构控制以促进Li的均匀形成,Li储存的可逆性得到了显着改善。而且,MOF衍生的PCF在循环过程中不会受到宏观体积变化的影响。这项工作表明,多孔碳结构的纳米结构工程与亲硫的元素配位相结合将是实现高容量,可逆锂金属阳极的有效方法。

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