N, F-enriched inorganic/organic composite interphases to stabilize lithium metal anodes for long-life anode-free cells

阳极 过电位 电解质 锂(药物) 材料科学 化学工程 复合数 聚乙烯醇 图层(电子) 纳米技术 化学 电化学 电极 复合材料 物理化学 内分泌学 工程类 医学
作者
Anjun Hu,Wei Chen,Yu Pan,Jun Zhu,Yinuo Li,Hui Yang,Runjing Li,Baihai Li,Yin Hu,Dongjiang Chen,Fei Li,Jianping Long,Chaoyi Yan,Tianyu Lei
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:648: 448-456 被引量:7
标识
DOI:10.1016/j.jcis.2023.06.021
摘要

The practical application of lithium metal batteries is considered to be one of the most promising successors for lithium-ion batteries due to their ability to meet the high-energy storage demands of modern society. However, their application is still hindered by the unstable solid electrolyte interphase (SEI) and uncontrollable dendrite growth. In this study, we propose a robust composite SEI (C-SEI) that consists of a fluorine doped boron nitride (F-BN) inner layer and an organic polyvinyl alcohol (PVA) outer layer. Both theoretical calculations and experimental results demonstrate that the F-BN inner layer induces the formation of favourable components (LiF and Li3N) at the interface, promoting rapid ionic transport and inhibiting electrolyte decomposition. The PVA outer layer acts as a flexible buffer in the C-SEI, ensuring the structural integrity of the inorganic inner layer during lithium plating and stripping. The C-SEI modified lithium anode shows a dendrite-free performance and stable cycle over 1200 h, with an ultralow overpotential (15 mV) at 1 mA cm-2 in this study. This novel approach also enhances the stability of capacity retention rate by 62.3% after 100 cycles even in anode-free full cells (C-SEI@Cu||LFP). Our findings suggest a feasible strategy for addressing the instability inherent in SEI, showing great prospects for the practical application of lithium metal batteries.
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