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基于简便表面化学的双功能人工固体电解质界面层用于稳定锂金属负极

A Dual Functional Artificial SEI Layer Based on a Facile Surface Chemistry for Stable Lithium Metal Anode.

作者信息

Ma Yue, Wu Feng, Chen Nan, Yang Tianyu, Liang Yaohui, Sun Zhaoyang, Luo Guangqiu, Du Jianguo, Shang Yanxin, Feng Mai, Wen Ziyue, Li Li, Chen Renjie

机构信息

Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China.

Advanced Technology Research Institute, Beijing Institute of Technology, Jinan 250300, China.

出版信息

Molecules. 2022 Aug 15;27(16):5199. doi: 10.3390/molecules27165199.

Abstract

Solid electrolyte interphase (SEI) on a Li anode is critical to the interface stability and cycle life of Li metal batteries. On the one hand, components of SEI with the passivation effect can effectively hinder the interfacial side reactions to promote long-term cycling stability. On the other hand, SEI species that exhibit the active site effect can reduce the Li nucleation barrier and guide Li deposition homogeneously. However, strategies that only focus on a separated effect make it difficult to realize an ideal overall performance of a Li anode. Herein, a dual functional artificial SEI layer simultaneously combining the passivation effect and the active site effect is proposed and constructed via a facial surface chemistry method. Simultaneously, the formed LiF component effectively passivates the anode/electrolyte interface and contributes to the long-term stable cycling performance, while the Li-Mg solid solution alloy with the active site effect promotes the transmission of Li and guides homogeneous Li deposition with a low energy barrier. Benefiting from these advantages, the Li||Li cell with the modified anode performs with a lower nucleation overpotential of 2.3 mV, and an ultralong cycling lifetime of over 2000 h at the current density of 1 mA cm, while the Li||LiFePO full battery maintains a capacity retention of 84.6% at rate of 1 C after 300 cycles.

摘要

锂负极上的固态电解质界面(SEI)对于锂金属电池的界面稳定性和循环寿命至关重要。一方面,具有钝化作用的SEI组分能够有效阻碍界面副反应,从而提升长期循环稳定性。另一方面,表现出活性位点效应的SEI物种能够降低锂成核势垒并引导锂均匀沉积。然而,仅关注单一效应的策略难以实现锂负极理想的整体性能。在此,通过一种简便的表面化学方法,提出并构建了一种同时兼具钝化效应和活性位点效应的双功能人工SEI层。同时,形成的LiF组分有效钝化了阳极/电解质界面,并有助于长期稳定的循环性能,而具有活性位点效应的Li-Mg固溶体合金促进了锂的传输,并以低能垒引导锂均匀沉积。受益于这些优势,具有改性负极的Li||Li电池在1 mA cm的电流密度下具有2.3 mV的较低成核过电位和超过2000 h的超长循环寿命,而Li||LiFePO全电池在1 C倍率下经过300次循环后容量保持率为84.6%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd05/9412686/70346294197b/molecules-27-05199-g001.jpg

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