{"title":"集成li20电极增强高性能锂金属电池富liff界面的吸附/除氟动力学","authors":"Guocheng Li, Xiang Feng, Yuanjian Li, Junmou Du, Junjie Fu, Chengjin Liu, Geng Chen, Yue Shen, Wei Xiao, Qianfan Zhang, Yongming Sun","doi":"10.1002/adfm.202523194","DOIUrl":null,"url":null,"abstract":"Regulating interfacial chemistry at lithium (Li) anodes is vital for constructing robust solid-electrolyte interphase (SEI) and achieving reliable Li metal batteries (LMBs). Herein, an electrode-based strategy is proposed to regulate adsorption/defluorination kinetics of fluorinated electrolyte species by incorporating mechanochemically generated Li<sub>2</sub>O nanoparticles into the Li/Li<sub>22</sub>Sn<sub>5</sub> composite electrode, thereby constructing a LiF-rich SEI. This approach fundamentally differs from conventional methods that rely on concentrated salts or complex electrolyte formulations. Spectroscopic characterizations combined with density functional theory simulations confirm that the integrated-Li<sub>2</sub>O nanoparticles strongly adsorb FEC and PF<sub>6</sub><sup>–</sup> anions and promote their spontaneous defluorination, facilitating the preferential formation of LiF within the SEI. This inorganic-rich interphase homogenizes Li deposition and mitigates electrolyte corrosion even at 60 °C. Consequently, the composite electrode delivers a high average Coulombic efficiency of 99.0% over 50 plating/stripping cycles in carbonate electrolyte at 1 mA cm<sup>−2</sup> and 1 mAh cm<sup>−2</sup>. Paired with LiCoO<sub>2</sub> cathodes, it achieves outstanding cyclability with 87.0% capacity-retention at a low negative-to-positive ratio of 2:1 and 84.8% capacity-retention under lean-electrolyte conditions (20 µL) after 200 cycles over a wide voltage range of 2.8–4.5 V. This work highlights regulating adsorption/defluorination kinetics as an effective route to engineer LiF-rich SEI and enable high-performance LMBs.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"56 1","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Li2O-Integrated Electrodes Enabling Enhanced Adsorption/Defluorination Kinetics Toward LiF-Rich Interphase for High-Performance Lithium Metal Batteries\",\"authors\":\"Guocheng Li, Xiang Feng, Yuanjian Li, Junmou Du, Junjie Fu, Chengjin Liu, Geng Chen, Yue Shen, Wei Xiao, Qianfan Zhang, Yongming Sun\",\"doi\":\"10.1002/adfm.202523194\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Regulating interfacial chemistry at lithium (Li) anodes is vital for constructing robust solid-electrolyte interphase (SEI) and achieving reliable Li metal batteries (LMBs). Herein, an electrode-based strategy is proposed to regulate adsorption/defluorination kinetics of fluorinated electrolyte species by incorporating mechanochemically generated Li<sub>2</sub>O nanoparticles into the Li/Li<sub>22</sub>Sn<sub>5</sub> composite electrode, thereby constructing a LiF-rich SEI. This approach fundamentally differs from conventional methods that rely on concentrated salts or complex electrolyte formulations. Spectroscopic characterizations combined with density functional theory simulations confirm that the integrated-Li<sub>2</sub>O nanoparticles strongly adsorb FEC and PF<sub>6</sub><sup>–</sup> anions and promote their spontaneous defluorination, facilitating the preferential formation of LiF within the SEI. This inorganic-rich interphase homogenizes Li deposition and mitigates electrolyte corrosion even at 60 °C. Consequently, the composite electrode delivers a high average Coulombic efficiency of 99.0% over 50 plating/stripping cycles in carbonate electrolyte at 1 mA cm<sup>−2</sup> and 1 mAh cm<sup>−2</sup>. Paired with LiCoO<sub>2</sub> cathodes, it achieves outstanding cyclability with 87.0% capacity-retention at a low negative-to-positive ratio of 2:1 and 84.8% capacity-retention under lean-electrolyte conditions (20 µL) after 200 cycles over a wide voltage range of 2.8–4.5 V. 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引用次数: 0
摘要
锂(Li)阳极的界面化学调节对于构建坚固的固-电解质界面相(SEI)和实现可靠的锂金属电池(lmb)至关重要。本文提出了一种基于电极的策略,通过将机械化学生成的Li2O纳米颗粒加入Li/Li22Sn5复合电极中,从而构建富liff SEI,来调节氟化电解质物种的吸附/除氟动力学。这种方法与依赖于浓缩盐或复杂电解质配方的传统方法有根本区别。光谱表征结合密度泛函理论模拟证实了集成li2o纳米颗粒对FEC和PF6 -阴离子的强吸附,促进了它们的自发脱氟,促进了SEI内LiF的优先形成。这种富含无机的界面相使Li沉积均匀,即使在60°C下也能减轻电解质腐蚀。因此,复合电极在1 mA cm - 2和1 mAh cm - 2的碳酸盐电解质中,在50次电镀/剥离循环中提供了99.0%的高平均库仑效率。与LiCoO2阴极配对,在低正负比为2:1的情况下,该材料具有出色的循环性能,在稀电解质条件下(20µL),在2.8-4.5 V宽电压范围内循环200次后,其容量保持率为87.0%,容量保持率为84.8%。这项工作强调了调节吸附/除氟动力学是设计富liff SEI和实现高性能lmb的有效途径。
Li2O-Integrated Electrodes Enabling Enhanced Adsorption/Defluorination Kinetics Toward LiF-Rich Interphase for High-Performance Lithium Metal Batteries
Regulating interfacial chemistry at lithium (Li) anodes is vital for constructing robust solid-electrolyte interphase (SEI) and achieving reliable Li metal batteries (LMBs). Herein, an electrode-based strategy is proposed to regulate adsorption/defluorination kinetics of fluorinated electrolyte species by incorporating mechanochemically generated Li2O nanoparticles into the Li/Li22Sn5 composite electrode, thereby constructing a LiF-rich SEI. This approach fundamentally differs from conventional methods that rely on concentrated salts or complex electrolyte formulations. Spectroscopic characterizations combined with density functional theory simulations confirm that the integrated-Li2O nanoparticles strongly adsorb FEC and PF6– anions and promote their spontaneous defluorination, facilitating the preferential formation of LiF within the SEI. This inorganic-rich interphase homogenizes Li deposition and mitigates electrolyte corrosion even at 60 °C. Consequently, the composite electrode delivers a high average Coulombic efficiency of 99.0% over 50 plating/stripping cycles in carbonate electrolyte at 1 mA cm−2 and 1 mAh cm−2. Paired with LiCoO2 cathodes, it achieves outstanding cyclability with 87.0% capacity-retention at a low negative-to-positive ratio of 2:1 and 84.8% capacity-retention under lean-electrolyte conditions (20 µL) after 200 cycles over a wide voltage range of 2.8–4.5 V. This work highlights regulating adsorption/defluorination kinetics as an effective route to engineer LiF-rich SEI and enable high-performance LMBs.
期刊介绍:
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