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Nitrile Electrolyte Strategy for 4.9 V-Class Lithium-Metal Batteries Operating in Flame

Energy & Environmental Materials 2023年第3期6卷 229-237页

作者： hyunseok moon Sung-Ju Cho Dae-Eun Yu Sang-Young Lee Department of Chemical and Biomolecular Engineering Yonsei UniversitySeoul 03722Korea Molecular Foundry Lawrence Berkeley National LaboratoryBerkeley CA USA Batteries R&D Center LG Energy SolutionDaejeon 34122Korea

Challenges facing high-voltage/high-capacity cathodes,in addition to the longstanding problems pertinent to lithium(Li)-metal anodes,should be addressed to develop high-energy-density Li-metal *** issue mostly stems from interfacial instability between electrodes and *** carbonate-or ether-based liquid electrolytes suffer from not only volatility and flammability but also limited electrochemical stability ***,we report a nitrile electrolyte strategy based on concentrated nitrile electrolytes(CNEs)with *** CNE consists of high-concentration lithium bis(fluorosulfonyl)imide(LiFSI)in a solvent mixture of succinonitrile(SN)/acetonitrile(AN).The SN/AN solvent mixture is designed to ensure high oxidation stability along with thermal stability,which are prerequisites for high-voltage Li-metal *** CNE exhibits interfacial stability with Li metals due to the coordinated solvation *** nitrate(LiNO_(3))and indium fluoride(InF_(3))are incorporated in the CNE as synergistic co-additives to further stabilize solid-electrolyte interphase(SEI)on Li *** resulting electrolyte(CNE+LiNO_(3)/InF_(3))enables stable cycling performance in Li||LiNi_(0.8)Co_(0.1)Mn_(0.1)and 4.9 V-class Li||LiNi_(0.5)Mn_(1.5)O_(4)***,the Li||LiNi_(0.5)Mn_(1.5)O_(4)cell maintains its electrochemical activity at high temperature(100℃)and even in flame without fire or explosion.

关键词： 4.9 V-class cathodes electrolyte-electrode interfaces lithium-metal batteries nitrile electrolytes safety

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An Anionic Covalent Organic Framework as an Electrostatic Molecular Rectifier for Stabilizing Mg Metal Electrodes

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CCS Chemistry 2023年第11期5卷 2567-2575页

作者： Zhongping Li hyunseok moon Seok-Kyu Cho Changqing Li Jeong-Min Seo Jong-Beom Baek Hong Xu Sang-Young Lee Department of Chemical and Biomolecular Engineering Yonsei UniversitySeoul 03772 School of Energy and Chemical Engineering Ulsan National Institute of Science and TechnologyUlsan 44919 UBATT Inc. Daejeon 34036 Institute of Nuclear and New Energy Technology Tsinghua UniversityBeijing 100084

Despite its potential as a high-capacity battery electrode,magnesium(Mg)metals are highly susceptible to electrolytes,resulting in the formation of unwanted passivation layers,which hinder charge transfer ***,we first report an anionic covalent organic framework(a-COF)as an electrostatic molecular rectifier(that can preferentially trap solvent molecules)to stabilize Mg metal *** to a neutral COF(n-COF)as a control sample,the a-COF enhances Mg^(2+)transport by facilitating the desolvation of Mg^(2+)-solvent complexes and cationic mobility through its negatively charged one-dimensional columns,thereby achieving an ionic conductivity eight times higher than that of the *** addition,the anionic porous frameworks in contact with Mg metal electrodes enable a uniform Mg^(2+)flux and interfacial stability with Mg metal ***,the a-COF exhibited reversible Mg plating/stripping cyclability on Mg metal electrodes compared to the n-COF,demonstrating the electrochemical viability of the anionic frameworks for Mg metal electrode stabilization.

关键词： anionic covalent organic framework Mg metal electrodes ion transport interfacial stability Mg plating/stripping

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