Electrolyte Design for High‐Voltage Lithium‐Metal Batteries with Synthetic Sulfonamide‐Based Solvent and Electrochemically Active Additives

Author:

Kim Saehun1,Jeon Ji Hwan2,Park Kyobin3,Kweon Seong Hyeon4,Hyun Jae‐Hwan5,Song Chaeeun1,Lee Donghyun1,Song Gawon3,Yu Seung‐Ho5,Lee Tae Kyung6,Kwak Sang Kyu5,Lee Kyu Tae3,Hong Sung You2,Choi Nam‐Soon1ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology (KAIST) Daejeon 34141 Republic of Korea

2. Department of Chemistry Graduate School of Carbon Neutrality Ulsan National Institute of Science and Technology (UNIST) Ulsan 44919 Republic of Korea

3. School of Chemical and Biological Engineering Institute of Chemical Processes Seoul National University (SNU) Seoul 08826 Republic of Korea

4. School of Energy of Chemical Engineering Ulsan National Institute of Science and Technology (UNIST) Ulsan 44919 Republic of Korea

5. Department of Chemical and Biological Engineering Korea University Seoul 02841 Republic of Korea

6. Department of Materials Engineering and Convergence Technology Gyeongsang National University (GNU) Jinju 52828 Republic of Korea

Abstract

AbstractConsidering practical viability, Li‐metal battery electrolytes should be formulated by tuning solvent composition similar to electrolyte systems for Li‐ion batteries to enable the facile salt‐dissociation, ion‐conduction, and introduction of sacrificial additives for building stable electrode–electrolyte interfaces. Although 1,2‐dimethoxyethane with a high‐donor number enables the implementation of ionic compounds as effective interface modifiers, its ubiquitous usage is limited by its low‐oxidation durability and high‐volatility. Regulation of the solvation structure and construction of well‐structured interfacial layers ensure the potential strength of electrolytes in both Li‐metal and LiNi0.8Co0.1Mn0.1O2 (NCM811). This study reports the build‐up of multilayer solid‐electrolyte interphase by utilizing different electron‐accepting tendencies of lithium difluoro(bisoxalato) phosphate (LiDFBP), lithium nitrate, and synthetic 1‐((trifluoromethyl)sulfonyl)piperidine. Furthermore, a well‐structured cathode–electrolyte interface from LiDFBP effectively addresses the issues with NCM811. The developed electrolyte based on a framework of highly‐ and weakly‐solvating solvents with interface modifiers enables the operation of Li|NCM811 cells with a high areal capacity cathode (4.3 mAh cm−2) at 4.4 V versus Li/Li+.

Funder

National Research Foundation of Korea

Korea Institute of Science and Technology Information

Ministry of Trade, Industry and Energy

Ministry of Science and ICT, South Korea

Publisher

Wiley

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