In situ formed polymer gel electrolytes for lithium batteries with inherent thermal shutdown safety features
文献情報
Hongyao Zhou, Haodong Liu, Yejing Li, Xiujun Yue, Xuefeng Wang, Matthew Gonzalez, Ying Shirley Meng, Ping Liu
Rechargeable lithium metal batteries based on organic electrolytes face challenges of both lithium metal cycling stability and the associated safety issues. Herein, we demonstrate an in situ formed polymer gel electrolyte which enables dendrite-free lithium metal cycling. Moreover, the gel electrolyte goes through further polymerization at elevated temperatures and loses its ionic conductivity, effectively shutting down the battery. When lithium iodide (LiI) is dissolved in vinylene carbonate (VC), LiI induces the polymerization of VC to form poly(vinylene carbonate) (polyVC). The electrolyte then transforms into a polymer gel electrolyte containing VC as the solvent and LiI as the salt. At room temperature, the gel electrolyte enables dendrite-free lithium metal cycling at current densities as high as 5 mA cm−2 for 500 cycles. Furthermore, a Li/Li4Ti5O12 (LTO) cell retains 50% of the initial capacity at the 700th cycle. When the cell is heated to 80 °C, the ionic resistance of the electrolyte increases by a factor of 103, resulting in the shutdown of the cell due to the complete polymerization of VC. The approach of using in situ polymerization to enable stable lithium cycling and to serve as a thermally triggered shutdown mechanism provides a new pathway for fabricating safer lithium metal batteries.
関連文献
NANOGOLD decorated by pHLIP peptide: comparative force field study
DOI: 10.1039/C5CP01136A
Electrical and thermal transport properties of Pb1−xSnxSe solid solution thermoelectric materials
Chao-Feng Wu, Tian-Ran Wei, Jing-Feng Li
DOI: 10.1039/C4CP06021K
Modelling bio-electrosynthesis in a reverse microbial fuel cell to produce acetate from CO2 and H2O
M. Kazemi, D. Biria, H. Rismani-Yazdi
DOI: 10.1039/C5CP00904A
Decomposition of nitroimidazole ions: experiment and theory
Johannes Postler, Athanasios Zavras, Paul Scheier, Stephan Denifl, Richard A. J. O'Hair
DOI: 10.1039/C5CP01014D
Physisorption of benzene derivatives on graphene: critical roles of steric and stereoelectronic effects of the substituent
Rui-Qin Zhang
DOI: 10.1039/C4CP05973E
New particle formation and growth from methanesulfonic acid, trimethylamine and water
Haihan Chen, Michael J. Ezell, Kristine D. Arquero, Mychel E. Varner, Matthew L. Dawson, R. Benny Gerber, Barbara J. Finlayson-Pitts
DOI: 10.1039/C5CP00838G
Experimental determination of the rate of V–V collisional relaxation in 14N2 in its ground (X1Σg+) electronic state between 77 and 300 K
R. Z. Martínez, D. Bermejo
DOI: 10.1039/C5CP01264C
Towards multielectron photocatalysis: a porphyrin array for lateral hole transfer and capture on a metal oxide surface
Bradley J. Brennan, Alec C. Durrell, Matthieu Koepf, Robert H. Crabtree, Gary W. Brudvig
DOI: 10.1039/C5CP01683E
Tuning the switching behavior of binary oxide-based resistive memory devices by inserting an ultra-thin chemically active metal nanolayer: a case study on the Ta2O5–Ta system
Shuang Gao, Fei Zeng, Minjuan Wang, Guangyue Wang, Cheng Song, Feng Pan
DOI: 10.1039/C5CP01235J
Water-wetting surfaces as hydrate promoters during transport of carbon dioxide with impurities
Tatiana Kuznetsova, Bjørnar Jensen, Bjørn Kvamme, Sara Sjøblom
DOI: 10.1039/C5CP00660K
こちらもおすすめ
オステニ二甲磺酸塩に適用される法規ガイドラインは何ですか?
オステニ二甲磺酸塩は、GHS分類に基づき corrosive 物質として分類されます。REACH規則では、該当物質の登録が要求される可能性があります。また、FD...
環丁基肼盐酸盐は安全ですか?
環丁基肼盐酸盐は毒性があり、吸入や皮膚接触は有害です。使用時の安全対策として、密閉システムを使用し、適切な排気設備を備えた場所で作業することが推奨されます。
N-(4-パリドン基ソニルフェニル)硫代イソシアネートを取り扱う際の実験室安全事項は何ですか?
N-(4-パリドン基ソニルフェニル)硫代イソシアネートは高毒性で、皮膚や吸入による毒性があります。取り扱う際は防毒マスク、保護用手袋、保護眼鏡などのPPEを着用...
5-ヒドロキシ-1,3-ジヒドロ-2H-インドン-2-酮の物理化学的性質は何ですか?
CAS番号3416-18-0の5-ヒドロキシ-1,3-ジヒドロ-2H-インドン-2-酮は、結晶性の白色粉末です。分子量は228.25であり、 aqueous m...
O-苄基-D-丝氨醇はどのように合成されますか?
O-苄基-D-丝氨醇は、D-アミノ酸とベンゼン環の経由で合成されます。触媒としてジメチルアミノピリジンが使用され、選択性は高いです。一般的な収率は約90%です。
ナトリウム3-ヒドロキシbutano酸とは何ですか?
ナトリウム3-ヒドロキシbutano酸は、CAS番号13613-65-5で登録されている化合物です。この化合物は、(3R)-3-ヒドロキシbutano酸とナトリ...
1-(二苯甲基)-4-甲基ベンゼンの物理化学的性質は何ですか?
CAS番号603-37-2の1-(二苯甲基)-4-甲基ベンゼンは、結晶性の固体で、分子量は244.28であり、水中的には微溶です。この化合物は有機反応において中...
ネアミン塩酸塩の物理化学的性質は何ですか?
ネアミン塩酸塩の分子量は321.19であり、結晶性の白色粉末です。この化合物は水に溶けやすく、pHが低くなると不溶性になります。反応活性は高く、水溶液中の酸化還...
偶氮二甲酰二哌啶の主な用途は何ですか?
偶氮二甲酰二哌啶は、医薬品、染料、高 Então 剤、触媒、溶媒、量論試薬など、様々な分野で使用されています。特に、高 Enough 反応において、グリコール酸...
掲載誌
Journal of Materials Chemistry A

Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. The journals have a strong history of publishing quality reports of interest to interdisciplinary communities and providing an efficient and rigorous service through peer review and publication. The journals are led by an international team of Editors-in-Chief and Associate Editors who are all active researchers in their fields. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C. More than one Journal of Materials Chemistry journal may be suitable for certain fields and researchers are encouraged to submit their paper to the journal that they feel best fits for their particular article. Example topic areas within the scope of Journal of Materials Chemistry A are listed below. This list is neither exhaustive nor exclusive. Artificial photosynthesis Batteries Carbon dioxide conversion Catalysis Fuel cells Gas capture/separation/storage Green/sustainable materials Hydrogen generation Hydrogen storage Photocatalysis Photovoltaics Self-cleaning materials Self-healing materials Sensors Supercapacitors Thermoelectrics Water splitting Water treatment














![(4-Methyl-1H-benzo[d]imidazol-2-yl)methanamine structure (4-Methyl-1H-benzo[d]imidazol-2-yl)methanamine structure](https://static.chemtradehub.com/structs/933/933756-31-1-7b0b.webp)