Covalent organic framework-based ultrathin crystalline porous film: manipulating uniformity of fluoride distribution for stabilizing lithium metal anode. Issue 6 (29th January 2020)
- Record Type:
- Journal Article
- Title:
- Covalent organic framework-based ultrathin crystalline porous film: manipulating uniformity of fluoride distribution for stabilizing lithium metal anode. Issue 6 (29th January 2020)
- Main Title:
- Covalent organic framework-based ultrathin crystalline porous film: manipulating uniformity of fluoride distribution for stabilizing lithium metal anode
- Authors:
- Zhao, Zedong
Chen, Wuji
Impeng, Sarawoot
Li, Mengxiong
Wang, Rong
Liu, Yicheng
Zhang, Long
Dong, Lei
Unruangsri, Junjuda
Peng, Chengxin
Wang, Changchun
Namuangruk, Supawadee
Lee, Sang-Young
Wang, Yonggang
Lu, Hongbin
Guo, Jia - Abstract:
- Abstract : In situ formed LiF grains are confined and evenly distributed throughout a covalent organic framework (COF) film, which exhibits cooperative effectiveness to greatly stabilize the lithium metal. Abstract : Lithium metal is regarded as the "Holy Grail" for rechargeable batteries yet it still suffers from low coulombic efficiency caused by its high reactivity toward the electrolyte. The so-formed solid-electrolyte interphases (SEIs) are ununiform and sluggish-ion-conducting further inducing severe dendrite growth. Herein, we report the in situ LiF-embedded covalent organic framework (COF) as a novel artificial lithium/electrolyte interphase. Briefly, an electrochemically active COF ultrathin film is synthesized by interfacial aldimine condensation, in which lithiophilic moieties reside in the high-surface-area COF film and can locally concentrate Li-salts from a dilute electrolyte. This promotes the electrochemical in situ formation of anion-derived LiF-rich SEI during the first cycling. Owing to the coaxially orientated microporous channels displayed in the COF, the as-formed LiF grains are confined in the micropores and evenly distributed throughout the COF matrix, thereby enhancing the mechanical strength of the SEI against dendrite growth as well as retaining flexibility to tolerate the anode volume change over cycling. Also, the Li + diffusion pathway is highly ordered along the 1D pore walls of the COF so as to spatially homogenize Li + flux. Therefore, theAbstract : In situ formed LiF grains are confined and evenly distributed throughout a covalent organic framework (COF) film, which exhibits cooperative effectiveness to greatly stabilize the lithium metal. Abstract : Lithium metal is regarded as the "Holy Grail" for rechargeable batteries yet it still suffers from low coulombic efficiency caused by its high reactivity toward the electrolyte. The so-formed solid-electrolyte interphases (SEIs) are ununiform and sluggish-ion-conducting further inducing severe dendrite growth. Herein, we report the in situ LiF-embedded covalent organic framework (COF) as a novel artificial lithium/electrolyte interphase. Briefly, an electrochemically active COF ultrathin film is synthesized by interfacial aldimine condensation, in which lithiophilic moieties reside in the high-surface-area COF film and can locally concentrate Li-salts from a dilute electrolyte. This promotes the electrochemical in situ formation of anion-derived LiF-rich SEI during the first cycling. Owing to the coaxially orientated microporous channels displayed in the COF, the as-formed LiF grains are confined in the micropores and evenly distributed throughout the COF matrix, thereby enhancing the mechanical strength of the SEI against dendrite growth as well as retaining flexibility to tolerate the anode volume change over cycling. Also, the Li + diffusion pathway is highly ordered along the 1D pore walls of the COF so as to spatially homogenize Li + flux. Therefore, the LiF-embedded COF interphase exhibits cooperative effectiveness to greatly stabilize the lithium metal anode. The full cell maintains its excellent performances with stable cycling and high efficiency in the close-to-practice conditions. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 8:Issue 6(2020)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 8:Issue 6(2020)
- Issue Display:
- Volume 8, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 6
- Issue Sort Value:
- 2020-0008-0006-0000
- Page Start:
- 3459
- Page End:
- 3467
- Publication Date:
- 2020-01-29
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ta13384d ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
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- 14579.xml