2022
DOI: 10.1016/j.nanoen.2022.107470
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In situ construction of Li3N-enriched interface enabling ultra-stable solid-state LiNi0.8Co0.1Mn0.1O2/lithium metal batteries

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Cited by 58 publications
(49 citation statements)
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“…Chen et al proposed a CSE with high ionic conductivity and low activation energy by using g-C 3 N 4 nanosheets reinforced with PVDF (Figure 3b). 44 The SEI with rich Li 3 N is in situ produced by g-C 3 N 4 reacting with Li during cycling, which significantly inhibits continuous side reactions and provides a fast lithium-ion transport channel. Moreover, to improve the interfacial compatibility and obtain rapid ions transport, Pan et al prepared a flexible ceramic/ polymer CSE via in situ coupling reactions (Figure 3c).…”
Section: Anode/se Interface Stabilitymentioning
confidence: 99%
“…Chen et al proposed a CSE with high ionic conductivity and low activation energy by using g-C 3 N 4 nanosheets reinforced with PVDF (Figure 3b). 44 The SEI with rich Li 3 N is in situ produced by g-C 3 N 4 reacting with Li during cycling, which significantly inhibits continuous side reactions and provides a fast lithium-ion transport channel. Moreover, to improve the interfacial compatibility and obtain rapid ions transport, Pan et al prepared a flexible ceramic/ polymer CSE via in situ coupling reactions (Figure 3c).…”
Section: Anode/se Interface Stabilitymentioning
confidence: 99%
“…, offer stable solid-electrolyte interfaces and improve the NCM811-based SSB performance. 226–229 Li et al have synthesized trifluoroethyl methacrylate (PTFEMA)–PEO by electropolymerization. 229 The PTFEMA layer modified the NCM811-electrolyte interface and plays the following roles: (i) offers undisrupted transport of Li + across the interface, (ii) mitigates the electrolyte oxidation at high voltage, (iii) prevents the microcrack formation and (iv) buffers the stress, generated by volume change in NCM811 particles during charge–discharge cycling.…”
Section: Ni-rich Ncms For Solid-state Libsmentioning
confidence: 99%
“…Various modied polymer electrolytes, such as g-C 3 N 4 nanosheet (GCN) reinforced poly(vinylidene uoride) (PVDF-GCN), poly(vinylidene-cotriuoroethylene) [P(VDF-TrFE)], decabromodiphenyl ethane (DBDPE) added poly(ethylene oxide) (PEO), triuoroethyl methacrylate (TFEMA)-PEO, etc., offer stable solid-electrolyte interfaces and improve the NCM811-based SSB performance. [226][227][228][229] Li et al have synthesized triuoroethyl methacrylate (PTFEMA)-PEO by electropolymerization. 229 The PTFEMA layer modied the NCM811-electrolyte interface and plays the following roles: (i) offers undisrupted transport of Li + across the interface, (ii) mitigates the electrolyte oxidation at high voltage, (iii) prevents the microcrack formation and (iv) buffers the stress, generated by volume change in NCM811 particles during charge-discharge cycling.…”
Section: Selection Of a Suitable Modification Strategymentioning
confidence: 99%
“…Great efforts focusing on the enhancement of interfacial compatibility and ionic conductivity have been made. It was reported that employing electrolyte additives [25][26][27] , adjusting the type of Li salts and solvent [28][29][30] , regulating the solvent content 17 and anchoring the solvent with llers 21 can suppress the side reactions effectively. Most recently, Xu et al reported that the PVDF-based electrolytes possess local high concentrated (LHC) structure, in which the high concentrated solution formed by Lithium bis(tri uoromethanesulfonyl) (LiTFSI) and dimethyl sulfoxide (DMSO) solvent is embedded inside the polymer spherulites, and the LHC structure of the PVDF electrolyte can mitigate the interfacial side reactions compared with the high concentrated solution due to the interactions between solvent and PVDF polymer 31 .…”
Section: Introductionmentioning
confidence: 99%