2022
DOI: 10.1016/j.ensm.2021.11.015
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Hexaoxacyclooctadecane induced interfacial engineering to achieve dendrite-free Zn ion batteries

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Cited by 75 publications
(40 citation statements)
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“…Under the competition of H + buffering/Mn 2+ complexing and ion diffusion/desolvation caused by steric hindrance of groups on carboxyl, the multiple factors induced comprehensive effect makes reaction thermodynamics and kinetics stand vividly. [42] As expected, the electrolyte containing propionic ions provides the highest specific charge capacity of 513.1 mA h g −1 at 0.5 A g −1 for the first cycles (inset in Figure 6a), while it also suffers the most serious capacity decay, maintaining a poor capacity retention of ≈45% after 300 cycles (Figure 6a). The Coulombic efficiencies remain nearly 100% during the whole cycles (Figure S19, Supporting Information), which indicates that the capacity decay is not attributed to irreversible manganese dissolution/deposition but the polarization, and the lower energy efficiency also reflects the high energy barrier (Figure S20, Supporting Information).…”
Section: Resultssupporting
confidence: 69%
“…Under the competition of H + buffering/Mn 2+ complexing and ion diffusion/desolvation caused by steric hindrance of groups on carboxyl, the multiple factors induced comprehensive effect makes reaction thermodynamics and kinetics stand vividly. [42] As expected, the electrolyte containing propionic ions provides the highest specific charge capacity of 513.1 mA h g −1 at 0.5 A g −1 for the first cycles (inset in Figure 6a), while it also suffers the most serious capacity decay, maintaining a poor capacity retention of ≈45% after 300 cycles (Figure 6a). The Coulombic efficiencies remain nearly 100% during the whole cycles (Figure S19, Supporting Information), which indicates that the capacity decay is not attributed to irreversible manganese dissolution/deposition but the polarization, and the lower energy efficiency also reflects the high energy barrier (Figure S20, Supporting Information).…”
Section: Resultssupporting
confidence: 69%
“…and organic materials especially for the covalent organic frameworks (COFs). [ 13 ] Excepting that, the effectiveness of introducing additive into aqueous electrolyte system also has been widely investigated, including the organic molecules [ 14–16 ] and inorganic salts. [ 17,18 ] Generally, electrolyte additive engineering can be expected to optimize the solvation structure and lowering the nucleation barrier.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, much research attention has been devoted to aqueous zinc-ion batteries (AZIBs), not only because the intrinsic safety, but also the high theoretical capacity and low redox potential of Zn metal anodes. These advantages offered the AZIBs great molecules [14][15][16] and inorganic salts. [17,18] Generally, electrolyte additive engineering can be expected to optimize the solvation structure and lowering the nucleation barrier.…”
Section: Introductionmentioning
confidence: 99%
“…34 Among them, manipulating the electrolyte with zincophilic organic additives represents an effective and economical strategy for stabilizing Zn anodes towards practical applications. 11,35 Theoretically, these zincophilic additives could not only adjust the solvation structure to decrease the water reactivity, [36][37][38] but also preferentially adsorb on the Zn surface to inhibit water adsorption and regulate random Zn 2+ diffusion, thus smoothing the Zn deposits. [38][39][40] For these reasons, various zincophilic organic additives have been rationally designed and they improve the reversibility of Zn plating/stripping, but their effectiveness at high current density and areal capacity is still limited.…”
Section: Introductionmentioning
confidence: 99%