The effect of S-functionalized and vacancies on V2C MXenes as anode materials for Na-ion and Li-ion batteries
The electrochemical properties of V2C and V2CT2 (T = O, S) MXenes with and without vacancy as anode materials for Na-ion and Li-ion batteries, have been studied using first-principles calculation. The present results indicate that the adsorption strength of Li-ion and Na-ion on V2CS2 are less than t...
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| Vydané v: | Current applied physics Ročník 20; číslo 2; s. 310 - 319 |
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| Hlavní autori: | , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
Elsevier B.V
01.02.2020
한국물리학회 |
| Predmet: | |
| ISSN: | 1567-1739, 1878-1675 |
| On-line prístup: | Získať plný text |
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| Shrnutí: | The electrochemical properties of V2C and V2CT2 (T = O, S) MXenes with and without vacancy as anode materials for Na-ion and Li-ion batteries, have been studied using first-principles calculation. The present results indicate that the adsorption strength of Li-ion and Na-ion on V2CS2 are less than that of O-functionalized, together with a lower diffusion barrier. Simultaneously, V2CS2 monolayer exhibits lower open-circuit voltage (OCV) values of 0.72 and 0.49 V for Li- and Na-ion, respectively. Interestingly, the presence of atomic vanadium vacancy on V2CS2 monolayer exerts more prominent effects on enhancing adsorption strength than that of carbon vacancy for Li-ion and Na-ion, but with an exception for the diffusion of Li-ion and Na-ion on V2CS2 monolayer. The finding suggests that the V2CS2 monolayer is expected to be a potential candidate as anode material for Li-ion and Na-ion battery due to its lower open-circuit voltages and diffusion barriers.
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•The S-group decreased the adsorption ability of Li- and Na-ion on V2C than O-group.•The vacancy has no effects to Li- and Na-ion diffusion property on V2CS2 monolayer.•The S-group significantly reduces the high diffusion barrier of Na-ion.•The storage capacity of Li- and Na-ion reaches to 301.12 mAh/g for V2CS2 monolayer. |
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| ISSN: | 1567-1739 1878-1675 |
| DOI: | 10.1016/j.cap.2019.11.025 |