Removing Fluoride-Terminations from Multilayered V2CTX MXene by Gas Hydrolyzation

被引:10
|
作者
Fagerli, Frode Hadegreesskjold [1 ]
Wang, Zhaohui [1 ,2 ]
Grande, Tor [1 ]
Kaland, Henning [1 ]
Selbach, Sverre M. [1 ]
Wagner, Nils Peter [1 ,2 ]
Wiik, Kjell [1 ]
机构
[1] NTNU Norwegian Univ Sci & Technol, Dept Mat Sci & Engn, NO-7034 Trondheim, Norway
[2] SINTEF Ind, NO-7034 Trondheim, Norway
来源
ACS OMEGA | 2022年
关键词
TOTAL-ENERGY CALCULATIONS; LI ION BATTERIES; ELECTRONIC-PROPERTIES; SURFACE TERMINATIONS; TI3C2; STORAGE; OXIDATION; ANODE; CAPACITY; METALS;
D O I
10.1021/acsomega.2c02441
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two-dimensional MXenes have shown great promise for many different applications, but in order to fully utilize their potential, control of their termination groups is essential. Here we demonstrate hydrolyzation with a continuous gas flow as a method to remove F-terminations from multilayered V2CTx particles, in order to prepare nearly F-free and partly bare vanadium carbide MXene. Density functional theory calculations demonstrate that the substitution of F-terminations is thermodynamically feasible and presents partly nonterminated V2CO as the dominating hydrolyzation product. Hydrolyzation at elevated temperatures reduced the F content but only subtly changed the O content, as inferred from spectroscopic data. The ideal hydrolyzation temperature was found to be 300 degrees C, as a degradation of the V2CTx phase and a transition to vanadium oxycarbides and V2O3 were observed at higher temperature. When tested as electrodes in Li-ion batteries, the hydrolyzed MXene demonstrated a reduced polarization compared with the pristine MXene, but no change in intercalation voltage was observed. Annealing in dry Ar did not result in the same F reduction, and the importance of water vapor was concluded, demonstrating hydrolyzation as a new and efficient method to control the surface terminations of multilayered V2CTx post etching. These results also provide new insights on the thermal stability of V2CTx MXene in hydrated atmospheres.
引用
收藏
页码:23790 / 23799
页数:10
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