TY - JOUR
T1 - Nitrogen and sulfur co-doped vanadium carbide MXene for highly reversible lithium-ion storage
AU - Zhang, Yajuan
AU - Li, Jinliang
AU - Gong, Zhiwei
AU - Xie, Junpeng
AU - Lu, Ting
AU - Pan, Likun
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/4
Y1 - 2021/4
N2 - As an emerging group of two-dimensional (2D) layered material, MXenes have received significant attention in the direction of energy storage. However, the restacking of MXene flakes severely hinders the ion transport within electrodes, which limits their application for lithium-ion batteries (LIBs). To address this issue, herein, we rationally designed and optimized the structure of N, S co-doped V2CTx MXene, which exhibits excellent electrochemical performance with a high reversible capacity of 590 mAh g−1 after 100 cycles at 0.1 A g−1 when used as anode of LIBs. Even at a high current density of 2 A g−1, a reversible capacity of 298 mAh g−1 is obtained after 300 cycles, which outperforms most of the V2CTx-based anode materials reported so far. The lithium-ion storage mechanism of N, S co-doped V2CTx MXene was studied by a series of characterizations. The results show that the significant improvement of electrochemical performance should be attributed to the facilitated charge transfer after N and S co-doping in V2CTx MXene, which can effectively improve the ion transfer kinetics during the lithiation-delithiation process. Furthermore, the expanded interlayer spacing of N, S co-doped V2CTx provides more active sites for the adsorption of lithium ions, promoting the insertion capacity of lithium ions. This work indicates that the N, S co-doped 2D V2CTx MXene should be a promising anode material for high-performance LIBs.
AB - As an emerging group of two-dimensional (2D) layered material, MXenes have received significant attention in the direction of energy storage. However, the restacking of MXene flakes severely hinders the ion transport within electrodes, which limits their application for lithium-ion batteries (LIBs). To address this issue, herein, we rationally designed and optimized the structure of N, S co-doped V2CTx MXene, which exhibits excellent electrochemical performance with a high reversible capacity of 590 mAh g−1 after 100 cycles at 0.1 A g−1 when used as anode of LIBs. Even at a high current density of 2 A g−1, a reversible capacity of 298 mAh g−1 is obtained after 300 cycles, which outperforms most of the V2CTx-based anode materials reported so far. The lithium-ion storage mechanism of N, S co-doped V2CTx MXene was studied by a series of characterizations. The results show that the significant improvement of electrochemical performance should be attributed to the facilitated charge transfer after N and S co-doping in V2CTx MXene, which can effectively improve the ion transfer kinetics during the lithiation-delithiation process. Furthermore, the expanded interlayer spacing of N, S co-doped V2CTx provides more active sites for the adsorption of lithium ions, promoting the insertion capacity of lithium ions. This work indicates that the N, S co-doped 2D V2CTx MXene should be a promising anode material for high-performance LIBs.
KW - Lithium storage mechanism
KW - Lithium-ion batteries
KW - N, S co-doping
KW - VCT MXene
UR - https://www.scopus.com/pages/publications/85098711866
U2 - 10.1016/j.jcis.2020.12.044
DO - 10.1016/j.jcis.2020.12.044
M3 - 文章
C2 - 33387843
AN - SCOPUS:85098711866
SN - 0021-9797
VL - 587
SP - 489
EP - 498
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -