TY - JOUR
T1 - An MXene/CNTs@P nanohybrid with stable Ti-O-P bonds for enhanced lithium ion storage
AU - Zhang, Shixue
AU - Liu, Huan
AU - Cao, Bin
AU - Zhu, Qizhen
AU - Zhang, Peng
AU - Zhang, Xin
AU - Chen, Renjie
AU - Wu, Feng
AU - Xu, Bin
N1 - Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - Two-dimensional transition metal carbides (MXenes) have a unique structure, excellent electronic conductivity and a low Li+ diffusion barrier, and show potential for application in energy storage. Especially, MXenes can act as a conductive matrix to achieve excellent lithium storage performance. Herein, a Ti3C2Tx MXene/carbon nanotubes@red phosphorus (Ti3C2Tx/CNTs@P) nanohybrid with stable Ti-O-P bonds is fabricated. The CNTs are introduced into Ti3C2Tx to construct a conductive network, and then the Ti3C2Tx/CNTs are combined with P by a ball-milling method. In this process, the surface oxygen-containing functional groups of Ti3C2Tx interact with P, forming Ti-O-P bonds. Owing to the large capacity contribution of P, the conductive network and buffering role of Ti3C2Tx/CNTs, and the effect of the Ti-O-P bond, the Ti3C2Tx/CNTs@P nanohybrid exhibits a superior reversible capacity of 2598 mA h g-1 at 0.05C (1C = 2600 mA g-1, based on the active material P), excellent cycling stability (2078 mA h g-1 after 500 cycles) and superior rate capability (454 mA h g-1 at 30C). These results demonstrate that the Ti3C2Tx/CNTs@P nanohybrid offers fascinating potential for high-performance lithium-ion batteries.
AB - Two-dimensional transition metal carbides (MXenes) have a unique structure, excellent electronic conductivity and a low Li+ diffusion barrier, and show potential for application in energy storage. Especially, MXenes can act as a conductive matrix to achieve excellent lithium storage performance. Herein, a Ti3C2Tx MXene/carbon nanotubes@red phosphorus (Ti3C2Tx/CNTs@P) nanohybrid with stable Ti-O-P bonds is fabricated. The CNTs are introduced into Ti3C2Tx to construct a conductive network, and then the Ti3C2Tx/CNTs are combined with P by a ball-milling method. In this process, the surface oxygen-containing functional groups of Ti3C2Tx interact with P, forming Ti-O-P bonds. Owing to the large capacity contribution of P, the conductive network and buffering role of Ti3C2Tx/CNTs, and the effect of the Ti-O-P bond, the Ti3C2Tx/CNTs@P nanohybrid exhibits a superior reversible capacity of 2598 mA h g-1 at 0.05C (1C = 2600 mA g-1, based on the active material P), excellent cycling stability (2078 mA h g-1 after 500 cycles) and superior rate capability (454 mA h g-1 at 30C). These results demonstrate that the Ti3C2Tx/CNTs@P nanohybrid offers fascinating potential for high-performance lithium-ion batteries.
UR - http://www.scopus.com/inward/record.url?scp=85072912798&partnerID=8YFLogxK
U2 - 10.1039/c9ta07357d
DO - 10.1039/c9ta07357d
M3 - Article
AN - SCOPUS:85072912798
SN - 2050-7488
VL - 7
SP - 21766
EP - 21773
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 38
ER -