TY - JOUR
T1 - In Situ Constructed NiFe-LDH@Ti3C2Tx with a Three-Dimensional Network Structure
T2 - Enhanced Li+/Na+ Storage via an Oxygen Bridge
AU - Jiang, Wei
AU - Li, Qian
AU - Xiao, Jian
AU - Ren, Jian
AU - Yang, Kai
AU - Xu, Yan
AU - Huang, Yiling
AU - Zhu, Xiaoxue
AU - Pan, Limei
AU - Yang, Jian
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/7/4
Y1 - 2024/7/4
N2 - In this work, we employed a one-step hydrothermal method, assisted by PVP and LAA additives, to synthesize NiFe-LDH@Ti3C2Tx in situ with a three-dimensional network structure. The crumpled NiFe-LDH nanoflakes were anchored on the Ti3C2Tx surface in close face-to-face contact by heterogeneous nucleation and growth with oxygen-containing functional groups as active sites. More importantly, an oxygen bridge was simultaneously formed at the interface between NiFe-LDH and Ti3C2Tx, which, as an electron migration channel to form a connected conductive network, significantly enhanced the structural stability and electron migration rate. Meanwhile, the open 3D network (SBET: 125.6 m2 g-1) facilitates the exposure of active sites and accelerates the ion migration rate, leading to excellent diffusion kinetics. As a consequence, NiFe-LDH@Ti3C2Tx demonstrates outstanding electrochemical stability as an anode for LIBs (987 mAh g-1 at 0.5 A g-1 up to 200 cycles and 912 mAh g-1 at 1 A g-1 up to 600 cycles) and SIBs (280 mAh g-1 at 0.5 A g-1 up to 200 cycles and 211 mAh g-1 at 1 A g-1 up to 2000 cycles).
AB - In this work, we employed a one-step hydrothermal method, assisted by PVP and LAA additives, to synthesize NiFe-LDH@Ti3C2Tx in situ with a three-dimensional network structure. The crumpled NiFe-LDH nanoflakes were anchored on the Ti3C2Tx surface in close face-to-face contact by heterogeneous nucleation and growth with oxygen-containing functional groups as active sites. More importantly, an oxygen bridge was simultaneously formed at the interface between NiFe-LDH and Ti3C2Tx, which, as an electron migration channel to form a connected conductive network, significantly enhanced the structural stability and electron migration rate. Meanwhile, the open 3D network (SBET: 125.6 m2 g-1) facilitates the exposure of active sites and accelerates the ion migration rate, leading to excellent diffusion kinetics. As a consequence, NiFe-LDH@Ti3C2Tx demonstrates outstanding electrochemical stability as an anode for LIBs (987 mAh g-1 at 0.5 A g-1 up to 200 cycles and 912 mAh g-1 at 1 A g-1 up to 600 cycles) and SIBs (280 mAh g-1 at 0.5 A g-1 up to 200 cycles and 211 mAh g-1 at 1 A g-1 up to 2000 cycles).
UR - http://www.scopus.com/inward/record.url?scp=85196533727&partnerID=8YFLogxK
U2 - 10.1021/acs.energyfuels.4c01437
DO - 10.1021/acs.energyfuels.4c01437
M3 - 文章
AN - SCOPUS:85196533727
SN - 0887-0624
VL - 38
SP - 12129
EP - 12139
JO - Energy and Fuels
JF - Energy and Fuels
IS - 13
ER -