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).
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Jiang et al. (2024) studied this question.
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