Aqueous rechargeable zinc-metal batteries are a promising candidate for next-generation energy storage devices due to their intrinsic high capacity, low cost, and high safety. However, uncontrollable dendrite formation is a serious problem, resulting in limited lifespan and poor coulombic efficiency of zinc-metal anodes. To address these issues, a 3D porous hollow fiber scaffold with well-dispersed TiO 2 , SiO 2 , and carbon is used as superzincophilic host materials for zinc anodes. The amorphous TiO 2 and SiO 2 allow for controllable nucleation and deposition of metal Zn inside the porous hollow fiber even at ultrahigh current densities. Furthermore, the as-fabricated interconnected conductive hollow SiO 2 and TiO 2 fiber (HSTF) possess high porosity, high conductivity, and fast ion transport. Meanwhile, the HSTF exhibits remarkable mechanical strength to sustain massive Zn loading during repeated cycles of plating/stripping. The HSTF with interconnected conductive network can build a uniform electric field, redistributing the Zn 2+ ion flux and resulting in smooth and stable Zn deposition. As a result, in symmetrical cells, the Zn@HSTF electrode delivers a long cycle life of over 2000 cycles at 20 mA cm −2 with low overpotential (≈160 mV). The excellent cycling lifespan and low polarization are also realized in Zn@HSTF//MnO 2 full cells.

MXene@Ag NW cellular composite films were successfully fabricated via a potassium ion induction and liquid nitrogen rapid pre-freezing strategy. The film delivers an ultrahigh EMI SE of 81.11 dB and a high thermal conductivity of 19.96 W m−1 K−1.

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To meet the increasing desire for a means of powering wearable and portable devices, the development of high‐performance flexible aqueous rechargeable lithium‐ion batteries (FARLIBs) would be greatly desirable. The design of binder‐free cathode materials with 3D architectures is the key to develop FARLIBs. Herein, self‐standing 3D Ni‐doped LiMn2O4 (NLMO) nanosheets are successfully prepared assembled by nanowall arrays (NWAs) directly grown on carbon cloth (CC) as the cathode for LIBs, which is performed to slow down the dissolution of Mn and the Jahn–Teller effect of LiMn2O4 during the reaction process. The as‐prepared NLMO NWAs/CC electrode delivers a high capacity of 113.27 mAh g−1 at a current density of 1 A g−1, and can also have a capacity retention rate of 81% after 500 cycles at 10 A g−1, both higher than that of pure LiMn2O4. The results of density functional theory simulation demonstrate that the Ni‐doped LiMn2O4 can significantly decrease the bandgap and Li ions diffusion barriers. A quasi‐solid‐state FARLIB is successfully constructed by using NLMO NWAs/CC as the positive electrode and rugby‐shaped NaTi2(PO4)3/CC as the negative electrode, exhibiting remarkable electrochemical performance and flexibility. These results offer a new opportunity for developing high‐performance FARLIB.