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Graphical abstract In situ-growth of 1T/2H-MoS 2 nanosheets on the CFC, ultra-small SnS 2 nanoparticles are anchored on the surface of MoS 2 nanosheets unifromly. When the SnS 2 /MoS 2 /CFC composites applied as a binder-free flexible anode, it exhibits excellent performances. A highly flexible full cell was fabricated, demonstrating remarkable flexibility and cycling stability. Highlights • In-situ growth SnS 2 /MoS 2 on CFC by a hydrothermal method and water bath process. • SnS 2 /MoS 2 shows a capacity of 1294 mA h g−1 at 0.1 A g−1 after 120 cycles. • The distribution of SnS 2 on 1T/2H-MoS 2 can enhance electrochemical properties. • A full cell is fabricated, showing high flexibility and electrochemical properties. Abstract Flexible lithium ion batteries are important for wearable electronic devices. Herein, 1T/2H phase MoS 2 nanosheets are grown on carbon fiber cloth, and the ultra-small SnS 2 nanoparticles are anchored in the surface of MoS 2 nanosheets uniformly. We fabricate the hierarchical nanostructures via a hydrothermal method then water bath process. During in-situ growth of 1T/2H phase MoS 2 , urea is used as the surfactant and NH4+ (produced by urea and ammonium molybdate tetrahydrate) is acted as insertion guest ions to stabilize 1T phase MoS 2. The synergistic effects between MoS 2 nanosheets and SnS 2 nanoparticles can improve structural stability of the electrode and significant enhance the transport of Li ions and electrons, thereby ameliorate the electrochemical properties. When applied as a binder-free, flexible Li-ion battery anode, it exhibits admirable cycling stability and excellent rate performance. Due to the presence of 1T phase MoS 2 and uniform distribution of ultra-small SnS 2 nanoparticles on MoS 2 nanosheets, the SnS 2 /MoS 2 /carbon fiber cloth composites maintain 1294 mA h g−1 when cycling at 100 mA g−1 after 120 cycles. A highly flexible battery based on SnS 2 /MoS 2 /carbon fiber cloth and LiCoO 2 is fabricated, demonstrating excellent mechanical flexibility and cycling stability. [ABSTRACT FROM AUTHOR]

[Display omitted] • Lamellar-structured CNT/MXene/SnO 2 host based on lithiophilic gradient is prepared. • Li deposition is guided in a bottom-up manner to inhibit dendrite growth. • The host accommodates metallic Li up to 8 mAh cm−2 with 4.6% volume expansion. • The anodes can be cycled at 40 mA cm−2 (symmetric cell) and 10C (full cell). Lithium (Li) metal batteries have attracted much attention due to extremely high energy density. However, safety concerns and limited lifetime associated with dendrite growth of Li anodes, especially at high capacity loadings and high rates, hamper their practical application. Here, we report the construction of lamellar-structured lithium host containing carbon nanotubes (CNTs), MXene nanosheets, and SnO 2 nanoparticles via a simple step-by-step vacuum filtration method. The architecture is based on the lithiophilic gradient of each component, in which highly-lithiophilic SnO 2 nanoparticles uniformly anchor on the lithiophilic MXene current collector, and lithiophobic CNTs act as the top protective layer. In this way, Li electrodeposition is spatially guided in a bottom-up mode free from dendrite growth. Consequently, the CNT/MXene/SnO 2 scaffold accommodates a high capacity loading of 8 mAh cm−2 with only 4.6 % volume expansion. Furthermore, the Li@CNT/MXene/SnO 2 electrode achieves fast-charging capability and long-term cycling stability in both symmetric cells (40 mA cm−2) and full cells (10C). This work demonstrates an efficient approach to construct dendrite-free anodes for durable and high-power lithium metal batteries. [ABSTRACT FROM AUTHOR]