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Controllable three-dimensional villose titanium dioxide architectures grown on carbon textiles are fabricated by a facile one-step in-situ hydrothermal method at low temperatures. It has in fact been proven to be an effective method to reduce self-aggregation and promote lithium-ion intercalate/extract via building 3D architectures based on 2D conductive materials. More importantly, the freestanding electrodes without any addition of conductive agents and polymeric binders reveal significant improvement in high-rate capacity and cycling performance.

This study demonstrates a robust and ultra-stable sodium infiltrated Fe2O3 coated carbon textile (SFCT) anode with excellent machinability. The obtained SFCT anode overcomes the disadvantage of Na electrodes, which is not easily processable, and exhibits more flat voltage profiles, lower stripping/plating overpotential, and better cycling stability in an additive-free carbonate-based electrolyte compared with bare Na electrodes.

We have demonstrate a facile strategy to achieve the controllable morphology transformation of TiO2 induced by the introduction of multi-walled carbon nanotubes. The intervention of functionalized carbon nanotubes (CNTs) is key to the formation of TiO2 nanopompons. Furthermore, the size of the obtained TiO2 nanopompons can be controlled by modulating the CNT amounts. The obtained TiO2 nanopompon-embedded CNT hybrid networks (TNP@CNT HNs) incorporate the advantages of hierarchical nanostructures and 3D interconnected conductive networks, including high surface area, uniform particle/pore size, short Li+ ion/electron transport pathway, and high electronic conductivity. These TNP@CNT HN-based anodes achieve a significant improvement in the insertion/extraction of Li+ ions and electrochemical performances via optimizing the CNT amounts and the size of the TiO2 nanopompons. The lithium-ion batteries based on the optimized TNP@CNT HNs exhibit excellent cycling stability (keeping approximately 200 mA h g−1 after 500 cycles at 2C rate, 1C = 170 mA g−1) and rate performance (approximately 125 mA h g−1 at 20C rate with a capacity retention of 77% after 2000 cycles).

The direct utilization of metallic lithium and sodium as the anodes for rechargeable batteries would be highly advantageous, which has been considered as one of the most promising choices for next-generation high-energy-density storage devices. Although the induced safety concerns, inferior rate, and cycling performance severely hinder the commercialization of lithium metal batteries (LMBs) and sodium metal batteries (SMBs), the recent development of nanotechnology-based solutions really revives the lithium/sodium metal anodes for high-energy batteries. In this work, an ultrastable carbon textile (CT)-based host with excellent infiltration for both metallic Li and Na has been designed and exhibits more flat voltage profiles, lower stripping/plating overpotential, and better cycling stability both in symmetric cell and full cell configurations, even in additive-free carbonate-based electrolyte compared with pure Li/Na electrodes. The highly conductive and mechanically robust three-dimensional CTs not only offer a stable scaffold against hyperactive lithium and sodium but also enable uniform nucleation and growth during stripping/plating process, which effectively suppress the dendrite growth and stabilize the electrode dimension. This facile strategy provides new insights into the design of stable hosts with prestored alkali metal to address the multifaceted issues in LMBs and SMBs simultaneously.