Multi‐wall Sn/SnO2@carbon hollow nanofibers evolved from SnO2 nanofibers are designed and programable synthesized by electrospinning, polypyrrole coating, and annealing reduction. The synthesized hollow nanofibers have a special wire‐in‐double‐wall‐tube structure with larger specific surface area and abundant inner spaces, which can provide effective contacting area of electrolyte with electrode materials and more active sites for redox reaction. It shows excellent cycling stability by virtue of effectively alleviating pulverization of tin‐based electrode materials caused by volume expansion. Even after 2000 cycles, the wire‐in‐double‐wall‐tube Sn/SnO2@carbon nanofibers exhibit a high specific capacity of 986.3 mAh g−1 (1 A g−1) and still maintains 508.2 mAh g−1 at high current density of 5 A g−1. This outstanding electrochemical performance suggests the multi‐wall Sn/SnO2@ carbon hollow nanofibers are great promising for high performance energy storage systems.

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Precisely regulating water and molecule permeation through membranes is of crucial significance in broad domains such as water filtration and smart reactors. Comparing with routine stiff membranes, stimuli‐response polymers endow porous membranes with various gating properties, but most of these membranes have only one‐way gating performance, that is, either positive or negative. Here poly(N‐isopropylacrylamide) (PNIPAM) grafted graphene oxide (GO) membranes with reversible positive/negative gating regularity are constructed by simply tuning the molecule grafting density. The water and small molecule permeance of the membranes can be regulated by adjusting environment temperature. Based on this tunable thermoresponsive gating regularity, a bidirectional fluidic controlling system is designed by integrating a positive membrane and a negative membrane, which can be employed as a self‐adaptive gating reactor. This strategy provides an insight into constructing smart gating membranes with extraordinary properties, showing promising applications in micro/nanofluidic valves and temperature sensitive biochemical reactors.

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One-dimensional (1D) hollow nanomaterials were widely used in the catalysis field. However, the inner surfaces of 1D hollow nanostructures could not be effectively utilized in liquid reaction because of diffusional limitation caused by the large ratio of length to diameter. In this work, a template-assisted coaxial electrospinning method was developed to prepare TiO2 hollow nanofibers with through-holes which were further employed as a carrier for Au nanoparticles. The Au/TiO2 hollow nanofibers with through-holes showed significant catalytic activity enhancement to the reduction of 4-nitrophenol in aqueous solution compared with solid and hollow nanofiber counterparts. The through-holes which provided unrestricted macropores for mass transfer in liquid solution were studied to be accounted for the catalytic activity enhancement. The through-hole structures can widen the application ranges and increase the efficiencies of zero-dimensional or 1D hollow nanomaterials.