One-dimensional nanomaterials can offer large surface area, facile strain relaxation upon cycling and efficient electron transport pathway to achieve high electrochemical performance. Hence, nanowires have attracted increasing interest in energy related fields. We designed the single nanowire electrochemical device for in situ probing the direct relationship between electrical transport, structure, and electrochemical properties of the single nanowire electrode to understand intrinsic reason of capacity fading. The results show that during the electrochemical reaction, conductivity of the nanowire electrode decreased, which limits the cycle life of the devices. We have developed a facile and high-yield strategy for the oriented formation of CNTs from metal−organic frameworks (MOFs). The appropriate graphitic N doping and the confined metal nanoparticles in CNTs both increase the densities of states near the Fermi level and reduce the work function, hence efficiently enhancing its oxygen reduction activity. Then, we fabricated a field-tuned hydrogen evolution reaction (HER) device with an individual MoS₂ nanosheet to explore the impact of field effect on catalysis. In addition, we demonstrated the critical role of structural H₂O on Zn²⁺ intercalation into bilayer V₂O₅·nH₂O. The results suggest that the H₂O-solvated Zn²⁺ possesses largely reduced effective charge and thus reduced electrostatic interactions with the V₂O₅ framework, effectively promoting its diffusion. We also identified the exciting electrochemical properties (including high electric conductivity, small volume change and self-preserving effect) and superior sodium storage performance of alkaline earth metal vanadates through preparing CaV₄O₉ nanowires. Our work presented here can inspire new thought in constructing novel one-dimensional structures and accelerate the development of energy storage applications.

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