Conductive and flexible CuS films with unique hierarchical nanocrystalline branches directly grown on three-dimensional (3D) porous Cu foam were fabricated using an easy and facile solution processing method without a binder and conductive agent for the first time. The synthesis procedure is quick and does not require complex routes. The structure and morphology of the as-deposited CuS/Cu films were characterized by X-ray diffraction and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy and transmission electron spectroscopy, respectively. Pure crystalline hexagonal structured CuS without impurities were obtained for the most saturated S solution. Electrochemical testing of CuS/Cu foam electrodes showed a reasonable capacity of 450 mAhg−1 at 0.1 C and excellent cyclability, which might be attributed to the unique 3D structure of the current collector and hierarchical nanocrystalline branches that provide fast diffusion and a large surface area.
New porous activated carbons with a high surface area as an anode material for lithium-ion batteries (LIBs) were synthesized by a one-step, sustainable, and environmentally friendly method. Four chemical activators—H2SO4, H3PO4, KOH, and ZnCl2—have been investigated as facilitators of the formation of the porous structure of activated carbon (AC) from an agar precursor. The study of the materials by Brunauer–Emmett–Teller (BET) and scanning electron microscopy (SEM) methods revealed its highly porous meso- and macro-structure. Among the used chemical activators, the AC prepared with the addition of KOH demonstrated the best electrochemical performance upon its reaction with lithium metal. The initial discharge capacity reached 931 mAh g−1 and a reversible capacity of 320 mAh g−1 was maintained over 100 cycles at 0.1 C. High rate cycling tests up to 10 C demonstrated stable cycling performance of the AC from agar.
The three-dimensional (3D) structure of batteries nowadays obtains a lot of attention because it provides the electrodes a vast surface area to accommodate and employ more active material, resulting in a notable increase in areal capacity. However, the integration of polymer electrolytes to complicated three-dimensional structures without defects is appealing. This paper presents the creation of a flawless conformal coating for a distinctive 3D-structured NiO/Ni anode using a simple thermal oxidation technique and a polymer electrolyte consisting of three layers of PAN-(PAN-PVA)-PVA with the addition of Al2O3 nanoparticles as nanofillers. Such a composition with a unique combination of polymers demonstrated superior electrode performance. PAN in the polymer matrix provides mechanical stability and corrosion resistance, while PVA contributes to excellent ionic conductivity. As a result, NiO/Ni@PAN-(PAN-PVA)-PVA with 0.5 wt% Al2O3 NPs configuration demonstrated enhanced cycling stability and superior electrochemical performance, reaching 546 mAh g−1 at a 0.1 C rate.
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