Roll-to-roll fabrication of organic nanorod electrodes for sodium ion batteries
نویسندگان
چکیده
0.1016/j.nanoen.2 lsevier Ltd. All rig thor. [email protected] Abstract Organic electroactive materials derived from biomasses are promising candidates for next generation rechargeable batteries due to the low cost, sustainability and environmental benignity. Since organic materials have very low electronic conductivity, they are normally synthesized into nano-scale and mixed with conductive carbon before electrode fabrication. Herein, we first reported a unique role-to-role fabrication technology by taking advantage of the high solubility of organic materials in water. The synthetic process of nano-size organic materials is merged into the organic electrode fabrication process. 2,5-Dihydroxy-1,4-benzoquinone disodium salt (DHBQDS) is used as a model, and the DHBQDS nanorod electrode is in situ formed by precipitating DHBQDS nanorods from DHBQDS–sodium alginate–carbon black aqueous slurry film on a Cu current collector during electrode drying process. Due to the fast ionic and electronic conductivity of DHBQDS– carbon nanocomposite, the DHBQDS nanorod electrodes deliver a reversible capacity of 167 mA h g 1 at a high current density of 200 mA g 1 after 300 cycles, which is 87% of its initial capacity (capacity decay rate of 0.051% per cycle). To reduce the dissolution of DHBQDS in the electrolyte upon cycling, a thin layer of Al2O3 with thickness of 1 nm or 2 nm is coated on the DHBQDS nanorod electrodes using atomic layer deposition (ALD). The Al2O3 coating remarkably suppresses the dissolution of DHBQDS nanorods as evidenced by the increased Coulombic efficiency from 94% to 100% at a low current density of 50 mA g . The reversible capacity of Al2O3 coated DHBQDS nanorod electrodes remains at 212 mA h g 1 after 300 cycles with a very low capacity decay rate of 0.049% per cycle. The ALD enhanced organic nanorods exhibit the best reversible capacity and cycle life among the organic electrodes reported for Na-ion batteries. & 2015 Elsevier Ltd. All rights reserved.
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