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A binary A(x)B(1-x) ionic alkaline pseudocapacitor system involving manganese, iron, cobalt, and nickel: formation of electroactive colloids via in situ electric field assisted coprecipitation

机译:一个二进制B (x) (1 - x)离子碱性pseudocapacitor系统包括锰、铁、钴、和镍:电活性通过胶体的形成原位电场辅助共同沉淀

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摘要

A new "combinatorial transition-metal cation pseudocapacitor" was demonstrated by designing combinatorial transition-metal cation pseudocapacitors with binary A(x)B(1-x) salt electrodes involving manganese, iron, cobalt, and nickel cations in an alkaline aqueous electrolyte. Binary multi-valence cations were crystallized in the colloidal state through an in situ coprecipitation under an electric field. These electroactive colloids absorbed by carbon black and the PVDF matrix are highly redox-reactive with high specific capacitance values, where the specific electrode configuration can create short ion diffusion paths to enable fast and reversible Faradaic reactions. This work shows huge promise for developing high-performance electrical energy storage systems via designing the colloidal state of electroactive cations. Multiple redox cations in the colloidal state can show high redox activities, making them more suitable for potential application in pseudocapacitor systems.
机译:一个新的“组合过渡金属阳离子pseudocapacitor”被设计了组合过渡金属阳离子与二进制pseudocapacitors B (x) (1 - x)盐电极包括锰、铁、钴、和镍离子在碱性水溶液电解液。通过在结晶的胶体状态现场共同沉淀在电场中。这些电活性胶体吸收碳黑色和PVDF矩阵是高度redox-reactive高的比电容值,具体的电极配置可以创建短的离子扩散使快速、可逆的感应电流的路径反应。开发高性能的电能通过设计胶体状态存储系统电活性阳离子。在胶态可以显示高氧化还原活动,使它们更适合pseudocapacitor系统的潜在应用。

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