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Selection and optimization of carbon-based electrode materials for flow-electrode capacitive deionization

电容去离子 材料科学 电极 碳纳米管 化学工程 海水淡化 石墨烯 碳纤维 介电谱 纳米技术 扫描电子显微镜 复合材料 化学 电化学 复合数 生物化学 物理化学 工程类
作者
Wanni Zhang,Wenchao Xue,Kang Xiao,Chettiyappan Visvanathan,Jialing Tang,Lu Li
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:315: 123649-123649 被引量:10
标识
DOI:10.1016/j.seppur.2023.123649
摘要

Flow-electrode capacitive deionization (FCDI) is an emerging desalination technology for its high desalination efficiency and continuous operation. This study systematically investigated the feasibility of various representative carbon-based materials and their combinations as the flow-electrode with the primary focus on their desalination efficiency and energy efficiency in FCDI. Among individual carbon-based electrode materials, namely activated carbon (AC), carbon fiber (CF), carbon black (CB), multi-walled carbon nanotubes (MWCNTs), and graphene nanoplatelets (GNPs), the nano-scale materials obviously outperformed micron-scale materials. Whereas, the combinations of AC + MWCNTs/GNPs provided superior desalination performance than AC + CB while working as blended flow-electrodes in FCDIs due to the different spatial configurations of three nano-scale particles. Furthermore, CB was tested as the base material in combination with MWCNTs and GNPs respectively. Approximately 110–130% increments in maximum salt adsorption rate were obtained for both blended electrodes compared to individual CB electrodes. The highest SARmax of 1.59 ± 0.02 μg cm−2 s−1 was observed in FCDI driven by the CB + GNPs electrode at a content of 1.5/0.5 wt%. Supported by the results of field emission scanning electron microscopy (FESEM) and electrical impedance spectroscopy (EIS), the 2D spatial morphologies of GNPs were able to build similar but more stable “bridges” between base electrode particles (i.e., AC or CB) as CNTs. Its sheet-like structure avoided agglomeration problems and largely promoted the conductivity of the product flow-electrodes.
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