4.7 Article

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

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 315, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2023.123649

Keywords

Flow-electrode capacitive deionization; Carbon-based electrode; Graphene nanoplatelets; Nanotube; Salt adsorption rate

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Flow-electrode capacitive deionization (FCDI) is an emerging desalination technology that offers high desalination efficiency and continuous operation. This study investigated the feasibility of different carbon-based materials as flow-electrodes in FCDI, focusing on their desalination efficiency and energy efficiency. The nano-scale materials, such as multi-walled carbon nanotubes (MWCNTs) and graphene nanoplatelets (GNPs), outperformed the micron-scale materials. Combinations of activated carbon (AC) with MWCNTs or GNPs showed superior desalination performance compared to combinations with carbon black (CB). The use of GNPs as a flow-electrode improved stability, conductivity, and salt adsorption rate in FCDI.
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 mu g 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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