沉淀
电极
混合(物理)
碳纤维
粒子(生态学)
电荷(物理)
流量(数学)
机械
万有引力
化学物理
环境科学
化学
化学工程
材料科学
物理
环境工程
经典力学
地质学
海洋学
复合材料
工程类
量子力学
物理化学
复合数
作者
Soumyadeep Paul,Yousif M. Alkhulaifi,Tomek Jaroslawski,Steven A. Hawks,Juan G. Santiago
标识
DOI:10.1021/acs.est.4c13987
摘要
Flowable carbon slurries are actively studied and under development for charge transport in various electrochemical systems including flow capacitors, capacitive deionization cells, semi-solid flow batteries, and lithium extraction. However, much less is known about in operando slurry flow dynamics and their corresponding effect on charge transport. We performed an experimental study of mixing and settling dynamics of slurry electrodes within an electrochemical flow cell during continuous operations. The electrochemical cell consisted of two horizontal co-flowing channels, separated by a cation-exchange membrane (CEM). We used high-speed optical imaging of planes parallel to gravity and simultaneous electrochemical measurements. At low flow rates, dense yet dynamic particle beds formed on the bottom electrode in each channel, which unexpectedly yielded the highest currents. This approach enables the operation of the flow cell at low system-average particle concentrations while leveraging gravity-driven particle settling to locally enhance carbon concentrations precisely at the current collector sites. Conversely, high flow rates were characterized by thin particle beds and well-mixed particle flows. In the latter case, the electrodes in closest proximity (located on either side of the CEM) achieved a current higher than the other electrode pairs. The observations have implications for slurry control and electrode designs in electrochemical systems.
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