微型多孔材料
离子键合
整改
离子
扩散
电荷密度
材料科学
电流密度
电场
离子流
表面电荷
电流(流体)
分析化学(期刊)
电压
化学物理
化学
热力学
色谱法
复合材料
物理
物理化学
有机化学
量子力学
作者
Long Ma,H. Y. Zhang,Bowen Ai,Jiakun Zhuang,Guanghua Du,Yinghua Qiu
摘要
Ionic current rectification (ICR) induced by electroosmotic flow (EOF) under concentration gradients can find many applications in micro/nanofluidic sensing and ionic circuits. Here, we focused on the cases with micropores of moderate length–diameter ratios. Through experimental research and systematic simulations, the EOF-induced ICR was found to exhibit voltage-dependent ratios. In the considered cases with a weak EOF or strong ionic diffusion, a large deviation appears between the ion concentration inside the micropore and the bulk value, which fails the prediction by solution conductivity gradients. Based on our simulation results, effective equations were developed for the theoretical description of ion concentration distributions along the micropore axis under a coupled concentration gradient and electric field. With the predicted ion distributions inside micropores, the ICR ratio can be conveniently calculated using the derived electrical resistance of the microfluidic system, which applies to micropores of 200–1000 nm in diameter. Because the surface charge density is the only unknown input parameter, our developed equations can be used to evaluate the surface charge density of micropores using the measured EOF-induced ICR ratio under concentration gradients.
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