Biwu Cai , Jianbang Ge , Zichen Zhang , Yang Gao , Shun Cao , Zhihao Cheng , Xin Lu , Shuqiang Jiao
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引用次数: 0
Abstract
Understanding mass transfer is of great importance to molten salt electrochemistry. However, natural convection has long been neglected in electrochemical measurements in stagnant molten salt systems due to the complex mathematical treatments. Here we reported the notable natural convection effects in molten LiF-NaF-KF during cyclic voltammetry and chronoamperometry tests. The established model showed that the convection-diffusion layer (CDL) convection dominated mass transfer under long time-scale tests in molten LiF-NaF-KF-EuF3. However, in the case of molten LiF-NaF-KF-K2TiF6, CDL convection predominated at dilute redox concentrations while density-driven convection came into dominance at high redox concentrations, because of the severe coordinate structure change of the redox couple. The derived thickness of the convection-diffusion layer, , ranged from 135 to 183 μm, much higher than that in aqueous solutions (220–250 μm). Moreover, the increase in system temperature greatly enhanced natural convection effects in molten fluorides. Lastly, the use of microelectrode (re<39.7 μm for =160 μm) was demonstrated to be an effective way to suppress the intense natural convection effects.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.