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铋作为一种新型的氯储存电极,实现了实用高容量脱盐电池的构建。

Bismuth as a New Chloride-Storage Electrode Enabling the Construction of a Practical High Capacity Desalination Battery.

机构信息

Department of Chemistry, University of Wisconsin-Madison , Madison, Wisconsin 53706, United States.

出版信息

J Am Chem Soc. 2017 Aug 16;139(32):11055-11063. doi: 10.1021/jacs.7b01119. Epub 2017 Aug 4.

DOI:10.1021/jacs.7b01119
PMID:28777553
Abstract

Materials that can selectively store Na and Cl ions in the bulk of their structures and release these ions with good cycle stability can enable the construction of a high capacity, rechargeable desalination cell for use in seawater desalination. In this study, the ability of a nanocrystalline Bi foam electrode to serve as an efficient and high capacity Cl-storage electrode using its conversion to BiOCl was investigated. When Bi as a Cl-storage electrode was coupled with NaTi(PO) as a Na-storage electrode, a new type of rechargeable desalination cell, which is charged during desalination and discharged during salination, was constructed. The resulting Bi-NaTi(PO) cell was tested under various salination and desalination conditions to investigate advantages and potential limitations of using Bi as a Cl-storage electrode. Slow Cl release kinetics of BiOCl in neutral conditions and an imbalance in Cl and Na storage (i.e., Cl storage requires three electrons/Cl, while Na storage requires one electron/Na) were identified as possible drawbacks, but strategies to address these issues were developed. On the basis of these investigations, optimum desalination and salination conditions were identified where the Bi/NaTi(PO) cell achieved a desalination/salination cycle at ±1 mA cm with a net potential input of only 0.20 V. The kinetics of Cl release from BiOCl was significantly improved by the use of an acidic solution, and therefore, a divided cell was used for the salination process. We believe that with further optimizations the Bi/BiOCl electrode will enable efficient and practical desalination applications.

摘要

材料可以选择性地在其结构主体中储存 Na 和 Cl 离子,并在良好的循环稳定性下释放这些离子,这可以实现构建一种高容量、可充电的脱盐电池,用于海水淡化。在这项研究中,研究了纳米晶 Bi 泡沫电极作为高效高容量 Cl 储存电极的能力,其通过转化为 BiOCl 来实现。当 Bi 作为 Cl 储存电极与 NaTi(PO) 作为 Na 储存电极结合时,构建了一种新型可充电脱盐电池,该电池在脱盐过程中充电,在盐化过程中放电。对所得的 Bi-NaTi(PO)电池进行了各种盐化和脱盐条件下的测试,以研究使用 Bi 作为 Cl 储存电极的优势和潜在局限性。在中性条件下 BiOCl 的缓慢 Cl 释放动力学和 Cl 和 Na 储存的不平衡(即,Cl 储存需要三个电子/Cl,而 Na 储存需要一个电子/Na)被认为是可能的缺点,但已开发出解决这些问题的策略。基于这些研究,确定了最佳的脱盐和盐化条件,在这些条件下,Bi/NaTi(PO)电池在±1 mA cm 的净电位输入仅为 0.20 V 的情况下实现了脱盐/盐化循环。通过使用酸性溶液,BiOCl 从 Bi 中的 Cl 释放动力学得到了显著改善,因此,为盐化过程使用了分置电池。我们相信,通过进一步优化,Bi/BiOCl 电极将能够实现高效且实用的脱盐应用。

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