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用于非对称电容去离子中有效捕获氯离子的基于MXene的阳极的层间结构与化学工程

Interlayer Structure and Chemistry Engineering of MXene-Based Anode for Effective Capture of Chloride Anions in Asymmetric Capacitive Deionization.

作者信息

Xu Wenyu, Tan Chang, Wang Ao, Hu Shengchun, Deng Libo, Boles Steven, Sun Kang, Li Bei, Hu Haibo

机构信息

School of Materials Science and Engineering, Anhui University, Hefei 230601, China.

Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China.

出版信息

ACS Appl Mater Interfaces. 2023 Mar 29;15(12):16266-16276. doi: 10.1021/acsami.2c23260. Epub 2023 Mar 14.

Abstract

Negatively charged surfaces and readily oxidizabile characteristics fundamentally restrict the use of MXene building blocks as anodes for anion intercalation. Herein, by embedding bacterial cellulose nanofibers with conformal polypyrrole coating (BC@PPy) and populating them between MXene (TiCT) interlayers, we enable the fabricated MXene/BC@PPy (MBP) composite films to be highly efficient anodes for Cl-capturing in asymmetric capacitive deionization (CDI) systems. Performance gains are realized due to the surface electronegativity of MXene nanosheets becoming compensated by positively charged BC@PPy nanofibers, alleviating electrostatic repulsion, thus realizing reversible Cl intercalation. More crucially, the anodization voltage of MBP is effectively enhanced as a result of the increase of the Ti valence state in MXene nanosheets with the addition of the BC@PPy spacer. Furthermore, BC@PPy nanopillars effectively enlarge the interlayer space for facile Cl de-/intercalation, improve the vertical electron transfer between loosely deposited MXene nanosheets, and perform as additional active materials for Cl-capturing. Consequently, the MBP anode exhibits a promising desalination capacity of up to 17.56 mg g at 1.2 V with a high capacity retention of 94.6% after 30 cycles in an asymmetric CDI system. This work offers a simple and effective strategy to unlock the application potential of MXene building blocks as anodes for Cl-capturing in electrochemical desalination.

摘要

带负电荷的表面和易于氧化的特性从根本上限制了MXene构建块作为阴离子嵌入阳极的应用。在此,通过将具有保形聚吡咯涂层的细菌纤维素纳米纤维(BC@PPy)嵌入并填充在MXene(TiCT)层间,我们使制备的MXene/BC@PPy(MBP)复合膜成为不对称电容去离子(CDI)系统中用于捕获Cl的高效阳极。由于带正电荷的BC@PPy纳米纤维补偿了MXene纳米片的表面电负性,减轻了静电排斥,从而实现了可逆的Cl嵌入,因此实现了性能提升。更关键的是,由于添加了BC@PPy间隔层,MXene纳米片中Ti价态增加,MBP的阳极氧化电压得到有效提高。此外,BC@PPy纳米柱有效地扩大了层间空间,便于Cl的脱嵌/嵌入,改善了松散沉积的MXene纳米片之间的垂直电子转移,并作为捕获Cl的额外活性材料。因此,在不对称CDI系统中,MBP阳极在1.2 V时表现出高达17.56 mg g的有前景的脱盐容量,经过30次循环后具有94.6%的高容量保持率。这项工作提供了一种简单有效的策略,以释放MXene构建块作为电化学脱盐中捕获Cl的阳极的应用潜力。

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