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用于超级电容器的金属有机框架纳米孔中限域聚苯胺的选择性形成

Selective Formation of Polyaniline Confined in the Nanopores of a Metal-Organic Framework for Supercapacitors.

作者信息

Song Yi-Da, Ho Wei Huan, Chen Yu-Chuan, Li Jun-Hong, Wang Yi-Sen, Gu Yu-Juan, Chuang Cheng-Hsun, Kung Chung-Wei

机构信息

Department of Chemical Engineering, National Cheng Kung University, 1 University Road, Tainan City, 70101, Taiwan.

出版信息

Chemistry. 2021 Feb 15;27(10):3560-3567. doi: 10.1002/chem.202004516. Epub 2021 Jan 18.

DOI:10.1002/chem.202004516
PMID:33166095
Abstract

In this study, a strategy that can result in the polyaniline (PANI) solely confined within the nanopores of a metal-organic framework (MOF) without forming obvious bulk PANI between MOF crystals is developed. A water-stable zirconium-based MOF, UiO-66-NH , is selected as the MOF material. The polymerization of aniline is initiated in the acidic suspension of UiO-66-NH nanocrystals in the presence of excess poly(sodium 4-styrenesulfonate) (PSS). Since the pore size of UiO-66-NH is too small to enable the insertion of the bulky PSS, the quick formation of pore-confined solid PANI and the slower formation of well dispersed PANI:PSS occur within the MOF crystals and in the bulk solution, respectively. By taking advantage of the resulting homogeneous PANI:PSS polymer solution, the bulk PANI:PSS can be removed from the PANI/UiO-66-NH solid by successive washing the sample with fresh acidic solutions through centrifugation. As this is the first time reporting the PANI solely confined in the pores of a MOF, as a demonstration, the obtained PANI/UiO-66-NH composite material is applied as the electrode material for supercapacitors. The PANI/UiO-66-NH thin films exhibit a pseudocapacitive electrochemical characteristic, and their resulting electrochemical activity and charge-storage capacities are remarkably higher than those of the bulk PANI thin films.

摘要

在本研究中,开发了一种策略,该策略可使聚苯胺(PANI)仅局限于金属有机框架(MOF)的纳米孔内,而不会在MOF晶体之间形成明显的块状聚苯胺。选择水稳定的锆基金属有机框架UiO-66-NH作为MOF材料。在过量的聚(4-苯乙烯磺酸钠)(PSS)存在下,在UiO-66-NH纳米晶体的酸性悬浮液中引发苯胺的聚合反应。由于UiO-66-NH的孔径太小,无法插入庞大的PSS,因此分别在MOF晶体内和本体溶液中快速形成孔内受限的固体聚苯胺和较慢形成分散良好的聚苯胺:PSS。通过利用所得的均匀聚苯胺:PSS聚合物溶液,通过离心用新鲜酸性溶液连续洗涤样品,可以从聚苯胺/UiO-66-NH固体中除去块状聚苯胺:PSS。由于这是首次报道聚苯胺仅局限于MOF的孔中,作为示例,将获得的聚苯胺/UiO-66-NH复合材料用作超级电容器的电极材料。聚苯胺/UiO-66-NH薄膜表现出赝电容电化学特性,并且它们产生的电化学活性和电荷存储容量明显高于块状聚苯胺薄膜。

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