Ferrocene-Based Porous Organic Polymer (FPOP): Synthesis, Characterization and an Electrochemical Study

Ž. Petrovski, Mateus P. Moreira, Andreia F. M. Santos, Sunny K. S. Freitas, N. Jordão, R. A. Maia, A. Nunes, L. Branco, Hugo Cruz, P. Esteves
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引用次数: 0

Abstract

Ferrocene-based porous organic polymers (FPOPs) were prepared from phenol-formaldehyde polymer (Bakelite) and phenol as starting materials; and two possible mechanisms for polymerization were discussed. Solid-state 13C CP-MAS NMR, FTIR, powder XRD, elemental analysis and ICP (Fe, Na, B) were performed to characterize the prepared materials. The two synthetic approaches produced polymers with different pore sizes: the FPOP synthesized through Bakelite presented a higher surface area (52 m2 g−1) when compared to the one obtained by the bottom-up polymerization from phenol (only 5 m2 g−1). Thermogravimetric analysis confirmed the thermal stability of the material, which decomposed at 350 °C. Furthermore, cyclic voltammetry (CV) of the new FPOP on modified electrodes, in ACN and 0.1 M TBAP as an electrolyte, showed fully reversible electron transfer, which is similar to that observed for the ferrocene probe dissolved in the same electrolyte. As a proof-of-concept for an electrochromic device, this novel material was also tested, with a color change detected between yellow/brownish coloration (reduced form) and green/blue coloration (oxidized form). The new hybrid FPOP seems very promising for material science, energy storage and electrochromic applications, as well as for plastic degradation.
二茂铁基多孔有机聚合物(FPOP):合成、表征及电化学研究
以酚醛聚合物(酚醛)和苯酚为原料制备了二茂铁基多孔有机聚合物(fpop);并讨论了两种可能的聚合机理。采用固态13C CP-MAS NMR、FTIR、粉末XRD、元素分析和ICP (Fe, Na, B)对制备的材料进行表征。两种合成方法产生的聚合物具有不同的孔径:通过酚醛合成的FPOP具有更高的表面积(52 m2 g−1),而由苯酚自下而上聚合得到的FPOP只有5 m2 g−1。热重分析证实了材料的热稳定性,该材料在350°C时分解。此外,在ACN和0.1 M ttbap作为电解质的修饰电极上,新FPOP的循环伏安(CV)显示出完全可逆的电子转移,这与在相同电解质中溶解的二茂铁探针所观察到的情况相似。作为电致变色装置的概念验证,这种新型材料也进行了测试,在黄色/褐色(还原形式)和绿色/蓝色(氧化形式)之间检测到颜色变化。这种新型混合FPOP在材料科学、储能和电致变色应用以及塑料降解方面似乎非常有前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.30
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