Synthesis of N-doped zeolite-templated carbons via depolymerized oligomer filling: applications in EDLC electrodes†

IF 3.2 Q2 CHEMISTRY, PHYSICAL Energy advances Pub Date : 2024-09-12 DOI:10.1039/D4YA00400K
Hiroyuki Itoi, Chika Matsuoka, Ginga Saeki, Hiroyuki Iwata, Shinichiroh Iwamura, Keigo Wakabayashi, Takeharu Yoshii, Hirotomo Nishihara and Yoshimi Ohzawa
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Abstract

Zeolite-templated carbons (ZTCs) are widely studied from basic research to applied research owing to their characteristic pore structures. To synthesize ZTCs, molecules with a size smaller than the pore sizes of template zeolites have been used as carbon sources for their carbonization in the zeolite pores. Therefore, the type of carbon sources has been limited to molecules with a size smaller than the pore sizes of zeolites. In this study, highly structurally regular N-doped zeolite-templated carbons are synthesized using propylene as a carbon source and chitin as both carbon and nitrogen sources via a depolymerized oligomer filling (DOF) mechanism. Chitin, the second most abundant biopolymer on the Earth, consists of N-acetylglucosamine (GlcNAc) as its unit structure and has a much larger size than the zeolite pores. NaY zeolite is used as a template without drying and mixed with chitin. The mixture is subjected to chemical vapor deposition (CVD) using propylene and subsequent heat treatment for graphitization, followed by HF etching for zeolite removal. Upon heating the mixture of the zeolite and chitin, chitin is catalytically depolymerized into chitin oligosaccharide radicals by the zeolite, and the radicals are absorbed into the zeolite pores below 450 °C, which is supported by electron spin resonance and N2 adsorption/desorption analyses. The ZTC structure is completed by propylene CVD for adequately filling carbon into the zeolite pores. A validation experiment is conducted using GlcNAc instead of chitin to confirm that the N-doped ZTC is synthesized via the DOF mechanism. The resulting N-doped ZTCs have high structural regularity and high surface areas ranging from 3420 to 3740 m2 g−1, and show a higher area-normalized capacitance than undoped ZTC as electric double-layer capacitor electrodes. Utilizing chitin from crustacean shells as one of the raw materials highlights an innovative approach to waste reduction and advances sustainable materials science, contributing to the circular economy and sustainable development goals.

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通过解聚低聚物填充合成掺杂 N 的沸石模板碳:在 EDLC 电极中的应用
沸石模板碳(Zeolite-templated carbons,ZTCs)因其特有的孔隙结构,从基础研究到应用研究都得到了广泛的研究。为了合成 ZTC,人们使用比模板沸石孔径更小的分子作为碳源,使其在沸石孔中碳化。因此,碳源类型仅限于比沸石孔径更小的分子。本研究以丙烯为碳源,甲壳素为碳源和氮源,通过解聚低聚物填充(DOF)机制合成了结构高度规整的掺氮沸石模板碳。甲壳素是地球上含量第二高的生物聚合物,由 N-乙酰葡糖胺(GlcNAc)作为单位结构组成,其尺寸远远大于沸石孔隙。NaY 沸石用作模板,无需干燥,然后与甲壳素混合。使用丙烯对混合物进行化学气相沉积(CVD),随后进行热处理使其石墨化,再用氢氟酸蚀刻去除沸石。在加热沸石和几丁质的混合物时,几丁质在沸石的催化下解聚成几丁质寡糖自由基,自由基在 450 °C 以下被沸石孔隙吸收,电子自旋共振和 N2 吸附/解吸分析证实了这一点。为了在沸石孔隙中充分填充碳,通过丙烯气相沉积完成了 ZTC 结构。使用 GlcNAc 代替几丁质进行了验证实验,以确认掺杂 N 的 ZTC 是通过 DOF 机制合成的。所得到的掺杂 N 的 ZTC 具有较高的结构规整性和 3420 至 3740 平方米 g-1 的高表面积,与未掺杂的 ZTC 相比,作为双层电容器电极显示出更高的面积归一化电容。利用甲壳类动物贝壳中的甲壳素作为原材料之一,是一种减少废物的创新方法,推动了可持续材料科学的发展,有助于实现循环经济和可持续发展目标。
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Correction: Steady states and kinetic modelling of the acid-catalysed ethanolysis of glucose, cellulose, and corn cob to ethyl levulinate. Back cover Fabrication methods, pseudocapacitance characteristics, and integration of conjugated conducting polymers in electrochemical energy storage devices Inside back cover Back cover
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