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酚醛树脂和硼酸协同增强多孔碳的电容性能

Synergistic Enhancement of Capacitive Performance in Porous Carbon by Phenolic Resin and Boric Acid.

作者信息

Xia Yingkai, Zhang Fengzhi, Wang Shuo, Wei Shuang, Zhang Xu, Dong Wei, Shen Ding, Tang Shuwei, Liu Fengxia, Chen Yuehui, Yang Shaobin

机构信息

School of Mining, Liaoning Technical University, Fuxin 123000, China.

Chengxi (Taizhou) Equipment Technology Co., Ltd., Jingjiang 214500, China.

出版信息

Molecules. 2025 Mar 9;30(6):1228. doi: 10.3390/molecules30061228.

Abstract

The study of pore structure regulation methods has always been a central focus in enhancing the capacitance performance of porous carbon electrodes in lithium-ion capacitors (LICs). This study proposes a novel approach for the synergistic regulation of the pore structure in porous carbon using phenol-formaldehyde (PF) resin and boric acid (BA). PF and BA are initially dissolved and adsorbed onto porous carbon, followed by hydrothermal treatment and subsequent heat treatment in a N atmosphere to obtain the porous carbon materials. The results reveal that adding BA alone has almost no influence on the pore structure, whereas adding PF alone significantly increases the micropores. Furthermore, the simultaneous addition of PF and BA demonstrates a clear synergistic effect. The CO and HO released during the PF pyrolysis contribute to the development of ultramicropores. At the same time, BA facilitates the N activation reaction of carbon, enlarging the small mesopores and aiding their transformation into bottlenecked structures. The resulting porous carbon demonstrates an impressive capacitance of 144 F·g at 1 A·g and a capacity retention of 19.44% at 20 A·g. This mechanism of B-catalyzed N-enhanced mesopore formation provides a new avenue for preparing porous carbon materials. This type of porous carbon exhibits promising potential for applications in Li-S battery cathode materials and as catalyst supports.

摘要

孔隙结构调控方法的研究一直是提高锂离子电容器(LIC)中多孔碳电极电容性能的核心关注点。本研究提出了一种使用酚醛(PF)树脂和硼酸(BA)对多孔碳孔隙结构进行协同调控的新方法。首先将PF和BA溶解并吸附到多孔碳上,然后进行水热处理,随后在N气氛中进行热处理以获得多孔碳材料。结果表明,单独添加BA对孔隙结构几乎没有影响,而单独添加PF会显著增加微孔。此外,同时添加PF和BA表现出明显的协同效应。PF热解过程中释放的CO和HO有助于超微孔的形成。同时,BA促进了碳的N活化反应,扩大了小介孔并促使它们转变为瓶颈状结构。所得多孔碳在1 A·g时表现出令人印象深刻的144 F·g电容,在20 A·g时容量保持率为19.44%。这种B催化N增强介孔形成的机制为制备多孔碳材料提供了一条新途径。这种类型的多孔碳在锂硫电池阴极材料和作为催化剂载体方面具有广阔的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdc/11946533/3237c4f4dac0/molecules-30-01228-g001.jpg

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