Promoting cross-linking reactivity of coal molecules via swelling strategy to realize high performance coal-derived hard carbon anode

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL Journal of Electroanalytical Chemistry Pub Date : 2025-05-01 Epub Date: 2025-03-04 DOI:10.1016/j.jelechem.2025.119060
JianZhang Niu , JiaYao Cheng , ZongLin Yi , ChangJun Wang , XiaoMing Li , JingPeng Chen , LiJing Xie , YongGang Chang , XiuChun Li , FangYuan Su , ChengMeng Chen
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Abstract

Cross-linking of coal is an effective method for the preparation of modified coal-derived hard carbon (HCs). However, the complex molecular structure and the lower reactivity of coal hinder its cross-linking, which is not beneficial to the preparation of high-performance coal-derived hard carbon. Herein, a swelling strategy is proposed to improve the reactivity of coal molecules with their cross-linking mechanisms with sucroce. It is found that swelling destroys the hydrogen bonding network in coal molecules, producing aliphatic structures and carboxyl functional groups. Therefore, it improves coal molecular reactivity which is conducive to the formation of an abundant C=O/O=C–O three-dimensional structure and a stable cross-linking structure during the high temperature carbonization procedure. The swelling treatment further enlarges the layer spacing of the carbon material, leading to a greater disorder in the carbon structure, and facilitates the development of pore structure. The HCs with optimal structure exhibit a high initial coulombic efficiency of 88.4 %, a reversible capacity of 304.7 mAh g−1, and a excellent rate performance (192 mAh g−1 at 1 A g−1). This work provides a molecular structure modulation strategy for the modification of coal-derived HCs with potential application in advanced sodium ion batteries.

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通过膨胀策略提高煤分子的交联反应性,实现高性能煤基硬炭阳极
煤的交联是制备改性煤系硬碳的有效方法。但由于煤的分子结构复杂,反应活性较低,阻碍了其交联,不利于制备高性能煤系硬碳。本文提出了一种膨胀策略,以提高煤分子与蔗糖交联机制的反应性。发现膨胀破坏了煤分子中的氢键网络,产生脂肪族结构和羧基官能团。因此,提高了煤的分子反应性,有利于在高温炭化过程中形成丰富的C=O/O=C - O三维结构和稳定的交联结构。膨胀处理进一步扩大了碳材料的层间距,导致碳结构更加无序,有利于孔隙结构的发育。具有最优结构的hc具有高达88.4%的初始库仑效率,304.7 mAh g−1的可逆容量和优异的倍率性能(在1 a g−1时可达192 mAh g−1)。本研究为煤源hc的改性提供了一种分子结构调制策略,有望应用于先进的钠离子电池。
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来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
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