{"title":"Boosting Closed Pores and Nitrogen Content in Hard Carbon via a Pre-Oxidation Approach for Fast-Charging Sodium-Ion Batteries","authors":"Shoucong Gao, Runyi Zhou, Yong Zhao, Chuang Bao, Mingrui Tian, Zhenhuan Wu, Meihui Wang, Zheng Bo, Huachao Yang","doi":"10.1002/cplu.70189","DOIUrl":null,"url":null,"abstract":"<p>Hard carbon has been widely recognized as a practical anode candidate for sodium-ion batteries because of its low cost, appropriate working potential, and structural stability. Nevertheless, its practical application remains limited by insufficient reversible capacity and poor high-rate performance. In this work, a nitrogen-enriched hard carbon with tuned structural order is synthesized from xylose via a simple air pre-oxidation step prior to carbonization, demonstrating fast-charging sodium-ion batteries. This pre-oxidation process introduces oxygen-containing groups in the precursor, enhances intermolecular cross-linking, and suppresses excessive structural fusion during pyrolysis, resulting in an optimized disordered/graphitic balance. Notably, this treatment improves nitrogen retention and modulates pore evolution, yielding enlarged interlayer spacing, smaller microcrystalline domains, and abundant closed ultramicropores, which are highly favorable for sodium storage in the plateau region. Benefiting from the synergistic effects of structural regulation and heteroatom doping, the optimized hard carbon electrode delivers a high reversible capacity of 397.4 mAh g<sup>−1</sup> and excellent rate capability of 148.5 mAh g<sup>−1</sup> at 5 A g<sup>−1</sup>. This work provides a straightforward and cost-effective strategy for engineering high-performance biomass-derived hard carbon anodes for advanced sodium-ion batteries.</p>","PeriodicalId":148,"journal":{"name":"ChemPlusChem","volume":"91 6","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2026-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPlusChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cplu.70189","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Hard carbon has been widely recognized as a practical anode candidate for sodium-ion batteries because of its low cost, appropriate working potential, and structural stability. Nevertheless, its practical application remains limited by insufficient reversible capacity and poor high-rate performance. In this work, a nitrogen-enriched hard carbon with tuned structural order is synthesized from xylose via a simple air pre-oxidation step prior to carbonization, demonstrating fast-charging sodium-ion batteries. This pre-oxidation process introduces oxygen-containing groups in the precursor, enhances intermolecular cross-linking, and suppresses excessive structural fusion during pyrolysis, resulting in an optimized disordered/graphitic balance. Notably, this treatment improves nitrogen retention and modulates pore evolution, yielding enlarged interlayer spacing, smaller microcrystalline domains, and abundant closed ultramicropores, which are highly favorable for sodium storage in the plateau region. Benefiting from the synergistic effects of structural regulation and heteroatom doping, the optimized hard carbon electrode delivers a high reversible capacity of 397.4 mAh g−1 and excellent rate capability of 148.5 mAh g−1 at 5 A g−1. This work provides a straightforward and cost-effective strategy for engineering high-performance biomass-derived hard carbon anodes for advanced sodium-ion batteries.
硬碳由于其成本低、工作电位适宜、结构稳定等优点,已被广泛认为是钠离子电池阳极的理想材料。然而,其实际应用仍然受到可逆容量不足和高速率性能差的限制。在这项工作中,通过炭化之前的简单空气预氧化步骤,以木糖为原料合成了结构顺序调整的富氮硬碳,展示了快速充电钠离子电池。这种预氧化过程在前驱体中引入了含氧基团,增强了分子间的交联,抑制了热解过程中过度的结构融合,从而优化了无序/石墨平衡。值得注意的是,该处理改善了氮潴留并调节了孔隙演化,使层间间距扩大,微晶畴变小,并产生大量封闭的超微孔,这对高原地区的钠储存非常有利。得益于结构调控和杂原子掺杂的协同效应,优化后的硬碳电极在5 a g-1下具有397.4 mAh g-1的高可逆容量和148.5 mAh g-1的优异倍率容量。这项工作为先进钠离子电池的高性能生物质衍生硬碳阳极的工程设计提供了一种简单而经济的策略。
期刊介绍:
ChemPlusChem is a peer-reviewed, general chemistry journal that brings readers the very best in multidisciplinary research centering on chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies.
Fully comprehensive in its scope, ChemPlusChem publishes articles covering new results from at least two different aspects (subfields) of chemistry or one of chemistry and one of another scientific discipline (one chemistry topic plus another one, hence the title ChemPlusChem). All suitable submissions undergo balanced peer review by experts in the field to ensure the highest quality, originality, relevance, significance, and validity.