{"title":"调节双原子掺杂多孔碳以实现高性能电容式存储设备","authors":"Jizhao Zou, Zhewen Deng, Jingyou Xu, Shunhong Chen, Xin Yu, Hongliang Wu and Fenglin Zhao","doi":"10.1039/D4TA02529F","DOIUrl":null,"url":null,"abstract":"<p >Zinc ion capacitors show impressive energy storage potential for well-balanced energy and power density, but exploring their implicit energy storage mechanism is crucial and still challenging. Herein, a new viewpoint is proposed for regulating nitrogen and oxygen dual-doped carbon with short-range order by sustaining the conductivity and synchronously boosting interfacial chemisorption sites. The artful nanoarchitecture engineering of a cross-linked carbon framework with a high specific surface area (2702.3 m<small><sup>2</sup></small> g<small><sup>−1</sup></small>) is beneficial for efficient electrolyte penetration and ion transfer, thus enhancing the electrode's capacitance and rate performance. Based on electrochemical capacitor properties and theoretical calculations, the optimized hetero-carbon used for zinc ion capacitors could deliver a high capacity of 241.1 mA h g<small><sup>−1</sup></small> at 0.1 A g<small><sup>−1</sup></small> and an energy density of 191.6 W h kg<small><sup>−1</sup></small>. The dynamic potential of zincate hydrated ion precipitation/dissolution behavior was explored by <em>ex situ</em> X-ray diffraction and photoelectron spectroscopy experiments. This work not only provides new perception integration with porousness and nanoarchitecture engineering in carbon materials, but also sheds light on the zinc-ion capacitor storage mechanism.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":null,"pages":null},"PeriodicalIF":10.7000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regulation of dual-atom doped porous carbon towards high-performance capacitive storage devices†\",\"authors\":\"Jizhao Zou, Zhewen Deng, Jingyou Xu, Shunhong Chen, Xin Yu, Hongliang Wu and Fenglin Zhao\",\"doi\":\"10.1039/D4TA02529F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Zinc ion capacitors show impressive energy storage potential for well-balanced energy and power density, but exploring their implicit energy storage mechanism is crucial and still challenging. Herein, a new viewpoint is proposed for regulating nitrogen and oxygen dual-doped carbon with short-range order by sustaining the conductivity and synchronously boosting interfacial chemisorption sites. The artful nanoarchitecture engineering of a cross-linked carbon framework with a high specific surface area (2702.3 m<small><sup>2</sup></small> g<small><sup>−1</sup></small>) is beneficial for efficient electrolyte penetration and ion transfer, thus enhancing the electrode's capacitance and rate performance. Based on electrochemical capacitor properties and theoretical calculations, the optimized hetero-carbon used for zinc ion capacitors could deliver a high capacity of 241.1 mA h g<small><sup>−1</sup></small> at 0.1 A g<small><sup>−1</sup></small> and an energy density of 191.6 W h kg<small><sup>−1</sup></small>. The dynamic potential of zincate hydrated ion precipitation/dissolution behavior was explored by <em>ex situ</em> X-ray diffraction and photoelectron spectroscopy experiments. This work not only provides new perception integration with porousness and nanoarchitecture engineering in carbon materials, but also sheds light on the zinc-ion capacitor storage mechanism.</p>\",\"PeriodicalId\":82,\"journal\":{\"name\":\"Journal of Materials Chemistry A\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2024-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry A\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ta/d4ta02529f\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ta/d4ta02529f","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
锌离子电容器以其均衡的能量和功率密度显示出惊人的储能潜力,但探索其隐含的储能机制仍是至关重要的挑战。本文提出了一种新观点,即通过维持导电性和同步增强界面化学吸附位点来调节氮氧双掺杂碳的短程有序性。具有高比表面积(2702.3 m2 g-1)的交联框架碳的巧妙纳米结构工程有利于电解质的有效渗透和离子转移,从而提高电极的电容和速率性能。根据电化学电容器特性和理论计算,用于锌离子电容器的优化杂化碳在 0.1 A g-1 的条件下可提供 241.1 mAh g-1 的高容量和 191.6 Wh kg-1 的能量密度。通过原位 X 射线衍射和光电子能谱实验,探索了锌酸盐水合离子沉淀/溶解行为的动态潜力。这项工作不仅提供了与碳材料多孔性和纳米结构工程相结合的新感知,还揭示了锌离子电容器的存储机理。
Regulation of dual-atom doped porous carbon towards high-performance capacitive storage devices†
Zinc ion capacitors show impressive energy storage potential for well-balanced energy and power density, but exploring their implicit energy storage mechanism is crucial and still challenging. Herein, a new viewpoint is proposed for regulating nitrogen and oxygen dual-doped carbon with short-range order by sustaining the conductivity and synchronously boosting interfacial chemisorption sites. The artful nanoarchitecture engineering of a cross-linked carbon framework with a high specific surface area (2702.3 m2 g−1) is beneficial for efficient electrolyte penetration and ion transfer, thus enhancing the electrode's capacitance and rate performance. Based on electrochemical capacitor properties and theoretical calculations, the optimized hetero-carbon used for zinc ion capacitors could deliver a high capacity of 241.1 mA h g−1 at 0.1 A g−1 and an energy density of 191.6 W h kg−1. The dynamic potential of zincate hydrated ion precipitation/dissolution behavior was explored by ex situ X-ray diffraction and photoelectron spectroscopy experiments. This work not only provides new perception integration with porousness and nanoarchitecture engineering in carbon materials, but also sheds light on the zinc-ion capacitor storage mechanism.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.