Jian Lu, Shuai Ruan, Xinping He*, Jiayuan Xiang, Fangfang Tu, Chen Wang, Wangjun Wan*, Hui Huang, Yongping Gan, Yang Xia, Jun Zhang, Xinhui Xia and Wenkui Zhang*,
{"title":"Plasma-Enhanced Chemical Vapor Deposition-Assisted Construction of Biomass-Derived Porous Carbon","authors":"Jian Lu, Shuai Ruan, Xinping He*, Jiayuan Xiang, Fangfang Tu, Chen Wang, Wangjun Wan*, Hui Huang, Yongping Gan, Yang Xia, Jun Zhang, Xinhui Xia and Wenkui Zhang*, ","doi":"10.1021/acs.energyfuels.5c0192510.1021/acs.energyfuels.5c01925","DOIUrl":null,"url":null,"abstract":"<p >Designing electrode materials that simultaneously exhibit excellent electrochemical performance and cost efficiency plays a vital role in enhancing both the capacity density and long cycle stability of energy storage systems. In this research, a novel strategy combining hydrothermal treatment and steam-assisted plasma-enhanced chemical vapor deposition (PECVD) is proposed to fabricate biomass-derived porous carbon (CC-PECVD) using corncob as the carbon source. Compared with conventional high-temperature carbonization, this method optimizes the pore structure significantly, leading to a higher specific surface area (373.4 m<sup>2</sup> g<sup>–1</sup>) and a more uniform mesopore distribution (∼5 nm), thereby enhancing ion diffusion efficiency and charge storage capacity. Structural analysis demonstrates that the application of PECVD facilitates the construction of a three-dimensional mesoporous framework with a honeycomb-like architecture while incorporating abundant oxygen/nitrogen functional groups onto the carbon surface simultaneously. These structural and chemical modifications significantly increase the number of active sites, thereby promoting ion transport and charge storage. Electrochemical properties reveal that the CC-PECVD electrode delivers outstanding capacitive behavior when applied in supercapacitor systems, achieving a specific capacitance of 250 F g<sup>–1</sup> at 1 A g<sup>–1</sup>. Moreover, when employed as an anode in sodium-ion battery systems, the CC-PECVD electrode shows a considerable reversible capacity of approximately 266 mAh g<sup>–1</sup>, along with excellent cycling durability. These results show that this approach not only offers an eco-friendly and effective way to transform agricultural biomass into high-value carbon materials but also creates a potential route for the efficient synthesis of carbon-based electrodes for future energy storage systems.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 21","pages":"10092–10102 10092–10102"},"PeriodicalIF":5.3000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c01925","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
Designing electrode materials that simultaneously exhibit excellent electrochemical performance and cost efficiency plays a vital role in enhancing both the capacity density and long cycle stability of energy storage systems. In this research, a novel strategy combining hydrothermal treatment and steam-assisted plasma-enhanced chemical vapor deposition (PECVD) is proposed to fabricate biomass-derived porous carbon (CC-PECVD) using corncob as the carbon source. Compared with conventional high-temperature carbonization, this method optimizes the pore structure significantly, leading to a higher specific surface area (373.4 m2 g–1) and a more uniform mesopore distribution (∼5 nm), thereby enhancing ion diffusion efficiency and charge storage capacity. Structural analysis demonstrates that the application of PECVD facilitates the construction of a three-dimensional mesoporous framework with a honeycomb-like architecture while incorporating abundant oxygen/nitrogen functional groups onto the carbon surface simultaneously. These structural and chemical modifications significantly increase the number of active sites, thereby promoting ion transport and charge storage. Electrochemical properties reveal that the CC-PECVD electrode delivers outstanding capacitive behavior when applied in supercapacitor systems, achieving a specific capacitance of 250 F g–1 at 1 A g–1. Moreover, when employed as an anode in sodium-ion battery systems, the CC-PECVD electrode shows a considerable reversible capacity of approximately 266 mAh g–1, along with excellent cycling durability. These results show that this approach not only offers an eco-friendly and effective way to transform agricultural biomass into high-value carbon materials but also creates a potential route for the efficient synthesis of carbon-based electrodes for future energy storage systems.
设计同时具有优异电化学性能和成本效益的电极材料对于提高储能系统的容量密度和长周期稳定性至关重要。本研究提出了一种结合水热处理和蒸汽辅助等离子体增强化学气相沉积(PECVD)的新策略,以玉米芯为碳源制备生物质衍生多孔碳(CC-PECVD)。与传统的高温碳化相比,该方法显著优化了孔隙结构,使其具有更高的比表面积(373.4 m2 g-1)和更均匀的介孔分布(~ 5 nm),从而提高了离子扩散效率和电荷存储能力。结构分析表明,PECVD的应用促进了具有蜂窝状结构的三维介孔框架的构建,同时在碳表面结合了丰富的氧/氮官能团。这些结构和化学修饰显著增加了活性位点的数量,从而促进了离子传输和电荷储存。电化学性能表明,CC-PECVD电极在超级电容器系统中应用时具有出色的电容性能,在1 a g-1时达到250 F - 1的比电容。此外,当用作钠离子电池系统的阳极时,CC-PECVD电极显示出相当大的可逆容量,约为266 mAh g-1,同时具有出色的循环耐久性。这些结果表明,这种方法不仅为将农业生物质转化为高价值碳材料提供了一种环保有效的方法,而且为未来储能系统的碳基电极的高效合成创造了一条潜在的途径。
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.