材料科学
碳化
微型反应器
石墨烯
超短脉冲
微波食品加热
储能
纳米技术
化学工程
工艺工程
有机化学
复合材料
催化作用
扫描电子显微镜
激光器
功率(物理)
化学
物理
工程类
量子力学
光学
作者
Dawei Sheng,Xiaoxu Liu,B. Liu,Tengsheng Zhang,Sheng Zhou,Hangtian Yin,Yongbin Wang,Ran Jing,Qianyu Zhang,Dongliang Chao,Peipei Ren
标识
DOI:10.1002/adfm.202508032
摘要
Abstract The traditional carbonization method for preparing carbon materials is hindered by high energy consumption and low efficiency. In this work, a microwave carbonization approach is employed to fabricate a carbonaceous electrode, comprising a graphene and hard carbon heterostructure (GHCH), by rapidly carbonizing waste paper in just 10 seconds using a graphene microreactor. A novel microwave carbonization mechanism is substantiated by combining experimental evidence with finite element simulations. Graphene absorbs microwaves, generating high‐frequency plasma electromagnetic waves, which “catalyze” the sample's rapid microwave absorption, leading to electric breakdown within the sample to initiate preliminary carbonization. Utilizing this ultra‐fast carbonization technique, the GHCH as anode of K‐ion batteries exhibits high reversible capacity and excellent cycle stability. Structural characterization confirms the orderly arrangement of carbon microcrystals, the presence of N and S heteroatoms, and a mesoporous structure within the GHCH electrode. In situ synchrotron X‐ray techniques are employed in this work to investigate the mesoporous structure of GHCH electrodes and the binding dynamics of K‐ions during the charge–discharge cycles. Density functional theory calculations further reveal that the incorporation of graphene facilitated K‐ion diffusion and electron transfer within the GHCH electrodes. In summary, microwave carbonization offers a sustainable and efficient pathway for synthesizing high‐performance carbon‐based electrode.
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