结晶度
石墨烯
X射线光电子能谱
氧化物
材料科学
拉曼光谱
微晶
剥脱关节
化学工程
傅里叶变换红外光谱
石墨
氧气
图层(电子)
密度泛函理论
亚氧化物
作者
Shivang Saxena,Akshay Kumar,Naveen Yadav,Subin Jung,Mohit K. Sharma,Sang‐Chae Jeon,Bon Heun Koo
标识
DOI:10.1021/acs.jpclett.5c02607
摘要
Oxidation of graphite layers is a crucial intermediate step during the chemical exfoliation of graphene, directly influencing the layer thickness, defect density, and functional group distribution. However, the mechanism governing structural and chemical changes in this stage remains insufficiently understood. In this work, graphene oxide (GO) was synthesized via the modified Hummer's method with controlled oxidation times of 6, 12, and 24 h, labeled as GO-T1, GO-T2, and GO-T3, respectively. XRD results showed nearly constant interlayer spacing but notable variations in crystallite size, indicating a time-dependent structural reorganization. FTIR and XPS analyses revealed that the overall oxygen content (C/O ratio) remained relatively stable, while the functional group distribution varied with oxidation time. Raman spectroscopy demonstrated a steady increase in the defect density over prolonged oxidation. Based on these findings, a time-dependent oxidation mechanism was proposed, offering a pathway to systematically understand and fine-tune GO properties through a controlled reaction time for practical applications.
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