石墨烯
位阻效应
氧化物
离域电子
化学物理
芘
化学
氢键
密度泛函理论
计算化学
光化学
材料科学
立体化学
纳米技术
分子
有机化学
作者
Jinrong Yang,Guosheng Shi,Yusong Tu,Haiping Fang
标识
DOI:10.1002/anie.201404144
摘要
Recent experiments have shown the coexistence of both large unoxidized and oxidized regions on graphene oxide (GO), but the underlying mechanism for the formation of the GO atomic structure remains unknown. Now, using density functional calculations, 52 oxidation pathways for local pyrene structures on GO were identified, and a kinetic profile for graphene oxidation with a high correlation between oxidation loci was proposed, which is different from the conventional view, which entails a random distribution of oxidation loci. The high correlation is an essential nature of graphene oxidation processes and can be attributed to three crucial effects: 1) breaking of delocalized π bonds, 2) steric hindrance, and 3) hydrogen-bond formation. This high correlation leads to the coexistence of both large unoxidized and oxidized regions on GO. Interestingly, even in oxidized regions on GO, some small areas of sp(2)-hybridized domains, similar to "islands", can persist because of steric effects.
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