石墨烯
吸附
X射线光电子能谱
氧化物
分子
材料科学
氧化石墨烯纸
选择性
化学工程
石墨烯纳米带
纳米技术
化学物理
化学
物理化学
有机化学
催化作用
工程类
冶金
作者
Vitalii I. Sysoev,A. V. Okotrub,А. В. Гусельников,Д. А. Смирнов,Lyubov G. Bulusheva
标识
DOI:10.1002/pssb.201700267
摘要
Graphene derivatives are promising sensor materials due to their high surface area available for molecule adsorption and conductivity changes under the adsorbate impact. The selectivity of such materials can be tuned through the attaching of certain functional groups preferably interacting with the defined gases. In the present work, we compare the reactivity of graphene oxide, oxyfluorinated graphene, and fluorinated graphene toward gaseous NO x molecules. The interaction of the molecules with the graphene‐based films was monitored by in situ X‐ray photoelectron and near‐edge X‐ray absorption fine structure spectroscopy measurements. The spectra before and after exposure of the films to a gaseous NO x mixture detected equal concentrations of adsorbed NO 2 and NO species on graphene oxide, the preferable interaction of oxyfluorinated graphene with NO 2 and the absence of the adsorbed molecules on the fluorinated graphene surface. These results are useful for the development of selective graphene‐based gas sensors.
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