材料科学
石墨烯
拉曼光谱
丙酮
X射线光电子能谱
兴奋剂
化学工程
旋涂
四方晶系
纳米颗粒
微晶
复合数
分析化学(期刊)
扫描电子显微镜
纳米技术
复合材料
薄膜
相(物质)
光电子学
有机化学
光学
冶金
工程类
物理
化学
作者
Suparat Singkammo,Anurat Wisitsoraat,Chakrit Sriprachuabwong,Adisorn Tuantranont,Sukon Phanichphant,Chaikarn Liewhiran
标识
DOI:10.1021/acsami.5b00161
摘要
In this work, flame-spray-made SnO2 nanoparticles are systematically studied by doping with 0.1–2 wt % nickel (Ni) and loading with 0.1–5 wt % electrolytically exfoliated graphene for acetone-sensing applications. The sensing films (∼12–18 μm in thickness) were prepared by a spin-coating technique on Au/Al2O3 substrates and evaluated for acetone-sensing performances at operating temperatures ranging from 150 to 350 °C in dry air. Characterizations by X-ray diffraction, transmission/scanning electron microscopy, Brunauer–Emmett–Teller analysis, X-ray photoelectron spectroscopy and Raman spectroscopy demonstrated that Ni-doped SnO2 nanostructures had a spheriodal morphology with a polycrystalline tetragonal SnO2 phase, and Ni was confirmed to form a solid solution with SnO2 lattice while graphene in the sensing film after annealing and testing still retained its high-quality nonoxidized form. Gas-sensing results showed that SnO2 sensing film with 0.1 wt % Ni-doping concentration exhibited an optimal response of 54.2 and a short response time of ∼13 s toward 200 ppm acetone at an optimal operating temperature of 350 °C. The additional loading of graphene at 5 wt % into 0.1 wt % Ni-doped SnO2 led to a drastic response enhancement to 169.7 with a very short response time of ∼5.4 s at 200 ppm acetone and 350 °C. The superior gas sensing performances of Ni-doped SnO2 nanoparticles loaded with graphene may be attributed to the large specific surface area of the composite structure, specifically the high interaction rate between acetone vapor and graphene–Ni-doped SnO2 nanoparticles interfaces and high electronic conductivity of graphene. Therefore, the 5 wt % graphene loaded 0.1 wt % Ni-doped SnO2 sensor is a promising candidate for fast, sensitive and selective detection of acetone.
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