石墨烯
离子液体
材料科学
氧化物
傅里叶变换红外光谱
无机化学
钯
纳米颗粒
介电谱
化学工程
电化学
催化作用
纳米技术
化学
电极
有机化学
物理化学
工程类
冶金
作者
Haleh Naeim,Farshad Kheiri,Mohammad Sirousazar,Arash Afghan
标识
DOI:10.1016/j.electacta.2018.05.204
摘要
Ionic liquids (ILs) were synthesized for the purpose of graphene oxide modification through π-π bonding and anchoring highly dispersed bimetallic Ni-Pd nanoparticles on reduced graphene oxide (RGO). Metallic ions (Pd2+ and Ni2+) were initially attached to an ionic liquid and graphene oxide composite. The ionic liquid served as a stabilizer following metal ions and graphene oxide sheets reduction by NaBH4, which produced an IL/RGO/Ni-Pd hybrid. The π-π interaction between the synthesized ionic liquid and graphene oxide was characterized by nuclear magnetic resonance spectroscopy (1H NMR), Fourier transform infrared spectroscopy (FTIR), and ultraviolet–visible spectroscopy (UV–vis). The result of transmission electron microscopy (TEM) demonstrated Ni-Pd NPs (3–5 nm in size) were uniformly dispersed on the IL/RGO composite. Electrochemical measurements revealed IL/RGO/Ni-Pd modified glassy carbon electrodes directly catalyzed glucose oxidation and displayed enhanced current response compared with RGO/Ni-Pd including a response time within 3 s, a linear range from 0.2 μM to 10 mM, good reproducibility, considerable stability, and excellent anti-interference to electro-active molecules. The superior catalytic activity and selectivity make the IL/RGO/Ni-Pd hybrid a promising nanomaterial for applications in direct detection of glucose.
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