کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7233520 | 1470972 | 2014 | 21 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
High loading Pt nanoparticles on functionalization of carbon nanotubes for fabricating nonenzyme hydrogen peroxide sensor
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
A very efficient, simple approach was developed to fabricate a high Pt nanoparticles-loading multiwall carbon nanotube (MWCNTs) amperometric sensor for hydrogen peroxide (H2O2) determination. In this strategy, MWCNTs were first functionalized with an anionic surfactant, sodium dodecyl sulfate (SDS); then the Pt nanoparticles (NPs) were loaded on MWCNTs-SDS by electrodepositing. The large amounts of Pt nanoparticles could be well deposited on the surface of the MWCNTs-SDS modified electrode, as revealed by scanning electron microscopy (SEM). In addition, the PtNPs/MWCNTs-SDS composite was also characterized by electrochemical methods including cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The experimental results demonstrated that the constructed electrode exhibited good catalytic activity toward the hydrogen peroxide, and obtained a wide linear range from 5.8Ã10â9 to 1.1Ã10â3Â M with a limit of detection (LOD) of 1.9Ã10â9Â M, which was superior to that obtained with other H2O2 electrochemical sensors reported previously. Moreover, it can also be applied to real samples analysis. The excellent performance of hydrogen peroxide sensor was ascribed to the MWCNTs-SDS composites being used as effective load matrix for the deposition of PtNPs and the synergistic amplification effect of the two kinds of nanomaterials-PtNPs and MWCNTs.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biosensors and Bioelectronics - Volume 59, 15 September 2014, Pages 221-226
Journal: Biosensors and Bioelectronics - Volume 59, 15 September 2014, Pages 221-226
نویسندگان
Xiaoyan Li, Xiuhui Liu, Weiwei Wang, Lin Li, Xiaoquan Lu,