کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
186070 459607 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Improved l-cysteine electrocatalysis through a sequential drop dry technique using multi-walled carbon nanotubes and cobalt tetraaminophthalocyanine conjugates
ترجمه فارسی عنوان
بهبود الکتروکاتالیزوری لسیستین با استفاده از تکنیک قطره خشک متوالی با استفاده از نانولوله های کربنی چندسانی و کنوبیات تترامینوفالتیسیانین کبالت
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
چکیده انگلیسی


• A glassy carbon electrode modified with multi-walled carbon nanotubes and cobalt tetraaminophthalocyanine by a sequential drop dry method.
• The modified surface gave a better catalytic response towards the oxidation of l-cysteine than when the individual components were mixed.
• Scanning electrochemical microscopy was employed for surface characterization.

Voltammetry, chronoamperometry, scanning electrochemical microscopy and electrochemical impedance spectroscopy methods are used for characterization of a glassy carbon electrode modified with multi-walled carbon nanotubes (MWCNTs)–cobalt tetraaminophthalocyanine (CoTAPc) mixture or sequential drop dry modification technique whereby the MWCNTs are first placed on to the electrode followed by CoTAPc. The sequential drop dry CoTAPc–MWCNTs modified surface gave better catalytic responses with a catalytic rate constant of 2.2 × 105 M−1 s−1, apparent electron transfer rate constant of 0.073 cm s−1, and a limit of detection of 2.8 × 10−7 M. Scanning electrochemical microscopy (SECM) surface characterization (topography and reactivity) further gave proof the better catalytic perfomance of the sequential drop dry CoTAPc–MWCNTs modified surface.

A sequential drop dry modification of a glassy carbon electrode where by multiwalled carbon nanotubes are first placed on to the electrode followed by cobalt tetraaminophthalocyanine gave a better catalytic response towards the oxidation of l-cysteine than when the two components were mixed, due to the higher catalytic activity of the former as judged by scanning electrochemical microscopy.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 128, 10 May 2014, Pages 32–40
نویسندگان
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