Direct electrocatalytic reduction of p-nitrophenol at room temperature ionic liquid modified electrode  被引量:5

Direct electrocatalytic reduction of p-nitrophenol at room temperature ionic liquid modified electrode

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作  者:Wei Sun Mao Xia Yang Qiang Jiang Kui Jiao 

机构地区:[1]College of Chemistry and Molecular Engineering, Key Laboratory of Eco-Chemical Engineering of Ministry of Education, Qingdao University of Science and Technology, Qingdao 266042, PR China

出  处:《Chinese Chemical Letters》2008年第10期1156-1158,共3页中国化学快报(英文版)

基  金:the National Natural Science Foundation of China(Nos.20405008,20635020)

摘  要:Direct electrochemical reduction ofp-nitrophenol (PNP) was investigated on a room temperature ionic liquid N-butylpyridinium hexafluorophosphate (BPPF6) modified carbon paste electrode (CILE). The cathodic peak potential was positively shifted and the peak currents were increased compared to that obtained on traditional carbon paste electrode (CPE). The results indicated that the presence of ionic liquid BPPF6 on the electrode surface showed excellent catalytic ability to the electrochemical reduction of PNP. The electrochemical behaviors of PNP on the CILE were investigated by cyclic voltammetry and the conditions such as the scan rate, the buffer pH, the substrate concentration were optimized. The electrochemical parameters were further calculated with the results of the electron transfer number (n), the charge-transfer coefficient (α) and the surface concentration (Гr) as 1.76, 0.37 and 2.47 × 10^-9 mol/cm^2, respectively, for the selected reductive peak. The results indicated that PNP showed an irreversible adsorption-controlled electrode process on the CILE.Direct electrochemical reduction ofp-nitrophenol (PNP) was investigated on a room temperature ionic liquid N-butylpyridinium hexafluorophosphate (BPPF6) modified carbon paste electrode (CILE). The cathodic peak potential was positively shifted and the peak currents were increased compared to that obtained on traditional carbon paste electrode (CPE). The results indicated that the presence of ionic liquid BPPF6 on the electrode surface showed excellent catalytic ability to the electrochemical reduction of PNP. The electrochemical behaviors of PNP on the CILE were investigated by cyclic voltammetry and the conditions such as the scan rate, the buffer pH, the substrate concentration were optimized. The electrochemical parameters were further calculated with the results of the electron transfer number (n), the charge-transfer coefficient (α) and the surface concentration (Гr) as 1.76, 0.37 and 2.47 × 10^-9 mol/cm^2, respectively, for the selected reductive peak. The results indicated that PNP showed an irreversible adsorption-controlled electrode process on the CILE.

关 键 词:N-Butylpyridinium hexafluorophosphate Ionic liquid P-NITROPHENOL Cyclic voltammetry ELECTROCATALYSIS 

分 类 号:O64[理学—物理化学]

 

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