Voltammetric and spectroelectrochemical characterization and electrocatalytic application of metallophthalocyanines carrying pendant bulky units

2009 ◽  
Vol 13 (06) ◽  
pp. 669-680 ◽  
Author(s):  
Atıf Koca ◽  
Hatice A. Dinçer ◽  
Ergün Gonca ◽  
Ahmet Gül

In this work, voltammetric, spectroelectrochemical, and electrocatalytic properties of the metallophthalocyanines bearing four chloro and four biphenyl-malonic ester bulky groups were investigated. Voltammetric and spectroelectrochemical measurements of the metallophthalocyanines show that while cobalt phthalocyanine presents both metal-based and ring-based redox processes, all other complexes give only ring-based reduction and oxidation processes. The redox processes have generally diffusion-controlled, reversible and one-electron transferred mechanisms. Cobalt phthalocyanine electrocoated easily on the glassy carbon working electrode during the repeating cycles, a very useful feature for application in fabrication of thin films. Electrocatalytic activity of cobalt phthalocyanine to hydrogen evolution reaction was studied in solution titrated with perchloric acid and on glassy carbon electrode modified with cobalt phthalocyanine in aqueous solution. Electrocatalytic measurements show that cobalt phthalocyanine has significant catalytic activities towards hydrogen evolution reaction. Moreover, the catalytic activity of the complex enhanced significantly when the complex was incorporated into the cation exchange Nafion polymeric matrix.

2013 ◽  
Vol 125 (41) ◽  
pp. 11067-11070 ◽  
Author(s):  
Junqiao Zhuo ◽  
Tanyuan Wang ◽  
Gang Zhang ◽  
Lu Liu ◽  
Liangbing Gan ◽  
...  

Author(s):  
Lifang Chen ◽  
Rizwan Ur Rehman Sagar ◽  
Jun Chen ◽  
Juan Liu ◽  
Sehrish Aslam ◽  
...  

CrystEngComm ◽  
2019 ◽  
Vol 21 (22) ◽  
pp. 3517-3524 ◽  
Author(s):  
Yu Feng ◽  
Ke Yu ◽  
Ziqiang Zhu

A new eight-awn star TaS2 with a specially designed fractal and cracked dendrite structure was prepared, which showed outstanding HER catalytic activities owing to its specially designed structure.


2011 ◽  
Vol 8 (2) ◽  
pp. 553-560 ◽  
Author(s):  
Mohammed Zidan ◽  
Tan Wee Tee ◽  
A. Halim Abdullah ◽  
Zulkarnain Zainal ◽  
Goh Joo Kheng

A MgB2microparticles modified glassy carbon electrode (MgB2/GCE) was fabricated by adhering microparticles of MgB2onto the electrode surface of GCE. It was used as a working electrode for the detection of paracetamol in 0.1 M KH2PO4aqueous solution during cyclic voltammetry. Use of the MgB2/GCE the oxidation process of paracetamol with a current enhancement significantly by about 2.1 times. The detection limit of this modified electrode was found to be 30 μM. The sensitivity under conditions of cyclic voltammetry is significantly dependent on pH, supporting electrolyte, temperature and scan rate. The current enhancement observed in different electrolytic media varied in the following order: KH2PO4> KCl > K2SO4> KBr. Interestingly, the oxidation of paracetamol using modified GC electrode remain constant even after 15 cycling. It is therefore evident that the MgB2modifiedGCelectrode possesses some degree of stability. A slope of 0.52 dependent of scan rate on current indicates that the system undergoes diffusion-controlled process.


2011 ◽  
Vol 2011 ◽  
pp. 1-11 ◽  
Author(s):  
Gopalakrishnan Gopu ◽  
Paramasivam Manisankar ◽  
Baladhandapani Muralidharan ◽  
Chinnapiyan Vedhi

Cyclic voltammetric behaviors of three analgesics, acetaminophen (AAP), acetylsalicylic acid (ASA), and dipyrone (DP), were studied using nano-riboflavin-modified glassy carbon electrode. One well-defined oxidation peak each for AAP and ASA and three oxidation peaks for DP were observed. The influence of pH, scan rate, and concentration reveals irreversible diffusion controlled reaction. The SEM analysis confirmed good accumulation of the drugs on the electrode surface. Calibration was made under the maximum peak current conditions. The concentration range studied for the determination of drugs was 0.02 to 0.4 μg mL−1for AAP and ASA and 0.025 to 0.4 μg mL−1for DP. The lower limit of detection observed for AAP, ASA, and DP was 0.016, 0.007 μg mL−1, and 0.013 μg mL−1, respectively. The suitability of the method for the determination of these analgesics in pharmaceutical preparations and urine samples was also ascertained.


Sign in / Sign up

Export Citation Format

Share Document