Electrochemical impedance study of polypyrrole modified electrodes bearing bathophenanthroline disulfonate in copper analysis

1997 ◽  
Vol 42 (3) ◽  
pp. 461-469 ◽  
Author(s):  
Kwok-Keung Shiu ◽  
Yingzhou Zhang
2021 ◽  
Author(s):  
◽  
Lekhetho Simon Mpeta

Conjugates of nanomaterials and metallophthalocyanines (MPcs) have been prepared and their electrocatalytic activity studied. The prepared nanomaterials are zinc oxide and silver nanoparticles, reduced graphene oxide nanosheets and semiconductor quantum dots. The MPcs used in this work are cobalt (II) (1a), manganese(III) (1b) and iron (II) (1c) 2,9(10),16(17),23(24)- tetrakis 4-((4-ethynylbenzyl) oxy) phthalocyaninato, 2,9(10),16(17),23(24)- tetrakis(5-pentyn-oxy) cobalt (II) phthalocyaninato (2), 9(10),16(17),23(24)- tris-[4-tert-butylphenoxy)-2- (4-ethylbezyl-oxy) cobalt (II) phthalocyaninato (3), 9(10),16(17),23(24)- tris-[4-tertbutylphenoxy)-2-(pent-4yn-yloxy)] cobalt (II) phthalocyaninato (4), cobalt (II) (5a) and manganese (III) (5b) 2,9(10),16(17),23(24)- tetrakis [4-(4-(5-chloro-1H-benzo [d]imidazol-2-yl)phenoxy] phthalocyaninato and 9(10),16(17),23(24)- tris tert butyl phenoxy- 2- [4-(4-(5-chloro-1H-benzo[d]imidazole-2-yl)phenoxy] cobalt (II) phthalocyaninato (6). Some of these MPcs (1a, 3 and 4) were directly clicked on azide grafted electrode, while some (1b, 1c, 2, 5a and 5b) were clicked to azide functionalised nanomaterials and then drop-dried on the electrodes. One phthalocyanine (5b) was drop-dried on the electrode then silver nanoparticles were electrodeposited on it taking advantage of metal-N bond. Scanning electrochemical microscopy, voltammetry, chronoamperometry, electrochemical impedance spectroscopy are among electrochemical methods used to characterise modified electrodes. Transmission electron microscopy, X-ray photoelectron spectroscopy, Xray diffractometry, Raman spectroscopy and infrared spectroscopy were employed to study surface functionalities, morphology and topography of the nanomaterials and complexes. Electrocatalytic activity of the developed materials were studied towards oxidation of 2-mercaptoethanol, hydrazine and hydrogen peroxide while the reduction study was based on oxygen and hydrogen peroxide. In general, the conjugates displayed superior catalytic activity when compared to individual materials. Complex 2 alone and when conjugated to zinc oxide nanoparticles were studied for their nonlinear optical behaviour. And the same materials were explored for their hydrazine detection capability. The aim of this study was to develop sensitive, selective and affordable sensors for selected organic waste pollutants. Conjugates were found to achieve the aim of the study compared to when individual materials were employed.


2017 ◽  
Vol 7 ◽  
pp. 413-419 ◽  
Author(s):  
N. Idusuyi ◽  
O.O. Ajide ◽  
O.O. Oluwole ◽  
O.A. Arotiba

2018 ◽  
Vol 528 ◽  
pp. 263-270 ◽  
Author(s):  
Mohammad Yaser Khani Meynaq ◽  
Britta Lindholm-Sethson ◽  
Solomon Tesfalidet

Batteries ◽  
2019 ◽  
Vol 5 (1) ◽  
pp. 16 ◽  
Author(s):  
Jonathan Schneider ◽  
Eduard Bulczak ◽  
Gumaa El-Nagar ◽  
Marcus Gebhard ◽  
Paul Kubella ◽  
...  

The performance of all-V redox flow batteries (VRFB) will decrease when they are exposed to dynamic electrochemical cycling, but also when they are in prolonged contact with the acidic electrolyte. These phenomena are especially severe at the negative side, where the parasitic hydrogen evolution reaction (HER) will be increasingly favored over the reduction of V(III) with ongoing degradation of the carbon felt electrode. Bismuth, either added to the electrolyte or deposited onto the felt, has been reported to suppress the HER and therefore to enhance the kinetics of the V(II)/V(III) redox reaction. This study is the first to investigate degradation effects on bismuth-modified electrodes in the negative half-cell of a VRFB. By means of a simple impregnation method, a commercially available carbon felt was decorated with Bi 2 O 3 , which is supposedly present as Bi(0) under the working conditions at the negative side. Modified and unmodified felts were characterized electrochemically using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in a three-electrode setup. Surface morphology of the electrodes and composition of the negative half-cell electrolyte were probed using scanning electron microscopy (SEM) and X-ray fluorescence spectroscopy (TXRF), respectively. This was done before and after the electrodes were subjected to 50 charge-discharge cycles in a battery test bench. Our results suggest that not only the bismuth catalyst is dissolved from the electrode during battery operation, but also that the presence of bismuth in the system has a strong accelerating effect on electrode degradation.


2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Lei Cheng ◽  
Youjun Fan ◽  
Xingcan Shen ◽  
Hong Liang

A hybrid and hierarchical nanocomposite was successfully prepared by the growth of zeolitic imidazolate framework-8 (ZIF-8) on the template of ionic liquid (IL, [Bmim][BF4]) functionalized reduced graphene oxide (IL-RGO). The structure and morphology of the IL-RGO/ZIF-8 nanocomposite were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FTIR), and Raman spectroscopy. The results showed that RGO sheets were refrained from restacking by IL, and ZIF-8 nanoparticles grew well on the surface of IL-RGO. Owing to the synergistic effect from large surface area and excellent electrocatalytic activity of ZIF-8 and great electrical conductivity of IL-RGO, a highly sensitive sensor for dopamine (DA) can be obtained. IL-RGO/ZIF-8-modified electrode exhibits good electrocatalytic activity and electroconductive properties towards DA which were investigated by cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). Compared with bare or IL-RGO-modified electrodes, the IL-RGO/ZIF-8-modified electrode effectively depressed the oxidation overpotential of DA. The linear response range of DA was from 1.0×10−7 to 1.0×10−4 mol/L with a low detection of limit 3.5×10−8 mol/L. In addition, the sensor was shown to provide satisfactory stability for the determination of DA.


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