Mechanisms of Charge Storage in Nanoparticulate TiO2 and Li4Ti5O12 Anodes: New Insights from Scan rate-dependent Cyclic Voltammetry

2015 ◽  
Vol 168 ◽  
pp. 125-132 ◽  
Author(s):  
Martin Opitz ◽  
Junpei Yue ◽  
Jens Wallauer ◽  
Bernd Smarsly ◽  
Bernhard Roling
2021 ◽  
Vol 883 ◽  
pp. 115056
Author(s):  
Alexander V. Kosov ◽  
Olga V. Grishenkova ◽  
Olga L. Semerikova ◽  
Vladimir A. Isaev ◽  
Yurii P. Zaikov

2021 ◽  
Vol 3 (6) ◽  
Author(s):  
Santanu Dey ◽  
Pradipta Chakraborty ◽  
Dhiraj Kumar Rana ◽  
Subhamay Pramanik ◽  
Soumen Basu

AbstractWe have synthesized carbon-supported silver (Ag/C) nanobars by a simple surfactant-free hydrothermal method using glucose as the reducing reagent as well as the source of carbon in Ag/C nanobars. Physicochemical characterization of the materials was performed by X-ray Diffraction (XRD), field emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The XRD pattern confirmed the presence of a pure metallic silver phase. No carbon phase was detected, which indicates that the carbon exists mainly in the amorphous form. The electrocatalytic activity of Ag/C in different electrolyte solutions such as 0.5 M NaOH, 0.5 M NaOH + 1 M ethanol (EtOH), 0.5 M NaOH + 1 M ethylene glycol (EG), and 0.5 M NaOH + 0.01 M NaBH4 (sodium borohydride) was studied by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronoamperometry (CA) study. Alcohol tolerance of the catalysts was also established in the presence of ethanol and ethylene glycol. The forward-to-backward current ratio from cyclic voltammetry (CV) study of Ag/C-20 (20 h) in 0.5 M NaOH + 1 M ethanol solution at 100 mV s−1 scan rate is 4.13 times higher compared to that of Ag/C-5 (5 h). Hence, Ag/C-20 is a better candidate for the tolerance of ethanol. In the presence of ethylene glycol (1 M) in 0.5 M NaOH solution, it is obtained that the forward-to-backward current ratio at the same scan rate for Ag/C-20 is lower than that in the presence of ethanol. The durability of the catalyst was studied by chronoamperometry measurement. We studied the electrochemical kinetics of Ag/C catalysts for borohydride oxidation in an alkaline medium. The basic electrochemical results for borohydride oxidation show that Ag/C has very well strength and activity for direct borohydride oxidation in an alkaline medium. The reaction of borohydride oxidation with the contemporaneous BH4−. hydrolysis was noticed at the oxidized silver surface. Among all the synthesized Ag/C catalysts, Ag/C-20 exhibited the best electrocatalytic performance for borohydride oxidation in an alkaline medium. The activation energy and the number of exchange electrons at Ag/C-20 electrode surface for borohydride electro-oxidation were estimated as 57.2 kJ mol−1 and 2.27, respectively.


2021 ◽  
Author(s):  
Xiangjun Pu ◽  
Dong Zhao ◽  
Chenglong Fu ◽  
Zhongxue Chen ◽  
Shunan Cao ◽  
...  

2019 ◽  
Vol 338 ◽  
pp. 5-11 ◽  
Author(s):  
Thiago A. Vieira ◽  
Jhonathan R. Souza ◽  
Denise T. Gimenes ◽  
Rodrigo A.A. Munoz ◽  
Edson Nossol

2020 ◽  
Vol 9 (2) ◽  
pp. 142-152
Author(s):  
Fitria Rahmawati ◽  
◽  
Dwi Aman Nur Romadhona ◽  
Syulfi Faiz ◽  
◽  
...  

Research to prepare NaFePO4 cathode material from iron sand was conducted. The iron sand consists of ilmenite FeTiO3 and hematite Fe2O3. A caustic fusion method used to precipitate iron as Fe(OH)3 and it increased Fe content up to 94.71 %. Phosphate precipitation successfully produced trigonal FePO4 and monoclinic FePO4 comply with ICSD#412736 and ICSD#281079. The prepared-FePO4 was then used as a precursor for Na insertion by applying cyclic voltammetry mode within 2.0 – 4.0 V with 0.05 mVs-1 of the scan rate. It produced orthorhombic olivine NaFePO4 and a secondary phase of orthorhombic Na0.7FePO4. Impedance analysis at 20 Hz – 5 MHz found that the material provided a semicircle at 100 Hz peak point, indicating electrode-bulk interface with a resistance value of 1735W, comparable to the electrical conductivity of 5.36 x 10-6 Scm-1. Even though the conductivity value is quite lower than NaFePO4 prepared from a commercial FePO4 that has been conducted in our previous research, however the electrical conductivity still reliable for cathode.


1989 ◽  
Vol 44 (10) ◽  
pp. 1199-1202 ◽  
Author(s):  
Harald Müller ◽  
Heinz P. Fritz ◽  
Anton Lerf ◽  
Jürgen O. Besenhard

The electrochemistry of BEDT-TTF+ was investigated by means of cyclic voltammetry in solvents most frequently used for the electrocrystallization of radical cations of this donor. It can be shown that the reversibility of redox reactions is decreasing with the scan rate, with a significant influence of solvent. The results presented allow conclusions about the mechanism of electrocrystallization.


1987 ◽  
Vol 65 (5) ◽  
pp. 1051-1057 ◽  
Author(s):  
Gordon N. Eccles ◽  
William C. Purdy

By using pulse cyclic voltammetry rather than cyclic voltammetry at a relatively high scan rate, an increase in sensitivity and a lowering of the detection limit by more than a factor of two are demonstrated for the ferricyanide–ferrocyanide couple at a carbon electrode. The test for reversibility based on peak shape or symmetry comparison is enhanced significantly with pulse cyclic voltammetry. Another reversibility test, by observing peak variations as a function of scan rate, was applied to pulse cyclic voltammetry and was found to be as diagnostically informative as the cyclic voltammetry test. These tests are illustrated by a study of the hydroquinone–quinone couple.


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.


2020 ◽  
Vol 1012 ◽  
pp. 147-152
Author(s):  
L.S.V. Silva ◽  
G.L. Mansani ◽  
D.S. Yoshikawa ◽  
J.C.S. Casini ◽  
R.N. Faria

The equivalent series resistances (ESR) and specific capacitances (Cs) of supercapacitors carbon electrodes have been investigated using cyclic voltammetry and electrochemical impedance spectroscopy. Commercial activated carbon electrodes employing organic electrolyte have been tested using a potential window in the range of 2.7–3.8 V. Specific capacitances were calculated from cyclic voltammetry curves at room temperature employing various scan rates (30 and 100mVs-1). Internal series resistances of the supercapacitors were measured using the galvanostatic curves at room temperature and above (25 and 50°C). The ESR increase to 9.8 Ω at 25° and 2.7V to 78.8 Ω at with operating temperature raise and also with overpotential. A compositional and morphological evaluation of these electrodes showed a very homogeneous structure. It has been shown that the specific capacitance decreased considerably with scan rate, current density, electrochemical potential window and working temperature.


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