A bulk micromachined silicon neural probe with nanoporous platinum electrode for low impedance recording

Author(s):  
Yi Jae Lee ◽  
Su Jin Lee ◽  
Hyo Sang Yoon ◽  
Jae Yeong Park
Nanoscale ◽  
2020 ◽  
Vol 12 (43) ◽  
pp. 22129-22139
Author(s):  
Zohreh Sadat Miripour ◽  
Parisa Aghaee ◽  
Reihane Mahdavi ◽  
Mohammad Ali Khayamian ◽  
Amir Mamdouh ◽  
...  

We present a new design on the Single Needle Electrochemical Therapy method by introducing some major improvements, including a nanoporous platinum electrode, tunable in situ anode size, and intratherapeutic impedance recording by the same needle.


Sensors ◽  
2008 ◽  
Vol 8 (10) ◽  
pp. 6154-6164 ◽  
Author(s):  
Yi-Jae Lee ◽  
Dae-Joon Park ◽  
Jae-Yeong Park ◽  
Younghun Kim

2018 ◽  
Vol 33 (21) ◽  
Author(s):  
Do Youn Kim ◽  
Yunseo Ku ◽  
Joong Woo Ahn ◽  
Chiheon Kwon ◽  
Hee Chan Kim

2009 ◽  
Vol 1 (2) ◽  
pp. 18-20
Author(s):  
Dahyunir Dahlan

Copper oxide particles were electrodeposited onto indium tin oxide (ITO) coated glass substrates. Electrodeposition was carried out in the electrolyte containing cupric sulphate, boric acid and glucopone. Both continuous and pulse currents methods were used in the process with platinum electrode, saturated calomel electrode (SCE) and ITO electrode as the counter, reference and working electrode respectively. The deposited particles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It was found that, using continuous current deposition, the deposited particles were mixture of Cu2O and CuO particles. By adding glucopone in the electrolyte, particles with spherical shapes were produced. Electrodeposition by using pulse current, uniform cubical shaped Cu2O particles were produced


1993 ◽  
Vol 28 (11-12) ◽  
pp. 473-480
Author(s):  
A. Heduit ◽  
B. Martin ◽  
I. Duchamp ◽  
D. R. Thevenot

Gold and platinum were compared to ascertain how they expressed a stabilized potential in activated sludge. The comparison was based on electrochemical determination of the electron transfer rate (i.e. equilibrium exchange current density) and recording of potentials against time. When both metals are treated in the same way, platinum gives equilibrium exchange current densities approx. 10 times higher than gold, both in aerated activated sludge and in treated water. For platinum, the equilibrium exchange current densities range from 0.1 to 0.25 µA/cm2 immediately after polishing and decrease during prolonged contact with activated sludge subjected to alternating aeration/anoxia sequences. The lower kinetics of electron transfer on gold go together with significant differences in response:- In an aerobic medium a gold electrode potential is lower than that of a platinum electrode. In a strongly anaerobic medium, the reverse is true. Consequently, the amplitude of the potential variation between aerobic and anaerobic media is smaller for gold than for platinum. Under our experimental conditions this amplitude was approx 350 mV for gold and 850 mV for platinum.- The slopes of the linear relationships between potential and pH or potential and the logarithm of the dissolved oxygen concentration are two or three times greater for platinum than for gold. Although the values obtained with platinum electrodes cannot represent a veritable equilibrium state, the platinum electrode zero-current potential would seem to be far more sensitive to variations in the medium than that of the gold electrode; it is, therefore, more suitable for use in activated sludge.


2000 ◽  
Vol 65 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Tomáš Loučka

The aim of this research was to study the oxidation and reduction of the adsorbed thiosulfate on the platinum electrode in a slightly alkaline medium. The adsorption was performed at the open circuit conditions. The reduction of the adsorbed layer in the hydrogen region is slower in a slightly alkaline medium than in acid. The mechanism of reduction and oxidation of adsorbed molecules is probably the same. The nonstationary currents measured in presence of thiosulfates showed that the change in the oxidation number does not take place during the adsorption in the double layer region. In the hydrogen region, thiosulfate replaces the adsorbed hydrogen while beeing reduced. Nonstationary currents at higher concentrations of thiosulfate indicate the presence of more layers on the electrode. Upon reaching higher concentrations of thiosulfate the oxidation reaction takes place between thiosulfate in solution and adsorbed product of its reduction. The open circuit potential of the platinum electrode measured in a thiosulfate solution was 0.780 and 0.783 V against the hydrogen electrode in the same solution.


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