International Scholarly Research Notices

Review Article

Electrosynthesis and Spectroscopic Characterization of Poly(o-Aminophenol) Film Electrodes

Table 1

Electropolymerization of o-aminophenol on different electrode materials and in different electrolyte media.


Electrode materials	Electrolyte medium	Electrosynthesis method	Reference

Pt, Au, and glassy carbon	0.1 M HClO₄ + 0.4 M NaClO₄ + 1 × 10⁻³M o-AP (1 < pH < 7)	Potentiodynamic cycling − 0.25 V and 0.70 V (SCE)	[10]

Pt electrode	0.4 mol cm⁻³ of NaClO₄ + 10⁻²mol dm⁻³ of o-AP	Potentiodynamic cycling −0.25 V and 0.75 V (SCE)	[12]

Carbon paste electrode	5 mM o-AP+ 0.5 M HClO₄ in the presence and in the absence of sodium dodecyl sulfate	Potentiodynamic cycling −0.1 V and 0.7 V (Ag/AgCl/KCl 3 M)	[13]

Platinum and glassy carbon electrodes	0.2 M NaClO₄ + 0.1 M HClO₄ + 5 × 10⁻³M o-AP solution	Potentiodynamic cycling 0.2 V and 1.3 V (RHE)	[14]

Glassy carbon electrodes chemical (nitric acid (67% wt/wt) and sulfuric acid (98% wt/wt) for 10 min) and electrochemically (1.85 V (SCE) for 5 min) pretreated before electropolymerization of o-AP	0.1 M H₂SO₄+ 0.05 M o-AP	Potentiodynamic method (−0.2 V and 0.7 V versus SCE)	[15]

Basal-plane pyrolytic graphite and In-Sn oxide conducting glass	0.5 M Na₂SO₄ solution (pH 1) + 50 mM o-AP	Potentiodynamic cycling (−0.4 and 1.0 V versus sodium chloride saturated calomel electrode)	[16]

Glassy carbon	1 M SO₄H₂+ 0.5 M Na₂SO₄ + 50 mM o-AP solution	Potentiodynamic cycling (−0.2 V and 1.0 V versus SCE)	[17]

Glassy carbon and Pt electrodes	0.05 M o-AP in a mixture of 1 M H₂SO₄ and 0.5 M Na₂SO₄	Potentiodynamic cycling (−0.2 V to 0.8 V versus SCE)	[18]

Pt and Au electrodes	0.05 M o-AP + 0.5 M H₂SO₄solution	Potentiostatic method ( V; 0.8 V and 0.9 V versus SCE	[19]

Pt and GC electrodes	0.05 M o-aminophenol solution in 0.5 M HClO_4. + 10 mM sulfonated nickel phtalocyanine	Potentiodynamic cycling (–0.25 and 0.7 V versus SCE)	[20]

GC electrodes	0.10 M HClO₄ + 0.10 M o-AP	Potentiodynamic (−0.10 V and 1.00 V versus SCE) and potentiostatic ( V for a given time) methods	[21]

Vitreous carbon, platinum, and copper	0.3 M NaOH hydroalcoholic solution (70 vol% H₂O, 30 vol% CH₃OH) + 0.1 M o-AP	Potentiodynamic cycling	[22]

Glassy carbon electrode or on a glass plate covered with semiconducting indium thin oxide	1 M phosphate buffer pH 5.55 solution containing 25 μg/mL of laccase and 10 mM o-AP	Potentiodynamic cycling (−0.1 V and 0.9 V versus Ag/AgCl)	[23]