Highly stable and redox active nano copper species stabilized functionalized-multiwalled carbon nanotube/chitosan modified electrode for efficient hydrogen peroxide detection

• Published in: Colloids and surfaces. A, Physicochemical and engineering aspects Vol. 395; pp. 207 - 216
• Main Authors: Annamalai, Senthil Kumar, Palani, Barathi, Chandrasekara Pillai, K.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 05.02.2012
• Subjects: ascorbic acid; carbon; carbon nanotubes; Chitosan; colloids; COMPOSITES; Copper; cysteine; ELECTRODES; electron transfer; energy-dispersive X-ray analysis; Functionalized carbon nanotube; Glassy carbon; glassy carbon electrode; HYDROGEN; HYDROGEN PEROXIDE; leaching; MICROSTRUCTURES; milk; Milk sample analysis; Nano copper species; Nanocomposites; Nanomaterials; Nanostructure; nitrites; OXIDES; SCANNING ELECTRON MICROSCOPY; transmission electron microscopy; TUBE; uric acid; X-ray photoelectron spectroscopy; Milk sample analysis; Functionalized carbon nanotube; Hydrogen peroxide; Chitosan; Nano copper species
• ISSN: 0927-7757; 1873-4359
• DOI: 10.1016/j.colsurfa.2011.12.032

[Display omitted] ► Very stable and highly redox active copper–CNT–chitosan modified electrode was prepared. ► The electrode showed selective electrocatalytic sensing of H 2O 2 in a physiological pH. ► H 2O 2 containing milk samples were tested. A highly redox active and stable nano copper species immobilized functionalized-multiwalled carbon nanotube (f-MWCNT) + chitosan (CHIT) film coated glassy carbon electrode (Cu@f-MWCNT + CHIT/GCE) was fabricated using a new preparation procedure, different from the conventional Cu 2+ + MWCNT + CHIT bulk electro-codeposition coupled glassy carbon surface activation method, for selective and sensitive amperometric estimation of H 2O 2 at −100 mV vs Ag/AgCl in physiological solution. Several copper modified film electrodes with nano copper species immobilized into films made of single component or different combinations of CNT and CHIT (i.e., Cu@f-MWCNT + CHIT/GCE, Cu@SWCNT + CHIT/GCE, Cu@f-MWCNT/GCE, Cu@MWCNT/GCE, Cu@CHIT/GCE and Cu/GCE) were characterized by cyclic voltammetry in a blank pH 7 phosphate buffer solution (PBS), and only the Cu@f-MWCNT + CHIT/GCE showed well-defined redox peak with an half-wave potential ( E 1/2) of −85 mV vs Ag/AgCl for the matrix immobilized Cu 2+/Cu + redox species with very good film stability and pronounced leaching resistance to copper. Transmission electron microscopy, scanning electron microscopy, energy dispersive X-ray analysis, X-ray photoelectron spectroscopy were used to give a complete characterization of the Cu@f-MWCNT + CHIT/GCE. Effect of potential scan rate and pH on the redox response of the Cu@f-MWCNT + CHIT/GCE was studied to probe the mechanism of Cu 2+/Cu + electron transfer process. The Cu@f-MWCNT + CHIT/GC electrode showed effective electrocatalytic reduction of H 2O 2 in pH 7 PBS. Amperometric i– t method of H 2O 2 detection yielded a calibration plot linear up to 125 μM with a current sensitivity of 0.463 A M −1 cm −2. The newly developed Cu@f-MWCNT + CHIT/GC electrode displayed remarkable tolerance to co-existing interferents, such as cysteine, ascorbic acid, uric acid and nitrite at the H 2O 2 detection potential in pH 7 PBS. The ability of the sensor electrode for routine analyses was demonstrated by the detection of H 2O 2 present in simulated milk samples with appreciable recovery values.