Fabrication of a sensitive amperometric sensor for NADH and H2O2 using palladium nanoparticles-multiwalled carbon nanotube nanohybrid.

Palladium nanoparticles decorated multiwalled carbon nanotubes (PdNPs-MWCNTs) were synthesized and simply cast on the surface of a glassy carbon electrode (GCE) to prepare an amperometric sensor. The fabricated sensor (PdNPs-MWCNTs/GCE) showed excellent electrocatalytic activity towards NADH and H2O2 oxidation and H2O2 reduction. A fast, linear and highly sensitive response was observed for NADH in the concentration range between 0.1 and 200 µM with a detection limit (S/N=3) of 32 nM. Also, the sensor exhibited fast and sensitive responses (<2 s) towards H2O2. The sensitivity and detection limit for H2O2 at the operating potential of +0.35 V were 167 nA µM(-1)cm(-2) and 1.2 µM, respectively and better than those obtained at the operating potential of -0.25 V (68 nA µM(-1)cm(-2) and 14 µM). Moreover, further modification of the proposed sensor by glucose oxidase led to the fabrication of a glucose biosensor with satisfactory performance.

Direct electron transfer of Phanerochaete chrysosporium cellobiose dehydrogenase at platinum and palladium nanoparticles decorated carbon nanotubes modified electrodes.

In the present work, platinum and palladium nanoparticles (PtNPs and PdNPs) were decorated on the surface of multi-walled carbon nanotubes (MWCNTs) by a simple thermal decomposition method. The prepared nanohybrids, PtNPs-MWCNTs and PdNPs-MWCNTs, were cast on the surface of spectrographic graphite electrodes and then Phanerochaete chrysosporium cellobiose dehydrogenase (PcCDH) was adsorbed on the modified layer. Direct electron transfer between PcCDH and the nanostructured modified electrodes was studied using flow injection amperometry and cyclic voltammetry. The maximum current responses (Imax) and the apparent Michaelis-Menten constants (K) for the different PcCDH modified electrodes were calculated by fitting the data to the Michaelis-Menten equation and compared. The sensitivity towards lactose was 3.07 and 3.28 µA mM(-1) at the PcCDH/PtNPs-MWCNTs/SPGE and PcCDH/PdNPs-MWCNTs/SPGE electrodes, respectively, which were higher than those measured at the PcCDH/MWCNTs/SPGE (2.60 µA mM(-1)) and PcCDH/SPGE (0.92 µA mM(-1)). The modified electrodes were additionally tested as bioanodes for biofuel cell applications.

Photocurrent generation from thylakoid membranes on osmium-redox-polymer-modified electrodes.

Thylakoid membranes (TMs) are uniquely suited for photosynthesis owing to their distinctive structure and composition. Substantial efforts have been directed towards use of isolated photosynthetic reaction centers (PRCs) for solar energy harvesting, however, few studies investigate the communication between whole TMs and electrode surfaces, due to their complex structure. Here we report on a promising approach to generate photosynthesis-derived bioelectricity upon illumination of TMs wired with an osmium-redox-polymer modified graphite electrode, and generate a photocurrent density of 42.4 µA cm(-2).

Sensitive and selective determination of hydrazine using glassy carbon electrode modified with Pd nanoparticles decorated multiwalled carbon nanotubes.

A glassy carbon electrode modified with palladium nanoparticles decorated multiwalled carbon nanotubes (GCE/nanoPd-MWCNTs) was fabricated. Incorporation of palladium nanoparticles onto the carbon nantube surface by thermal decomposition of palladium acetate led to the fabrication of a sensor with a significant decrease in hydrazine electrooxidation potential. The sensor exhibited low detection limits, high sensitivity and selectivity, rapid response, and good stability toward hydrazine detection.

Fabrication of bulk-modified carbon paste electrode containing alpha-PW12O40(3-) polyanion supported on modified silica gel: Preparation, electrochemistry and electrocatalysis.

Alpha-PW(12)O(40)(3-) (PW(12)) supported on the surface of silica gel derivatized by 3-aminopropyl(triethoxy)silane (devoted briefly as SiNH(3)PW(12)) was synthesized and used as bulk modifier to fabricate a renewable three-dimensional chemically modified electrode. The electrochemical behavior of the modified electrode was characterized by cyclic voltammetry. There is an ionic bonding character between PW(12) and the surface amino groups of modified silica, which greatly improves the stability of SiNH(3)PW(12)-modified carbon paste electrode due to insolubility of silica gel in water. The SiNH(3)PW(12) bulk-modified carbon paste electrode not only maintains the electrochemical activity of PW(12), but also exhibits remarkable advantages of renewability, as well as simple preparation and inexpensive material. The modified electrode offers an excellent and stable electrocatalytic response for the reduction of IO(3)(-) and hydrogen peroxide. The SiNH(3)PW(12)-CPE is successfully applied as an electrochemical detector to monitor IO(3)(-) in flow injection analysis (FIA). The catalytic peak current was found to be linear with the IO(3)(-) concentration in the range 5x10(-6) to 1x10(-3)molL(-1). The detection limit of the proposed method was found to be 3.1x10(-6)molL(-1) for IO(3)(-) determination.