Efficient generation of photocurrents by using CdS/carbon nanotube assemblies on electrodes.
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Biomedical subjects
Publications and source records attributed to Laila Sheeney-Haj-Ichia.
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Magnetic nanoparticles consisting of undecanoate-capped magnetite (average diameter approximately 4.5 nm; saturated magnetization, M(s), 38.5 emu g(-1)) are used to control and switch the hydrophobic or hydrophilic properties of the electrode surface. A two-phase system consisting of an aqueous buffer solution and a toluene phase that includes the suspended capped magnetic nanoparticles is used to control the interfacial properties of the electrode surface. The magnetic attraction of the functionalized particles to the electrode by means of an external magnet yields a hydrophobic interface that acts as an insulating layer, prohibiting interfacial electron transfer. The retraction of the magnetic particles from the electrode to the upper toluene phase by means of the external magnet generates a hydrophilic electrode that reveals effective interfacial electron transfer. The electron-transfer resistance and double-layer capacitance of the electrode surface upon the attraction and retraction of the functionalized magnetic particles to and from the electrode, respectively, by means of the external magnet were probed by Faradaic impedance spectroscopy (R(et) = 170 Omega and C(dl) = 40 microF sm(-2) in the hydrophilic state of the electrode and R(et) = 22 k Omega and C(dl) = 0.5 microF sm(-2) in the hydrophobic state of the interface). The magnetoswitchable control of the interface enables magnetic switching of the bioelectrocatalytic oxidation of glucose in the presence of glucose oxidase and ferrocene dicarboxylic acid to "ON" and "OFF" states.
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Magnetic switching of redox reactions and bioelectrocatalytic transformations is accomplished in the presence of relay-functionalized magnetite particles (Fe(3)O(4)). The electrochemistry of a naphthoquinone (1), pyrroloquinoline quinone (2; PQQ), microperoxidase-11 (3), a ferrocene derivative (4) and a bipyridinium derivative (5), functionalized magnetic particles, is switched "ON" and "OFF" by an external magnet upon the attraction of the magnetic particles to an electrode or their retraction from the electrode, respectively. The magneto-switchable activation and deactivation of the electrochemical oxidation of the ferrocene-functionalized magnetic particles and the electrochemical reduction of the bipyridinium-functionalized magnetic particles are used for the triggering of mediated bioelectrocatalytic oxidation of glucose, in the presence of glucose oxidase (GOx), and bioelectrocatalytic reduction of nitrate (NO(3) (-)), in the presence of nitrate reductase (NR), respectively. Magnetic particles functionalized with a PQQ-NAD(+) dyad are used for the magnetic switching of the bioelectrocatalytic oxidation of lactate in the presence of lactate dehydrogenase (LDH). The coupling of these particles with a ferrocene-monolayer-functionalized electrode allows the dual and selective sensing of lactate and glucose in the presence of LDH and GOx, respectively, by using an external magnet to switch the detection mode.