Bimodal Electrochemiluminescence of G-CNQDs in the Presence of Double Coreactants for Ascorbic Acid Detection.

How to improve the accuracy of target detection substance in low-content and complex of real sample, which is still a major challenge in the analysis field. There is no doubt that the internal standard method is the best choice in the analysis methods. The internal standard method of ECL strategy can furnish more accurate detection results in the changeable complex environment, and it can dispel the primary vaguest interference in the system through the self-calibration of two emission spectra.

New Insight into Procedure of Interface Electron Transfer through Cascade System with Enhanced Photocatalytic Activity.

Recombination of photogenerated electron-hole pairs is extremely limited in the practical application of photocatalysis toward solving the energy crisis and environmental pollution. A rational design of the cascade system (i.e.

Preparation of GO-COOH/AuNPs/ZnAPTPP nanocomposites based on the π-π conjugation: Efficient interface for low-potential photoelectrochemical sensing of 4-nitrophenol.

The GO-COOH/AuNPs/ZnAPTPP nanocomposites were constructed using zinc monoamino porphyrin (ZnAPTPP) through π-π conjugation with carboxylated graphene oxide (GO-COOH) loaded with Au nanoparticles (AuNPs). Prepared materials were characterized by H NMR spectra, UV-vis absorption spectroscopy and electrochemical impedance spectroscopy. ITO electrode surface was modified with the prepared nanocomposites showed a good photocurrent response when the bias potential, -0.

Behaviors of the Interfacial Consecutive Multistep Electron Transfer Controlled by Varied Transition Metal Ions in Porphyrin Cores.

Almost all life activities involve the process of multistep electron transfer (ET) which occurs on biomembrane. Metalloporphyrins (MTPPs) are a class of molecules which are closely related to life course. Here, the n-step (n = 1, 2) ET behaviors controlled by different metal ions in porphyrin cores were investigated by thin-layer cyclic voltammetry (TLCV).

Porphyrin aggregates decorated MWCNT film for solar light harvesting: influence of J- and H-aggregation on the charge recombination resistance, photocatalysis, and photoinduced charge transfer kinetics.

J- and H-aggregates of zinc tetraphenylporphyrin (ZnTPP) on carbon nanotube films (CNTFs) were prepared using the mixed solvent method. This resulted in completely different structures, such as the four-leaf clover and flower, on the CNTF, which were observed by recording SEM images. Characteristic changes in the electronic spectra of the ZnTPP monomer appeared when it underwent J- and H-aggregation.

Electrochemiluminescence behavior of meso-tetra(4-sulfonatophenyl)porphyrin in aqueous medium: its application for highly selective sensing of nanomolar Cu(2.).

The cathodic electrochemiluminescence (ECL) behavior of meso-tetra(4-sulfonatophenyl)porphyrin (TSPP) with potassium peroxydisulfate (K2S2O8) as the coreactant in aqueous solution with strong and stable emission was exploited to determine Cu(2+) down to nanomolar concentration. Two possible reaction mechanisms have been proposed to understand the generation of ECL by the TSPP/K2S2O8 system. The effects of the concentration of TSPP and K2S2O8, pH of the medium, and scan rate on the ECL intensity were studied in detail.

Micelle mediated trace level sulfide quantification through cloud point extraction.

A simple cloud point extraction protocol has been proposed for the quantification of sulfide at trace level. The method is based on the reduction of iron (III) to iron (II) by the sulfide and the subsequent complexation of metal ion with nitroso-R salt in alkaline medium. The resulting green-colored complex was extracted through cloud point formation using cationic surfactant, that is, cetylpyridinium chloride, and the obtained surfactant phase was homogenized by ethanol before its absorbance measurement at 710 nm.

Micellar-mediated extractive spectrophotometric determination of hydrogen sulfide/sulfide through Prussian Blue reaction: application to environmental samples.

A sensitive surfactant-mediated extractive spectrophotometric method has been developed, based on the reaction of ferric iron with sulfide to form ferrous iron and its subsequent reaction with ferricyanide to form Prussian Blue, to quantify trace levels of hydrogen sulfide/sulfide in environmental samples. The method obeys Beer's law in the concentration range 2-10 microg of sulfide in 25 mL of aqueous phase with molar absorptivity (epsilon) of 3.92 x 10(4) L mol(-1) cm(-1).