Xiao-mei Chen

Nonenzymatic amperometric sensing of glucose by using palladium nanoparticles supported on functional carbon nanotubes

A nonenzymatic electrochemical method was developed for glucose detection using an electrode modified with palladium nanoparticles (PdNPs)-functional carbon nanotubes (FCNTs). PdNPs were homogeneously modified on FCNTs through a facile spontaneous redox reaction and characterized by transmission electron microscopy. Based on the voltammetric and amperometric results, PdNPs efficiently catalyzed the oxidation of glucose at 0.40 V in the presence of 0.2M NaCl and showed excellent resistance towards poisoning from such interfering species as ascorbic acid, uric acid, and p-acetamidophenol. This anti-poisoning ability was investigated using analysis of the electrocatalytic products by in situ subtractively normalized interfacial Fourier transform infrared reflection spectroscopy, and the results indicated that no strongly adsorbed CO(ad) species could be found in the oxidation products, which was obviously different from the results obtained using Pt-based electrodes. In order to verify the sensor reliability, it was applied to the determination of glucose in urine samples. The results indicated that the proposed approach provided a highly sensitive, wide linear range, more facile method with good reproducibility for glucose determination, promising the development of Pd-based material in nonenzymatic glucose sensing.

Graphene and graphene-based nanomaterials: the promising materials for bright future of electroanalytical chemistry

Similar to its popular older cousins of fullerene and carbon nanotubes (CNTs), the latest form of nanocarbon, graphene, is inspiring intensive research efforts in its own right. As an atomically thin layer of sp(2)-hybridized carbon, graphene possesses spectacular electronic, optical, magnetic, thermal and mechanical properties, which make it an exciting material in a variety of important applications. In this review, we present the current advances in the field of graphene electroanalytical chemistry, including the modern methods of graphene production, and graphene functionalization. Electrochemical (bio) sensing developments using graphene and graphene-based materials are summarized in more detail, and we also speculate on their future and discuss potential progress for their applications in electroanalytical chemistry.

Non-enzymatic electrochemical glucose sensor based on platinum nanoflowers supported on graphene oxide

A non-enzymatic electrochemical method was developed for glucose detection using a glassy carbon electrode modified with platinum nanoflowers supported on graphene oxide (PtNFs-GO). PtNFs-GO was synthesized using a nontoxic, rapid, one-pot and template-free method. Low-cost, green solvent ethanol acted as the reductant, and the advanced and effective 2D carbon material-GO nanosheet acted as the stabilizing material. Their morphologies were characterized using transmission electron microscopy. Cyclic voltammetry and amperometric methods were used to evaluate the electrocatalytic activity towards glucose in neutral media. The modified electrode exhibited strong and sensitive amperometric responses to glucose even in the presence of a high concentration of chloride ions. The response time was within 5s. The interference effects from ascorbic acid and uric acid were comparatively small when operated at suitable potential. Under optimal detection potential (0.47 V with a saturated calomel reference electrode) the PtNFs-GO modified electrode performed a current response towards glucose at a broad concentration range from 2 μM to 20.3mM. Two linear regions could be observed at 2 μM to 10.3mM with a sensitivity of 1.26 μA mM(-1)cm(-2) (correlation coefficient 0.9968), and at 10.3mM to 20.3mM with a sensitivity of 0.64 μA mM(-1)cm(-2)(correlation coefficient 0.9969). The LOD of 2 μM was lower than many non-enzymatic electrochemical glucose sensors. The modified electrode was also applied to the determination of glucose in glucose injection solutions, and the satisfactory results obtained indicated that it was promising for the development of a novel non-enzymatic electrochemical glucose sensor.

An electrochemical ascorbic acid sensor based on palladium nanoparticles supported on graphene oxide

In this study, an electrochemical ascorbic acid (AA) sensor was constructed based on a glassy carbon electrode modified with palladium nanoparticles supported on graphene oxide (PdNPs-GO). PdNPs with a mean diameter of 2.6 nm were homogeneously deposited on GO sheets by the redox reaction between PdCl(4)(2-) and GO. Cyclic voltammetry and amperometric methods were used to evaluate the electrocatalytic activity towards the oxidation of AA in neutral media. Compared to a bare GC or a Pd electrode, the anodic peak potential of AA (0.006 V) at PdNPs-GO modified electrode was shifted negatively, and the large anodic peak potential separation (0.172 V) of AA and dopamine (DA), which could contribute to the synergistic effect of GO and PdNPs, was investigated. A further amperometric experiment proved that the proposed sensor was capable of sensitive and selective sensing of AA even in the presence of DA and uric acid. The modified electrode exhibited a rapid response to AA within 5s and the amperometric signal showed a good linear correlation to AA concentration in a broad range from 20 μM to 2.28 mM with a correlation coefficient of R=0.9991. Moreover, the proposed sensor was applied to the determination of AA in vitamin C tablet samples. The satisfactory results obtained indicated that the proposed sensor was promising for the development of novel electrochemical sensing for AA determination.

Platinum nanoflowers supported on graphene oxide nanosheets: their green synthesis, growth mechanism, and advanced electrocatalytic properties for methanol oxidation

This paper reports a nontoxic, rapid, one-pot and template-free synthesis of three-dimensional (3D) Pt nanoflowers (PtNFs) with high yield and good size monodispersity supported on graphene oxide (GO) nanosheets. The key synthesis strategy employed a low-cost, green solvent, ethanol as the reductant and an advanced, powerful 2D carbon material, GO nanosheets as the stabilizing material. The resulting PtNFs-GO nanosheets were characterized by transmission electron microscopy (TEM), high-resolution TEM, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and electrochemical techniques. It was found that the monodispersed, porous PtNFs supported on GO nanosheets were a uniform size of 30 nm and each was composed of numerous “clean” and small (4 nm) Pt nanoparticles, which revealed an unusually high activity for methanol oxidation reaction compared to commercial Pt black. Furthermore, based on a systematic study of the PtNFs growth conditions, a possible mechanism, and especially the importance of GO in the formation was proposed. Our study demonstrates that GO is a promising support material for developing next-generation advanced Pt based fuel cells and their relevant electrodes in the field of energy.

A novel non-enzymatic ECL sensor for glucose using palladium nanoparticles supported on functional carbon nanotubes

A novel non-enzymatic electrochemiluminescence (ECL) sensor based on palladium nanoparticles (PdNPs)-functional carbon nanotubes (FCNTs) was discovered for glucose detection. PdNPs were homogeneously modified on FCNTs using a facile spontaneous redox reaction method. Their morphologies were characterized by transmission electron microscopy (TEM). Based on ECL experimental results, the PdNPs-FCNTs-Nafion film modified electrode displayed high electrocatalytic activity towards the oxidation of glucose. The free radicals generated by the glucose oxidation reacted with the luminol anion (LH(-)), and enhanced the ECL signal. Under the optimized conditions, the linear response of ECL intensity to glucose concentration was valid in the range from 0.5 to 40 micromol L(-1) (r(2)=0.9974) with a detection limit (S/N=3) of 0.09 micromol L(-1). In addition, the modified electrode presented high resistance towards the poisoning of chloride ion, high selectivity and long-term stability. In order to verify the sensor reliability, it was applied to the determination of glucose in glucose injection samples. The results indicated that the proposed approach provided a highly sensitive, more facile method with good reproducibility for glucose determination, promising the development of a non-enzymatic ECL glucose sensor.

A facile synthesis of palladium nanoparticles supported on functional carbon nanotubes and its novel catalysis for ethanol electrooxidation

In this study, a novel material, palladium nanoparticles-carboxylic functional carbon nanotubes (PdNPs-CFCNTs), based on PdNPs supported on CFCNTs was synthesized by a facile spontaneous redox method. The material reveals high electrochemical activity and excellent catalytic characteristic for alcohol electrooxidation on a glassy carbon electrode (GCE) in an alkaline medium. The preparation mechanism was studied by the galvanic cell effect between PdCl(4)(2-) and functional defect sites on CFCNTs. Results from UV-visible absorption spectroscopy and electrochemical impedance spectroscopy revealed that the reduction of PdCl(4)(2-) to metallic Pd was successfully achieved. Morphologies of PdNPs supporting on CFCNTs (PdNPs-CFCNTs) were also characterized by transmission electron micrograph. PdNPs-CFCNTs with the best electrocatalytic characteristics were obtained under the condition as: the weight ratio of Pd to CFCNTs was kept at 2:1, the temperature was kept at 70 degrees C in the synthesis, and the scan rate of the applied potential was selected at 60 mV s(-1). The results indicate that PdNPs-CFCNTs could be a great potential material in direct ethanol fuel cells and ethanol sensors.

Fabrication of a Colorimetric Electrochemiluminescence Sensor

A colorimetric electrochemiluminescence (ECL) sensor was fabricated for the first time, based on a dual-color system including a strong red Ru(bpy)(3)(2+) ECL and a green reference light from a light emitting diode. Traditional ECL intensity information can be easily transformed into a color variation with this sensor, and the color variation can be directly monitored using the naked eye or a commercial CCD camera. The sensor has been successfully used to determine the concentration of tripropylamine, proline (enhancing system), and dopamine (quenching system). The results indicated that the color variation obtained corresponded to the concentration of target analytes. This sensor has potential application in rapid and semiquantitative ECL analysis.

Electrogenerated chemiluminescence ethanol biosensor based on alcohol dehydrogenase functionalized Ru(bpy)32+ doped silica nanoparticles

An ethanol biosensor, based on the electrogenerated chemiluminescence of Ru(bpy)(3)(2+)-doped silica nanoparticles (RuSiNPs), was investigated in this study. The biosensor was a modified glassy carbon electrode, where alcohol dehydrogenase was crosslinked to RuSiNPs, and then immobilized on the electrode surface using chitosan. The results indicated that the biosensor exhibited excellent performance during ethanol determination with a wide linear range (10(-7) to 10(-2) M), low detection limit (5.0x10(-8) M) and good stability.

A novel electrochemiluminescence tetracyclines sensor based on a Ru(bpy)32+-doped silica nanoparticles/Nafion film modified electrode

A novel method for the determination of tetracyclines (TCs) using electrochemiluminescence (ECL) based on a Ru(bpy)3(2+)-doped silica nanoparticles (RuSiNPs)/Nafion film modified electrode is presented in this paper. The RuSiNPs were prepared by a water-in-oil microemulsion method. The characterization results indicated that the thus-prepared RuSiNPs presented a uniform size of 45 nm and retained the original electrochemical properties of Ru(bpy)3(2+). Importantly, the ECL response on RuSiNPs/Nafion film modified electrode was greatly enhanced by TCs. Under the optimum conditions, the ECL intensity versus the concentration of TCs was found to be linear over the range of 1-100 μmol L(-1) for tetracycline (TC), 0.1-100 μmol L(-1) for oxytetracycline (OTC) and 1-100 μmol L(-1) for chlortetracycline (CTC). The detection limits (S/N=3) were 0.23 μmol L(-1) for TC, 0.10 μmol L(-1) for OTC and 0.16 μmol L(-1) for CTC. Moreover, due to the electrostatic interaction between Ru(bpy)3(2+) and silica matrix, the leaching of Ru(bpy)3(2+) was greatly reduced, therefore, the ECL sensor exhibited excellent repeatability and stability in the detection of TCs. Based on these investigations, the proposed ECL approach was successfully used to analyze the TCs content in drugs.