Yuanyuan Jiang

Novel blue light emitting graphene oxide nanosheets fabricated by surface functionalization

Graphene and graphene oxide (GO) attract increasing attention due to their unique physical and chemical properties and thus the potential applications in optics and electronics. However, the gapless band structure greatly limits their wide applications in opto-electronic devices. Surface functionalization was found to be an effective method to tune the properties of graphene and GO. In the present report, GO hybrid materials with blue-emission were fabricated through the GO surface functionalization with aryl diazonium salts of 2-aminoanthracene. The obtained hybrids were carefully characterized with atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), Fourier-transformed infrared spectroscopy (FTIR), Raman spectroscopy and UV-Vis absorption spectroscopy. Significantly different from the cyan emission (∼491 nm) of monomeric 2-aminoanthracene, the as-synthesized GO hybrid composites exhibited strong blue photoluminescence centered at ca. 400 nm. The large blue shift of the luminescence (∼91 nm) obtained from the functionalized GO could be partly ascribed to the rigid chemical environment with anthryl moieties chemically bonded onto GO surface. Such surface-functionalized GO hybrids with unique optical properties render them exciting materials for opto-electronic devices.

Functionalization of graphene with electrodeposited Prussian blue towards amperometric sensing application

Prussian blue (PB) was grown compactly on graphene matrix by electrochemical deposition. The as-prepared PB-graphene modified glassy carbon electrode (PB-graphene/GCE) showed excellent electrocatalytic activity towards both the reduction of hydrogen peroxide and the oxidation of hydrazine, which could be attributed to the remarkable synergistic effect of graphene and PB. The PB-graphene/GCE showed sensitive response to H(2)O(2) with a wide linear range of 10-1440 μM at 0.0V, and to hydrazine with a wide linear range of 10-3000 μM at 0.35 V. The detection limit was 3 μM and 7 μM, respectively, and both of them had rapid response within 5s to reach 95% steady state response. The wide linear range, good selectivity and long-time stability of the PB-graphene/GCE make it possible for the practical amperometric detection of hydrogen peroxide and hydrazine.

Green-synthesized gold nanoparticles decorated graphene sheets for label-free electrochemical impedance DNA hybridization biosensing

Sensitive electrochemical impedance assay of DNA hybridization by using a novel graphene sheets platform was achieved. The graphene sheets were firstly functionalized with 3,4,9,10-perylene tetracarboxylic acid (PTCA). PTCA molecules separated graphene sheets efficiently and introduced more negatively-charged -COOH sites, both of which were beneficial to the decoration of graphene with gold nanoparticles. Then amine-terminated ionic liquid (NH₂-IL) was applied to the reduction of HAuCl₄ to gold nanoparticles. The green-synthesized gold nanoparticles, with the mean diameter of 3 nm, dispersed uniformly on graphene sheets and its outer layer was positively charged imidazole termini. Due to the presence of large graphene sheets and NH₂-IL protected gold nanoparticles, DNA probes could be immobilized via electrostatic interaction and adsorption effect. Electrochemical impedance value increased after DNA probes immobilization and hybridization, which was adopted as the signal for label-free DNA hybridization detection. Unlike previously anchoring DNA to gold nanoparticles, this label-free method was simple and noninvasive. The conserved sequence of the pol gene of human immunodeficiency virus 1 was satisfactorily detected via this strategy.

Hollow Ag@Pd core-shell nanotubes as highly active catalysts for the electro-oxidation of formic acid.

Ag nanowires are prepared as templates by a polyol reduction process. Then Ag nanotubes coated with a thin layer of Pd are synthesized through sequential reduction accompanied with the galvanic displacement reaction. The products show a hollow core-shell nanotubular structure, as demonstrated by detailed characterizations. The Ag@Pd can significantly improve the electrocatalytic activity towards the electro-oxidation of formic acid and enhance the stability of the Pd component. It is proposed that the enhanced electrochemically active surface area and modulated electron structure of Pd by Ag are responsible for the improvement of electrocatalytic activity and durability. The results obtained in this work are different from those previous reports, in which alloy walls with hollow interiors are usually formed. This work provides a new and simple method for synthesizing novel bimetallic core-shell structure with a hollow interior, which can be applied as high-performance catalysts for the electro-oxidation of formic acid.

Flexible solid state lithium batteries based on graphene inks

Different formulations of solution-processable graphene have been characterised as electrode materials for use in electrochemical energy storage devices. Graphene was fabricated by chemical reduction of exfoliated graphene oxide (GO), and modified with either p-type (e.g. polyaniline) or n-type anionic groups (poly(styrenesulfonate) (PSS−) and poly[2,5-bis(3-sulfonatopropoxy)-1,4-ethynylphenylene-alt-1,4-ethynylphenylene] sodium salt (PPE-SO3−) anion). Solutions of these graphene compounds were deposited on charge collecting electrodes and used as battery cathodes. Electrodes using the anionically-modified graphene inks containing anatase titanate (TiO2) nanoparticles show improved performance over pristine graphene ink as well as the p-type conducting polymer modified ones. In addition, the open circuit voltage of batteries based on TiO2 has been boosted over 3 V with good cyclability when mixed with the graphene ink. Combined with a polymer electrolyte, this work suggests a feasible route towards fully printable rechargeable lithium batteries based on graphene inks. This approach is both versatile and scalable and is adaptable to a wide variety of applications.