Tianhong Lu

Nonenzymatic Electrochemical Detection of Glucose Based on Palladium−Single-Walled Carbon Nanotube Hybrid Nanostructures

A new electrocatalyst, palladium nanoparticle-single-walled carbon nanotube (Pd-SWNTs) hybrid nanostructure, for the nonenzymatic oxidation of glucose was developed and characterized by X-ray diffraction (XRD) and the transmission electron microscope (TEM). The hybrid nanostructures were prepared by depositing palladium nanoparticles with average diameters of 4-5 nm on the surface of single-walled carbon nanotubes (SWNTs) via chemical reduction of the precursor (Pd(2+)). The electrocatalyst showed good electrocatalytic activity toward the oxidation of glucose in the neutral phosphate buffer solution (PBS, pH 7.4) even in the presence of a high concentration of chloride ions. A nonenzymatic amperometric glucose sensor was developed with the use of the Pd-SWNT nanostructure as an electrocatalyst. The sensor had good electrocatalytic activity toward oxidation of glucose and exhibited a rapid response (ca.3 s), a low detection limit (0.2 +/- 0.05 microM), a wide and useful linear range (0.5-17 mM), and high sensitivity (approximately 160 microA mM(-1) cm(-2)) as well as good stability and repeatability. In addition, the common interfering species, such as ascorbic acid, uric acid, 4-acetamidophenol, 3,4-dihydroxyphenylacetic acid, and so forth did not cause any interference due to the use of a low detection potential (-0.35 V vs SCE). The sensor can also be used for quantification of the concentration of glucose in real clinical samples. Therefore, this work has demonstrated a simple and effective sensing platform for nonenzymatic detection of glucose.

Three-Dimensional Interconnected Network of Graphene-Wrapped Porous Silicon Spheres: In Situ Magnesiothermic-Reduction Synthesis and Enhanced Lithium-Storage Capabilities

A novel type of 3D porous Si-G micro/nanostructure (i.e., 3D interconnected network of graphene-wrapped porous silicon spheres, Si@G network) was constructed through layer-by-layer assembly and subsequent in situ magnesiothermic-reduction methodology. Compared with bare Si spheres, the as-synthesized Si@G network exhibits markedly enhanced anodic performance in terms of specific capacity, cycling stability, and rate capability, making it an ideal anode candidate for high-energy, long-life, and high-power lithium-ion batteries.

Autocatalysis and selective oxidative etching induced synthesis of platinum-copper bimetallic alloy nanodendrites electrocatalysts.

The controllable synthesis of noble metal alloy nanostructures with highly branched morphology has attracted much attention because of their specific physical and chemical properties. This article reports the synthesis of platinum-copper bimetallic alloy nanodendrites (Pt-Cu BANDs) by a facile, one-pot, templateless, and seedless hydrothermal method in the presence of poly(allylamine hydrochloride) (PAH) and formaldehyde (HCHO). The morphology, composition, and structure of Pt-Cu BANDs are fully characterized by various physical techniques, demonstrating Pt-Cu BANDs are highly alloying, porous, and self-supported nanostructures. The formation/growth mechanism of Pt-Cu BANDs is explored and discussed based on the experimental observations. The autocatalytic growth and interdiffusion are responsible for the formation of Pt-Cu alloy whereas selective oxidative etching results in dendritic morphology of Pt-Cu alloy nanostructures. In addition, the electrocatalytic activity and stability of Pt-Cu BANDs for the methanol oxidation reaction (MOR) are investigated by various electrochemical techniques. The synthesized Pt-Cu BANDs show higher electrocatalytic activity and stability than commercially available Pt black.

Platinum–Cobalt alloy networks for methanol oxidation electrocatalysis

Three-dimensional (3D) platinum–cobalt alloy networks nanostructures with a high alloying degree were synthesized through a room temperature wet-chemical synthetic method using the K2PtCl4/K3Co(CN)6 cyanogel as reaction precursor in the absence of surfactants and templates. The size, morphology and surface composition of platinum–cobalt alloy networks nanostructures were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectrum (EDS), selected area electron diffraction (SAED), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The 3D backbone structure and double-metallic property of the K2PtCl4/K3Co(CN)6 cyanogel are responsible for the 3D structure and the high alloying degree of the as-prepared products, respectively. Compared to the pure Pt nanoparticles, 3D platinum–cobalt alloy networks nanostructures exhibit superior electrocatalytic activity and stability for the methanol oxidation reaction (MOR), which is ascribed to their unique 3D structure and alloy properties.

One-pot synthesis of three-dimensional platinum nanochain networks as stable and active electrocatalysts for oxygen reduction reactions

Three-dimensional platinum nanochain network (Pt-3NCNW) nanostructures are synthesized through a thermal decomposition method using platinum(IV)-complexes as reaction precursors in the absence of surfactants and templates. The size, morphology and surface composition of Pt-3NCNWs are investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). These spectral studies confirm the as-papered products are three-dimensionally interconnected network nanostructures with primary Pt nanochains as building blocks, and the Pt nanochains grow from the primary spheric Pt nanoparticles via oriented attachment. Compared to the commercial Pt black catalyst, the Pt-3NCNW nanostructures exhibit superior electrocatalytic activity and stability towards oxygen reduction reactions, which is ascribed to their unique properties such as the few surface defect sites and the low hydroxyl surface coverage on one-dimensional Pt nanochains, as well as fast O2 diffusion in three-dimensional structures.

Synthesis and electrocatalytic activity of Au@Pd core-shell nanothorns for the oxygen reduction reaction

AbstractBimetallic core-shell nanostructures with porous surfaces have drawn considerable attention due to their promising applications in various fields, including catalysis and electronics. In this work, Au@Pd core-shell nanothorns (CSNTs) with rough and porous surfaces were synthesized for the first time through a facile co-chemical reduction method in the presence of polyallylamine hydrochloride (PAH) and ethylene glycol (EG) at room temperature. The size, morphology, and composition of Au@Pd CSNTs were investigated by transmission electron microscopy (TEM), X-ray diffraction (XRD), energy dispersive spectroscopy (EDX), EDX mapping, and X-ray photoelectron spectroscopy (XPS). The electrochemical properties of as-synthesized Au@Pd CSNTs were also studied by various electrochemical techniques. Au@Pd CSNTs exhibited remarkably high electrocatalytic activity and durability for the oxygen reduction reaction (ORR) in the alkaline media, owing to the unique porous structure and the synergistic effect between the Au core and Pd shell.

Self-Assembly of Tetrakis (3-Trifluoromethylphenoxy) Phthalocyaninato Cobalt(II) on Multiwalled Carbon Nanotubes and Their Amperometric Sensing Application for Nitrite

In this work, the soluble cobalt phthalocyanine functionalized multiwalled carbon nanotubes (MWCNTs) are synthesized by π-π stacking interaction between tetrakis (3-trifluoromethylphenoxy) phthalocyaninato cobalt(II) (CoPcF) complex and MWCNTs. The physical properties of CoPcF-MWCNTs hybrids are evaluated using spectroscopy (UV-vis, XPS, and Raman) and electron microscopy (TEM and SEM). Subsequently, an amperometric nitrite electrochemical sensor is designed by immobilizing CoPcF-MWCNTs hybrids on the glassy carbon electrode. The immobilized CoPcF complex shows the fast electron transfer rate and excellent electrocatalytic activity for the oxidation of nitrite. Under optimum experimental conditions, the proposed nitrite electrochemical sensor shows the fast response (less than 2 s), wide linear range (9.6 × 10(-8) to 3.4 × 10(-4) M) and low detection limit (6.2 × 10(-8) M) because of the good mass transport, fast electron transfer rate, and excellent electrocatalytic activity.

One-pot, water-based and high-yield synthesis of tetrahedral palladium nanocrystal decorated graphene

This paper reports a facile, water-based and one-pot synthesis of tetrahedral Pd nanocrystals (Pd-TNPs) with high yield and good size monodispersity supported on reduced graphene oxide (RGO) nanosheets via a co-chemical reduction method. The key synthetic strategy employed a positively charged polyallylamine-Pd(II) complex (PAH-Pd(II)) with un-coordinated amine groups as a linker molecule to immobilize Pd(II) species on the negatively charged graphene oxide (GO) surface through electrostatic interaction. As characterized by transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Raman spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) techniques, well-defined Pd-TNPs with an average size of 9 nm were uniformly distributed on the RGO surface. The as-prepared Pd-TNPs/RGO nanohybrid with excellent colloidal stability in aqueous solution exhibits superior catalytic activity towards the degradation of methylene blue (MB) compared to both unsupported Pd-TNPs and Pd black. Thus, the resultant Pd-TNPs/RGO nanohybrid, as a promising heterogeneous catalyst, might have wide potential applications in water-based catalysis systems for the future.

Pt‐Pd‐Co Trimetallic Alloy Network Nanostructures with Superior Electrocatalytic Activity towards the Oxygen Reduction Reaction

Pt alloy nanostructures show great promise as electrocatalysts for the oxygen reduction reaction (ORR) in fuel cell cathodes. Herein, three-dimensional (3D) Pt-Pd-Co trimetallic network nanostructures (TNNs) with a high degree of alloying are synthesized through a room temperature wet chemical synthetic method by using K2 PtCl4 /K3 Co(CN)6 -K2 PdCl4 /K3 Co(CN)6 mixed cyanogels as the reaction precursor in the absence of surfactants and templates. The size, morphology, and surface composition of the Pt-Pd-Co TNNs are investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected-area electron diffraction (SAED), energy dispersive spectroscopy (EDS), EDS mapping, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The 3D backbone structure, solid nature, and trimetallic properties of the mixed cyanogels are responsible for the 3D structure and high degree of alloying of the as-prepared products. Compared with commercially available Pt black, the Pt-Pd-Co TNNs exhibit superior electrocatalytic activity and stability towards the ORR, which is ascribed to their unique 3D structure, low hydroxyl surface coverage and alloy properties.

Arginine-Assisted Synthesis and Catalytic Properties of Single-Crystalline Palladium Tetrapods

Noble metallic nanocrystals (NMNCs) with highly branched morphologies are an exciting new class of nanomaterials because of their great potential application in catalysis, sensing, optics, and electronics originating from their unique structures. Herein, we report a facile water-based method to synthesize high-quality palladium (Pd) tetrapods with the assistance of arginine molecule, which is more economical and environmentally friendly than the previous reported carbon monoxide (CO)-assisted synthesis in the organic system. During the synthesis, arginine molecule plays an essential role in controlling the tetrapod-like morphology. The as-synthesized Pd tetrapods have a potential application in the formic acid (HCOOH)-induced reduction of highly toxic hexavalent chromium (Cr(VI)) owing to their improved catalytic performance for the HCOOH decomposition.