The shape-controlled synthesis of gallium-palladium (GaPd2) nanomaterials as high-performance electrocatalysts for the hydrogen evolution reaction.

Recently, great efforts have been focused on developing more active and stable Pd-based electrocatalysts to partially or completely replace rare and costly Pt. We developed a facile hot injection method and successfully synthesized well-dispersed and shape-controlled GaPd2 nanomaterials including polyhedrons, nanoparticles and nanowires. All the as-synthesized catalysts exhibit superior HER activity compared to commercial pure Pd catalysts and are stable in acidic media. Among them, the GaPd2 nanoparticles required only 24.3 mV overpotential to achieve a 10 mA cm-2 current density, which is outstanding compared to most Pt-based nanomaterials. Also, cycling tests over 10 000 CV sweep cycles (-0.3 to 0.2 vs. RHE) and durability testing for 24 hours were applied, with the GaPd2 catalysts exhibiting similar i-V curves and stable current densities to those obtained in the initial tests. We further evaluated the mass activities of the GaPd2 catalysts, and it is fascinating that the GaPd2 polyhedrons, nanoparticles and nanowires achieved factors of 3.7, 5 and 2.3 enhancement in mass activity at -0.1 V vs. RHE compared with a commercial Pd black catalyst. Meanwhile, with the assistance of a reduced graphene oxide (rGO) support, the GaPd2 nanoparticles/rGO (20 wt%) electrocatalyst presents outstanding HER activity comparable with that of a carbon-supported Pt catalyst (20% Pt/C). This work provides an avenue to develop effective and stable Pd-based catalysts with reduced Pd usage and high HER performance.

Sub-1 nm PtSn ultrathin sheet as an extraordinary electrocatalyst for methanol and ethanol oxidation reactions.

Sub-1 nm PtSn nanosheets of 0.6-0.9 nm in thickness were synthesized via a solution colloidal method and were applied as electrooxidation catalysts for methanol oxidation reaction (MOR) and ethanol oxidation (EOR) in alkaline and acid environments. Owing to the specific structural and compositional characteristics, the as-prepared PtSn nanosheets exhibits superior activity and durability relative to commercial Pt black and Pt/carbon catalysts. PtSn nanosheets not only exhibit an outstanding mass activity in MOR (871.6 mA mg Pt-1), which is 2.3 times (371 mA mg Pt-1) and 10.1 times (86.1 mA mg Pt-1) higher than that of commercial Pt/carbon and Pt black respectively, but also display an mass activity in EOR (673.6 mA mg Pt-1) with 5.3 times higher commercial Pt black (127.7 mA mg Pt-1) and 2.3 times higher than commercial Pt/C catalyst (295 mA mgPt-1). The reported value is the highest activity in both MOR and EOR examinations compared to the reported PtSn-based electrocatalysts,. The improved performance may be due to the highly-reactive exposed (1 1 1) facet sites resulted from its sub-1 nm 2D sheet like morphology.

Au@CdSe heteroepitaxial nanorods: An example of metal nanorods fully covered by a semiconductor shell with strong photo-induced interfacial charge transfer effects.

Synthesis of metal@semiconductor heteroepitaxial nanorods fully covered by a semiconductor shell remains challenging due to the large lattice mismatch between the two components. Here, we prepared Au@CdSe heteroepitaxial nanorods by employing pre-growth of Ag2Se as an intermediate layer that favored the formation of a complete CdSe shell via a cation-exchange process. The optical properties of these hybrid nanostructures can be tailored by changing the shell thickness with thicker shells resulting in a redshift of the longitudinal surface plasmon resonance. The resonance energy, intensity, and linewidth of the longitudinal surface plasmon resonance were measured by single-particle dark-field scattering spectroscopy, confirming significant electron transfer from the Au nanorod to the CdSe shell. In addition, we also studied the dependence of the catalytic reactivity on shell thickness in photocatalysis of methylene blue under UV illumination. These studies revealed that a thinner shell thickness resulted in higher photocatalytic activity.

Synthesis of germanium-platinum nanoparticles as high-performance catalysts for spray-deposited large-area dye-sensitized solar cells (DSSC) and the hydrogen evolution reaction (HER).

GePt3 and Ge2Pt nanoparticles were synthesized via a solution colloidal method as catalysts for dye-sensitized solar cells (DSSC) and the hydrogen evolution reaction (HER). The shape, size, arrangement, phases and crystalline structures of Ge-Pt nanoparticles were determined, and the ability to be dispersed in nonpolar solvents enabled them to form a catalyst ink with a stable ejection for the spray coating technique. A series of electrochemical analyses confirmed the catalytic properties of Ge-Pt nanoparticles toward the I-/I3- redox reaction system. The DSSC using GePt3 nanoparticles as the counter electrode exhibited excellent power conversion efficiency (PCE) of 8.04% at 0.16 cm2, which was comparable to that of a DSSC using Pt as the counter electrode (8.0%); it also exhibited an average PCE of 7.26% even at a large working area (2 cm2). In addition, the GePt3 catalyst exhibited excellent HER electrocatalytic performance with a large current density and a low Tafel slope, and it could stably operate at a working area of up to 5 cm2 with a low over potential (<0.06 V) to achieve 10 mA cm-2 cathodic current. This study provides fundamental insights into the preparation of germanium-platinum intermetallic compound catalysts at the nanoscale, which can be beneficial for the design and development of clean energy devices.

Binary halide, ternary perovskite-like, and perovskite-derivative nanostructures: hot injection synthesis and optical and photocatalytic properties.

A variety of crystalline colloid binary halide, ternary perovskite-like and ternary perovskite-derivative nanostructures with well-defined morphologies were synthesized, thus expanding materials chemistry to the new category of nanomaterials. The optical and photocatalytic properties of ternary nanostructures were investigated.

Alexander disease causing mutations in the C-terminal domain of GFAP are deleterious both to assembly and network formation with the potential to both activate caspase 3 and decrease cell viability.

Alexander disease is a primary genetic disorder of astrocyte caused by dominant mutations in the astrocyte-specific intermediate filament glial fibrillary acidic protein (GFAP). While most of the disease-causing mutations described to date have been found in the conserved α-helical rod domain, some mutations are found in the C-terminal non-α-helical tail domain. Here, we compare five different mutations (N386I, S393I, S398F, S398Y and D417M14X) located in the C-terminal domain of GFAP on filament assembly properties in vitro and in transiently transfected cultured cells. All the mutations disrupted in vitro filament assembly. The mutations also affected the solubility and promoted filament aggregation of GFAP in transiently transfected MCF7, SW13 and U343MG cells. This correlated with the activation of the p38 stress-activated protein kinase and an increased association with the small heat shock protein (sHSP) chaperone, αB-crystallin. Of the mutants studied, D417M14X GFAP caused the most significant effects both upon filament assembly in vitro and in transiently transfected cells. This mutant also caused extensive filament aggregation coinciding with the sequestration of αB-crystallin and HSP27 as well as inhibition of the proteosome and activation of p38 kinase. Associated with these changes were an activation of caspase 3 and a significant decrease in astrocyte viability. We conclude that some mutations in the C-terminus of GFAP correlate with caspase 3 cleavage and the loss of cell viability, suggesting that these could be contributory factors in the development of Alexander disease.