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The electrodeposition of Pt nanoparticles (NPs) on two-dimensional single walled carbon nanotube (SWNT) network electrodes is investigated as a means of tailoring electrode surfaces with a well-defined amount of electrocatalytic material. Both Pt NP deposition and electrocatalytic studies are undertaken using the microcapillary electrochemical method (MCEM), enabling multiple microscale measurements to be performed quickly and easily on the same SWNT sample. Using this approach, Pt catalysts with high specific surface areas relative to the geometric electrode area (defined by the meniscus contact of the MCEM probe with the Si/SiO 2 substrate bearing the SWNT network) can be controlled precisely over three orders of magnitude. This enables the influence of the specific surface area of an electrocatalyst on activity to be investigated, as demonstrated by studies of the oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR). [ABSTRACT FROM AUTHOR]

We report a single-step route to co-deposit Cu nanoparticles with a graphitic carbon nitride (gCN) support using nanosecond Ce:Nd:YAG pulsed laser ablation from a Cu metal target coated using acetonitrile (CH3CN). The resulting Cu/gCN hybrids showed strong optical absorption in the visible to near-IR range and exhibited surface-enhanced Raman or resonance Raman scattering (SERS or SERRS) enhancement for crystal violet (CV), methylene blue (MB), and rhodamine 6G (R6G) used as probe analyte molecules adsorbed on the surface. We have characterized the Cu nanoparticles and the nature of the gCN support materials using a range of spectroscopic, structural, and compositional analysis techniques. [ABSTRACT FROM AUTHOR]

• Operando synchrotron X-ray study on Phosphorus and Platinum migration. • Graphene-related-material applied as interventional materials for comparison. • X-ray Absorption Near Edge Structure applied to study chemical structural change. • Conducting mechanistic studies via the three-phase interface. • Performance and durability of high-temperature proton exchange membrane fuel cells. The application of high-temperature proton exchange membrane fuel cells (HT-PEMFCs) addresses challenges in water management, fuel purity, and overheating under high current density. However, phosphoric acid (PA) migration hinders their development. This study uses synchrotron-based X-ray fluorescence spectroscopy to investigate PA and catalyst migration. Interventions with single-layer graphene and electrochemically exfoliated graphene oxide improve performance and durability. X-ray absorption spectroscopy provides insights into relevant mechanisms, advancing understanding of membrane electrode assembly preparation and the intricate influences of PA and catalyst migration on performance and durability in HT-PEMFCs. [ABSTRACT FROM AUTHOR]

There is currently an enormous drive to move away from the use of Pt group metals in catalysis, particularly for fuel cells, because of their increasing rarity and cost. Simultaneously, there have been advances in the application of graphene supported nanoparticular catalysts. However, these Pt-free, graphene supported catalysts can be complex to produce, show poor catalytic activity and degrade quickly due to particle agglomeration or isolation. Herein, we report a one-pot synthesis of silver nanoparticles (NPs) tethered to a reduced graphene oxide (rGO) template via organic linkages. This is one of the few silver precursor formations that have been combined with graphene oxide (GO) to simultaneously establish linkage binding sites, reduce GO and yield tethered nanoparticles. These materials are shown to efficiently catalyze the oxygen reduction reaction in alkaline environments, with aminoethanol linkages to 21.55 ± 2.88 nm Ag particles exhibiting the highest catalytic activity via the four-electron pathway. This method, therefore, offers a straightforward route to produce effective catalysts from inexpensive precursors, which could be developed further for significant industrial application. [ABSTRACT FROM AUTHOR]

The article provides information on a study which demonstrated rapid transport of molecular H2O through nanometer-sized voids ordered within the layers of crystalline carbon nitride with a polytriazine imide structure by combining neutron spectroscopy and first-principles calculations. Topics discussed include synthesis and characterization of intercalant-free (IF-)-polytriazine imide (PTI) and PTI-H2O, and quasi-elastic neutron scattering (QENS) analysis of water dynamics in PTI-H2O.

Carbon nitride materials with graphitic to polymeric structures (gCNH) were investigated as catalyst supports for the proton exchange membrane (PEM) water electrolyzers using IrO2 nanoparticles as oxygen evolution electrocatalyst. Here, the performance of IrO2 nanoparticles formed and deposited in situ onto carbon nitride support for PEM water electrolysis was explored based on previous preliminary studies conducted in related systems. The results revealed that this preparation route catalyzed the decomposition of the carbon nitride to form a material with much lower N content. This resulted in a significant enhancement of the performance of the gCNH-IrO2 (or N-doped C-IrO2) electrocatalyst that was likely attributed to higher electrical conductivity of the N-doped carbon support. [ABSTRACT FROM AUTHOR]