Publications by authors named "G N Parkinson"

A survey of industry groups including nutritionists, producers, feed manufacturers, and technical personnel in broiler and layer operations within the Australian poultry industry was completed to determine the industry's present views of max-profit and stochastic feed formulation and the barriers they see to implementing these techniques. A total of 32 responses were collected, made up of 17 nutritionists, 4 feed manufacturers, 5 producers, and 6 technical personnel. The survey revealed interest and need to implement stochastic and max-profit feed formulation techniques and identified the key barriers to the implementation of these feed formulation techniques.

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In polarizable materials, electronic charge carriers interact with the surrounding ions, leading to quasiparticle behavior. The resulting polarons play a central role in many materials properties including electrical transport, interaction with light, surface reactivity, and magnetoresistance, and polarons are typically investigated indirectly through these macroscopic characteristics. Here, noncontact atomic force microscopy (nc-AFM) is used to directly image polarons in FeO at the single quasiparticle limit.

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Water-solid interfaces pervade the natural environment and modern technology. On some surfaces, water-water interactions induce the formation of partially dissociated interfacial layers; understanding why is important to model processes in catalysis or mineralogy. The complexity of the partially dissociated structures often makes it difficult to probe them quantitatively.

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Article Synopsis
  • The study examines how carbon hydride (CH) interacts with a model catalyst, Rh/FeO(001), focusing on various coordination environments of rhodium (Rh) atoms.* -
  • Researchers used surface-sensitive techniques and density functional theory (DFT) calculations to analyze how different Rh species react during the thermal evolution of the system.* -
  • Results show that CH binds strongest to 2-fold coordinated Rh sites, but unexpected desorption occurs at lower temperatures due to Rh atoms migrating to less stable sites; 5-fold coordinated Rh sites exhibit a less pronounced interaction.*
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Article Synopsis
  • Understanding the local coordination of active sites is crucial for effectively modeling single-atom catalysts (SACs), but it's challenging with powder-based systems.
  • This study explores how platinum (Pt) atoms interact with the (11̅02) facet of α-FeO, revealing that Pt modifies the lattice structure to achieve a favorable pseudolinear coordination with surface oxygen.
  • The findings suggest that the linear O-Pt-O configuration is prevalent in reactive Pt-based SACs, striking a balance between stability and the ability to interact with gas-phase reactants; thus, extensive structural searches are essential for identifying realistic active site geometries.
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