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Cerium oxide nanoparticles (CeNPs) are versatile materials with unique and unusual properties that vary depending on their surface chemistry, size, shape, coating, oxidation states, crystallinity, dopant, structural and surface defects. This review details advances made over the past twenty years in the development of CeNPs and ceria-based nanostructures, the structural determinants affecting their activity, and translation of these distinct features into applications. The two-oxidation states of nanosized CeNPs (Ce3+/Ce4+) coexisting at the nanoscale level, facilitate formation of oxygen vacancies and defect states which confer extremely high reactivity and oxygen buffering capacity, and the ability to act as catalysts for oxidation and reduction reactions. However, the method of synthesis, surface functionalization, surface coating and defects are important factors in determining their properties. This review highlights the key properties of CeNPs, their synthesis, interactions and reaction pathways, and provides examples of emerging applications. Due to their unique properties, CeNPs have become quintessential candidates for catalysis, chemical mechanical planarization (CMP), sensing, biomedical applications and environmental remediation, with tremendous potential to create novel products and translational innovations in a wide range of industries. This review highlights the timely relevance and the transformative potential of these materials in addressing societal challenges and driving technological advancements across these fields. 

Abstract Gold screen printed electrodes (Au‐SPEs) were treated electrochemically to produce a micro‐rough pattern increasing the real electrode surface. The procedure based on the Dynamic Hydrogen Bubble Template (DHBT) method included electrochemical deposition of Au layers onto the surface of the Au‐SPEs, followed by a reductive process at −3 V (vs. Ag/AgCl) leading to formation of H₂bubbles, which produced pores in the Au multilayer. The morphology of the micro‐porous Au electrode was characterized by scanning electron microscopy (SEM), surface mapping, surface profilometry, and confocal microscopy. The electrode surface morphology was controlled by the time of the electrode reductive treatment (H₂evolution) and the optimized condition resulting in the best surface structuring was found. Notably, the surface roughness leading to the highest electrode surface area was significantly increased compared to previously reported results with Au‐SPEs.