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Jamie Ford

Publications and source records attributed to Jamie Ford.

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Site-selective enhancement of Eu emission in delta-doped GaN

Europium-doped gallium nitride (GaN:Eu) is a promising platform for classical and quantum optoelectronic applications. When grown using organometallic vapor-phase epitaxy, the dominant red emission from Eu exhibits an inhomogeneous photoluminescence (PL) spectrum due to contributions from several non-equivalent incorporation sites that can be distinguished with combined excitation emission spectroscopy. Energy transfer from the GaN bandgap to the majority site is inefficient, limiting the performance of GaN:Eu LEDs and resulting in an inhomogeneous emission spectrum dominated by disproportionate contributions from minority sites. In this work, we use site-selective spectroscopy to characterize the photoluminescence properties of delta-doped structures with alternating doped and undoped layers of varying thicknesses and demonstrate that they selectively enhance emission from the majority site when compared to uniformly-doped samples. Samples with 2-nm and 10-nm doped layers show much greater PL intensity per Eu concentration as well as more efficient energy transfer to the majority site, which are both highly desirable for creating power-efficient LEDs. Meanwhile, a sample with 1-nm doped layers shows emission only from the majority site, resulting in a narrow, homogeneous emission spectrum that is desirable for quantum technologies. This utilization of delta-doping has the potential to be broadly applicable for engineering desirable defect properties in rare-earth doped semiconductors.

cond-mat.mtrl-sci

Comprehensive Structural Characterization of Charged Polymers Involved in Moisture-Driven Direct Air Capture

The rise in atmospheric carbon dioxide (CO2) levels has led to urgent calls for effective carbon capture methods, with direct air capture (DAC) emerging as a promising solution. This study focuses on the structural characterization of commercially available alkaline anion-exchange membrane (AEM) polymers, Fumasep FAA-3 and IRA 900, for use in low-energy, moisture-driven DAC applications. A combination of X-ray diffraction, small and wide-angle X-ray scattering (SAXS/WAXS), atomic force microscopy (AFM), focused ion beam-scanning electron microscopy (FIB-SEM), and transmission electron microscopy (TEM) were employed to explore the structural features of these materials. X-ray scattering analysis revealed molecular ordering and large-scale structural organization in both materials, while humidity-induced changes highlighted the impact of moisture on structural properties. AFM surface analysis further indicated the presence of clustering, porosity, and swelling, which were corroborated by FIB-SEM and TEM imaging. These structural insights offer a deeper understanding of the behavior of AEM-DAC materials during CO2 capture and release, emphasizing the role of moisture in these processes. This work lays the foundation for the development of more energy-efficient DAC polymers, paving the way for improved CO2 capture technologies.

cond-mat.mtrl-sci

Hydrazine-Free Precursor for Solution-Processed All-Inorganic Se and Se1-xTex Photovoltaics

Selenium (Se) has reemerged as a promising absorber material for indoor and tandem photovoltaics (PVs), and its alloys with Te (Se1-xTex) offer a widely tunable bandgap. Solution processing of this materials system offers a route to low-cost fabrication. However, solution processing of Se has, thus far, only used hydrazine, which is an extremely hazardous solvent. In this work, we prepare and isolate propylammonium poly-Se and poly-Se-Te precursors from a safer thiol-amine solvent system. We formulate molecular inks by dissolving the precursor n,n-dimethylformamide (DMF) with a monoethanolamine (EA) additive and process high-quality Se and Se1-xTex films with bandgaps ranging from 1.20 eV to 1.86 eV. We fabricate PVs from these films using TiO2 and MoO3 charge transport layers (CTLs) to achieve power conversion efficiencies as high as 2.73% for Se and 2.33% for Se0.7Te0.3 under solar simulation. Se devices show excellent stability with no degradation after 1 month in air, enabled by the excellent stability of Se and the use of inorganic CTLs. This work represents an important step towards low-cost solution-phase processing of Se and Se1-xTex alloys for PVs and photodetectors with low toxicity and high bandgap tunability.

cond-mat.mtrl-sci