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CHEM2018RODRIGUEZ3379 CHEM

Formation of New Perovskite Nanostructures Templated by Porous Silicon

Type: Undergraduate
Author(s): Adriana Rodriguez Chemistry & Biochemistry
Advisor(s): Jeff Coffer Chemistry & Biochemistry

A recent and promising development in solar energy involves a class of materials known as organometal halide perovskites, capable of efficiencies (>20%) comparable to the current industry standard of silicon. These materials also demonstrate strong light emission, a key property associated with energy-efficient sources of lighting, suggesting potential applications in light-emitting devices such as light-emitting diodes (LED). The goal of this project was to investigate the fundamental photoluminescence (PL) properties of perovskites housed in a nanoporous material known as semiconducting porous silicon (pSi).

pSi provides a nanoscale template to control the growth of the light-emitting perovskite structure and is an electrically-responsive host matrix, ideally regulating the flow of charge to/from the perovskite. Samples were prepared within the pores of surface oxidized pSi and hydride-terminated pSi, each with a mesoporous width in the 5 – 50 nm range. The perovskite-loaded pSi was fabricated through solution-loading of perovskite precursors into warmed pSi (60ºC), removal of excess reactant solution, and drying. While perovskites can feature a wide range of halide compositions (including mixed halides), this research thus far has focused on methylammonium lead iodide (MAPbI3) perovskite.

These perovskite nanostructures formed within pSi were characterized using a variety of techniques. Following synthesis, the stability of each prepared sample was monitored for 3 weeks through tracking its relative photoluminescence intensity at its maximum value. Perovskite morphology was evaluated by SEM (scanning electron microscope) and TEM (transmission electron microscope) imaging, crystalline structure was evaluated by XRD (x-ray powder diffraction), and elemental analysis was evaluated by EDX (energy-dispersive x-ray spectroscopy).

In this study, SEM imaging showed consistent perovskite particle size and ununiformed perovskite infiltration. It is found that the emission intensity for MAPbI3 formed within hydride-terminated pSi (at ~730nm) and oxidized pSi (at ~740nm) were relatively stable over a 3 week period, but the emission intensity for perovskite microrods formed in the absence of any pSi template actually decreased over time. More detailed measurements of the long term stability of these new nanoscale materials are currently under evaluation.

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CHEM2018TRETTE12261 CHEM

Fabrication Methods of Polycaprolactone (PCL) Fibers and their Thermal Properties

Type: Undergraduate
Author(s): Sayre Trette Chemistry & Biochemistry Nelli Bodiford Chemistry & Biochemistry Nathan Shurtleff Chemistry & Biochemistry
Advisor(s): Jeffery Coffer Chemistry & Biochemistry

Significant increases in average life expectancy in the last century have brought a growth in human illnesses related to aging: chronic wounds, bone diseases, eye diseases and cancer. In this work, we demonstrate fabrication of biodegradable polymer scaffolds that can be used for drug delivery and tissue engineering to treat the above-mentioned ailments. Tissue engineering can be defined as the use of a combination of engineering and materials methods and appropriate biochemical factors to improve or replace biological tissues.
This project includes fabrication of solid and porous fibers from the biocompatible PCL polymer. This polymer is currently used for surgical sutures, nerve guides and three-dimensional scaffolds for use in tissue engineering. The drug release rate is faster when it is loaded into porous PCL fibers compared to solid PCL fibers, creating an advantage for porous fiber fabrication. Use of a technique known as electrospinning of a solution of PCL and chloroform results in solid fibers that are 4 (± 2.0) micrometers (μm) in diameter. The porous fiber scaffolds are fabricated using a 50% weight of PCL compared to volume of solvent (w/v) solution prepared in a mixture of solvents 9:1 dichloromethane (DCM):dimethyl sulfoxide (DMSO) and 60% w/v PCL in 8:2 DCM:DMSO. The porous fibers are collected at 0-5 oC with a pore size of 50.0 (± 10.0) nanmoeters (nm) and fiber diameter of 3.0 (± 1.0) μm. The porosity for 50% w/v PCL and 60% w/v PCL fibers ranges from 40-50%.
Fiber surface morphology is characterized using field emission scanning electron microscopy (FESEM). In addition, the melting temperature and percent crystallinity are determined via differential scanning calorimetry (DSC). The melting temperature was collected of PCL bulk, 30%w/w PCL solid fibers, 50% w/v PCL and 60% w/v PCL. The crystallinity of PCL in solid fiber and porous fiber forms ranges from 52-55%, compared to the 60% crystallinity of PCL bulk. Solid PCL fibers showed to be more crystalline compared to porous PCL fibers, which in turn can effect the degradation time.
In order for these composites to be identified as a major technological advancement, the aging and degradation of the polymer scaffold must also be understood. The degradation of a given polymer matrix impacts the potential drug delivery behavior when testing in vitro. Degradation studies of the above mentioned materials are currently ongoing.

(Presentation is private)

CHEM2018VILLEGAS47591 CHEM

The Anomalous Stabilization of the Cis-2-Butenyl Anion by both Through-Space and Through-Bond Interactions

Type: Undergraduate
Author(s): Hector Villegas Chemistry & Biochemistry
Advisor(s): Benjamin Janesko Chemistry & Biochemistry

While cis/Z-substituted alkenes are usually less stable than their trans/E-substituted counterparts, the cis-2-butenyl anion shows a higher preference over the trans-isomer. Calculations suggest that the discrepancy is due to two cooperating effects: electrostatic interactions between the anionic center (C1) to the methyl group (C4) and coupling between the C=C pi* antibonding orbital and both the CH2 pz and CH3 C-H sigma bonds. Supporting the charge transfer is the fact that substitution on C1 with EDG stabilizes the cis more while substitution on C4 with EWG stabilizes the cis more. For the coupling interaction the C=C bond was stretched which increased the cis stabilization by lowering the pi* orbital energy and increasing the coupling between the lone pair on C1 and pi*.

(Presentation is private)

COSC2018COX17551 COSC

RAFTER: Software for the Geological Analysis of River Stream Data

Type: Undergraduate
Author(s): Connor Cox Computer Science Kaitlin Hendrick Computer Science Kiet Nguyen Computer Science Jim Pfluger Computer Science
Advisor(s): Lisa Ball Computer Science

Geology is better known for work done in the field than software applications, but by combining software with science, researchers can acquire results more efficiently and make better determinations about data. Stream input data, which consists of variables like stream size, depth, and sediment density, can be used to predict the location of oil deposits. Without a software application to automate the process, this is difficult to calculate manually.
This application will provide a useful resource and tool by which researchers can input geological data and have results returned based on that input. Specifically, users will enter data about streams and select one of two primary methods of calculation which will return results that refine sediment discharge estimates and give the user the yearly averaged bankfull flow duration. To achieve this we have implemented a database to store all of the necessary information concerning the stream data, such as location, climate ID, and Koeppen classification, established software to function as middleware between the database and the user interface, and built a web application that can be readily accessed online. With no knowledge of the middleware or database, the expected user can simply go on the website, select the desired method of calculation, and have the data returned to them in an easily understandable format.

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COSC2018GONZALEZ13220 COSC

Naturally Curly Cook Baking Application

Type: Undergraduate
Author(s): Rebecca Gonzalez Computer Science Daniel Fletcher Computer Science Ford McDonald Computer Science Luke Reddick Computer Science
Advisor(s): Lisa Ball Computer Science

Naturally Curly Cook is a baking business that does catering, standing coffee shop orders, and Farmer’s Markets. Currently, Naturally Curly Cook is having difficulty with its current pen and paper ordering system and inefficient invoicing. The purpose of the Naturally Curly Cook Team is to create an iOS application that streamlines ordering and invoicing. The application will display a daily baking list and what the bakers must bake with a check box system to ensure everything has been baked. It will also display weekly orders. Orders can be added, edited, and deleted while still maintaining the orders that do not change week to week. Excel will act as the database for all customers, orders and quantities to be stored. In addition to the ordering process, an invoicing process will allow invoices to be automatically generated from the week’s orders. The new invoicing process will be generated from Excel and will allow for different pricing options and it will update with week to week changes. The intent of this project is to create a more automatic and efficient business while cutting costs and most importantly retaining data integrity.

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