ABSTRACT
Scientific success in the field of chemistry depends upon the mastery of a wide range of soft skills, most notably scientific writing and speaking. However, training for scientific communication is typically limited at the undergraduate level, where students struggle to express themselves in a clear and logical manner. The underlying issue is deeper than basic technical skills; rather, it is a problem of students' unawareness of a fundamental and strategic framework for writing and speaking with a purpose. The methodology has been implemented for individual mentorship and in our regional summer research program to deliver a blueprint of thought and reasoning that endows students with the confidence and skills to become more effective communicators. Our didactic process intertwines undergraduate research with the scientific method and is partitioned into six steps, referred to as "phases", to allow for focused and deep thinking on the essential components of the scientific method. The phases are designed to challenge the student in their zone of proximal development so they learn to extract and ultimately comprehend the elements of the scientific method through focused written and oral assignments. Students then compile their newly acquired knowledge to create a compelling and logical story, using their persuasive written and oral presentations to complete a research proposal, final report, and formal 20 min presentation. We find that such an approach delivers the necessary guidance to promote the logical framework that improves writing and speaking skills. Over the past decade, we have witnessed both qualitative and quantitative gains in the students' confidence in their abilities and skills (developed by this process), preparing them for future careers as young scientists.
ABSTRACT
Stainless steel 316L is widely used as a biomedical implant material; however, there is concern about the corrosion of metallic implants in the physiological environment. The corrosion process can cause mechanical failure due to resulting cracks and cavities in the implant. Alkyl phosphonic acid forms a thin film by self-assembly on the stainless steel surface and this report conclusively shows that thermal treatment of the octadecylphosphonic acid (ODPA) film greatly enhances the stability of the ODPA molecules on the substrate surface. AFM images taken from the modified substrates revealed that thermally treated films remain intact after methanol, THF, and water flushes, whereas untreated films suffer substantial loss. Water contact angles also show that the hydrophobicity of thermally treated films does not diminish after being incubated in a dynamic flow of water for a 3-hour period, whereas the untreated film becomes increasingly hydrophilic due to loss of ODPA. IR spectra taken of both treated and untreated films after water and THF flushes show that the remaining film retains its initial crystallinity. A model is suggested to explain the stability of ODPA film enhanced by thermal treatment. An ODPA molecule is physisorbed to the surface weakly by hydrogen bonding. Heating drives away water molecules leading to the formation of strong monodentate or mixed mono/bi-dentate bonds of ODPA molecule to the surface.
ABSTRACT
Development of coatings to minimize unwanted surface adsorption is extremely important for their use in applications, such as sensors and medical implants. Self-assembled monolayers (SAMs) are an excellent choice for coatings that minimize nonspecific adsorption because they can be uniform and have a very high surface coverage. Another equally important characteristic of such coatings is their stability. In the present study, both the bonding mechanism and the stability of stearic acid SAMs on two aluminum oxides (single-crystal C-plane aluminum oxide (sapphire) and amorphous aluminum oxide (alumina)) are investigated. The adsorption mechanism is investigated by ex situ X-ray photoelectron spectroscopy and infrared (IR) spectroscopy. The results revealed that stearic acid binds to sapphire surfaces via a bidentate interaction of carboxylate with two oxygen atoms while it binds to alumina surfaces via both bidentate and monodentate interactions. Desorption kinetics of stearic acid self-organized on both aluminum oxide surfaces into water is explored by ex situ tapping mode atomic force microscopy, IR spectroscopy, and contact angle measurements. The results exhibit that the SAMs of stearic acid formed on sapphire are not stable in water and are continuously lost through desorption. Water contact angle measurements of SAMs that are immersed in water further indicate that the desorption rate of adsorbates from atomically smooth terrace sites is substantially faster than that of adsorbates from the sites of surface defects due to weaker molecular interaction with the smooth surface. A time-dependent desorption profile of SAMs grown on amorphous alumina reveals that contact angles decrease monotonically without any regional distinction, providing further evidence for the presence of adsorption sites with different types of affinity on the amorphous alumina surface.
ABSTRACT
The surfaces of the magnetic data storage hard disks used in computers are coated with a thin film of amorphous carbon and a layer of perfluoropolyalkyl ether (PFPE) lubricant. Both protect the surface of the magnetic layer from contact with the read-write head flying over the disk surface. Although the most commonly used carbon films are amorphous hydrogenated carbon, a-CH(x), it has been suggested that the thermal properties of amorphous fluorinated carbon films, a-CF(x), might be superior. This work has probed the interaction of small fluorinated ethers and alcohols with the surfaces of a-CF(x) films to understand the effects of carbon film fluorination on the interaction of the lubricant with its surface. Temperature-programmed desorption was used to measure the desorption energies of small fluorocarbons from the a-CF(x) surface and to compare their desorption energies with those from the surfaces of a-CH(x) films. These measurements reveal that, similarly to a-CH(x) films, a-CF(x) films expose a heterogeneous surface on which fluorocarbons adsorb at sites with a range of binding energies. The fluorocarbon ethers all have lower heats of adsorption than their hydrocarbon counterparts, suggesting that the ethers adsorb by donation of electron density from the oxygen lone-pair electrons to sites on the surface. Fluorinated alcohols have roughly the same heats of adsorption as their hydrocarbon counterparts. There is little significant difference between the interactions of fluorinated ethers (or alcohols) with the surfaces of either a-CF(x) or a-CH(x) films.
ABSTRACT
Reduction of the interfacial friction for the contact of a silicon oxide surface with sodium borosilicate in aqueous solutions has been accomplished through the adsorption of poly(L-lysine)-graft-poly(ethylene glycol) on one or both surfaces. Spontaneous polymer adsorption has been achieved via the electrostatic attraction of the cationic polylysine polymer backbone and a net negative surface charge, present for a specific range of solution pH values. Interfacial friction has been measured in aqueous solution, in the absence of wear, and on a microscopic scale with atomic force microscopy. The successful investigation of the polymer-coated interfaces has been aided by the use of sodium borosilicate microspheres (5.1 microm diameter) as the contacting probe tip. Measurements of interfacial friction as a function of applied load reveal a significant reduction in friction upon the adsorption of the polymer, as well as sensitivity to the coated nature of the interface (single-sided versus two-sided) and the composition of the adsorbed polymer. These measurements demonstrate the fundamental opportunity for lubrication in aqueous environments through the selective adsorption of polymer coatings.
