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  <title><![CDATA[PhD Proposal by Adam Vitale]]></title>
  <body><![CDATA[<p>MSE PhD Proposal - Adam Vitale</p><p>&nbsp;</p><p>Date/Time: Wednesday August 19<sup>th</sup> at 5 p.m.</p><p>&nbsp;</p><p>Location:&nbsp; Room 3515, Hightower Conference Room, MRDC</p><p>&nbsp;</p><p>Committee:</p><p>•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Faisal Alamgir (Advisor, Materials Science and Engineering)</p><p>•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Meilin Liu (Materials Science and Engineering)</p><p>•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Preet Singh (Materials Science and Engineering)</p><p>•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Eric Vogel (Materials Science and Engineering)</p><p>•&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Krista Walton (Chemical &amp; Biomolecular Engineering)</p><p>&nbsp;</p><p>Thesis Title: Near Surface Evaluation of Structural, Electronic and Chemical Properties of Templated Pt Monolayers</p><p>&nbsp;</p><p>Abstract: Platinum group metals are the choice catalysts for a wide variety of catalytic reactions, including oxygen reduction. The focus of this study is to explore the dimensional aspect of both electronic and structure-driven surface properties of Pt monolayers grown via templating on Au. Surface limited redox replacement is used to provide precise layer-by-layer growth of Pt to synthesize well-controlled ‘core-shell’ catalyst architectures.</p><p>&nbsp;</p><p>The interaction between core and shell manifests itself through both a structural contribution of epitaxial strain and d-electron orbital mixing. The cumulative effect of the secondary support on the surface Pt and its interaction with adsorbate species is referred to as a ligand effect. The main goal of the research is to investigate how these ligand effects contribute to the structural and electronic properties of Pt monolayer catalysts.</p><p>&nbsp;</p><p>One focus of our study is to explore the incorporation of two dimensional materials into the core-shell catalyst architecture. Materials such as single-layer graphene and transition metal dichalcogenides have shown potential for increased activity and stability when used as supports. We have found that fully wetted 4-5 monolayer Pt films can be grown on graphene, maximizing the exposed catalyst surface with high Pt utilization. The research also looks to investigate the use of single-layer graphene as an intimate capping sheet to prevent surface dissolution of electrode metals into the electrolyte, without adversely affecting activity. </p><p>&nbsp;</p><p>X-ray photoelectron spectroscopy and extended x-ray absorption fine structure techniques are used to examine surface composition and local atom-atom correlations (bond distance, strain, coordination) as well as core-shell charge transfer effects. Cyclic voltammetry and the oxygen reduction reaction are used as probes to examine the electrochemically active area of Pt monolayers and catalyst activity, respectively. </p><p> </p>]]></body>
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