• Owrutsky, Jeff
• Yesinowski, James P.
• Glaser, Evan R.
• Pitman, Catherine L.
• Pietron, Jeremy
• Dunkelberger, Adam D.
• Desario, Paul
• Brintlinger, Todd
• Rolison, Debra
• Melinger, Joseph S.
• Johannes, Michelle
• Miller, Joel

Abstract

We describe the opportunity to deploy aerogels-an ultraporous nanoarchitecture with co-continuous networks of meso/macropores and covalently bonded nanoparticulates-as a platform to address the nature of the electronic, ionic, and mass transport that underlies catalytic activity. As a test case, we fabricated Au||TiO2 junctions in composite guest-host aerogels in which ∼5 nm Au nanoparticles are incorporated either directly into the anatase TiO2 network (Au "in" TiO2, AuIN-TiO2 aerogel) or deposited onto preformed TiO2 aerogel (Au "on" TiO2, AuON/TiO2 aerogel). The metal-meets-oxide nanoscale interphase as visualized by electron tomography feature extended three-dimensional (3D) interfaces, but AuIN-TiO2 aerogels impose a greater degree of Au contact with TiO2 particles than does the AuON/TiO2 form. Both aerogel variants enable transport of electrons over micrometer-scale distances across the TiO2 network to Au||TiO2 junctions, as evidenced by electron paramagnetic resonance (EPR) and ultrafast visible pump-IR probe time-resolved absorption spectroscopy. The siting of gold nanoparticles in the TiO2 network more effectively disperses trapped electrons. Density functional theory (DFT) calculations find that increased physical contact between Au and TiO2, induced by oxygen vacancies, produces increased hybridization of midgap states and quenches unpaired trapped electrons. We assign the apparent differences in electron-transport capabilities to a combination of the relatively better-wired Au||TiO2 junctions in AuIN-TiO2 aerogels, which have a greater capacity to dilute accumulated charge over a larger interfacial surface area, with an enhanced ability to discharge the accumulated electrons via catalytic reduction of adsorbed O2 to O2- at the interface. Solid-state 1H nuclear magnetic resonance experiments show that proton spin-lattice relaxation times and possibly proton diffusion are strongly coupled to Au||TiO2 interfacial design, likely through spin coupling of protons to unpaired electrons trapped at the TiO2 network. Taken together, our results show that Au||TiO2 interfacial design strongly impacts charge carrier (electron and proton) transport over mesoscale distances in catalytic aerogel architectures.

Topics

• nanoparticle
• density
• surface
• theory
• experiment
• Oxygen
• tomography
• gold
• composite
• density functional theory
• electron spin resonance spectroscopy
• interfacial surface area