Ionic liquids on oxide surfaces.

Ionic liquids (ILs) supported on oxide surfaces are being investigated for numerous applications including catalysis, batteries, capacitors, transistors, lubricants, solar cells, corrosion inhibitors, nanoparticle synthesis and biomedical applications. The study of ILs with oxide surfaces presents challenges both experimentally and computationally. The interaction between ILs and oxide surfaces can be rather complex, with defects in the oxide surface playing a key role in the adsorption behaviour and resulting electronic properties.

Interactions and stabilisation of acetone, sulfur dioxide and water with 1-octyl-3-methylimidazolium tetrafluoroborate [OMIM][BF] at low temperatures.

The interactions between three small molecules, water (HO), sulfur dioxide (SO) and acetone ((CH)CO), with the ionic liquid (IL) 1-octyl-3-methylimidazolium tetrafluoroborate, [OMIM][BF], have been determined using line of sight temperature programmed desorption (LOSTPD) from a gold surface. Multilayers of the IL were deposited by physical vapour deposition with multilayers of the small molecular species (adsorbed from the gas phase) at 90 K. LOSTPD was then carried out with the small molecular species desorbing first from the mixed multilayer, followed at higher temperatures by desorption of the IL from the gold surface.

Ionic Liquid Ordering at an Oxide Surface.

The interaction of the ionic liquid [C C Im][BF ] with anatase TiO , a model photoanode material, has been studied using a combination of synchrotron radiation photoelectron spectroscopy and near-edge X-ray absorption fine structure spectroscopy. The system is of interest as a model for fundamental electrolyte-electrode and dye-sensitized solar cells. The initial interaction involves degradation of the [BF ] anion, resulting in incorporation of F into O vacancies in the anatase surface.

Adsorption, Desorption, and Reaction of 1-Octyl-3-methylimidazolium Tetrafluoroborate, [C₈C₁Im][BF₄], Ionic Liquid Multilayers on Cu(111).

Multilayers of 1-octyl-3-methylimidazolium tetrafluoroborate [C8C1Im][BF4] have been deposited on a Cu(111) surface by evaporation in UHV. XPS shows that [C8C1Im][BF4] adsorbs without decomposition for substrate temperatures < 300 K. XPS and UPS data indicate that ionic liquid (IL) deposition onto a 120 K Cu(111) surface results in the IL forming multilayers by a simultaneous-multilayer growth process.

Surface properties of nanocrystalline PbS films deposited at the water-oil interface: a study of atmospheric aging.

Nanocrystalline thin films of PbS are obtained in a straightforward reaction by precipitation at the interface between toluene (containing a Pb precursor) and water (containing Na2S). Lead thiobiuret [Pb(SON(CN(i)Pr2)2)2] and lead diethyldithiocarbamate [Pb(S2CNEt2)2] precursors are used. The films are characterized by X-ray diffraction and electron microscopy, revealing typical particle sizes of 10-40 nm and preferred (200) orientation.

Dynamics in next-generation solar cells: time-resolved surface photovoltage measurements of quantum dots chemically linked to ZnO (101[combining macron]0).

The charge dynamics at the surface of the transparent conducting oxide and photoanode material ZnO are investigated in the presence and absence of light-harvesting colloidal quantum dots (QDs). The time-resolved change in surface potential upon photoexcitation has been measured in the m-plane ZnO (101[combining macron]0) using a laser pump-synchrotron X-ray probe methodology. By varying the oxygen annealing conditions, and hence the oxygen vacancy concentration of the sample, we find that dark carrier lifetimes at the ZnO surface vary from hundreds of μs to ms timescales, i.

Adsorption studies of p-aminobenzoic acid on the anatase TiO₂(101) surface.

The adsorption of p-aminobenzoic acid (pABA) on the anatase TiO2(101) surface has been investigated using synchrotron radiation photoelectron spectroscopy, near edge X-ray absorption fine structure (NEXAFS) spectroscopy, and density functional theory (DFT). Photoelectron spectroscopy indicates that the molecule is adsorbed in a bidentate mode through the carboxyl group following deprotonation. NEXAFS spectroscopy and DFT calculations of the adsorption structures indicate the ordering of a monolayer of the amino acid on the surface with the plane of the ring in an almost upright orientation.

Adsorption of dopamine on rutile TiO2 (110): a photoemission and near-edge X-ray absorption fine structure study.

Synchrotron radiation photoelectron spectroscopy and near-edge X-ray absorption fine structure (NEXAFS) techniques have been used to study the adsorption of dopamine on a rutile TiO2 (110) single crystal. Photoemission results suggest that dopamine bonds through the oxygen molecules in a bidentate fashion. From the data, it is ambiguous whether the oxygens bond to the same 5-fold coordinated surface titanium atom or bridges across two, although based on the bonding of pyrocatechol on rutile TiO2 (110), it is likely that the dopamine bridges two titanium atoms.

PEGylation of nanosubstrates (titania) with multifunctional reagents: at the crossroads between nanoparticles and nanocomposites.

Titania (anatase) nanoparticles were successfully PEGylated through the use of catechol (dopamine)-terminated PEG derivatives. The resulting materials were characterized by excellent stability at neutral pH and extremely low toxicity (phagocytic and nonphagocytic cell lines). In particular, we focused on the comparison between mono- and bis-catechol PEGs.

Adsorption of organic molecules on rutile TiO2 and anatase TiO2 single crystal surfaces.

The interaction of organic molecules with titanium dioxide surfaces has been the subject of many studies over the last few decades. Numerous surface science techniques have been utilised to understand the often complex nature of these systems. The reasons for studying these systems are hugely diverse given that titanium dioxide has many technological and medical applications.

Surface characterization of SLActive dental implants.

The aim of the study was to characterize the surface chemistry, hydration capacity, topography and roughness of the root part of a hydrophilic sandblasted and acid-etched titanium dental implant (SLActive). Implants as received (SAR), after water rinsing (SAW) and after ultrasonication in water (SAU) were subjected to x-ray photoelectron spectroscopy (XPS) elemental and binding state analysis. Scanning electron microscopy plus energy dispersive x-ray microanalysis (SEM/EDX), reflection Fourier transform infrared microspectroscopy (RFTIRM) and hydration/ dehydration cycling by environmental scanning electron microscopy (ESEM), were performed in SAR, whereas SAU implants were subjected to 3D-optical profilometry and SEM.