Anoma Mudalige

Orientation of phenylphosphonic acid self-assembled monolayers on a transparent conductive oxide: a combined NEXAFS, PM-IRRAS, and DFT study.

Self-assembled monolayers (SAMs) of dipolar phosphonic acids can tailor the interface between organic semiconductors and transparent conductive oxides. When used in optoelectronic devices such as organic light emitting diodes and solar cells, these SAMs can increase current density and photovoltaic performance. The molecular ordering and conformation adopted by the SAMs determine properties such as work function and wettability at these critical interfaces. We combine angle-dependent near-edge X-ray absorption fine structure (NEXAFS) spectroscopy and polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) to determine the molecular orientations of a model phenylphosphonic acid on indium zinc oxide, and correlate the resulting values with density functional theory (DFT). We find that the SAMs are surprisingly well-oriented, with the phenyl ring adopting a well-defined tilt angle of 12-16° from the surface normal. We find quantitative agreement between the two experimental techniques and density functional theory calculations. These results not only provide a detailed picture of the molecular structure of a technologically important class of SAMs, but also resolve a long-standing ambiguity regarding the vibrational-mode assignments for phosphonic acids on oxide surfaces, thus improving the utility of PM-IRRAS for future studies.

Modification of BaTiO3 thin films: adjustment of the effective surface work function

Sputter-deposited BaTiO3 thin films have been modified with an alkylphosphonic acid and a partially-fluorinated alkylphosphonic acid in order to model the surface composition of similarly modified BaTiO3 nanoparticles. We present here the surface characterization of these modified films by a combination of X-ray photoelectron spectroscopy (XPS) and UV-photoelectron spectroscopy (UPS). BaTiO3 layers of average thicknesses ca. 2 nm were prepared by radio frequency (rf) magnetron sputter deposition on Ag films, to avoid charging effects during XPS/UPS characterization. Octadecylphosphonic acid (ODPA) and 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl phosphonic acid (perfluorohexyloctyl phosphonic acid, FHOPA), molecules with quite different molecular dipole moments, were chemisorbed from solution to the BaTiO3 surface. Polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS) of the modified BaTiO3 films indicated bidentate bonding of the alkylphosphonic acid to the oxide. Modification of the BaTiO3 surface with the partially-fluorinated alkylphosphonic acid (versus the normal alkylphosphonic acid) significantly changes the BaTiO3 interface dipole as revealed by UPS/XPS measurements, which, in turn, changes the frontier orbital offsets between the oxide and the organic modifier.

Evaporative deposition patterns of bacteria from a sessile drop: effect of changes in surface wettability due to exposure to a laboratory atmosphere.

Evaporative deposition from a sessile drop is a simple and appealing way to deposit materials on a surface. In this work, we deposit living, motile colloidal particles (bacteria) on mica from drops of aqueous solution. We show for the first time that it is possible to produce a continuous variation in the deposition pattern from ring deposits to cellular pattern deposits by incremental changes in surface wettability which we achieve by timed exposure of the mica surface to the atmosphere. We show that it is possible to change the contact angle of the drop from less than 5 degrees to near 20 degrees by choice of atmospheric exposure time. This controls the extent of drop spreading, which in turn determines the architecture of the deposition pattern.

PM-IRRAS Determination of Molecular Orientation of Phosphonic Acid Self-Assembled Monolayers on Indium Zinc Oxide

Self-assembled monolayers (SAMs) of phosphonic acids (PAs) on transparent conductive oxide (TCO) surfaces can facilitate improvement in TCO/organic semiconductor interface properties. When ordered PA SAMs are formed on oxide substrates, interface dipole and electronic structure are affected by the functional group properties, orientation, and binding modes of the modifiers. Choosing octylphosphonic acid (OPA), F13-octylphosphonic acid (F13OPA), pentafluorophenyl phosphonic acid (F5PPA), benzyl phosphonic acid (BnPA), and pentafluorobenzyl phosphonic acid (F5BnPA) as a representative group of modifiers, we report polarization modulation-infrared reflection-absorption spectroscopy (PM-IRRAS) of binding and molecular orientation on indium-doped zinc oxide (IZO) substrates. Considerable variability in molecular orientation and binding type is observed with changes in PA functional group. OPA exhibits partially disordered alkyl chains but on average the chain axis is tilted ∼57° from the surface normal. F13OPA tilts 26° with mostly tridentate binding. The F5PPA ring is tilted 23° from the surface normal with a mixture of bidentate and tridentate binding; the BnPA ring tilts 31° from normal with a mixture of bidentate and tridentate binding, and the F5BnPA ring tilts 58° from normal with a majority of bidentate with some tridenate binding. These trends are consistent with what has been observed previously for the effects of fluorination on orientation of phosphonic acid modifiers. These results from PM-IRRAS are correlated with recent results on similar systems from near-edge X-ray absorption fine structure (NEXAFS) and density functional theory (DFT) calculations. Overall, these results indicate that both surface binding geometry and intermolecular interactions play important roles in dictating the orientation of PA modifiers on TCO surfaces. This work also establishes PM-IRRAS as a routine method for SAM orientation determination on complex oxide substrates.

Thickness, composition, and molecular structure of residual thin films formed by forced dewetting of Ag from glycerol/D2O solutions

The thickness, composition, and interfacial molecular structure of residual thin films retained on the surface of polycrystalline Ag substrates after being forcibly dewet from glycerol/D2O solutions are investigated using contact angle measurements, ellipsometry, and polarization modulation-infrared reflection-absorption spectroscopy (PM-IRRAS). Residual film thicknesses are rationalized on the basis of the relevant long-range van der Waals and structural forces leading to residual film formation along with the interfacial glycerol and D2O structure. Unique interfacial composition, wherein glycerol preferentially segregates to the residual film interfaces, is substantiated by PM-IRRAS. Thus, the residual films possess composition and molecular structure that differ from those of bulk solution. Specifically, in the thinnest residual films, glycerol interacts strongly with the Ag substrate, leading to glycerol that is more ordered than the bulk liquid that coexists with bulk-like D2O. In thicker residual films, the glycerol mole fraction is still enhanced relative to the bulk solution, but both ordered and liquid-like glycerol species are observed along with D2O that is more strongly hydrogen-bonded than in the bulk. The creation of residual films by forced dewetting and their interrogation by spectroscopic methods are thus demonstrated to represent a powerful approach for characterizing interfacial liquid molecular structure near solid surfaces but beyond the first monolayer under ambient conditions.

Infrared Reflectance−Absorbance Spectroscopy of Thin Films Formed by Forced Dewetting of Solid−Fluid Interfaces

An infrared reflectance-absorbance spectroscopy method for characterizing the ultrathin fluid film retained on a surface upon forced dewetting from a fluid has been developed for investigation of interfacial molecular structure at reflective substrates. This report details the optical considerations and constraints necessary to acquire IR spectral data from nanometer-thick films retained upon forced dewetting of a solid substrate from a fluid into a vapor-saturated environment. The feasibility of this method is demonstrated through successful spectral acquisition from Ag surfaces modified with 11-mercaptoundecanol forcibly dewet from water. The IR spectral results clearly illustrate that information is acquired only from the interfacial region with no contribution from the bulk liquid. Residual layer thicknesses calculated from IR absorbance values are substantiated by ellipsometry. The spectra make clear that the molecular structure of the residual layer is distinctly different from that of the bulk liquid, confirming that this method is viable for interfacial structure elucidation of thin fluid films at a variety of solid substrates.