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We develop and harness a phase field simulation method to study liquid filling on grooved surfaces. We consider both short-range and long-range liquid-solid interactions, with the latter including purely attractive and repulsive interactions, as well as those with short-range attraction and long-range repulsion. This allows us to capture complete, partial and pseudo-partial wetting states, demonstrating complex disjoining pressure profiles over the full range of possible contact angles as previously proposed in the literature. Applying the simulation method to study liquid filling on grooved surfaces, we compare the filling transition for the three different classes of wetting states as we vary the pressure difference between the liquid and gas phases. The filling and emptying transition is reversible for the complete wetting case, while significant hysteresis is observed for the partial and pseudo-partial cases. In agreement with previous studies, we also show that the critical pressure for the filling transition follows the Kelvin equation for the complete and partial wetting scenarios. Finally, we find the filling transition can display a number of distinct morphological pathways for the pseudo-partial wetting cases, as we demonstrate here for varying groove dimensions., 11 pages, 6 figures, accepted in the Journal of Chemical Physics

Reactive molecular dynamics simulations of MoS2 crystallization from amorphous precursor materials showed that crystal domain size decreased because of excess S or O, relative to the stoichiometric...

Economical CO 2 capture demands low-energy separation strategies. We use a liquid-infused surface (LIS) approach to immobilize reactive liquids, such as amines, on a textured and thermally conductive solid substrate with high surface-area to volume ratio (A/V) continuum geometry. The infused, micrometer-thick liquid retains that high A/V and directly contacts the gas phase, alleviating mass transport resistance typically encountered in mesoporous solid adsorbents. We name this LIS class “solid with infused reactive liquid” (SWIRL). SWIRL-amine requires no water dilution or costly mixing unlike the current liquid-based commercial approach. SWIRL–tetraethylenepentamine (TEPA) shows stable, high capture capacities at power plant CO 2 concentrations near flue gas temperatures, preventing energy-intensive temperature swings needed for other approaches. Water vapor increases CO 2 capacity of SWIRL-TEPA without compromising stability.

The ability to predict liquid transport rates on textured surfaces is key to the design and optimization of devices and processes such as oil recovery, coatings, reaction-separation, high-throughput screening, and thermal management. In this work we develop a fully analytical model to predict the propagation coefficients for liquids hemiwicking through micropillar arrays. This is carried out by balancing the capillary driving force and a viscous resistive force and solving the Navier-Stokes equation for representative channels. The model is validated against a large data set of experimental hemiwicking coefficients harvested from the literature and measured in-house using high-speed imaging. The theoretical predictions show excellent agreement with the measured values and improved accuracy compared to previously proposed models. Furthermore, using lattice Boltzmann (LB) simulations, we demonstrate that the present model is applicable over a broad range of geometries. The scaling of velocity with texture geometry, implicit in our model, is compared against experimental data, where good agreement is observed for most practical systems. The analytical expression presented here offers a tool for developing design guidelines for surface chemistry and microstructure selection for liquid propagation on textured surfaces.

The morphology, composition, and bonding character (carbon hybridization state) of continuous, ultra-thin (thickness ∼60 nm) nanocrystalline diamond (NCD) membranes are reported. NCD films were deposited on a silicon substrate that was pretreated using an optimized, two-step seeding process. The surface after each of the two steps, the as-grown NCD topside and the NCD underside (revealed by etching away the silicon substrate) is examined by X-ray PhotoElectron Emission spectroMicroscopy (X-PEEM) combined with X-ray absorption near edge structure (XANES) spectroscopy, X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM). The first step in the seeding process, a short exposure to a hydrocarbon plasma, induces the formation of SiC at the diamond/Si interface along with a thin, uniform layer of hydrogenated, amorphous carbon on top. This amorphous carbon layer allows for a uniform, dense layer of nanodiamond seed particles to be spread over the substrate in the second step. This facilitates the growth of a homogeneous, continuous, smooth, and highly sp 3 -bonded NCD film. We show for the first time that the underside of this film possesses atomic-scale smoothness (RMS roughness: 0.3 nm) and N98% diamond content, demonstrating the effectiveness of the two-step seeding method for diamond film nucleation. © 2007 Elsevier B.V. All rights reserved.

Additive explanation for anti-wear Additives in oil are vital for protecting engines from wear by forming films at sliding interfaces. Zinc dialkydithiophosphate (ZDDP) has been used for decades to reduce engine wear. Now there is a strong incentive for finding a replacement for ZDDP: Its breakdown products shorten catalytic converter lifetime. Gosvami et al. examined exactly how ZDDP produces an anti-wear film under high stress or elevated temperature (see the Perspective by Schwarz). Understanding these mechanisms will help in the development of higher-performance and more effective additives. Science , this issue p. 102 ; see also p. 40

This paper reports the recent development and applications of conductive boron-doped ultrananocrystalline diamond (BD-UNCD). The authors have determined that BD-UNCD can be synthesized with an H-rich gaseous chemistry and a high CH4/H2 ratio, which is opposite to previously reported methods with Ar-rich or H-rich gas compositions but utilizing very low CH4/H2 ratios. The BD-UNCD reported here has a resistivity as low as 0.01 ohm cm, with low roughness (

Highly $s{p}^{3}$-bonded, nearly hydrogen-free carbon-based materials can exhibit extremely low friction and wear in the absence of any liquid lubricant, but this physical behavior is limited by the vapor environment. The effect of water vapor on friction and wear is examined as a function of applied normal force for two such materials in thin film form: one that is fully amorphous in structure (tetrahedral amorphous carbon, or ta-C) and one that is polycrystalline with $l10$ nm grains [ultrananocrystalline diamond (UNCD)]. Tribologically induced changes in the chemistry and carbon bond hybridization at the surface are correlated with the effect of the sliding environment and loading conditions through ex situ, spatially resolved near-edge x-ray absorption fine structure (NEXAFS) spectroscopy. At sufficiently high relative humidity (RH) levels and/or sufficiently low loads, both films quickly achieve a low steady-state friction coefficient and subsequently exhibit low wear. For both films, the number of cycles necessary to reach the steady-state is progressively reduced for increasing RH levels. Worn regions formed at lower RH and higher loads have a higher concentration of chemisorbed oxygen than those formed at higher RH, with the oxygen singly bonded as hydroxyl groups (C-OH). While some carbon rehybridization from $s{p}^{3}$ to disordered $s{p}^{2}$ bonding is observed, no crystalline graphite formation is observed for either film. Rather, the primary solid-lubrication mechanism is the passivation of dangling bonds by OH and H from the dissociation of vapor-phase H${}_{2}$O. This vapor-phase lubrication mechanism is highly effective, producing friction coefficients as low as 0.078 for ta-C and 0.008 for UNCD, and wear rates requiring thousands of sliding passes to produce a few nanometers of wear.

The impressively low friction and wear of diamond in humid environments is debated to originate from either the stability of the passivated diamond surface or sliding-induced graphitization/rehybridization of carbon. We find ultralow friction and wear for ultrananocrystalline diamond surfaces even in dry environments, and observe negligible rehybridization except for a modest, submonolayer amount under the most severe conditions (high load, low humidity). This supports the passivation hypothesis, and establishes a new regime of exceptionally low friction and wear for diamond.

Extended abstract of a paper presented at Microscopy and Microanalysis 2012 in Phoenix, Arizona, USA, July 29 – August 2, 2012.

Extended abstract of a paper presented at Microscopy and Microanalysis 2011 in Nashville, Tennessee, USA, August 7–August 11, 2011.

Extended abstract of a paper presented at Microscopy and Microanalysis 2011 in Nashville, Tennessee, USA, August 7–August 11, 2011.

Extended abstract of a paper presented at Microscopy and Microanalysis 2011 in Nashville, Tennessee, USA, August 7–August 11, 2011.

Extended abstract of a paper presented at Microscopy and Microanalysis 2011 in Nashville, Tennessee, USA, August 7–August 11, 2011.

We perform a quantitative investigation of the energetics of thermally induced sp3→sp2 conversion of carbon-carbon bonds in tetrahedral amorphous carbon (ta-C) films by using near-edge x-ray absorption fine structure (NEXAFS) and Raman spectroscopy. We investigate the evolution of the bonding configuration in ta-C thin films subjected to high temperature annealing in flowing Argon gas using a rapid thermal annealing furnace over the range of 200–1000 °C. We observe no substantial change in bonding structure below 600 °C. Changes in the NEXAFS and Raman spectra start to appear above 600 °C, and by 1000 °C a significant increase in the sp2 bonding in the film is observed. No oxygen bonding is detected in the NEXAFS spectra, but we do observe an isosbestic point, demonstrating that the thermally driven sp3→sp2 conversion reaction occurs without passing through an intermediate transition state. This allows us to use NEXAFS spectra of thermally annealed ta-C films to quantitatively determine that the activation energy for directly converting the sp3-bonded carbon to the sp2-bonded configuration is 3.5±0.9 eV.

This letter describes the fundamental process underlying the synthesis of ultrananocrystalline diamond (UNCD) films, using a new low-pressure, heat-assisted bias-enhanced nucleation (BEN)/bias enhanced growth (BEG) technique, involving H2∕CH4 gas chemistry. This growth process yields UNCD films similar to those produced by the Ar-rich/CH4 chemistries, with pure diamond nanograins (3–5nm), but smoother surfaces (∼6nm rms) and higher growth rate (∼1μm∕h). Synchrotron-based x-Ray absorption spectroscopy, atomic force microscopy, and transmission electron microscopy studies on the BEN-BEG UNCD films provided information critical to understanding the nucleation and growth mechanisms, and growth condition-nanostructure-property relationships.