Noncovalently assembled nanotubular porous layers for delaying of heating surface failure.

Thermal management to prevent extreme heat surge in integrated electronic systems and nuclear reactors is a critical issue. To delay the thermal surge on the heater effectively, we report the benefit of a three dimensional nanotubular porous layer via noncovalent interactions (hydrophobic forces and hydrogen bonds). To observe the contribution of individual noncovalent interactions in a porous network formation, pristine carbon nanotubes (PCNTs) and oxidatively functionalized carbon nanotubes (FCNTs) were compared. Hydrogen-bonded interwoven nanotubular porous layer showed approximately two times critical heat flux (CHF) increase compared to that of a plain surface. It is assumed that the hydrophilic group-tethered nanotubular porous wicks and enhanced fluidity are the main causes for promoting the CHF increase. Reinforced hydrophilicity assists liquid spreading and capillarity-induced liquid pumping, which are estimated by using Electrochemical Impedance Spectroscopy. Also, shear induced thermal conduction, thermal boundary reduction, and rheology of nanoparticles could attribute to CHF enhancement phenomena.

Enhancing dropwise condensation through bioinspired wettability patterning.

Dropwise condensation (DWC) heat transfer depends strongly on the maximum diameter (Dmax) of condensate droplets departing from the condenser surface. This study presents a facile technique implemented to gain control of Dmax in DWC within vapor/air atmospheres. We demonstrate how this approach can enhance the corresponding heat transfer rate by harnessing the capillary forces in the removal of the condensate from the surface. We examine various hydrophilic-superhydrophilic patterns, which, respectively, sustain and combine DWC and filmwise condensation on the substrate. The material system uses laser-patterned masking and chemical etching to achieve the desired wettability contrast and does not employ any hydrophobizing agent. By applying alternating straight parallel strips of hydrophilic (contact angle ∼78°) mirror-finish aluminum and superhydrophilic regions (etched aluminum) on the condensing surface, we show that the average maximum droplet size on the less-wettable domains is nearly 42% of the width of the corresponding strips. An overall improvement in the condensate collection rate, up to 19% (as compared to the control case of DWC on mirror-finish aluminum) was achieved by using an interdigitated superhydrophilic track pattern (on the mirror-finish hydrophilic surface) inspired by the vein network of plant leaves. The bioinspired interdigitated pattern is found to outperform the straight hydrophilic-superhydrophilic pattern design, particularly under higher humidity conditions in the presence of noncondensable gases (NCG), a condition that is more challenging for maintaining sustained DWC.

Biologically inspired tunable hydrophilic/hydrophobic surfaces: a copper oxide self-assembly multitier approach.

In this study, a fabrication method for biologically inspired superhydrophobic micro- and nano-structured tier surfaces, each made of a self-assembled copper oxide, is presented. The method is controllable and applicable to bulk production when compared to existing high-end fabrication techniques. By modulating wet chemistry, different shapes and scales of tier structures were created. We demonstrated that their wetting behaviors are closely related to morphological information such as pitch, height and shape. To characterize their wetting behaviors, several experiments were designed and executed. In static water contact angle (WCA) measurements, morphological modulation led to wide WCA range (17°-95°). After hydrophobic self-assembly monolayer of 1-dodecanethiol, their WCA was escalated into superhydrophobic regime. In dynamic WCA, the contact angle hysteresis is greatly reduced by hybridizing the micro- and nano-tier (multiple tiers) when compared to utilizing a single tier. Also, the modification of the surface structure influences the rate of evaporation. In an analytical approach, the multiple tiers show a lower surface free energy compared to that of the single tier. By hybridizing different scales and shapes of tiers-such as hemispheric and conic shapes-the multiple tiers can efficiently reduce the surface energy barrier. Eventually, these manipulations lead to a subtle WCA hysteresis during the liquid motion testing. The analytical results are consistent with the dynamic WCA measurements. The multiple tiers also stabilize the Cassie regime and result in an increased hydrophobicity, which is more than when a single tier is employed.

Dendritic molecular switch: chiral folding and helicity inversion.

Appropriately designed chemical architectures can fold to adopt well-defined secondary structures without the need for structural motifs of biological origin. We have designed tris(N-salicylideneaniline)-based hyperbranched molecules that spontaneously collapse to compact three-blade propeller geometry of either (P)- or (M)-handedness. For a homologous series of compounds, a direct correlation was established between the absolute screw sense, either (P)- or (M)-, of this helical folding and the absolute configuration, either (R)- or (S)-, of the chiral alcohol groups introducing local asymmetric bias to the conformationally restricted molecular backbone. 1H NMR and CD spectroscopic studies provided significant insights into structural folding and unfolding of these chiral molecules in solution, which proceed via reversible assembly and disassembly of the C3-symmetric hydrogen-bonding network. Notably, solvents profoundly influenced this dynamic process. A strong correlation between the solvent donor number (DN) or solvent basicity (SB) parameters and the change in the Cotton effects pointed toward specific O-H...solvent interactions that drive structural unfolding and eventual refolding to apparently opposite helicity. This unusual chirality inversion process could also be induced by installation of chemical protecting groups that simulate specific solvent-solute interactions. Removal of this covalent mimic of the solvent shell restored the original screw sense of the parent molecule, thus establishing the feasibility of covalently triggered helicity inversion as a new mode of operation for chiroptical molecular switches.