Quanzi Yuan

Measurement of the Rate of Water Translocation through Carbon Nanotubes

We present an approach for measuring the water flow rate through individual ultralong carbon nanotubes (CNTs) using field effect transistors array defined on individual tubes. Our work exhibits a rate enhancement of 882-51 and a slip length of 53-8 nm for CNTs with diameters of 0.81-1.59 nm. We also found that the enhancement factor does not increase monotonically with shrinking tube diameter and there exists a discontinuous region around 0.98-1.10 nm. We believe that these single-tube level results would help understand the intrinsic nanofluidics of water in CNTs.

Hydroelectric Voltage Generation Based On Water-Filled Single-Walled Carbon Nanotubes

A DFT/MD mutual iterative method was employed to give insights into the mechanism of voltage generation based on water-filled single-walled carbon nanotubes (SWCNTs). Our calculations showed that a constant voltage difference of several mV would generate between the two ends of a carbon nanotube, due to interactions between the water dipole chains and charge carriers in the tube. Our work validates this structure of a water-filled SWCNT as a promising candidate for a synthetic nanoscale power cell, as well as a practical nanopower harvesting device at the atomic level.

Hierarchical self-assembly of achiral amino acid derivatives into dendritic chiral nanotwists.

The organogel formation and self-assembly of a glycine-based achiral molecule were investigated. It has been found that the compound could gel organic solvents either at a lower temperature with lower concentration or at room temperature with higher concentration, which showed different self-assembled nanostructures. At a low temperature of -15 °C, the compound self-assembled into fibrous structures, whereas it formed distinctive flat microbelts at room temperature. When the organogel with nanofibers formed at -15 °C was brought into an ambient condition, chiral twist nanostructures were immediately evolved, which subsequently transferred to a giant microbelt through a hierarchical dendritic twist with the time. Although the compound is achiral, it formed chiral twist with both left- and right-handed twist structures simultaneously. When a trace analogical chiral trigger, L-alanine or D-alanine derivative, was added, a complete homochiral dendritic twist was obtained. Interestingly, a reverse process, i.e. the transformation of the microbelts into twists, could occur upon dilution of the organogel with microbelt structure. During the dilution, both left- and right-handed chiral twists could be formed again. Interestingly, the same branch from the microbelt formed the twist with the same handedness. A combination of the density functional theory (DFT), molecular mechanics (MM), and molecular dynamics (MD) simulations demonstrates that the temperature-induced twisting of the bilayer is responsible for the morphological transformation and evolution of the dendrite twist. This research sheds new light on the hierarchical transformation of the chiral structures from achiral molecules via controlled self-assembly.

Topology-dominated dynamic wetting of the precursor chain in a hydrophilic interior corner

The topology-dominated dynamic wetting of a droplet in a hydrophilic interior corner was explored using molecular dynamics simulations and molecular kinetic theory. A wetting transition in the interior corner of a single-file water-molecule precursor chain (PC), which eliminated the stress singularity and advanced much faster than the precursor film, was controlled by the interior angle. Owing to the confinement in the interior corner, the potential surface is lower and smoother. The one-dimensional hydrogen-bond chain transferred the disjoining pressure to drive the PC to slip-like ice. As an example, a stable and long metallic monatomic chain was formed using the unique transport properties of the PC for the first time. Our results may help in understanding the topology-dominated dynamic wetting in a hydrophilic interior corner, expand ‘Taylor conjecture’ to nanoscale and develop new applications at nanoscale.

Molecular dynamics simulations of the enhanced recovery of confined methane with carbon dioxide

For the first time, the enhanced recovery of confined methane (CH4) with carbon dioxide (CO2) is investigated through molecular dynamics simulations. The adsorption energy and configuration of CH4 and CO2 on the carbon surface were compared, which shows that CO2 is a good candidate in displacing confined CH4. The energy barrier required for displacing CH4 by CO2 injection was found to depend on the displacement angle. When CO2 approached vertically to the carbon surface, the displacement of CH4 occurred most easily. The curvature and size effects of the carbon nanopores on CH4 recovery were revealed and indicated that there exists an optimum pore size making the displacement occur most efficiently. The underlying mechanisms of these phenomena were uncovered. Our findings and related analyses may help to understand CO2 enhanced gas recovery from the atomic level and assist the future design in engineering.

Growth Mechanism And Joint Structure Of Zno Tetrapods

Regular zinc oxide (ZnO) tetrapods with a flat plane have been obtained on Si(1 0 0) substrate via the chemical vapour deposition approach. The x-ray diffraction result suggests that these tetrapods are all single crystals with a wurtzite structure that grow along the (0 0 0 1) direction and corresponding electron backscatter diffraction analysis reveals the crystal orientation of growth and exposed surface. Furthermore, we find some ZnO tetrapods with some legs off and the angles between every two legs are measured with the aid of scanning electron microscopy and image analysis, which benefit to reveal the structure of ZnO tetrapods joint. The structure model and growth mechanism of ZnO tetrapods are proposed. Besides, the stable model of the interface was obtained through the density-functional theory calculation and the energy needed to break the twin plane junction was calculated as 5.651 J m(-2).Regular zinc oxide (ZnO) tetrapods with a flat plane have been obtained on Si(1?0?0) substrate via the chemical vapour deposition approach. The x-ray diffraction result suggests that these tetrapods are all single crystals with a wurtzite structure that grow along the (0?0?0?1) direction and corresponding electron backscatter diffraction analysis reveals the crystal orientation of growth and exposed surface. Furthermore, we find some ZnO tetrapods with some legs off and the angles between every two legs are measured with the aid of scanning electron microscopy and image analysis, which benefit to reveal the structure of ZnO tetrapods joint. The structure model and growth mechanism of ZnO tetrapods are proposed. Besides, the stable model of the interface was obtained through the density-functional theory calculation and the energy needed to break the twin plane junction was calculated as 5.651?J?m?2.

Dynamic spreading on pillar-arrayed surfaces: Viscous resistance versus molecular friction

The dynamic spreading of a liquid droplet on micropillar-arrayed surfaces is experimentally investigated. A theoretical model is proposed to include energy dissipations raised from both the viscous resistance at mesoscale and the molecular friction at microscale in the triple-phase region. The scaling laws and spreading shape of the droplet change with the variation of the liquid viscosity because of the competition between these two mechanisms of energy dissipations at the moving contact line. The Laplace pressures at the interior corner and at the wavy contact line are the answers to the excess driving energy and the superwetting on pillar-arrayed surfaces. The formation and evolution of the bulk and the fringe are also analyzed in detail. Our results may help to understand the wetting dynamics on microtextured surfaces and assist the future design of engineered surfaces in practical applications.

Tuning structural and mechanical properties of two-dimensional molecular crystals: the roles of carbon side chains.

A key requirement for the future applicability of molecular electronics devices is a resilience of their properties to mechanical deformation. At present, however, there is no fundamental understanding of the origins of mechanical properties of molecular films. Here we use quinacridone, which possesses flexible carbon side chains, as a model molecular system to address this issue. Eight molecular configurations with different molecular coverage are identified by scanning tunneling microscopy. Theoretical calculations reveal quantitatively the roles of different molecule-molecule and molecule-substrate interactions and predict the observed sequence of configurations. Remarkably, we find that a single Youngs modulus applies for all configurations, the magnitude of which is controlled by side chain length, suggesting a versatile avenue for tuning not only the physical and chemical properties of molecular films but also their elastic properties.

Transport properties and induced voltage in the structure of water-filled single-walled boron-nitrogen nanotubes

Density functional theorymolecular dynamics simulations were employed to give insights into the mechanism of voltage generation based on a water-filled single-walled boron-nitrogen nanotube (SWBNNT). Our calculations showed that (1) the transport properties of confined water in a SWBNNT are different from those of bulk water in view of configuration, the diffusion coefficient, the dipole orientation, and the density distribution, and (2) a voltage difference of several millivolts would generate between the two ends of a SWBNNT due to interactions between the water dipole chains and charge carriers in the tube. Therefore, this structure of a water-filled SWBNNT can be a promising candidate for a synthetic nanoscale power cell as well as a practical nanopower harvesting device.

Phase transitions of a water overlayer on charged graphene: from electromelting to electrofreezing

We show by using molecular dynamics simulations that a water overlayer on charged graphene experiences first-order ice-to-liquid (electromelting), and then liquid-to-ice (electrofreezing) phase transitions with the increase of the charge value. Corresponding to the ice-liquid-ice transition, the variations of the order parameters indicate an order-disorder-order transition. The key to this novel phenomenon is the surface charge induced change of the orientations of water dipoles, which leads to the change of the water-water interactions from being attractive to repulsive at a critical charge value qc. To further uncover how the orientations of water dipoles influence the interaction strength between water molecules, a theoretical model considering both the Coulomb and van der Waals interactions is established. The results show that with the increase of the charge value, the interaction strength between water molecules decreases below qc, then increases above qc. These two inverse processes lead to electromelting and electrofreezing, respectively. Combining this model with the Eyring equation, the diffusion coefficient is obtained, the variation of which is in qualitative agreement with the simulation results. Our findings not only expand our knowledge of the graphene-water interface, but related analyses could also help recognize the controversial role of the surface charge or electric field in promoting phase transitions of water.