Flapping and powering characteristics of a flexible piezoelectric nanogenerator at Reynolds number range simulating ocean current.

For effective ocean energy harvesting, it is necessary to understand the coupled motion of the piezoelectric nanogenerator (PENG) and ocean currents. Herein, we experimentally investigate power performance of the PENG in the perspective of the fluid-structure interaction considering ocean conditions with the Reynolds number (Re) values ranging from 1 to 141,489. A piezoelectric polyvinylidene fluoride micromesh was constructed via electrohydrodynamic (EHD) jet printing technique to produce the ß-phase dominantly that is desirable for powering performance. Water channel was set to generate water flow to vibrate the flexible PENG. By plotting the Re values as a function of nondimensional bending rigidity (KB) and the structure-to-fluid mass ratio (M*), we could find neutral curves dividing the stable and flapping regimes. Analyzing the flow velocities between the vortex and surroundings via a particle image velocimetry, the larger displacement of the PENG in the chaotic flapping regime than that in the flapping regime was attributed to the sharp pressure gradient. By correlating M*, Re, KB, and the PENG performance, we conclude that there is critical KB that generate chaotic flapping motion for effective powering. We believe this study contributes to the establishment of a design methodology for the flexible PENG harvesting of ocean currents.

Experimental, Theoretical, and Numerical Investigation of the Electric Field and Surface Wettability Effects on the Penetration Length in Capillary Flow.

This study addressed the dynamics of capillary-driven flow for different surface wettabilities by concentrating on the influence of electric potential. The capillary flow dynamics were investigated by varying the wettability (plasma-treated, hydrophobic, hydrophilic, and superhydrophilic) of a capillary surface, and the applied electric potential to the liquid ranged from 0 to 500 V. When an electric potential was applied to the liquid, the fluid flow penetration length increased by 30-50% due to the electrohydrodynamic (EHD)-driven flow by the Maxwell (electric) pressure gradient effect. The results showed that the EHD effect enhanced the fluid penetration through narrow gaps. The maximum fluid penetration was attained for every surface at 500 V, particularly for the superhydrophilic surface, which exhibited the highest value. The combined effect of the electric field and wettability resulted in an enhanced fluid penetration speed, reducing the underfill time. In addition, theoretical and numerical models were developed for comparison with the experimental results. The proposed models reinforce the observed fluid flow phenomenon on various surfaces under the influence of an electric field. These findings can provide alternative strategies for controlling the dynamic features of capillary imbibition by introducing an electric field and wettability effects, which has practical implications in flip-chip packaging, microfluidic devices, and the manipulation of biocells.

Infiltrated thin film structure with hydrogel-mediated precursor ink for durable SOFCs.

The hydrogel of biomolecule-assisted metal/organic complex has the superior ability to form a uniform, continuous, and densely integrated structure, which is necessary for fine thin film fabrication. As a representative of nature-originated polymers with abundant reactive side chains, we select the gelatin molecule as an element for weaving the metal cations. Here, we demonstrate the interaction between the metal cation and gelatin molecules, and associate it with coating quality. We investigate the rheological property of gelatin solutions interacting with metal cation from the view of cross-linking and denaturing of gelatin molecules. Also, we quantitatively compare the corresponding interactions by monitoring the absorbance spectrum of the cation. The coated porous structure is systematically investigated from the infiltration of gelatin-mediated Gd0.2Ce0.8O2-δ (GDC) precursor into Sm0.5Sr0.5CoO3-δ (SSC) porous scaffold. By applying the actively interacting gelatin-GDC system, we achieve a thin film of GDC on SSC with excellent uniformity. Compare to the discrete coating from the typical infiltration process, the optimized thin film coated structure shows enhanced performance and stability.

Characterization and Comparison of Two Complete Plastomes of Rosaceae Species (Potentilla dickinsii var. glabrata and Spiraea insularis) Endemic to Ulleung Island, Korea.

Potentilla dickinsii var. glabrata and Spiraea insularis in the family Rosaceae are species endemic to Ulleung Island, Korea, the latter of which is listed as endangered. In this study, we characterized the complete plastomes of these two species and compared these with previously reported plastomes of other Ulleung Island endemic species of Rosaceae (Cotoneaster wilsonii, Prunus takesimensis, Rubus takesimensis, and Sorbus ulleungensis). The highly conserved complete plastomes of P. dickinsii var. glabrata and S. insularis are 158,637 and 155,524 base pairs with GC contents of 37% and 36.9%, respectively. Comparative phylogenomic analysis identified three highly variable intergenic regions (trnT-UGU/trnL-UAA, rpl32/trnL-UAG, and ndhF/rpl32) and one variable genic region (ycf1). Only 14 of the 75 protein-coding genes have been subject to strong purifying selection. Phylogenetic analysis of 23 representative plastomes within the Rosaceae supported the monophyly of Potentilla and the sister relationship between Potentilla and Fragaria and indicated that S. insularis is sister to a clade containing Cotoneaster, Malus, Pyrus, and Sorbus. The plastome resources generated in this study will contribute to elucidating the plastome evolution of insular endemic Rosaceae on Ulleung Island and also in assessing the genetic consequences of anagenetic speciation for various endemic lineages on the island.

Redox-Active Tyrosine-Mediated Peptide Template for Large-Scale Single-Crystalline Two-Dimensional Silver Nanosheets.

Although self-assembly of various peptides has been widely applied, it is challenging to obtain single-crystalline and layer-by-layered nanostructures in a two-dimensional system. Here, we report a method for controlling the morphology and crystal growth at room temperature by a redox-active peptide template that can specifically co-assemble with metal ions. During the crystal growth, a silver ion-coordinated α-helical peptide (+3HN-YYACAYY-COO-) induces long-range atomic ordering at the air/water interface, which leads to multilayered single-crystalline silver nanosheets without an additional annealing process. Furthermore, this peptide template can facilitate efficient electron transfer between the independent metal nanosheets to improve electrochemical properties. We expect that this peptide template-based single-crystal growth method can be extended to synthesize other materials.