Changkronborg5964

Robust and inexpensive dry adhesives have a great potential in multitudinous industrial applications. RIN1 However, to date, the fabrication of dry adhesives, prepared using high aspect ratio structures in general, requires specific equipment and time-consuming processes, which limit their practicable utilization. Inspired from human fingerprints, in this study, we created durable single-component elastomer surfaces with symmetric and multiple concentric-shaped wrinkled patterns that exhibit isotropic dry adhesion capabilities. The dynamic interfacial release-induced surface wrinkling property of a rigid degradable polymeric capping layer [i.e., poly(l-lactide) (PLLA)] was exploited on a soft elastomer substrate [i.e., polydimethylsiloxane (PDMS)] to spontaneously form wrinkled PLLA/PDMS bilayer composites. After conducting a two-step thermal curing process on the composite and hydrolysis of the PLLA capping layer, a single-component microwrinkled PDMS surface with a large area and symmetric patterns could be generated. The patterns show flexible, durable, and isotropic dry adhesion capabilities that could be controlled by tuning their geometrical parameters (wrinkle wavelengths and amplitudes) and elastic modulus. In particular, the formation of symmetrically wrinkled patterns without using expensive lithography for patterning and costly material precursors is an advantage and could be extended to other industrial applications, such as damage-free transportation, biomimetic climbing robots, and biocompatible medical patches.In this work, the effect of carbon dots (C-dots) on the performance of NiO-based dye-sensitized solar cells (DSSCs) was explored. NiO nanoparticles (NPs) with a rectangular shape (average size 11.4 × 16.5 nm2) were mixed with C-dots, which were synthesized from citric acid (CA) and ethylenediamine (EDA). A photocathode consisting of a composite of C-dots with NiO NPs (NiO@C-dots) was then used to measure the photovoltaic performance of a DSSC. A power conversion efficiency (PCE) of 9.85% (430 nm LED@50 mW/cm2) was achieved by a DSSC fabricated via the adsorption of N719 sensitizer with a C-dot content of 12.5 wt % at a 1.51 EDA/CA molar ratio. This PCE value was far larger than the PCE value (2.44 or 0.152%) obtained for a NiO DSSC prepared without the addition of C-dots or N719, respectively, indicating the synergetic effect by the co-adsorption of C-dots and N719. This synergetically higher PCE of the NiO@C-dot-based DSSC was due to the larger amount of sensitizer adsorbed onto the composites with a larger specific surface area and the faster charge transfer in the NiO@C-dot working electrode. In addition, the C-dots bound to the NiO NPs shorten the band gap of the NiO NPs due to energy transfer and give rise to faster charge separation in the electrode. The most important fact is that C-dots are the main sensitizer, while N719 tightly adsorbs on C-dots and NiO behaves as an accelerator of a positive electron transfer and a restrainer of the electron-hole recombination. These results reveal that C-dots are a remarkable enhancer for NiO NPs in DSSCs and that NiO@C-dots are promising photovoltaic electrode materials for DSSCs.The utilization of nonprecious metal electrocatalysts for water-splitting may be the ultimate solution for sustainable and clean hydrogen energy. MXene, an emerging two-dimensional material, exhibits many unique properties such as possible metal-like conductivity, hydrophilic surface, and rich chemistry, rendering a group of promising catalysts and catalyst support materials. In this study, exfoliated Ti3C2 MXenes serve as a substrate to perpendicularly grow uniform mesoporous NiCoP nanosheets through an in situ interface-growth strategy and subsequent phosphorization. The obtained Ti3C2@mNiCoP materials with a stable hierarchical sandwich structure possess excellent conductivity, large surface area, and uniform mesopores with high pore volume. With these beneficial properties, the Ti3C2@mNiCoP material exhibits superior overall water-splitting performance compared with that of its building-block counterparts, matching the state-of-the-art water-splitting electrocatalysts.Herein, we present the cathodic paths of the Group-7 metal complex [Re(3,3'-DHBPY)(CO)3Cl] (3,3'-DHBPY = 3,3'-dihydroxy-2,2'-bipyridine) producing a moderately active catalyst of electrochemical reduction of CO2 to CO. The combined techniques of cyclic voltammetry and IR/UV-vis spectroelectrochemistry have revealed significant differences in the chemistry of the electrochemically reduced parent complex compared to the previously published Re/4,4'-DHBPY congener. The initial irreversible cathodic step in weakly coordinating THF is shifted toward much less negative electrode potentials, reflecting facile reductive deprotonation of one hydroxyl group and strong intramolecular hydrogen bonding, O-H···O-. The latter process occurs spontaneously in basic dimethylformamide where Re/4,4'-DHBPY remains stable. The subsequent reduction of singly deprotonated [Re(3,3'-DHBPY-H+)(CO)3Cl]- under ambient conditions occurs at a cathodic potential close to that of the Re/4,4'-DHBPY-H+ derivative. However, for the stabilized 3HBPY)(CO)3(PrCN)]+ that also smoothly deprotonates by the initial reduction to [Re(3,3'-DHBPY-H+)(CO)3(PrCN)]. The latter complex ultimately converts at the second cathodic wave to [Re(3,3'-DHBPY-2H+)(CO)3(PrCN)]3- via a counterintuitive ETC step generating the 1e- radical of the parent complex, viz., [Re(3,3'-DHBPY)(CO)3(PrCN)]. The same alternative reduction path is also followed by [Re(3,3'-DHBPY-H+)(CO)3Cl]- at the onset of the second cathodic wave, where the ETC step results in the intermediate [Re(3,3'-DHBPY)(CO)3Cl]•- further reducible to [Re(3,3'-DHBPY-2H+)(CO)3]3- as the CO2 catalyst.The task-specific ionic liquid (IL), 1-ethyl-3-methylimidazolium 2-cyanopyrolide ([EMIM][2-CNpyr]), was encapsulated with polyurea (PU) and graphene oxide (GO) sheets via a one-pot Pickering emulsion, and these capsules were used to scrub CO2 (0-5000 ppm) from moist air. Up to 60 wt % of IL was achieved in the synthesized capsules, and we demonstrated comparable gravimetric CO2 capacities to zeolites and enhanced absorption rates compared to those of bulk IL due to the increased gas/liquid surface-to-volume area. The reactive IL capsules show recyclability upon mild temperature increase compared to zeolites that are the conventional absorber materials for CO2 scrubbing. The measured breakthrough curves in a fixed bed under 100% relative humidity establish the utility of reactive IL capsules as moisture-stable scrubber materials to separate CO2 from air, outperforming zeolites owing to their higher selectivity. It is shown that thermal stability, CO2 absorption capacity, and rate of uptake by IL capsules can be further modulated by incorporating low-viscosity and nonreactive ILs to the capsule core.