Highly active, durable, and inexpensive nanostructured catalysts are crucial for achieving efficient and economical electrochemical water splitting. However, developing efficient approaches to further improve the catalytic ability of the well-defined nanostructured catalysts is still a big challenge. Herein, we report a facile and universal cation-exchange process for synthesizing Fe-doped Ni(OH)2 and Co(OH)2 nanosheets with enriched active sites toward enhanced oxygen evolution reaction (OER). In comparison with typical NiFe layered double hydroxide (LDH) nanosteets prepared by the conventional one-pot method, Fe-doped Ni(OH)2 nanosheets evolving from Ni(OH)2 via an Fe3+/Ni2+ cation-exchange process possess nanoporous surfaces with abundant defects. Accordingly, Fe-doped Ni(OH)2 nanosheets exhibit higher electrochemical active surface area (ECSA) and improved surface wettability in comparison to NiFe LDH nanosheets and deliver significantly enhanced catalytic activity over NiFe LDH. Specifically, a low overpotential of only 245 mV is required to reach a current density of 10 mA cm-2 for Ni0.83Fe0.17(OH)2 nanosheets with a low Tafel slope of 61 mV dec-1, which is greatly decreased in comparison with those of NiFe LDH (310 mV and 78 mV dec-1). Additionally, this cation-exchange process is successfully extended to prepare Fe-doped Co(OH)2 nanosheets with improved catalytic activity for oxygen evolution. The results suggest that this cation-exchange process should have great potential in the rational design of defect-enriched catalysts toward high-performance electrocatalysis.

With the impacts of climate change and impending crisis of clean drinking water, designing functional materials for water harvesting from fog with large water capacity has received much attention in recent years. Nature has evolved different strategies for surviving dry, arid, and xeric conditions. Nature is a school for human beings. In this contribution, inspired by the Stenocara beetle, superhydrophilic/superhydrophobic patterned surfaces are fabricated on the silica poly(dimethylsiloxane) (PDMS)-coated superhydrophobic surfaces using a pulsed laser deposition approach with masks. The resultant samples with patterned wettability demonstrate water-harvesting efficiency in comparison with the silica PDMS-coated superhydrophobic surface and the Pt nanoparticles-coated superhydrophilic surface. The maximum water-harvesting efficiency can reach about 5.3 g cm h . Both the size and the percentage of the Pt-coated superhydrophilic square regions on the patterned surface affect the condensation and coalescence of the water droplet, as well as the final water-harvesting efficiency. The present water-harvesting strategy should provide an avenue to alleviate the water crisis facing mankind in certain arid regions of the world.

No abstract

A triphenylamine-based organic luminophor (TPA-CO) with a highly distorted structure has been designed and effortlessly obtained by an Ullmann reaction. The luminophor exhibits a stimuli-induced emission enhancement effect and intramolecular charge transfer properties. The fluorescence efficiency of its crystals is dramatically increased from 0.4% to 12.3% upon grinding. The emission enhancement is also realized by a heating process. The "bright" state can recover its original state and turn "dark". The luminescence "on-off" behaviour is repeatedly transformed by a grinding-vapour process or by a heating process. The XRD patterns of the "bright" and "dark" states show that the change of emission intensity is related to the reversible transition between the crystalline state and the metastable amorphous state. At the molecular level, the emission enhancement upon external stimuli may be attributed to conformational planarization and weak intermolecular interactions.

Chemomechanical effects are known to initiate fluid oscillations in certain liquid metals; however, they typically produce an irregular motion that is difficult to deactivate or control. Here we show that stimulating liquid gallium with electrochemistry can cause a metal drop to exhibit a heart beating effect by shape shifting at a telltale frequency. Unlike the effects reported in the past for mercury, the symmetry-breaking forces generated by using gallium propel the drop several millimeters with velocities of the order of 1 cm per second. We demonstrate pulsating dynamics between 0 and 610 beats per minute for 50-150  μL droplets in a NaOH electrolyte at 34 °C. The underlying mechanism is a self-regulating cycle initiated by fast electrochemical oxidation that adjusts the drop's surface tension and causes a transformation from spherical to pancake form, followed by detachment from the circular electrode. As the beat frequency can be activated and controlled using a dc voltage, the electrochemical mechanism opens the way for fluid-based timers and actuators.

No abstract

A low-cost and reusable novel superhydrophilic and underwater superoleophobic NiO/Ni mesh with a micro/nanoscale hierarchical structure exhibits superior oil/water separation in harsh environments.

Electrode surface wettability is critically important for heterogeneous electrochemical reactions taking place in aqueous and nonaqueous media. Herein, electrochemically inert g-C 3 N 4 (GCN) is successfully demonstrated to significantly enhance water oxidation by constructing a superhydrophilic catalyst surface and promoting substantial exposure of active sites. As a proofof-concept application, superhydrophilic GCN/Ni(OH) 2 (GCNN) hybrids with monodispersed Ni(OH) 2 nanoplates strongly anchored on GCN are synthesized for enhanced water oxidation catalysis. Owing to the superhydrophilicity of functionalized GCN, the surface wettability of GCNN (contact angle 0°) is substantially improved as compared with bare Ni(OH) 2 (contact angle 21°). Besides, GCN nanosheets can effectively suppress Ni(OH) 2 aggregation to help expose more active sites. Benefiting from the well-defined catalyst surface, the optimal GCNN hybrid shows significantly enhanced electrochemical performance over bare Ni(OH) 2 nanosheets, although GCN is electrochemically inert. In addition, similar catalytic performance promotion resulting from wettability improvement induced by incorporation of hydrophilic GCN is also successfully demonstrated on Co(OH) 2 . The present results demonstrate that, in addition to developing new catalysts, building efficient surface chemistry is also vital to achieve extraordinary water oxidation performance.