Solvothermal Synthesis and Pyrolysis Toward Heteroatom-Doped Carbon Microspheres for Zinc-Ion Hybrid Capacitors.

Heteroatom-doped porous carbon materials have investigated to promote the energy density of zinc-ion hybrid capacitors (ZICs). Yet, the quest for high-performance carbon materials or cathodes brings to light the question of which dopants facilitate fast energy storage kinetics and various types of pseudocapacitive reactions. Investigation of carbon materials with precise quantitative dopants as the key variable represents an effective appropriate approach to comprehending the intricate role of dopants in energy storage areas. Here, a straightforward solvothermal strategy is demonstrated for a variety of pristine and iron-incorporated polymer microspheres, used as precursors for durable spherical carbons intended for cathode applications in ZICs. The strategy effectively governs the incorporation of dopants within the carbon materials, whilewhile maintaining consistent morphology, microtexture, and pore structure across different carbon variations. The synergistic effect of various dopants enhance the pseudocapacitance and facilitate the ion storage process. In consequence, the optimal cathode delivers considerable capacity (178.8 mAh g-1 at 0.5 A g-1), good energy density (120.2 Wh kg-1 at 336 W kg-1), and excellent cycling stability (101.5% capacity retention at 35 000 cycles). The demonstration showcases a viable method for crafting carbon materials with precise dopants to accommodate the zinc anode, thus enabling high-capacity and high-energy ZICs.

Optical vector fields with kaleidoscopic quasicrystal structures by multiple beam interference.

An easily accessible approach is proposed to create structured beams with various quasicrystal structures and polarization distributions based on multi-beam interference. By controlling the azimuthally-dependent polarization for Q evenly and circularly distributed beams to be interfered, the intensity and polarization structures for the generated quasicrystal field with Q-fold rotational symmetry are flexibly adjusted. Using the diffraction theory for interfering Q vector Gaussian beams, an analytical wave function is derived to reconstruct the polarization-resolved intensities and the distributions of Stokes parameters measured in the experiment. With good agreement between the numerical and experimental results, the derived wave function is further employed to characterize the propagation-variant states of polarization, providing fundamentally important information for the vector quasicrystal beams.

Stretchable Hydrogels with Low Hysteresis and High Fracture Toughness for Flexible Electronics.

Stretchable materials, especially hydrogels, are emerging in various fields recently. Many applications demand low hysteresis and high fracture toughness of the materials to be used under dynamic mechanical loads. Herein, the authors report a hydrogel with high fracture toughness and low hysteresis through using a strong metal coordination bond and relatively high crosslinking density. This design allows the sacrificial bond to remain intact under normal operation, while fracturing to dissipate mechanical energy in the fracture zone to prevent propagation of the cracks. The obtained hydrogel exhibits a low hysteresis (≈1.5%) and a high fracture toughness (≈2,164 J m-2 ). Moreover, the hydrogel possesses a high fatigue threshold of ≈141 J m-2 and a reasonable conductivity. This study provides a worth-adopted approach to synthesize hydrogels with low hysteresis and high fracture toughness.

Improved electrochemical conversion of CO2 to multicarbon products by using molecular doping.

The conversion of CO2 into desirable multicarbon products via the electrochemical reduction reaction holds promise to achieve a circular carbon economy. Here, we report a strategy in which we modify the surface of bimetallic silver-copper catalyst with aromatic heterocycles such as thiadiazole and triazole derivatives to increase the conversion of CO2 into hydrocarbon molecules. By combining operando Raman and X-ray absorption spectroscopy with electrocatalytic measurements and analysis of the reaction products, we identified that the electron withdrawing nature of functional groups orients the reaction pathway towards the production of C2+ species (ethanol and ethylene) and enhances the reaction rate on the surface of the catalyst by adjusting the electronic state of surface copper atoms. As a result, we achieve a high Faradaic efficiency for the C2+ formation of ≈80% and full-cell energy efficiency of 20.3% with a specific current density of 261.4 mA cm-2 for C2+ products.

Metal Oxy-Hydroxides with a Hierarchical and Hollow Structure for Highly Efficient Solar-Thermal Water Evaporation.

Solar-thermal water evaporation is a promising technology for pure water production. However, the design of low-cost systems for efficient antifouling solar-thermal water evaporation remains a challenge. Herein, an evaporator based on metal oxy-hydroxides with a hierarchical and hollow structure is rationally designed through material selection and structural engineering. The obtained evaporator possesses good light absorption performance, excellent antifouling property against oil, and enhanced heat localization ability. Consequently, the water evaporation rate reaches as high as 1.65 kg m-2 h-1 with a solar-thermal conversion efficiency up to 82.3% under 1 sun illumination. More importantly, the evaporator exhibits almost identical evaporation performance in oily wastewater and natural seawater due to its superhydrophilicity and underwater superoleophobicity. This work provides a worth-adopted approach to prepare solar-thermal evaporators with high efficiency and anti-oil-fouling property, highlighting the new application of metal oxy-hydroxide-based materials and the importance of a hierarchical and hollow structure for efficient solar-thermal water evaporation.

Polycyclopentene-Crystal-Decorated Carbon Nanotubes by Convenient Large-Scale In Situ Polymerization and their Lotus-Leaf-Like Superhydrophobic Films.

In situ Pd-catalyzed cyclopentene polymerization in the presence of multi-walled carbon nanotubes (MWCNTs) is demonstrated to effectively render, on a large scale, polycyclopentene-crystal-decorated MWCNTs. Controlling the catalyst loading and/or time in the polymerization offers a convenient tuning of the polymer content and the morphology of the decorated MWCNTs. Appealingly, films made of the decorated carbon nanotubes through simple vacuum filtration show the characteristic lotus-leaf-like superhydrophobicity with high water contact angle (>150°), low contact angle hysteresis (<10°), and low water adhesion, while being electrically conductive. This is the first demonstration of the direct fabrication of lotus-leaf-like superhydrophobic films with solution-grown polymer-crystal-decorated carbon nanotubes.