Gentle fabrication of colorful superhydrophobic bamboo based on metal-organic framework.

The efficient use of abundant renewable bamboo as high value-added decoration and building materials is of great significance for mitigating carbon dioxide emissions and maintaining sustainable development. The key challenge is to explore efficient and gentle methods to improve the undesirable surface properties of bamboo. Herein, a colorful and superhydrophobic bamboo is gently fabricated by a facile in-situ growth and conversion method based on metal-organic framework (for constructing micro-nano composite structures) and subsequent coating of sodium laurate (for reducing surface energy) at room temperature. The resulting sodium laurate-coated cobalt-nickel double hydroxide layer (CoNi-DH-La) is demonstrated as an efficient superhydrophobic layer to exhibit excellent chemical and mechanical stability. Impressively, the as-obtained CoNi-DH-La-coated bamboo sheet (BS-CoNi-DH-La) shows positive performances in terms of mildew resistance, flame retardancy, and self-cleaning. More importantly, this gentle method can endow bamboo with multiple unfading colors by changing the type of inorganic salts during the preparation process and display good potential for large-scale production.

Rational design of cobalt-nickel double hydroxides for flexible asymmetric supercapacitor with improved electrochemical performance.

Rational design of micro-nano morphology and suitable crystalline structure are highly desired for metal hydroxides to achieve overall high-performance in the advanced electrodes for flexible supercapacitors. Herein, a novel wisteria flower-like microstructure of cobalt-nickel double hydroxide (CoNi-DH) is successfully constructed on carbon cloth (CC) using an in-situ hydrolysis-induced exchange process between hydroxide ions and organic ligands of the Co-MOF in four different kinds of solutions containing Ni2+. The as-prepared wisteria flower-like microstructure grown on CC shows vertically aligned arrays with high specific area and abundant active sites, which not only guarantee the CoNi-DH active materials to be thoroughly exposed in the electrolyte, resulting in highly effective pseudocapacitive energy storage, but also are beneficial to rapid and reversible redox kinetics and thus give rise to high-rate capability. In addition, compared to Ni(NO3)2, NiCl2, and Ni(CH3COO)2 solutions, the Ni2SO4 solution is found to facilitate the formation of the most regular morphology and the largest interlayer spacing on (003) plane of the layered nickel hydroxide phase in the resultant CoNi-DH. As a result, the optimal CoNi-DH-S@CC (CoNi-DH prepared in Ni2SO4) serves as an advanced electrode to show high-rate capability (only 13% Cs decay after a 15-fold current elevation) and a superior specific capacity (Cs) of 929.4 C g-1, which remarkably exceeds those of CoNi-DH-N (823.1 C g-1, in Ni(NO3)2), CoNi-DH-Cl (798.4 C g-1, in NiCl2), CoNi-DH-C (803.8 C g-1, in Ni(CH3COO)2), and other similar metal hydroxides. Moreover, with this CoNi-DH-S electrode as the positive electrode, the as-prepared asymmetric supercapacitor (ASC) delivers an impressive capacity of 204.8 C g-1, a superior energy density of 42.5 Wh kg-1, and satisfactory cycle life (81.5% reservation after 7500 cycles). As a proof-of-concept application, a quasi-solid-state ASC is further successfully fabricated based on the CoNi-DH-S electrode to exhibit encouraging application potential.

Aluminum-doping-based method for the improvement of the cycle life of cobalt-nickel hydroxides for nickel-zinc batteries.

The unsatisfactory cycle life of nickel-based cathodes hinders the widespread commercial usage of nickel-zinc (Ni-Zn) batteries. The most frequently used methods to improve the cycle life of Ni-based cathodes are usually complicated and/or involve using organic solvents and high energy consumption. A facile process based on the hydrolysis-induced exchange of the cobalt-based metal-organic framework (Co-MOF) was developed to prepare aluminum (Al)-doped cobalt-nickel double hydroxides (Al-CoNiDH) on a carbon cloth (CC). The entire synthesis process is highly efficient, energy-saving, and has a low negative impact on the environment. Compared to undoped cobalt-nickel double hydroxide (Al-CoNiDH-0%), the as-prepared Al-CoNiDH as the electrode material displays a remarkably improved cycling stability because the Al-doping successfully depresses the transition in the crystal phase and microstructure during the long cycling. Benefiting from the improved performance of the optimal Al-CoNiDH electrode (Al-CoNiDH-5% electrode), the as-constructed aqueous Ni-Zn battery with Al-CoNiDH-5% as the cathode (Al-CoNiDH-5%//Zn) displays more than 14% improvement in the cycle life relative to the Al-CoNiDH-0%//Zn battery. Moreover, this Al-CoNiDH-5%//Zn battery achieves a high specific capacity (264 mAh g-1), good rate capability (72.4% retention at a 30-fold higher current), high electrochemical energy conversion efficiency, superior fast-charging ability, and strong capability of reversible switching between fast charging and slow charging. Furthermore, the as-assembled quasi-solid-state Al-CoNiDH-5%//Zn battery exhibits a decent electrochemical performance and satisfactory flexibility.

Facile Construction of Superhydrophobic Surfaces by Coating Fluoroalkylsilane/Silica Composite on a Modified Hierarchical Structure of Wood.

Constructing superhydrophobic surfaces by simple and low-cost methods remains a challenge in achieving the large-scale commercial application of superhydrophobic materials. Herein, a facile two-step process is presented to produce a self-healing superhydrophobic surface on wood to improve water and mildew resistance. In this process, the natural hierarchical structure of wood is firstly modified by sanding with sandpaper to obtain an appropriate micro/nano composite structure on the surface, then a fluoroalkylsilane/silica composite suspension is cast and dried on the wood surface to produce the superhydrophobic surface. Due to the full use of the natural hierarchical structure of wood, the whole process does not need complicated equipment or complex procedures to construct the micro/nano composite structure. Moreover, only a very low content of inorganic matter is needed to achieve superhydrophobicity. Encouragingly, the as-obtained superhydrophobic surface exhibits good resistance to abrasion. The superhydrophobicity can still be maintained after 45 abrasion cycles under the pressure of 3.5 KPa and this surface can spontaneously recover its superhydrophobicity at room temperature by self-healing upon damage. Moreover, its self-healing ability can be restored by spraying or casting the fluoroalkylsilane/silica composite suspension onto this surface to replenish the depleted healing agents. When used for wood protection, this superhydrophobic surface greatly improves the water and mildew resistance of wood, thereby prolonging the service life of wood-based materials.

Electrochemically Stable Cobalt⁻Zinc Mixed Oxide/Hydroxide Hierarchical Porous Film Electrode for High-Performance Asymmetric Supercapacitor.

Construction of electrochemically stable positive materials is still a key challenge to accomplish high rate performance and long cycling life of asymmetric supercapacitors (ASCs). Herein, a novel cobalt⁻zinc mixed oxide/hydroxide (CoZn-MOH) hierarchical porous film electrode was facilely fabricated based on a cobalt⁻zinc-based metal⁻organic framework for excellent utilization in ASC. The as-constructed hierarchical porous film supported on conductive Ni foam possesses a rough surface and abundant macropores and mesopores, which allow fast electron transport, better exposure of electrochemically active sites, and facile electrolyte access and ion diffusion. Owing to these structural merits in collaboration, the CoZn-MOH electrode prepared with a zinc feeding ratio up to 45% at 110 min of heating time (CoZn-MOH-45-110) exhibited a high specific capacitance of 380.4 F·g-1, remarkable rate capability (83.6% retention after 20-fold current increase), and outstanding cycling performances (96.5% retention after 10,000 cycles), which exceed the performances of similar active electrodes. Moreover, an ASC based on this CoZn-MOH-45-110 electrode exhibited a high specific capacitance of 158.8 F·g-1, an impressive energy density of 45.8 Wh·kg-1, superior rate capability (83.1% retention after 50-fold current increase), and satisfactory cycling stability (87.9% capacitance retention after 12,000 cycles).

Facile Activation of Commercial Carbon Felt as a Low-Cost Free-Standing Electrode for Flexible Supercapacitors.

High cost, low capacitance, and complicated synthesis process are still the key limitations for carbon-negative materials to meet their industrial production and application in high-energy-density asymmetric supercapacitors (ASCs). In this work, we demonstrate the facile preparation of ultrahigh-surface-area free-standing carbon material from low-cost industrial carbon felt (CF) and its application for flexible supercapacitor electrode with outstanding performance. Through a simple freeze-drying-assisted activation method, the as-prepared activated CF (ACF) was endowed with satisfactory flexibility, ultrahigh specific surface area of 2109 m2 g-1, good electric conductivity (311 S m-1), and excellent wettability to aqueous electrolyte. Owing to these merits, the ACF expressed an ultrahigh areal capacitance of 1441 mF cm-2, a high specific capacitance ( Cs) of 280 F g-1 based on the mass of the whole electrode, and an impressive cycling stability (87% retention after 5000 cycles). When applied as a flexible freestanding electrode for MnO2//ACF ASCs, the ACF-based device provided satisfactory areal energy densities of 0.283 and 0.104 mWh cm-2 in aqueous and quasi-solid electrolytes, respectively. The values outperform many previously reported carbon-based electrochemical devices. The low cost of raw material and the facile fabrication process, together with the high electrochemical performance, make our ACF electrode highly applicable for the mass production of flexible energy-storage devices.