A comparative study of α-Ni(OH)2 and Ni nanoparticle supported ZIF-8@reduced graphene oxide-derived nitrogen doped carbon for electrocatalytic ethanol oxidation.

Ethanol electrooxidation is an important reaction for fuel cells, however, the major obstacle to ethanol electrocatalysis is the splitting of the carbon-carbon bond to CO2 at lower overpotentials. Herein, a ZIF-8@graphene oxide-derived highly porous nitrogen-doped carbonaceous platform containing zinc oxide was attained for supporting a non-precious Ni-based catalyst. The support was doped with the disordered α-phase Ni(OH)2 NPs and Ni NPs that are converted to Ni(OH)2 through potential cycling in alkaline media. The Ni-based catalysts exhibit high electroactivity owing to the formation of the NiOOH species which has more unpaired d electrons that can bond with the adsorbed species. From CV curves, the EOR onset potential of the α-Ni(OH)2/ZNC@rGO electrode is strongly shifted to negative potential (Eonset = 0.34 V) with a high current density of 8.3 mA cm-2 relative to Ni/ZNC@rGO. The high catalytic activity is related to the large interlayer spacing of α-Ni(OH)2 which facilitates the ion-solvent intercalation. Besides, the porous structure of the NC and the high conductivity of rGO facilitate the kinetic transport of the reactants and electrons. Finally, the catalyst displays a high stability of 92% after 900 cycles relative to the Ni/ZNC@rGO and commercial Pt/C catalysts. Hence, the fabricated α-Ni(OH)2/ZNC@rGO catalyst could be regarded as a potential catalyst for direct EOR in fuel cells.

Stable polyethylene glycol/biochar composite as a cost-effective photothermal absorber for 24 hours of steam and electricity cogeneration.

Seawater desalination powered by solar energy is the most environmentally and economical solution in responding to the global water and energy crisis. However, solar desalination has been negatively impacted by intermittent sun radiation that alternates between day and night. In this study, sugarcane bagasse (SCB) was recycled via the pyrolysis process to biochar as a cost-effective solar absorber. Besides, polyethylene glycol (PEG) as a phase change material was encapsulated in the abundant pore structure of biochar to store the thermal energy for 24 hours of continuous steam generation. The BDB/1.5 PEG evaporator exhibited an evaporation rate of 2.11 kg m-2 h-1 (98.1% efficiency) under 1 sun irradiation. Additionally, the BDB/1.5 PEG evaporator incorporated by the TEC1-12706 module for continuous steam and electricity generation with a power density of 320.41 mW m-2. Moreover, 10 continuous hours of evaporation were applied to the composite demonstrating outstanding stability. The composite exhibited high water purification efficiency through solar desalination due to the abundant functional groups on the biochar surface. Finally, the resulting low-cost and highly efficient PCM-based absorber can be used on a wide scale to produce fresh water and energy.

Construction of thickness-controllable bimetallic sulfides/reduced graphene oxide as a binder-free positive electrode for hybrid supercapacitors.

Devices for electrochemical energy storage with exceptional capacitance and rate performance, outstanding energy density, simple fabrication, long-term stability, and remarkable reversibility have always been in high demand. Herein, a high-performance binder-free electrode (3D NiCuS/rGO) was fabricated as a supercapacitor by a simple electrodeposition process on a Ni foam (NF) surface. The thickness of the deposited materials on the NF surface was adjusted by applying a low cycle number of cyclic voltammetry (5 cycles) which produced a thin layer and thus enabled the easier penetration of electrolytes to promote electron and charge transfer. The NiCuS was anchored by graphene layers producing nicely integrated materials leading to a higher electroconductivity and a larger surface area electrode. The as-fabricated electrode displayed a high specific capacitance (2211.029 F g-1 at 5 mV s-1). The NiCuS/rGO/NF//active carbon device can achieve a stable voltage window of 1.5 V with a highly specific capacitance of 84.3 F g-1 at a current density of 1 A g-1. At a power density of 749 W kg-1, a satisfactory energy density of 26.3 W h kg-1 was achieved, with outstanding coulombic efficiency of 100% and an admirable life span of 96.2% after 10 000 GCD cycles suggesting the significant potential of the as-prepared materials for practical supercapacitors.

Cesium salt of tungstophosphoric acid/mesoporous (zirconia-silica) composite for highly efficient synthesis of 7-hydroxy-4-methyl coumarin and removal of methylene blue.

The removal of harmful organic dyes from aqueous solutions has drawn the attention of scientists because of the substantial threat they pose to society's worldwide health. Hence, it is crucial to design an adsorbent that is both very effective in removing dyes and has the benefit of being inexpensive. In the present work, Cs salts of tungstophosphoric acid (CPW) supported mesoporous Zr-mSiO2 (mZS) with varying extents of Cs ions have been prepared by a two-step impregnation technique. Accordingly, a lowering in the surface acidity modes was observed after Cs exchanged protons of H3W12O40 and formed salts immobilized on the mZS support. After exchanging the protons with Cs ions, the characterization results revealed that the primary Keggin structure was unaltered. Moreover, the Cs exchanged catalysts had higher surface area than the parent H3W12O40/mZS, suggesting that Cs reacts with H3W12O40 molecules to create new primary particles with smaller sizes possessing inter-crystallite centers with a higher dispersion degree. With an increase in Cs content and thus a decrease in the acid strength and surface acid density, the methylene blue (MB) monolayer adsorption capacities on CPW/mZS catalysts were increased and reached an uptake capacity of 359.9 mg g-1 for Cs3PW12O40/mZS (3.0CPW/mZS). The catalytic formation of 7-hydroxy-4-methyl coumarin was also studied at optimum conditions and it is found that the catalytic activity is influenced by the amount of exchangeable Cs with PW on the mZrS support, which is in turn influenced by the catalyst acidity. The catalyst kept approximately the initial catalytic activity even after the fifth cycle.

Silver sulfide decorated carbonaceous sawdust/ES-PANI composites as salt-resistant solar steam generator.

Solar steam generation (SSG) is a potential approach for resolving the global water and energy crisis while causing the least amount of environmental damage. However, using adaptable photothermal absorbers with salt resistance through a simple, scalable, and cost-effective production approach is difficult. Herein, taking advantage of the ultra-fast water transportation in capillaries, and the large seawater storage capacity of wood, we develop a highly efficient natural evaporator. The wood wastes (sawdust) were carbonized at low temperatures to fabricate a green and low-cost carbonaceous porous material (CW). To enhance the salt resistance in high saline water, this evaporator was coated with polyaniline emeraldine salt (ES-PANI) which was synthesized through facile and cost-effective one-step oxidation of aniline. Furthermore, the composite was decorated with silver sulfide to increase the evaporation rate which reached up to 1.1 kg m-2 h-1 under 1 sun irradiation with 91.5% efficiency. Besides, the evaporator performs exceptionally well over 10 cycles due to the salt resistance capability of ES-PANI which generates a "Donnan exclusion" effect against cations in saline water. The Ag2S@PANI/CW evaporator may be a viable large-scale generator of drinking water due to its high efficiency for energy conversion, simple and low-cost fabrication approach, salt-resistance, and durability.

High efficiency solar desalination and dye retention of plasmonic/reduced graphene oxide based copper oxide nanocomposites.

Water desalination via solar-driven interfacial evaporation is one of the most essential technologies to limit the problem of global freshwater scarcity. Searching for a highly efficient, stable, eco-friendly, and cost-effective solar-absorber material that can collect the full solar spectrum is critically important for solar steam generation. This study reports the development of a new solar thermal evaporation system based on plasmonic copper oxide/reduced graphene oxide (rGO). The silver nanoparticles in the composite exhibit a very strong solar absorption. Also, rGO and CuO nanoparticles offer excellent thermal absorptivity. Polyurethane was used as the support and as a thermal insulator. Moreover, filter paper was used for fast water delivery to the surface of the solar absorber. Ag/CuO-rGO nanocomposite is manifested to be one of the most efficient solar-absorbers reported to date for solar desalination which exhibits an average 2.6 kg m-2 h-1 evaporation rate with solar thermal efficiency up to 92.5% under 1 sun irradiation. Furthermore, the composite has excellent stability and durability as it displays stable evaporation rates for more than 10 repeated cycles in use, with no significant decrease in the activity. Besides, the successful removal of various organic dyes from contaminated water is also revealed, resulting in the production of clean condensed freshwater. Finally, this work commences a new avenue of synthesizing cost-effective thermal absorbers based on metal oxides.