2D Cobalt Chalcogenide Heteronanostructures Enable Efficient Alkaline Hydrogen Evolution Reaction.

The development of high-efficiency non-precious metal electrocatalysts for alkaline electrolyte hydrogen evolution reactions (HER) is of great significance in energy conversion to overcome the limited supply of fossil fuels and carbon emission. Here, a highly active electrocatalyst is presented for hydrogen production, consisting of 2D CoSe2 /Co3 S4 heterostructured nanosheets along Co3 O4 nanofibers. The different reaction rate between the ion exchange reaction and redox reaction leads to the heterogeneous volume swelling, promoting the growth of 2D structure. The 2D/1D heteronanostructures enable the improved the electrochemical active area, the number of active sites, and more favorable H binding energy compared to individual cobalt chalcogenides. The roles of the different composition of the heterojunction are investigated, and the electrocatalysts based on the CoSe2 /Co3 S4 @Co3 O4 exhibited an overpotential as low as 165 mV for 10 mA cm-2 and 393 mV for 200 mA cm-2 in 1 m KOH electrolyte. The as-prepared electrocatalysts remained active after 55 h operation without any significant decrease, indicating the excellent long-term operation stability of the electrode. The Faradaic efficiency of hydrogen production is close to 100% at different voltages. This work provides a new design strategy toward Co-based catalysts for efficient alkaline HER.

Tailoring Zeolite L-Supported-Cu Catalysts for CO2 Hydrogenation: Insights into the Mechanism of CH3OH and CO Formation.

The utilization of Cu-based catalysts in CO2 conversion into valuable chemicals is of significant interest due to their potential in mitigating greenhouse gas emissions. However, the controllable design of Cu-based catalysts and the regulation of their mechanism remain challenging. In this study, a series of efficient Cu/L catalysts were prepared for this process, and the intrinsic influencing factors on the reaction routes were systematically revealed. Various techniques revealed that Cu particles in L-supported catalysts exhibited higher dispersion and formed Cu-O(OH)-K interfacial sites. However, with increasing Cu loading, the dispersion of Cu particles and the percentage of Cu-O(OH)-K interfaces decreased. Kinetic investigations revealed that the adsorption configuration and electronic structure of Cu species codetermined the reaction pathways and resulting selectivity. Cu/L catalysts possessing Cu-O(OH)-K interfaces and small particles demonstrated the preferential formation of formate species, promoting methanol formation. However, larger Cu particles generated carboxylate intermediates, resulting in higher CO selectivity..

Determination of carbohydrate content in kenaf degumming wastewater and converting them to carbon dots.

The traditional textile degumming process produces abundant wastewater, which contains a lot of monosaccharides and oligosaccharides. It is of great economic and environmental significance to utilize these carbohydrates in high value. In this study, high performance liquid chromatography (HPLC) was used to analyze the carbohydrate components in kenaf degumming wastewater, and then the production of C-dots using the wastewater was explored. The results showed that the types and content in the degumming wastewater were monosaccharides (glucose, xylose and arabinose) and oligosaccharides (dextran, xylan and araban). The carbohydrate (mainly glucan and xylan) content in wastewater accounted for 91.16 % of the total carbohydrates weight loss in kenaf degumming process. By using hydrolysis and hydrothermal reaction on kenaf degumming wastewater, blue-green carbon dots (C-dots) with good performance were prepared and successfully applied to anti-counterfeiting printing. In particular, the as-prepared C-dots prepared from kenaf degumming wastewater with urea added (WUC-dots) showed an excitation-dependent photoluminescence (PL) spectrum and quantum yield (QY) of 2.4 % in aqueous solution. The fluorescent code exhibited a clear outline, excitation-tunable color and good stability, showing a great potential for anti-counterfeiting system.

Microwave-assisted solid-state pretreatment for fabrication of hemp fibres using ethanolamine at low temperature.

Conventional methods faced challenges in pretreating natural cellulose fibres due to their high energy consumption and large wastewater drainage. This research devised an efficient solid-state pretreatment method for pretreating hemp fibres using ethanolamine (ETA) assisted by microwave (MW) heating. This method produced a notable removal rate of lignin (85.4 %) with the highest cellulose content (83.0 %) at a high solid content (30 %) and low temperature (70 °C). Both FT-IR and XRD analyses indicated that the pretreatment did not alter the structure of cellulose within the hemp fibres but increased crystallinity as the CrI increased from 84 % in raw hemp fibre to 89 % in pretreated fibre. As a result, it produced hemp fibres with impressive fineness (4.6 dtex) and breaking strength (3.81 cN/dtex), meeting the requirement of textile fibre. In addition, an improvement in glucose concentration (15.6 %) was observed in enzymatic hydrolysis of the MW pretreated hemp fibres compared to the fibres pretreated without MW. Furthermore, the FT-IR and NMR data confirmed that the amination of lignin occurred even at low temperature, which contributed to the high lignin removal rate. Thus, this study presents a potentially effective energy-saving, and environmentally sustainable solid-state method for pretreating hemp fibres.

Elastic and compressible Al2O3/ZrO2/La2O3 nanofibrous membranes for firefighting protective clothing.

Developing ceramic nanofibrous membranes for the thermal insulation layer of firefighting protective clothing is vital. However, previous ceramic nanofibrous membranes were brittle and easy to break during service in high-temperature environments. The lack of elastic and compressible properties has limited the high-end applications of ceramic nanofibrous membranes. In this work, elastic and compressible Al2O3/ZrO2/La2O3 nanofibrous membranes were fabricated via sol-gel electrospinning and calcination in air at different temperatures. The as-fabricated Al2O3/ZrO2/La2O3 nanofibrous membranes can maintain excellent elasticity and compressibility in the temperature ranging from -196 to 1400 °C. Moreover, they have low thermal conductivity and high working temperatures. These favorable characteristics make the Al2O3/ZrO2/La2O3 nanofibrous membranes a promising candidate for the thermal insulation layer of firefighting protective clothing.

The behavior between fluid and structure from coupling system of bile, bile duct, and polydioxanone biliary stent: A numerical method.

The performance and effects of 12 different structures of stents in the bile duct were compared and used the finite element method. Numerical models of the 12 kinds of fluid-structure interaction(FSI) coupling systems were established to investigate the relationship between three aspects (velocity distribution of bile, wall shear stress (WSS) distribution of bile, and Von Mises Stress(VMS) distribution on the stent and bile duct) and the structural parameters of the stent (monofilament diameter and the number of braiding heads). After calculating and analyzing the simulation results yielding distributions of velocity, WWS, and VMS and regions of bile duct susceptibility to stenosis, they were consistent with previous findings on the locations of restenosis occurring after stent removal, indicating that the simulation results could provide a useful reference for studying biliary stents. The results of the simulations showed that (i) eddy currents were prone to occur at the stent ends regions; (ii) the WSS distribution of the bile fluid in contact with the stent and bile duct related to the stent structure; (iii) the high VMS on the stent and bile duct was prone to occur at the stent ends. The simulation results of 12 FSI coupling systems were studied and two superior stent model structures were obtained by comprehensive evaluation.

Sustainable Production of Lactic Acid from Cellulose Using Au/W-ZnO Catalysts.

The catalytic conversion of cellulose to lactic acid (LA) has garnered significant attention in recent years due to the potential of cellulose as a renewable and sustainable biomass feedstock. Here, a series of Au/W-ZnO catalysts were synthesized and employed to transform cellulose into LA. Through the optimization of reaction parameters and catalyst compositions, we achieved complete cellulose conversion with a selectivity of 54.6% toward LA over Au/W-ZnO at 245 °C for 4 h. This catalyst system also proved effective at converting cotton and kenaf fibers. Structural and chemical characterizations revealed that the synergistic effect of W, ZnO, and Au facilitated mesoporous architecture generation and the establishment of an adequate acidic environment. The catalytic process proceeded through the hydrolysis of cellulose to glucose, isomerization to fructose, and its subsequent conversion to LA, with glucose isomerization identified as the rate-limiting step. These findings provide valuable insights for developing high-performance catalytic systems to convert cellulose.

Photothermal and Concus Finn capillary assisted superhydrophobic fibrous network enabling instant viscous oil transport for crude oil cleanup.

Rapid and effective removal of highly viscous oil spills from the sea remains a great challenge globally. Superhydrophobic materials are attractive candidates for handling oil spills, but they are restrained to recover oils with low viscosity exclusively. Herein, we report a novel polypyrrole wrapped superhydrophobic fibrous network using cross-shaped polyester fibers as starting blocks. The polypyrrole coating enables the absorbent to convert light to heat, ensuring that the viscosity of heavy oils in the proximity can be easily controlled. In the meanwhile, the special structure of the starting fibers initiates Concus Finn (CFin) capillary allowing instant oil transport in the network. When the absorbent is exposed to light oils (0-500 mPa.s), the oils can be transported instantly via CFin capillary. Interestingly, under synergistic effect of light-to-heat conversion and CFin capillary, a drawing-sticking crude oil strip (105 mPa.s) is sucked instantly against gravity by the absorbent. The absorbent is successfully applied to efficiently separate both oil/water mixtures and oil/water emulsions (efficiency > 99%). Such absorbent can absorb 62.99-74.23 g/g light oils on average and up to 123.3 g/g crude oil under 0-2 sun illumination, holding a huge potential in managing oil spills.

A sustainable layered nanofiber/sheet aerogels enabling repeated life cycles for effective oil/water separation.

Discarded oil-containing absorbents, which has been used in handling oil spills, are tricky to deal with and have rose global environmental concerns regarding release of microplastics. Herein, we developed a facile strategy to fabricate sustainable absorbents by a gas-inflating method, through which 2D electrospinning polycaprolactone nanofiber membranes were directly inflated into highly porous 3D nanofiber/sheet aerogels with layered long fiber structure. The membranes were inflated rapidly from a baseline porosity of 81.98% into 97.36-99.42% in 10-60 min. The obtained aerogels were further wrapped with -CH3 ended siloxane structures using CH3SiCl3. This hydrophobic absorbent (CA ≈ 145°) could rapidly trap oils from water with sorption range of 25.60-42.13 g/g and be recycled by simple squeeze due to its mechanical robustness. As-prepared aerogels also showed high separation efficiency to separate oils from both oil/water mixtures and oil-in-water emulsions (>96.4%). Interestingly, the oil-loaded absorbent after cleaning with absolute ethanol could be re-dissolved in selected solvents and promptly reconstituted by re-electrospinning and gas-inflation. The reconstituted aerogels were used as fire-new oil absorbents for repeated life cycles. The novel design, low cost and sustainability of the absorbent provides an efficient and environmentally-friendly solution for handling oil spills.

Biomass Chitosan-Based Tubular/Sheet Superhydrophobic Aerogels Enable Efficient Oil/Water Separation.

Water pollution, which is caused by leakage of oily substances, has been recognized as one of the most serious global environmental pollutions endangering the ecosystem. High-quality porous materials with superwettability, which are typically constructed in the form of aerogels, hold huge potential in the field of adsorption and removal of oily substances form water. Herein, we developed a facile strategy to fabricate a novel biomass absorbent with a layered tubular/sheet structure for efficient oil/water separation. The aerogels were fabricated by assembling hollow poplar catkin fiber into chitosan sheets using a directional freeze-drying method. The obtained aerogels were further wrapped with -CH3-ended siloxane structures using CH3SiCl3. This superhydrophobic aerogel (CA ≈ 154 ± 0.4°) could rapidly trap and remove oils from water with a large sorption range of 33.06-73.22 g/g. The aerogel facilitated stable oil recovery (90.07-92.34%) by squeezing after 10 sorption-desorption cycles because of its mechanical robustness (91.76% strain remaining after 50 compress-release cycles). The novel design, low cost, and sustainability of the aerogel provide an efficient and environmentally friendly solution for handling oil spills.

Biomass-derived oriented neurovascular network-like superhydrophobic aerogel as robust and recyclable oil droplets captor for versatile oil/water separation.

Using tubular kapok fibers (KF) and sodium alginate (SA) as the natural building block, we put forward a novel oriented neurovascular network-like superhydrophobic aerogel with robust dry and wet compression resilience by directional freeze-drying and chemical vapor deposition. In the block, SA forms aligned channel structures providing space for rapid oil transmission, while KF serves as vascular-like capillaries acting as instant "tentacle" to capture the tiny oil droplets in water, facilitating fascinating oil capture efficiency for versatile oil/water separation, The aerogel after dry and wet compression (under a strain of 60%) can recover 96.0% and 97.3% its original, respectively, facilitating stable oil recovery (81.1-89.8%) by squeezing, high separation efficiency (99.04-99.64%) and permeation flux separating oil contaminants from water. A pump-supported experiment shows the aerogel efficiently collecting oil contaminants from the water's surface and bottom by 11503-25611 L·m-2·h-1. Particularly, the aerogel as robust oil droplets captor facilely achieves isolation of 99.39-99.68% emulsified oils from oil/water emulsions by novel oil trapping mechanism which simply involves exerting kinetic energy on emulsified oils through repeated oscillation, potentially indicating a simple and efficient alternative to membrane-based oily wastewater remediation via filtration.

Biomimetic Fibrous Leaf-Vein Membrane Enabling Unidirectional Water Penetration and Effective Antibacterial PM Filtration.

Air pollution induced by pathogenic particulate matter (PM) has posed a serious threat to public health worldwide. Advanced air filters are thus required, not only exhibiting high PM capture efficiency, low breathing resistance, and high internal moisture transferring performance but also isolating and inactivating external pathogenic aerosols. In this study, we demonstrated a facile approach to construct a biomimetic fibrous leaf-vein membrane with unidirectional water penetration and effective antibacterial PM filtration by one-step electrospinning of poly(vinylidene fluoride) (PVDF)-based multilayer nanofibers. With ultrathin fibers penetrating the skeletal framework of bimodal thick fibers, the membranes showed gradient interconnected porous structures and achieved a highly efficient and stable (in an acid and alkali environment) PM0.3 interception (>99.98%) with low air drag (51-71 Pa). In addition, the gradient narrow pores of the membranes contributed to a gradient higher hydrophilicity. The subsequent unidirectional water motion effectively isolates pathogenic aerosols typically generated by external individuals or ultrafast water penetration from the inverse face. Moreover, the membranes demonstrated an antibacterial efficacy (>99.99%) in a 5 min contact, inactivating the intercepted airborne pathogens efficiently. The test results proved that the proposed membranes were promising advanced air filters for respirator applications.

Platinum Cluster/Carbon Quantum Dots Derived Graphene Heterostructured Carbon Nanofibers for Efficient and Durable Solar-Driven Electrochemical Hydrogen Evolution.

Large scale solar-driven hydrogen production is a crucial step toward decarbonizing society. However, the solar-to-hydrogen (STH) conversion efficiency, long-term stability, and cost-effectiveness in hydrogen evolution reaction (HER) still need to be improved. Herein, an efficient approach is demonstrated to produce low-dimensional Pt/graphene-carbon nanofibers (CNFs)-based heterostructures for bias-free, highly efficient, and durable HER. Carbon dots are used as efficient building blocks for the in situ formation of graphene along the CNFs surface. The presence of graphene enhances the electronic conductivity of CNFs to ≈3013.5 S m-1  and simultaneously supports the uniform Pt clusters growth and efficient electron transport during HER. The electrode with a low Pt loading amount (3.4 µg cm-2 ) exhibits a remarkable mass activity of HER in both acidic and alkaline media, which is significantly better than that of commercial Pt/C (31 µg cm-2  of Pt loading). In addition, using a luminescent solar concentrator-coupled solar cell to provide voltage, the bias-free water splitting system exhibits an STH efficiency of 0.22% upon one-sun illumination. These results are promising toward using low-dimensional heterostructured catalysts for future energy storage and conversion applications.

Surface chemistry in calcium capped carbon quantum dots.

Colloidal carbon quantum dots (C-dots) have attracted a lot of attention because of their excellent optical properties for various types of applications. Due to the complicated structure of C-dots, the photoluminescence (PL) mechanism of C-dots is still unclear. In particular, it is still a big challenge to understand well the surface chemistry of C-dots. In this work, we used a vacuum-heating approach to produce high-quality C-dots. With different purification procedures, the surface chemistry of C-dots can be well-controlled. Removal of Ca2+ by Na2CO3 led to the disappearance of the absorption at 405 nm and a decrease of the quantum yield. In addition, the Na2CO3 treated C-dots exhibited an excitation-dependent PL behavior. These results confirmed that Ca2+ can interact with the surface functional group of C[double bond, length as m-dash]O of the C-dots, forming a stable structure surrounding the C-dot core, which contributed to a high quantum yield (QY) of 65%, excitation-independent PL behavior and absorption at 405 nm. Furthermore, the PL of the C-dots is strongly dependent on the pH, indicating that the Ca2+ capped C-dots could be used as pH indicators. Our finding provides clear evidence for the surface-chemistry dependent PL behavior of C-dots.

Research on Chemically Deuterated Cellulose Macroperformance and Fast Identification.

Chemically deuterated cellulose fiber was expected to provide novel applications due to its spectral, biological, and kinetic isotope effect. In this research, the performance of the chemically deuterated cotton fibers, including their mechanical property, enzymatic degradation performance, effect on bacterial treatment, and fast identification (near-infrared modeling) was investigated. The breaking tenacity of the deuterated cotton fibers was slightly lower, which might be attributed to the structural damage during the chemical deuteration. The glucose yield by enzymatic hydrolysis was less than that of the protonic cotton fibers, implying the deuterated fibers are less sensitive to enzymatic degradation. Furthermore, the deuterated fibers could promote the growth of bacteria such as Escherichia. coli, which was associated with the released low-level deuterium content. At last, the near-infrared technique combined with partial least squares regression successfully achieved a fast identification of the protiated and deuterated cotton fibers, which significantly promoted the potential application of deuterated cellulose as anticounterfeiting materials (e.g., special paper).

Near-infrared heavy-metal-free SnSe/ZnSe quantum dots for efficient photoelectrochemical hydrogen generation.

Solar-driven photoelectrochemical (PEC) hydrogen production is one of the most effective strategies for solar-to-hydrogen energy conversion. Among various types of semiconductors used for PEC anodes, colloidal quantum dots (QDs) have been widely used as new and promising absorbers for PEC and other optoelectronic devices. However, currently, most efficient optoelectronic devices contain toxic Pb/Cd elements or non-earth-abundant elements (In/Ag). It is still a challenge to produce Pb/Cd-free QDs without using any toxic and non-earth-abundant elements. Here, we synthesized SnSe QDs via a diffusion-controlled hot injection approach and further stabilized the as-prepared SnSe QDs via a cation exchange reaction. The as-synthesized Zn-stabilized SnSe QDs (SnSe/ZnSe) have an orthorhombic crystal structure with indirect bandgaps ranging from 1 to 1.37 eV. Zn stabilization can significantly decrease the number of QD surface metallic Sn bonds, thereby decreasing the number of recombination centers of defects/traps. As a proof-of-concept, SnSe/ZnSe QDs are used as light absorbers for PEC hydrogen production, leading to a saturated photocurrent density of 7 mA cm-2, which is comparable to best values reported for PEC devices based on toxic-metal-free QDs. Our results indicate that Zn-stabilized SnSe QDs have great potential for use in emerging optoelectronic devices.

Concus Finn Capillary driven fast viscous oil-spills removal by superhydrophobic cruciate polyester fibers.

Developing functional materials integrating multi-tasking oil/water separation performances is significant but challenging for the remediation of large-scale oil spills causing pernicious environmental damages. Herein, a novel Concus Finn Capillary driven oil sorbent (OSCPF) fabricated by aligning superhydrophobic cruciate polyester fibers based on yarn spinning mechanism is designed to realize the clean-up of oil spills and various oil/water mixtures at high speeds. Instantaneous oil diffusion is achieved by abrupt Concus Finn Capillary driven oil-flows along aligned channels. This advance reduces the penetrating time for viscous crude oils by 95.00% comparing with that of non-oriented circular polyester fibers. The OSCPF possess great oil sorption capacity of 54.36-124.71 g/g and can separate oils from immiscible oil/water mixtures, including seawater, soap-water, CuCl2-water, and KMnO4-water, and surfactant-stabilized O/W emulsions by the way of adsorption with satisfactory separation efficiency (99.41-99.83%). Especially, the OSCPF is effectively used to enclose oil spills to prevent rapid oil diffusion and in-situ continuously collect the spillages from water surface and underwater by pumping device with recovery rates of 15,727-104,227 L·m-2·h-1. Considering the unique structural design, fast oil sorption speed, and low operating cost, this work provides a prospective oil remover addressing the remediation of catastrophic multi-tasking oil/water pollutions.

Biodegradable and Reusable Cellulose-Based Nanofiber Membrane Preparation for Mask Filter by Electrospinning.

Environmentally friendly face masks with high filtration efficiency are in urgent need to fight against the COVID-19 pandemic, as well as other airborne viruses, bacteria and particulate matters. In this study, coaxial electrospinning was employed to fabricate a lithium chloride enhanced cellulose acetate/thermoplastic polyurethanes (CA/TPU-LiCl) face mask nanofiber filtration membrane, which was biodegradable and reusable. The analysis results show that the CA/TPU-LiCl membrane had an excellent filtration performance: when the filtration efficiency reached 99.8%, the pressure drop was only 52 Pa. The membrane also had an outstanding reusability. The filtration performance maintained at 98.2% after 10 test cycles, and an alcohol immersion disinfection treatment showed no effect on its filtration performance. In summary, the CA/TPU-LiCl nanofiber membrane made in this work is a promising biodegradable and reusable filtration material with a wide range of potential applications, including high-performance face mask.

Ag NPs-Assisted Synthesis of Stable Cu NPs on PET Fabrics for Antibacterial and Electromagnetic Shielding Performance.

In this study, Cu/Ag/polydopamine (PDA)/polyester (PET) fabrics were fabricated for multi-functional textiles. The PET fabrics were firstly modified by dopamine to form a polydopamine (PDA) layer on the fiber surface, then Ag nanoparticles (Ag NPs) were anchored on fiber surface through chelation between PDA and Ag+ ions, and the Ag NPs were further used as catalytic seeds for in situ reduction of Cu nanoparticles (Cu NPs). The surface morphology, chemistry, and crystalline structure of the prepared PET fabrics were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). As expected, Cu NPs were evenly dispersed on the surface of fibers. The Cu/Ag/PDA/PET fabrics showed good antibacterial property against Escherichia coli and exhibited excellent electromagnetic interference (EMI) shielding ability. The Cu/Ag/PDA/PET fabrics with high performance antibacterial and EMI shielding properties can be applied as functional protective textiles.

Facile Fabrication of Marine Algae-Based Robust Superhydrophobic Sponges for Efficient Oil Removal from Water.

Water pollution caused by oil spillages has aroused worldwide attention. Therefore, it is of great significance to develop low-cost, environmentally friendly materials to remove oil contaminants from water. Herein, a "green" superhydrophobic sponge made from marine algae was fabricated by one-step growth of silicone nanofilaments onto a AgNP-decorated alginate sponge via chemical vapor deposition of an azeotrope of (CH3)3SiCl and SiCl4. The reaction of the azeotrope with the alginate sponge was termed "instant", as it took only a few minutes (5 min) at room temperature to achieve superhydrophobicity (152.0°). Such sponges resist high temperatures, UV irradiation, organic solvents, and mechanical abrasion without losing the superhydrophobicity. The sponges absorbed oil droplets within seconds (1.3-7.0 s) with 11.7-17.1 g/g of sorption capacities for oils of different viscous levels (0.56-1775.00 mPa·s). These sponges could retain 90% of the initial oil sorption capacities after 10 consecutive oil sorption/desorption cycles. Benefiting from the superhydrophobicity and superoleophilicity, the sponges also exhibited high efficiency in oil/water mixture separation. Once the oil/water mixture was injected into the sponge, oil drops were retained in inner pores while water was rejected and spouted from the surface. These excellent performances make the resultant sponge a competitive material for oil spill emergency remediation.