Bacterial cellulose impregnated with andaliman (Zanthoxylum acanthopodium) microencapsulation as diabetic wound dressing.

Diabetic foot ulcer (DFU) is a common complication of diabetes mellitus which can cause infection, amputation and even death. One of many treatments that can be applied to support the DFU healing processes is by using wound dressings. Bacterial cellulose (BC) is a good material to be used as a wound dressing. However, some of the limitations of BC to be applied as wound dressing are does not possess antibacterial properties and support the healing process. Andaliman (Zanthoxylum acanthopodium) is known to have antioxidant, antibacterial and anti-inflammatory abilities that can support BC as a wound dressing. This research focused on the manufacture of BC/Z. acanthopodium microencapsulated wound dressing composites and evaluate their potential as a DFU wound dressing with a variety of gelatin composition in microencapsulation. The results of FTIR and SEM analysis showed that the Z. acanthopodium impregnation process in BC was successful. The variation of gelatine that used in microencapsulation affected the morphological and effectiveness of the wound dressing. However, overall, the wound dressings showed good antibacterial effect on E. coli and S. aureus bacteria and accelerating the wound closure process 8 times faster (BCAMc12) on the 17th day compared to wounds that did not receive any treatment.

Sustainable utilization of Sedum plumbizincicola as superior hydrochar for efficient nutrients recovery.

To realize sound disposal of hyperaccumulator harvested from phytoremediation, hydrothermal carbonization (HTC) has been employed to obtain superior hydrochar adsorbents for removal of phosphate and ammonium from water body. A series of hydrochars have been prepared under tuned HTC conditions to tailor hydrochar with desired properties. Generally, increased temperature and prolonged reaction time facilitated acidic oxygen functional groups on hydrochars, thereby improving adsorption capacity of hydrochar. In single solute system, a superior hydrochar, derived from HTC under 260 °C for 2 h, achieved a maximum phosphate and ammonium adsorption capacity of 52.46 mg/g and 27.56 mg/g at 45 °C, respectively. In binary system, synergistic adsorption was observed only in lower solute concentration, whereas competitive adsorption occurred under higher solute concentration. Characterization and adsorption kinetics suggested chemisorption may dominate the adsorption process, thus the adsorption capacity could be improved by tuning pHpzc of hydrochar. This study firstly demonstrates the sustainable utilization of hyperaccumulators into nutrients-enriched hydrochar as fertilizer for in-situ phytoremediation of contaminated sites with minimized environmental risks towards circular economy.

Photocatalytic Degradation of Methylene Blue Using N-Doped ZnO/Carbon Dot (N-ZnO/CD) Nanocomposites Derived from Organic Soybean.

This study reports on successful synthesis of carbon dots (CDs), nitrogen-doped zinc oxide (N-ZnO), and N-ZnO/CD nanocomposites as photocatalysts for degradation of methylene blue. The first part was the synthesis of CDs utilizing a precursor from soybean and ethylenediamine as a dopant by a hydrothermal method. The second part was the synthesis of N-ZnO with urea as the nitrogen dopant carried out by a calcination method in a furnace at 500 °C for 2 h in an N2 atmosphere (5 °C min-1). The third part was the synthesis of N-ZnO/CD nanocomposites. The characteristics of CDs, N-ZnO, and N-ZnO/CD nanocomposites were analyzed through Fourier transform infrared (FTIR), UV-vis absorbance, photoluminescence (PL), high-resolution transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), thermal gravimetry analysis (TGA), field-emission scanning electron microscopy energy-dispersive spectroscopy (FESEM EDS), X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) analysis. Based on the HR-TEM analysis, the CDs had a spherical shape with an average particle size of 4.249 nm. Meanwhile, based on the XRD and HR-TEM characterization, the N-ZnO and N-ZnO/CD nanocomposites have wurtzite hexagonal structures. The materials of N-ZnO and N-ZnO/CD show increased adsorption in the visible light region and low energy gap E g. The E g values of N-ZnO and N-ZnO/CDs were found to be 2.95 and 2.81 eV, respectively, whereas the surface area (S BET) values 3.827 m2 g-1 (N-ZnO) and 3.757 m2 g-1(N-ZnO/CDs) belonged to the microporous structure. In the last part, the photocatalysts of CDs, N-ZnO, and N-ZnO/CD nanocomposites were used for degradation of MB (10 ppm) under UV-B light irradiation pH = 7.04 (neutral) for 60 min at room temperature. The N-ZnO/CD nanocomposites showed a photodegradation efficiency of 83.4% with a kinetic rate of 0.0299 min-1 higher than N-ZnO and CDs. The XRD analysis and FESEM EDS of the N-ZnO/CDs before and after three cycles confirm the stability of the photocatalyst with an MB degradation of 58.2%. These results have clearly shown that the N-ZnO/CD nanocomposites could be used as an ideal photocatalytic material for the decolorization of organic compounds in wastewater.

Acetylated lignin from oil palm empty fruit bunches and its electrospun nanofibres with PVA: Potential carbon fibre precursor.

The electrospinning of acetylated lignin/polyvinyl alcohol (PVA) nanofibres was carried out to expand the application of lignin materials obtained from oil palm empty fruit bunches (OPEFB). Lignin was isolated by the steam explosion method and subsequently precipitated using H2SO4. Acetylated lignin was produced by mixing acetic anhydride and pyridine at a 2:1 v/v ratio. Following the acetylation process, FTIR analysis showed the absorption of the C=O carbonyl group at wavenumber 1714.6 cm-1. The chemical structures of isolated and acetylated lignin were established using 1H NMR spectral analysis, and XRD examination demonstrated their amorphous character. The electrospinning process of acetylated lignin and PVA solution was then carried out at 15 kV voltage, 0.8 mL/h flow rate, and 12 cm distance between the needle and collector. The sample exhibited electrical conductivity of 443 µS/cm and viscosity of 2.8 × 10-3 Pa s. The morphology analysis showed that there were more beads on the surface of lignin/PVA nanofibres than acetylated lignin/PVA nanofibres. In addition, acetylated lignin/PVA nanofibre was more stable than lignin/PVA. The G-band of carbonized material increased with the presence of lignin. The works presented suggest the potential of using waste materials such as OPEFB as a suitable precursor for the preparation of carbon fibre.

Nanocomposite Foams with Balanced Mechanical Properties and Energy Return from EVA and CNT for the Midsole of Sports Footwear Application.

Polymer foam that provides good support with high energy return (low energy loss) is desirable for sport footwear to improve running performance. Ethylene-vinyl acetate copolymer (EVA) foam is commonly used in the midsole of running shoes. However, EVA foam exhibits low mechanical properties. Conventional mineral fillers are usually employed to improve EVA's mechanical performance, but the energy return is sacrificed. Here, we produced nanocomposite foams from EVA and multi-walled carbon nanotubes (CNT) using a chemical foaming process. Two kinds of CNT derived from the upcycling of commodity plastics were prepared through a catalytic chemical vapor deposition process and used as reinforcing and nucleating agents. Our results show that EVA foam incorporated with oxygenated CNT (O-CNT) demonstrated a more pronounced improvement of physical, mechanical, and dynamic impact response properties than acid-purified CNT (A-CNT). When CNT with weight percentage as low as 0.5 wt% was added to the nanocomposites, the physical properties, abrasion resistance, compressive strength, dynamic stiffness, and rebound performance of the EVA foams were improved significantly. Unlike the conventional EVA formulation filled with talc mineral fillers, the incorporation of CNT does not compromise the energy return of the EVA foam. From the long-cycle dynamic fatigue test, the CNT/EVA foam displays greater properties retention as compared to the talc/EVA foam. This work demonstrates a good balanced of mechanical-energy return properties of EVA nanocomposite foam with very low CNT content, which presents promising opportunities for lightweight-high rebound midsoles for running shoes.

Conformal Noble Metal High-Entropy Alloy Nanofilms by Atomic Layer Deposition for an Enhanced Hydrogen Evolution Reaction.

The current synthesis methods of high-entropy alloy (HEA) thin-film coatings face huge challenges in facile preparation, precise thickness control, conformal integration, and affordability. These challenges are more specific and noteworthy for noble metal-based HEA thin films where the conventional sputtering methods encounter thickness control and high-cost issues (high-purity noble metal targets required). Herein, for the first time, we report a facile and controllable synthesis process of quinary HEA coatings consisting of noble metals (Rh, Ru, Pt, Pd, and Ir), by sequential atomic layer deposition (ALD) coupled with electrical Joule heating for post-alloying. Furthermore, the resulting quinary HEA thin film with a thickness of ∼50 nm and an atomic ratio of 20:15:21:18:27 shows promising potential as a platform for catalysis, exhibiting enhanced electrocatalytic hydrogen evolution reaction (HER) performances with lower overpotentials (e.g., from 85 to 58 mV in 0.5 M H2SO4) and higher stability (by retaining more than 92% of the initial current after 20 h with a current density of 10 mA/cm2 in 0.5 M H2SO4) than other noble metal-based structure counterparts in this work. The enhanced material properties and device performances are attributed to the efficient electron transfer of HEA with the increased number of active sites. This work not only presents RhRuPtPdIr HEA thin films as promising HER catalysts but also sheds light on controllable fabrication of conformal HEA-coated complex structures toward a broad range of applications.

The New Materials for Battery Electrode Prototypes.

In this article, we present the performance of Copper (Cu)/Graphene Nano Sheets (GNS) and C-π (Graphite, GNS, and Nitrogen-doped Graphene Nano Sheets (N-GNS)) as a new battery electrode prototype. The objectives of this research are to develop a number of prototypes of the battery electrode, namely Cu/GNS//Electrolyte//C-π, and to evaluate their respective performances. The GNS, N-GNS, and primary battery electrode prototypes (Cu/GNS/Electrolyte/C-π) were synthesized by using a modified Hummers method; the N-doped sheet was obtained by doping nitrogen at room temperature and the impregnation or the composite techniques, respectively. Commercial primary battery electrodes were also used as a reference in this research. The Graphite, GNS, N-GNS, commercial primary batteries electrode, and battery electrode prototypes were analyzed using an XRD, SEM-EDX, and electrical multimeter, respectively. The research data show that the Cu particles are well deposited on the GNS and N-GNS (XRD and SEM-EDX data). The presence of the Cu metal and electrolytes (NH4Cl and MnO2) materials can increase the electrical conductivities (335.6 S cm-1) and power density versus the energy density (4640.47 W kg-1 and 2557.55 Wh kg-1) of the Cu/GNS//Electrolyte//N-GNS compared to the commercial battery (electrical conductivity (902.2 S cm-1) and power density versus the energy density (76 W kg-1 and 43.95 W kg-1). Based on all of the research data, it may be concluded that Cu/GNS//Electrolyte//N-GNS can be used as a new battery electrode prototype with better performances and electrical activities.

Sustainable Production of Molybdenum Carbide (MXene) from Fruit Wastes for Improved Solar Evaporation.

Invited for the cover of this issue is the group of Edison Huixiang Ang at the National Institute of Education, an institute of Nanyang Technological University, Singapore. The image depicts the sustainable fabrication of two-dimensional MXene sheets from the upcycling of fruit waste for solar desalination. Read the full text of the article at 10.1002/chem.202203184.

Sustainable Production of Molybdenum Carbide (MXene) from Fruit Wastes for Improved Solar Evaporation.

Freshwater production using solar-driven interfacial evaporation is regarded as a green and sustainable strategy. The biggest barrier to practical deployment of solar desalination, however, continues to be the lack of options for renewable materials. Herein, we present a facile two-step carbonization approach that is sustainable for developing innovative two-dimensional (2D) molybdenum carbide (Mo2 C) materials derived from carbonized fruit wastes. The resultant 2D Mo2 C photothermal layer has an efficient water evaporation rate of 1.52 kg m-2 h-1 with a photothermal conversion efficiency of 94 % under one sun irradiation, which is among the best reported values so far. The broad solar absorption band, high specific surface area (555.1 m2 g-1 ) with large micro- and meso porosity, of the Mo2 C photothermal layer are responsible for these outstanding results. The conversion of food wastes into valuable products, in this case MXene, can potentially inspire greener developments of advanced materials for solar water evaporator.

Noble metal alloy thin films by atomic layer deposition and rapid Joule heating.

Metal alloys are usually fabricated by melting constituent metals together or sintering metal alloy particles made by high energy ball milling (mechanical alloying). All these methods only allow for bulk alloys to be formed. This manuscript details a new method of fabricating Rhodium-Iridium (Rh-Ir) metal alloy films using atomic layer deposition (ALD) and rapid Joule heating induced alloying that gives functional thin film alloys, enabling conformal thin films with high aspect ratios on 3D nanostructured substrate. In this work, ALD was used to deposit Rh thin film on an Al2O3 substrate, followed by an Ir overlayer on top of the Rh film. The multilayered structure was then alloyed/sintered using rapid Joule heating. We can precisely control the thickness of the resultant alloy films down to the atomic scale. The Rh-Ir alloy thin films were characterized using scanning and transmission electron microscopy (SEM/TEM) and energy dispersive spectroscopy (EDS) to study their microstructural characteristics which showed the morphology difference before and after rapid Joule heating and confirmed the interdiffusion between Rh and Ir during rapid Joule heating. The diffraction peak shift was observed by Grazing-incidence X-ray diffraction (GIXRD) indicating the formation of Rh-Ir thin film alloys after rapid Joule heating. X-ray photoelectron spectroscopy (XPS) was also carried out and implied the formation of Rh-Ir alloy. Molecular dynamics simulation experiments of Rh-Ir alloys using Large-Scale Atomic/Molecular Massively Parallel Simulator (LAMMPS) were performed to elucidate the alloying mechanism during the rapid heating process, corroborating the experimental results.

Nd-Nb Co-doped SnO2/α-WO3 Electrochromic Materials: Enhanced Stability and Switching Properties.

The fabrication of Nd-Nb co-doped SnO2/α-WO3 electrochromic (EC) materials for smart window applications is presented in the present paper. Nb is a good dopant candidate for ECs owing to its ability to introduce active sites on the surface of α-WO3 without causing much lattice strain due to the similar ionic radius of Nb5+ and W6+. These active sites introduce more channels for charge insertion or removal during redox reactions, improving the overall EC performance. However, Nb suffers from prolonged utilization due to the Li+ ions trapped within the ECs. By coupling Nd with Nb, the co-dopants would transfer their excess electrons to SnO2, improving the electronic conductivity and easing the insertion and extraction of Li+ cations from the ECs. The enhanced Nd-Nb co-doped SnO2/α-WO3 exhibited excellent visible light transmission (90% transmittance), high near-infrared (NIR) contrast (60% NIR modulation), rapid switching time (∼1 s), and excellent stability (>65% of NIR modulation was retained after repeated electrochemical cycles). The mechanism of enhanced EC performance was also investigated. The novel combination of Nd-Nb co-doped SnO2/α-WO3 presented in this work demonstrates an excellent candidate material for smart window applications to be used in green buildings.

Atomic layer deposition of rhodium and palladium thin film using low-concentration ozone.

Rhodium (Rh) and palladium (Pd) thin films have been fabricated using an atomic layer deposition (ALD) process using Rh(acac)3 and Pd(hfac)2 as the respective precursors and using short-pulse low-concentration ozone as the co-reactant. This method of fabrication does away with the need for combustible reactants such as hydrogen or oxygen, either as a precursor or as an annealing agent. All previous studies using only ozone could not yield metallic films, and required post treatment using hydrogen or oxygen. In this work, it was discovered that the concentration level of ozone used in the ALD process was critical in determining whether the pure metal film was formed, and whether the metal film was oxidized. By controlling the ozone concentration under a critical limit, the fabrication of these noble metal films was successful. Rhodium thin films were deposited between 200 and 220 °C, whereas palladium thin films were deposited between 180 and 220 °C. A precisely controlled low ozone concentration of 1.22 g m-3 was applied to prevent the oxidation of the noble metallic film, and to ensure fast growth rates of 0.42 Å per cycle for Rh, and 0.22 Å per cycle for Pd. When low-concentration ozone was applied to react with ligand, no excess ozone was available to oxidize the metal products. The surfaces of deposited films obtained the RMS roughness values of 0.30 nm for Rh and 0.13 nm for Pd films. The resistivities of 18 nm Rh and 22 nm Pd thin films were 17 µΩ cm and 63 µΩ cm.

One-step construction of heterostructured metal-organics@Bi2O3 with improved photoinduced charge transfer and enhanced activity in photocatalytic degradation of sulfamethoxazole under solar light irradiation.

A facile one-step assembly method was developed for the preparation of metal-organics @Bi2O3 composites for photocatalysis. Two kinds of metal-organics (Ti-bdc and Cu-btc)@Bi2O3 composites were synthesized via the coordination of btc3-/bdc2- and metal ions (Ti4+/Cu2+) as well as OH on the surface of Bi2O3. Compared with pure Bi2O3, Ti-bdc@Bi2O3 shows a 1.7 times higher photocatalytic activity in the degradation of sulfamethoxazole (SMX) under a simulated solar irradiation with a cumulative removal of 62% within 60 min. The high photocatalytic activity could be attributed to the high charge separation, enhanced electron transfer as well as the low recombination rate of photo-generated electrons and holes due to the construction of hetero-structures. The stability test showed that Ti-bdc@Bi2O3 is more stable in water than Cu-btc@Bi2O3. Furthermore, through the radical-trapping experiments and main intermediates detection, it is demonstrated that the photo-generated holes as well as the OH and O2- formed dominate the photocatalytic decomposition of SMX. These findings demonstrate the potential usage of a facile method to synthesize metal-organics and metal oxides composites, some of which possess high water stability and thus could be employed for water treatment.

Magnetically recyclable Bi/Fe-based hierarchical nanostructures via self-assembly for environmental decontamination.

Pristine bismuth ferrite usually possesses weak magnetic properties (e.g., saturation magnetization Ms < 3 emu g(-1)) for practical magnetic separation applications. Herein, a superparamagnetic bismuth ferrite with coral-like hierarchical morphology (BFO-M) was fabricated through methanol solvothermal treatment of the as-prepared Bi2Fe4O9 nanoclusters (P-BFO). The BFO-M shows a higher Ms of ∼31 emu g(-1) compared to that of P-BFO treated in water (BFO-A), in ethanol (BFO-E) and in ethylene glycol (BFO-G). Compared to single-crystalline Bi2Fe4O9 (PS) and Bi2Fe4O9 clusters (NSP), BFO-M shows an excellent organic pollutant removal rate by virtue of its high adsorption capacity and catalytic activity when methyl orange (MO) is used as the model organic pollutant. BFO-M also exhibits good visible light photo-Fenton oxidation rates for pharmaceuticals and pesticides. Even at a low catalyst loading of 0.12 g L(-1), the removal rate of organic pollutants (e.g., 5-fluorouracil, isoproturon) can be ∼99% in 100 min under visible light irradiation. Besides, BFO-M is also a good adsorbent for different kinds of heavy metal ions (Pb(ii), Cr(iii), Cu(ii), As(v), etc.). For example, its maximal adsorption capacity for Pb(ii) is 214.5 mg g(-1). The used BFO-M can be recovered via magnetic separation. The outstanding performances of BFO-M can be ascribed to its coral-like hierarchical morphology which consists of the self-assembly of 1D nanowires (∼6 nm in diameter) and 2D ultrathin nanoflakes (∼4.5 nm in thickness). A schematic illustration of its morphology formation is proposed.

Ag-decorated TiO2 photocatalytic membrane with hierarchical architecture: photocatalytic and anti-bacterial activities.

Ag-decorated TiO2 (Ag-TiO2) photocatalytic membranes have been fabricated by using Pluronic P-123 as a pore-forming and structure-directing agent. Six different hierarchical architectures were obtained by multilayer coating of different Ag-TiO2 sols. The porous structure of the resulting layers could be fine-tuned by altering the amounts of P-123 and AgNO3 added during the preparation of TiO2 sols. Physico-chemical and morphological properties of different Ag-TiO2 layers were thoroughly investigated. Ag nanoparticles were successfully incorporated into the TiO2 matrix. The Ag-TiO2 membranes possessed multi-functionality of membrane retention, Ag-enhanced TiO2 photocatalytic activity and anti-bacterial action. They were evaluated through experiments using a batch reactor and a photocatalytic membrane reactor (PMR). The best performing membrane was able to remove up to 1007 mg m(-2) h(-1) of Rhodamine B in the PMR. Two phenomena (photocatalytic degradation and adsorptive-membrane retention) that were responsible for the RhB removal were evaluated. In the batch reactor operated in dark, the membranes were able to remove greater than 5-logs of Escherichia coli. The membrane with the highest percentage of Ag incorporated was able to remove close to 7-logs of E. coli when operated in the PMR.