Cellulose-based functional hydrogels derived from bamboo for product design.

Hydrogels have outstanding research and application prospects in the field of product design. Among them, the design and preparation of cellulose-based functional hydrogels derived from bamboo have attracted increasing research interest. Cellulose-based hydrogels not only have the skeleton function of hydrogels, but also retain excellent specificity, smart structural design, precise molecular recognition ability, and superior biocompatibility. Cellulose-based hydrogels show important application prospects in various fields, such as environmental protection, biomedicine, and energy. What's more, they are potentially viable for application in food packaging and plant agriculture, such as fertilizers release and crop production. Recently, researchers have extracted cellulose from bamboo and generated a variety of cellulose-based functional hydrogels with excellent properties by various cross-linking methods. In addition, a variety of multifunctional hybrid cellulose-based hydrogels have been constructed by introducing functional components or combining them with other functional materials, thus expanding the breadth and depth of their applications. Herein, we elaborate on advances in the field of cellulose-based hydrogels and highlight their applications in food packaging and plant agriculture. Meanwhile, the existing problems and prospects are summarized. The review provides a reference for the further development of cellulose-based hydrogels.

Crystal Orientation Modulation and Defect Passivation for Efficient and Stable Methylammonium-Free Dion-Jacobson Quasi-2D Perovskite Solar Cells.

Dion-Jacobson (DJ) quasi-2D perovskite solar cells (PSCs) have received increasing attention due to their greater potentials in realizing efficient and stable quasi-2D PSCs relative to their Ruddlesden-Popper counterpart. The substitution of methylammonium (MA+) with formamidinium is expected to be able to further increase the stability and power conversion efficiency (PCE) of DJ quasi-2D PSCs. Herein, we report a multifunctional additive strategy for preparing high-quality MA-free DJ quasi-2D perovskite films, where 1,1'-carbonyldi(1,2,4-triazole) (CDTA) molecules are incorporated into the perovskite precursor solution. CDTA modification can control phase distribution, enlarge grain size, modulate crystallinity and crystal orientation, and passivate defects. After CDTA modification, more favorable gradient phase distribution and accordingly gradient band alignment are formed, which is conducive to carrier transport and extraction. The improved crystal orientation can facilitate carrier transport and collection. The enlarged grain size and effective defect passivation contribute to reduced defect density. As a result, the CDTA-modified device delivers a PCE of 16.07%, which is one of the highest PCEs ever reported for MA-free DJ quasi-2D PSCs. The unencapsulated device with CDTA maintains 92% of its initial PCE after aging under one sun illumination for 360 h and 86% after aging at 60 °C for 360 h.

Multistage Extraction of Star Anise and Black Pepper Derivatives for Antibacterial, Antioxidant, and Anticancer Activity.

Recently, natural resources have attracted considerable interest for their applications in food security and human health problems. Traditional natural spices, such as star anise and black pepper, played important roles in the pharmaceutical and food industries due to their strong pharmacological activity, antioxidant potential and rare complications. In order to achieve biomasses from the natural product with multiple bioactivities, we developed the multistage extraction method to extract and separate various bioactive compounds from these natural plants. Our work demonstrated that various bioactive-rich extractives were achieved using steam distilled- or oxidative-extraction methods with high extraction yields and purity. Furthermore, the extractives in each step can be used not only as bioactive compounds, but also as a resource to further prepare different derivatives during the next extractive step, providing biomass-saving to a great extent. The extractives obtained with high yields and purities (>82%) were identified by 1H NMR, 13C NMR, FTIR, UV-vis, fluorescence spectroscopy, and high-performance liquid chromatography (HPLC). Moreover, these biomasses display potent antibacterial activities against some types of microorganisms such as S.aureus, S.pyogenes, E.coli, and S.typhi with a lowest MIC of 400 µg/ml for the development of antibacterial agents, significant antioxidant activity as the natural antioxidant for enhancing food shelf-life, and excellent anticancer activity that induces significant cancer cell apoptosis. This work showed the different multistage extracts from natural products, which enable them to be applied in the fields of the pharmaceutical industry and the food industry.

Upgrading of bio-oil via solar pyrolysis of the biomass pretreated with aqueous phase bio-oil washing, solar drying, and solar torrefaction.

In this study, three types of biomass were first pretreated with an aqueous phase bio-oil instead of traditional acid washing. Then, the washed samples were pretreated with drying (100 â„ƒ, 30 min) and torrefaction (250 â„ƒ, 30 min) using a parabolic-trough solar receiver system. The subsequent pyrolysis was performed at 550 â„ƒ for 10 min using a parabolic-dish solar receiver system. Results showed that the solar energy can effectively ensure the temperature required for biomass drying, torrefaction, and pyrolysis, having thus a potential to replace the conventional electric heating or fossil fuel heating. Such a strategy combines the advantages of the independent pretreatments, i.e., leaching out of metallic species and reduction of oxygen content. Consequently, the high heating value of bio-oil increased remarkably, the generation of acids was strongly inhibited, whereas the formation of phenols and anhydrosugars was promoted. Therefore, the method proposed herein is promising for upgrading of biomass and bio-oil.

Water, a Green Solvent for Fabrication of High-Quality CsPbBr3 Films for Efficient Solar Cells.

Water has been labeled as a devil in fabrication and stability of perovskite solar cells. The inherent cognition impels researchers to prepare perovskite films in water-controlled conditions. Herein, water is used as a green solvent to prepare CsPbBr3 films through a two-step spin-coating method. Due to the high solubility of CsBr but low solubility of PbBr2 in water, it provides a possibility to deposit CsBr onto PbBr2 from water solution without destroying the film. Here, high-quality CsPbBr3 films are fabricated by spin-coating concentrated CsBr/H2O solution onto the PbBr2 film followed by annealing. As a result, the solar cells basing on a configuration of FTO/TiO2/CsPbBr3/Carbon exhibit a power conversion efficiency of 6.12%. This work provides a simple and easy way to prepare high-quality CsPbBr3 films for efficient solar cells. It makes a solid step toward reducing the solvent toxicity in the fabrication process of perovskite solar cells. It also breaks the forbidden zone for fabricating perovskite films from water and updates the inherent understanding of water in the research study of perovskite solar cells.

A Review of the Role of Solvents in Formation of High-Quality Solution-Processed Perovskite Films.

Recently, perovskite solar cells have attracted great attention because of their outstanding photovoltaic performance and ease of fabrication. High-quality perovskite films hold a key in getting highly efficient perovskite solar cells. Solution-processed fabrication technique is the most widely adopted for preparing perovskite films because of its low cost. In the solution-proceed perovskite films, solvents not only play the role of dissolving the solute but also participate in the crystallization of perovskite. In the one-step method, solvents play key roles in controlling morphology, widening process window, and achieving room-temperature crystallization of perovskite films. In addition, the solvents play important roles in controlling the nuclei/growth, suppressing volume expansion during the two-step method. Especially, the solvent can induce grain coarsening during the annealing process. A deep understanding of the multiplicity of roles during the formation of perovskite films will help understand the formation mechanism of perovskite films. Here, a systematic review on the progress in fabrication of high-quality perovskite films by making use of solvent to control the crystallization is presented. Meanwhile, we elucidate the key roles of solvent in the fabrication of high-quality perovskite films.

High annealing temperature induced rapid grain coarsening for efficient perovskite solar cells.

Thermal annealing plays multiple roles in fabricating high quality perovskite films. Generally, it might result in large perovskite grains by elevating annealing temperature, but might also lead to decomposition of perovskite. Here, we study the effects of annealing temperature on the coarsening of perovskite grains in a temperature range from 100 to 250 °C, and find that the coarsening rate of the perovskite grain increase significantly with the annealing temperature. Compared with the perovskite films annealed at 100 °C, high quality perovskite films with large columnar grains are obtained by annealing perovskite precursor films at 250 °C for only 10 s. As a result, the power conversion efficiency of best solar cell increased from 12.35% to 16.35% due to its low recombination rate and high efficient charge transportation in solar cells.

Perovskite Solar Cells Fabricated by Using an Environmental Friendly Aprotic Polar Additive of 1,3-Dimethyl-2-imidazolidinone.

Perovskite solar cells (PSCs) have great potentials in photovoltaics due to their high power conversion efficiency and low processing cost. PSCs are usually fabricated from PbI2/dimethylformamide solution with some toxic additives, such as N-methyl pyrrolidone and hexamethylphosphoramide. Here, we use an environmental friendly aprotic polar solvent, 1,3-dimethyl-2-imidazolidinone (DMI), to fabricate perovskite films. By adding 10 vol% DMI in the precursor solution, high-quality perovskite films with smooth surface are obtained. By increasing annealing temperature from 100 to 130 °C, the average grain size of the perovskite increases from ~ 216 to 375 nm. As a result, the efficiency of the PSCs increases from 10.72 to 14.54%.

Elucidating the Key Role of a Lewis Base Solvent in the Formation of Perovskite Films Fabricated from the Lewis Adduct Approach.

High-quality perovskite films can be fabricated from Lewis acid-base adducts through molecule exchange. Substantial work is needed to fully understand the formation mechanism of the perovskite films, which helps to further improve their quality. Here, we study the formation of CH3NH3PbI3 perovskite films by introducing some dimethylacetamide into the PbI2/N,N-dimethylformamide solution. We reveal that there are three key processes during the formation of perovskite films through the Lewis acid-base adduct approach: molecule intercalation of solvent into the PbI2 lattice, molecule exchange between the solvent and CH3NH3I, and dissolution-recrystallization of the perovskite grains during annealing. The Lewis base solvents play multiple functions in the above processes. The properties of the solvent, including Lewis basicity and boiling point, play key roles in forming smooth perovskite films with large grains. We also provide some rules for choosing Lewis base additives to prepare high-quality perovskite films through the Lewis adduct approach.

In Situ Observation of Crystallization of Methylammonium Lead Iodide Perovskite from Microdroplets.

It is of great importance to investigate the crystallization of organometallic perovskite from solution for enhancing performance of perovskite solar cells. Here, this study develops a facile method for in situ observation of crystallization and growth of the methylammonium lead iodide (MAPbI3 ) perovskite from microdroplets ejected by an alternating viscous and inertial force jetting method. It is found that there are two crystallization modes when MAPbI3 grows from the CH3 NH3 I (MAI)/PbI2 /N,N-dimethylformamide (DMF) solution: needle precursors and granular perovskites. Generally, needle Lewis adduct of MAPbI3 ·DMF tends to nucleate and grow from the solution due to low solubility of PbI2 . The growth of MAPbI3 ·DMF depends on both the concentration of MAI and temperature. It tends to form large perovskite domains on substrates at high temperature. The MAPbI3 ·DMF coverts to nanocrystalline perovskite due to lattice shrinkage when DMF molecules escape from the Lewis adduct. Granular perovskite can also directly nucleate from the solution at high concentration of MAI due to compositional segregation.

Enhanced performance of perovskite solar cells by modulating the Lewis acid-base reaction.

The Lewis acid-base reaction between PbI2 and solvent molecules is popular in fabricating PbI2 films by a two-step method for making perovskite solar cells. Here, we control the microstructure of PbI2 films through modulating the Lewis acid-base reaction by adding a small amount of N-methyl pyrrolidone into PbI2/DMF solution. PbI2 films with excellent crystallinity and full coverage are fabricated by spin-coating the mixed solution on the substrate, which leads to high quality perovskite layers with low recombination rate and high efficiency for carrier transfer. As a result, the power conversion efficiency of the best perovskite solar cells increases from 13.3% to 17.5%.

Magnetic properties of fluffy Fe@α-Fe2O3 core-shell nanowires.

: Novel fluffy Fe@α-Fe2O3 core-shell nanowires have been synthesized using the chemical reaction of ferrous sulfate and sodium borohydride, as well as the post-annealing process in air. The coercivity of the as-synthesized nanowires is above 684 Oe in the temperature range of 5 to 300 K, which is significantly higher than that of the bulk Fe (approximately 0.9 Oe). Through the annealing process in air, the coercivity and the exchange field are evidently improved. Both the coercivity and the exchange field increase with increasing annealing time (TA) and reach their maximum values of 1,042 and 78 Oe, respectively, at TA = 4 h. The magnetic measurements show that the effective anisotropy is increased with increasing the thickness of theα-Fe2O3 by annealing. The large values of coercivity and exchange field, as well as the high surface area to volume ratio, may make the fluffy Fe@α-Fe2O3 core-shell nanowire a promising candidate for the applications of the magnetic drug delivery, electrochemical energy storage, gas sensors, photocatalysis, and so forth.

[Analysis of membrane fouling genesis in nanofiltration process for advanced treatment of dyeing and finishing wastewater].

In order to investigate the types and genesis of membrane fouling of nanofiltration desalination system treating dyeing and finishing wastewater of cotton knit textile, comprehensive analysis, using ICP-AES, SEM-EDX, FTIR, TGA, high optical microscope and XRF, was carried out based on tests of influent water quality, and tests of the membrane fouling states of different processes and tests of membrane cleaning. The results showed that the types of membrane fouling included inorganic fouling, organic fouling and microbial fouling. The mass percents of bound water, organic substance and inorganic substance of dry foulants, dried at 105 degrees C, were 8.2%, 41.0% and 50.8% respectively. Ferric salt was the most serious inorganic fouling salt, and the main functional groups, found from organic foulants, were -OH, -CH and -C =C. Several kinds of protozoa were found from the membrane foulants as well as metazoan. The analysis of short-term and long-term membrane fouling indicated that it need a long time cumulative effect for the formation of organic fouling and microbial fouling. The results of NF cleaning tests showed that the mainly reason lead to the decline of membrane flux were organic fouling and microbial fouling, which took 53.3%.