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Self-healing hydrogels have attracted wide attention because of their potential applications in various fields. However, the complex processes, environmental requirements, and insufficient functionality limit their practical application. Herein, we synthesized a chitosan quaternary ammonium salt-oxidized sodium alginate-glycerol-calcium ion (HACC-OSA-Gly-Ca 2+ ) biobased hydrogel with a multi-network structure that exhibits excellent self-healing abilities. This was achieved by utilizing reversible dynamic imine bonding, electrostatic interactions, Ca 2+ ions as crosslinking points, and hydrogen bonding. The oxidation of sodium alginate (SA) with sodium periodate was carried out to obtain oxidized sodium alginate (OSA) with varying oxidation degrees. The resulting OSAs were then introduced into a glycerol-water solvent system containing chitosan quaternary ammonium salt (HACC) and calcium chloride, and this reaction successfully prepared the biobased eco-friendly self-healing hydrogel. The impacts of the oxidation degree (OD) of OSA on the microscopic morphology, mechanical properties, viscoelastic properties, swelling properties, and self-healing properties of the corresponding synthetic hydrogels were investigated. The outcomes indicated that the optimal HACC-OSA-Gly-Ca 2+ hydrogel possessed good mechanical properties, with a tensile stress of 0.0132 MPa and elongation at break of 551.38%. Furthermore, the multiple bond interactions led to a high self-healing ratio (100%), with an elongation at break of about 614.29%, and excellent adhesion ability (average peel strength of 6.38 kN m -1 ) on various substrates. Additionally, the composite hydrogels exhibited excellent water retention, thermal stability, and resilience, making them promising for various potential applications. Moreover, the properties of the composite hydrogels could be facilely and finely tuned by varying the oxidation degree of OSA and ratio of each component. Thus, the presented strategy could enrich the construction as well as application of biopolymer-based self-healing hydrogels., Competing Interests: The authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)

Metal-organic frameworks, a type of porous architecture, have caught wide attention for their pore-rich and special metal-active centres. However, the non-conductive MOFs show limitations in lithium-sulfur batteries (LSBs). Herein, we first synthesized a lamellar nickel-based MOF and subsequently conducted pre-carbonization to attain a conductive Ni-carbon (Ni@C) catalyst. On account of the retained three-dimensional architecture and elevated conductivity, using Ni@C as the interlayer can realize polysulfide-regulated and kinetically promoted LSBs. This work offers a viable strategy to extend the implementation of MOFs in state-of-the-art LSB systems.

Porphyromonas gingivalis causes various health issues through oral infections. This study investigates the antibacterial activities of food-derived dihydrochalcone flavonoids against Porphyromonas gingivalis and their mechanisms of antibacterial action through comparative transcriptome profiling. Susceptibility tests showed that two typical dihydrochalcone flavonoids (phloretin and phlorizin) had much lower minimum inhibitory concentrations (12.5 μg mL -1 and 50 μg mL -1 , respectively) than the common flavanone naringenin (100 μg mL -1 ). SEM observations and the LDH activity assay indicated obvious anomalies in cell morphology and increased cell membrane permeability, indicating the destructive effect of those compounds on the cell structure. These compounds might also induce apoptosis in P. gingivalis , as shown by the CLSM fluorescence images. Transcriptomic analysis revealed that the flavonoid treatment impacted DNA function and oxidative damage. These flavonoids may activate antioxidant-related pathways that are lethal to anaerobic bacteria like P. gingivalis . Additionally, the compounds resulted in the silencing of transposition-related genes, potentially inhibiting resistance-gene acquisition and expression. Phloretin regulated fatty acid metabolism pathways, which are related to the construction and maintenance of the cell membrane. This suggests a relationship between the structure and antibacterial activities of the tested compounds that share a flavonoid skeleton but differ in the C-ring and glucose moiety. This is the first report of the antibacterial activities and mechanisms of action of food-derived dihydrochalcone flavonoids at the transcriptome level, offering a promising approach for the development of new antibacterial agents from natural products and enhancing their applicability in treating diseases associated with oral pathogens as a substitute for antibiotics.

Background : Employing citric acid/dimethyl formamide (CA/DMF), two distinct types of carbon quantum dots (CQDs), tree-shaped/fingerprinted (TF-CQDs) and fullerene-like (F) were synthesized from both cellulose and carboxymethyl cellulose (CMC). Methods : Fluorescence microscopy revealed different emission colors: blue for TF-CQDs and green for F, highlighting the structural influence on light properties. Transmission electron microscopy (TEM) confirmed the intricate fingerprinted and tree-like morphology of TF-CQDs and the spherical nature of F derived from CMC. The adsorption behavior and kinetics of Cr(vi) removal from water by TF-CQDs and F were evaluated. Significant findings : Both samples demonstrated rapid Cr(vi) uptake; TF-CQDs reached equilibrium within 120 minutes compared to 240 minutes for F. Subsequent leaching led to decreased adsorption after these initial periods. Kinetic analysis revealed a first-order model for TF-CQDs, implying physical adsorption dominance. Conversely, F exhibited a better fit to pseudo-first and second-order models, suggesting combined chemical and physical mechanisms., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Tin phosphide has gained extensive attention as a prospective anode for lithium/potassium ion batteries because of its high theoretical capacity. Nevertheless, the fast capacity fading, which is induced by the huge volume expansion and poor electrical conductivity during cycling, severely restricts its practical applications. In this work, a SnP 3 -CNTs/KB composite with a SnP 3 content as high as 90 wt% was successfully synthesized by a two-step ball milling method. SnP 3 nanoparticles were tightly encapsulated in multi-geometric composite carbon layers to efficiently relieve the volume changes and enhance conductivity. Specifically, the resulting SnP 3 -CNTs/KB anode showed a specific capacity up to 998.6 mA h g -1 after 100 cycles at 50 mA g -1 and 810.4 mA h g -1 after 500 cycles at 1000 mA g -1 for lithium ion batteries. For potassium ion batteries, a high reversible capacity of 200.2 mA h g -1 was achieved after 200 cycles at 1000 mA g -1 . This work affords a new insight for exploring excellent support structures of tin phosphide-based anodes.

This work deals with the fabrication of lignin containing cellulose nanofiber (LCNF)/Ag 2 Se films for thermoelectric applications. Ag 2 Se nanoparticles were synthesized within the LCNF network through in situ methods, employing Na 2 SeO 3 and AgNO 3 along with microwave energy treatment. LCNF/Ag 2 Se films fabricated with two LCNF : Ag 2 Se weight percent ratios ( i.e. , 50 : 50 and 30 : 70) were used to construct a flexible thermoelectric module. The obtained Ag 2 Se nanoparticles displayed a uniform size distribution in the LCNF network with smaller dimensions from the microwave energy treated group. The microstructure of LCNF/Ag 2 Se films was improved by hot-pressing, leading to enhanced film density thermoelectric properties. At a differential temperature of 50 K, films with 50% and 70% of Ag 2 Se exhibited output voltages of 18 and 21 mV; and Seebeck coefficients of -60 and -70 μV K -1 at 350 K, respectively. When microwave energy was applied, the films at 50% and 70% Ag 2 Se showed highest output voltages of 19 and 33 mV, respectively, and Seebeck coefficients of -63.3 and -110 μV K -1 at 350 K. The low-cost fabrication process associated with this module opens a pathway for applications such as energy harvesting., Competing Interests: No conflicts require declaration., (This journal is © The Royal Society of Chemistry.)

This study promotes the use of nanobiochar (NBC) as an environmentally friendly substitute to conventional fillers to improve various properties of biopolymers such as their mechanical strength, thermal stability and crystallization properties. TGA analysis showed a slight increase in onset thermal degradation temperature of the composites by up to 5 °C with the addition of 4 wt% NBC. Non-isothermal DSC analysis determined that the addition of NBC into PHBHHx increases the crystallization temperature and degree of crystallinity of PHBHHx while isothermal DSC analysis demonstrated higher crystallization rate in PHBHHx/NBC composited by up to 54%. PHBHHx incorporated with NBC also exhibited superior tensile strength and modulus versus neat PHBHHx. Increase in mechanical strength was further proven via DMA where PHBHHx/NBC composites maintained higher storage modulus at higher temperatures when compared to neat PHBHHx. PHBHHx/NBC also exhibited no cytotoxicity effect against HaCat cells. This study demonstrates the ability of biochar to act as both nucleating agents and reinforcing agents in biodegradable polymers such as PHBHHx, which could be suitable for packaging application., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

A W/ZSM-5 zeolite was successfully prepared by incorporating tungsten transition metal into a zeolite structure using a conventional impregnation method. The as-obtained W/ZSM-5 zeolite was characterized using several characterization techniques such as XRD, IR and SEM-EDS. The catalyst was then applied to a cascade, single-batch reaction to synthesize bio-polyol from sunflower oils using H 2 O 2 in isopropanol solvent. The obtained results indicated that the W/ZSM-5 zeolite had high catalytic efficiency in the epoxidation of the double bond of vegetable oil and the epoxy ring opening reaction to form bio-polyol. The effect of different reaction conditions on bio-polyol synthesis, such as the dosage of the catalyst and reaction time, were investigated. Bio-polyol was obtained from sunflower oil with a hydroxyl number of 160 mg KOH per g and functionality of 2.9 OH groups per mol. The as-synthesized sunflower oil-based polyol was used to replace fossil-based polyol in the fabrication of a bio-polyurethane-based composite with high oil uptake capacity. The oil adsorption capacity of the porous polyurethane-corn stalk composite was relatively high, up to 15.07 g g -1 . In comparison with neat polyurethane and lignocellulosic materials, the new porous bio-composite had higher oil uptake capacity., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Environment-friendly and biodegradable packaging materials have attracted widespread attention. Development of green solutions to extend the fruit shelf life and address fruit preservation thus has a far-reaching impact. In this study, high-barrier white cardboard (WC) was prepared by a facile coating method. Compared with the WC substrate, the WVP value of the polyvinylidene chloride (PVDC) emulsion-coated WC (3.46 × 10 -11 g m m -2 s -1 kPa -1 ) decreased 73.8% and the OP value (14.8 cm 3 m -2 day -1 ·Pa -1 ) decreased 61.9%. In addition, the mechanical properties of the PVDC emulsion-coated WC increased significantly. The weight loss rate and decay rate of the stored fruits packaged with PVDC emulsion-coated WC decreased by about 5%. The high barrier PVDC emulsion-coated WC with excellent mechanical properties, good barrier effect, and preservation function was successfully prepared. Benefitting from these investigated characteristics, the obtained coated WC can be used to package fruits to reduce water loss and delay ripening, and thus extend their shelf life, exhibiting a favorable effect on blueberry and grape storage. Overall, the fabricated eco-friendly coated white cardboard has shown great potential for biodegradable packaging applications. We believe the current work presents an approach to address perishable fruit preservation and provide a supplement alternative., Competing Interests: The authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)

Subcritical water extraction (SWE) is an emerging green and efficient hydrothermal technology, that offers superior performance in active material extraction, scalability, and reduction of harsh process chemicals, in biomass conversion. Regarding biomaterials, traditional isolation methods for cellulose nanocrystals (CNCs) are reliant on harsh chemicals ( i.e. , strong acid), which are expensive with little to no recyclability. This paper explores SWE as a nanotechnology platform to produce CNCs under the principle of "less is more" - by using low content (1 wt%) of phosphoric acid under subcritical conditions. Acid-catalyzed digestion of woody biomass afforded CNCs desirable physico-chemical features that are dependent on the process parameters (temperature, pressure, and time). Process temperature had a major impact on the reduction of fiber sizes (macroscale to nanoscale), fiber degradation, and fiber coloration (white to black). Electron microscopy revealed rod-like structures, with varying particle size distribution (100-500 nm), dominated by process time. However, colloidal stability was low ( versus acid-hydrolyzed CNCs) due to the low charges on the surface of CNCs. Interestingly, vibrational spectroscopy reveals the effect of process pressure on biomass conversion to CNCs (with cellulose I structure) evidenced by Raman spectroscopy and solid-state fluorometry. The produced (bio)nanomaterials possessed a degree of crystallinity (∼70%) comparable to those produced via acid hydrolysis, with higher thermal stability, enhancing their applicability over a wide range of heat-intensive processes required for nanocomposite applications in biomedical and automotive industries, among others., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

In this study, we developed a multi-site acylation strategy to improve the lipophilicity and cellular uptake of troxerutin, a natural flavonoid with many health-promoting bioactivities. By clarifying the acylation properties of troxerutin catalyzed by lipases from different sources, a series of troxerutin ester derivatives acylated at different sites was synthesized, including troxerutin dipropyl (TDP), tripropyl (TTP), tetrapropyl (TEP), dibutyl (TDB), monohexyl (TMH), monooctyl (TMO) and monodecyl (TMD) esters. Interestingly, the troxerutin esters acylated at multiple sites with shorter fatty chains (TDP, TTP and TEP) had similar lipophilicity to the mono-acylated esters bearing longer fatty chains (TMH, TMO and TMD, respectively) and meanwhile demonstrated surprisingly lower cytotoxicity than that of the long fatty-chain mono-esters. In particular, the multi-acylated esters with shorter fatty chains showed remarkably higher cellular uptake than the mono-esters with long fatty chains. In vitro gastrointestinal digestion suggested that the multi-acylated esters of troxerutin were more resistant to gastrointestinal degradation than the mono-esters. These results indicated that multi-site acylation with short fatty chains could be an effective alternative to introducing one-site mono-acylation for the modification of troxerutin and other flavonoid compounds.

Paper-based materials with precisely designed wettabilities show great potential for fluid transport control, separation, and sensing. To tune the wettability of paper, paper sheets are usually modified after the paper manufacturing process. This limits the complexity of the local wettability design. We combined the wettability design of the individual fibres with subsequent paper sheet fabrication through either fibre deposition or fibre printing. Using silica-based cellulose fibre functionalization, the wettability of the paper sheets, containing only one specific fibre type, could be gradually tuned from highly hydrophilic to highly hydrophobic, resulting in water exclusion. The development of a silica-functionalized fibre library containing mesoporous or dense silica coatings, as well as silica with varying precursor compositions, further enabled the variation of the paper wettability and fluid flow. By combining this fibre library with the paper fabrication process by (i) fibre deposition or (ii) fibre printing, the paper wettability architecture and thus the local fibre composition were adjusted without any further processing steps. This enabled the fabrication of papers with wettability integration, such as a wettability pattern or a Janus paper design, containing wettability gradients along the paper sheet cross section. This asymmetric wettability along all three spatial dimensions enabled side-selective oil-water separation., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Biomass-based hydrogels have displayed excellent potential in flexible strain sensors due to their adequacy, biocompatibility, nontoxic and degradability. Nevertheless, their inferior mechanical properties, particularly at cryogenic temperatures, impeded their extensive utilization. Herein, we reported a rationally designed strain sensor fabricated from a gelatin and cellulose-derived hydrogel with superior mechanical robustness, cryogenic endurance, and flexibility, owing to a triple dynamic bond strategy (TDBS), namely the synergistic reinforcement among potent hydrogen bonds, imine bonds, and sodium bonds. Beyond conventional sacrificing bonds consisting of hydrogen bonds, dynamic covalent bonds and coordinate bonds, synergetic triple dynamic bonds dominated by strong hydrogen bonds and assisted by imine and sodium bonds with higher strength can dissipate more mechanical energy endowing the hydrogel with 38-fold enhancement in tensile strength (6.4 MPa) and 39-fold improvement in toughness (2.9 MPa). We further demonstrated that this hydrogel can work as a robust and biodegradable strain sensor exhibiting remarkable flexibility, broad detection range, considerable sensitivity and excellent sensing stability. Furthermore, owing to the improved nonfreezing performance achieved from incorporating sodium salts, the sensor delivered outstanding sensing properties under subzero conditions such as -20 and -4 °C. It is anticipated that the TDBS can create diverse high-performance soft-electronics for broad applications in human-machine interfaces, energy and healthcare.

Stimuli-responsive aggregation-induced emission (AIE) materials are highly sensitive and rapidly responsive to external signals, making them ideal solid materials for anti-counterfeiting encryption. However, the limited conformational and packing variations resulting from regio-isomerization with a single substituent restricts the stimuli-responsive behavior of these materials. In this work, several AIE-active regio-structural isomers based on the salicylaldehyde Schiff base scaffold have been straightforwardly obtained through multiple substitutions with bromide and triphenylamine moieties. Solvent-effect experiments demonstrate their different orders of charge-transfer and excited-state intramolecular proton transfer upon photoexcitation, indicating the regulation of excited-state processes via multi-site isomerization. These isomers also demonstrate mechanochromism and acidichromism, allowing for adjustable stimuli-responsive effects. As a demonstration, p -Br-TPA with both mechanochromism and acidichromism can be synergistically utilized for multi-level decryption. This study successfully regulates the evolution of excited states through multi-site isomerization, offering a general approach for achieving tunable stimuli-responsive properties in AIE-active salicylaldehyde Schiff bases toward multi-level decryption., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Triboelectric nanogenerators (TENGs) have been utilized in a wide range of applications, including smart wearable devices, self-powered sensors, energy harvesting, and high-voltage power sources. The surface morphology and structure of TENGs play a critical role in their output performance. In this review, we analyze the working mechanism of TENGs with the aim to improve their output performance and systematically summarize the morphological engineering and structural design strategies for TENGs. Additionally, we present the emerging applications of TENGs with specific structures and surfaces. Finally, we discuss the potential future development and industrial application of TENGs. By deeply exploring the surface and structural design strategy of high-performance TENGs, it is conducive to further promote the application of TENGs in actual production. We hope that this review provides insights and guidance for the morphological and structural design of TENGs in the future.

The interest of scientists in the carbazole core has risen steadily over the last 30 years, particularly over the last decade given its presence in several active pharmaceutical ingredients, functional materials and a wide range of biologically active natural products. The continuous development of more efficient, more (regio-)selective and "greener" methodologies to access the carbazole core is thus imperative. This review compares and evaluates synthetic strategies towards the carbazole core that have been reported since 2013, with a focus on their applicability towards the total synthesis of carbazole-containing natural products.

Reversed-electrowetting based droplet electricity generator (REWOD-DEG) shows merits in high power densities, tunable output formats, and wide adaptability to diverse mechanical energies. However, the surface charge trapping and dielectric failure, which are also common challenges for electrowetting system, hinders the development of reliable REWOD-DEGs for long-term running. We innovatively introduce a slippery lubricant-infused porous surface (SLIPS) into REWOD-DEG. Benefits from the significant inhibitory effect for surface charge trapping and ambient contamination, self-healing characteristic given by SLIPS, and robust reversed-electrowetting based energy harvesting were achieved. The SLIPS enhanced REWOD-DEG experienced 100 days of intermittent energy harvesting without deterioration. In addition, the device shows robust performances when exposed to a variety of extreme working conditions, like low temperature, pH, humidity, fouling, and even scratching. This work may address the core application challenges of REWOD based devices, and inspire the development of other robust droplet-based electricity generators., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Solvent-controlled extraction and precipitation are the most fundamental methods for obtaining hemicellulose from lignocellulosic biomass and purification processes. However, the dissolution and precipitation mechanisms involved have scarcely been mentioned. In this study, the molecular scale behavior of xylan-type hemicellulose during solvent-controlled extraction and precipitation is investigated using molecular dynamics (MD) simulations and density functional theory (DFT) calculations. To bring the model closer to the real extracted xylan, a high degree of polymerization (DP100) of xylan is established, and hemicelluloses with low DP (DP15 and DP50) are also investigated. Four phenomena are explained at the molecular level, including the influence of the polymerization degree and side chain on the solubility of xylan in water, the improvement of the xylan's solubility in NaOH, the precipitation of xylan in ethanol, and the acetyl group preservation of xylan in DMSO. This study contributes to an increased understanding of the dissolution and precipitation mechanisms of hemicellulose and provides a resource for the simulation of high DP hemicellulose, which gives a theoretical basis for the efficient extraction of high-purity hemicellulose as well as economic biorefining.

Cu/SiO 2 is one of the most promising catalysts for the furfural (FF) hydrogenation reaction but suffers from the difficulty of tailoring the microstructure and surface properties. Herein, we developed a MOF-derived Cu/SiO 2 catalyst (Cu/SiO 2 -MOF) for FF hydrogenation to 2-methyl furan (2-MF). In comparison with Cu/SiO 2 catalysts prepared from ammonia evaporation (Cu/SiO 2 -AE) and traditional impregnation (Cu/SiO 2 -TI), the copper species in Cu/SiO 2 -MOF could not only be anchored on the silica surface via forming Cu-O-Si bonds but also exposed many more active sites. In this way, a higher ratio of Cu + /(Cu + + Cu 0 ) and richer oxygen defects were constructed via strong metal-support interactions, which were responsible for the superior catalytic performance. In addition, it was found that the solvent effect on product distribution played an important role in adjusting the selectivity to 2-MF and cyclopentanone (CPO). The present work not only provides a deep insight into the catalytic mechanism of Cu/SiO 2 -MOF for the FF hydrogenation reaction but also sheds light on the design and synthesis of highly efficient catalysts for other heterogeneous catalysis fields.

By a hydroamination-induced tandem annulation process, we herein report a new three-component reaction for room temperature construction of carbo-bridged polyheterocycles with exclusive diastereoselectivity, which features readily available feedstocks, catalyst-free conditions, good substrate and functionality compatibility, no need for transition metal catalysts, and high step and atom efficiency. The products are formed via initial formation of 1,2-dihydro-3 H -pyrazol-3-one nucleophiles from but-2-ynedioates and hydrazine followed by 2,4-difunctionalization of N -heteroarenium salts. Given that the obtained products possess structurally important tetrahydroquinoline and pyranopyrazole motifs, the developed chemistry is anticipated to be further applied to the discovery of functional molecules including biomedical ones.

Sustainable bimetallic nanoparticles (NPs) have attracted particular attention in the past decade. However, the efficiency and environmental concerns are associated with their synthesis and properties optimization. We report herein biosynthesis of bimetallic ZnO@SeO NPs based on green and ecofriendly methods using pomegranate peel extract (PPE). Pyrochemical ultraviolet-visible (UV-vis), Fourier-transform infrared (FTIR) and X-ray diffraction (XRD) spectroscopy as well as TEM and EDX supported successful synthesis. Antibacterial, antifungal, and cytotoxic activities were indicative of biological worth of sustainable bimetallic ZnO@SeO NPs, exhibiting antibacterial activity compared to monometallic ZnO and SeO NPs. The values of Minimum Inhibitory Concentration (MIC) of bimetallic ZnO@SeO NPs toward E. coli , P. aeruginosa , B. subtilis and S. aureus were 3.9, 15.62, 3.9 and 7.81 μg ml -1 , respectively. Likewise, a promising antifungal activity against Candida albicans , Aspergillus flavus , A. niger and A. fumigatus was achieved (MICs: 31.25, 1.95, 15.62 and 15.62 μg ml -1 , respectively). The cytotoxicity results suggest that bimetallic ZnO@SeO NPs are non-toxic and biomedically safe, evidenced by in vitro anticancer activity against human liver carcinoma (Hep-G2) cell line (with a half-maximal inhibitory concentration (IC50) > 71 μg ml -1 ). The bimetallic ZnO@SeO NPs successfully biosynthesized using PPE showed a high potential for biomedical engineering., Competing Interests: The authors declare that they have no conflict to interests., (This journal is © The Royal Society of Chemistry.)

The efficient production of γ-valerolactone (GVL) from renewable lignocellulose that is synthesized in plants by photosynthesis to replace the declining fossil resources conforms to the principles of circular economy. Compared to direct hydrogenation by H 2 molecules, catalytic transfer hydrogenation (CTH) of levulinic acid (LA) and/or its esters to GVL with organic alcohols as a hydrogen source is a much milder route. The synergistic catalysis between Lewis and Brønsted acids is indispensable in the CTH process. Considering that unsaturated coordinated Zr species could act as Lewis acid sites and phosphotungstic acid (PTA) could dissociate protons as Brønsted acid sites, UiO-66 (Zr) was thus "acidified" by encapsulating PTA in its channels to tune the ratio of Brønsted to Lewis acid sites as a bifunctional catalyst so as to better understand the catalytic structure-performance relationship in the CTH process. To address the dilemma of encapsulated PTA that is prone to leach, a rapid surface sealing strategy was adopted to establish a polyimide (PI) coating over the surface of UiO-66 introducing a space confinement effect via an anhydride-amine coupling reaction. The as-synthesized PTA/UiO-66@PI catalyst exhibited 100% of LA conversion, a 93.2% of GVL yield and high recyclability for at least five consecutive cycles. Moreover, a reaction pathway followed by esterification, hydrogenation and dealcoholization as well as a catalytic hydrogenation mechanism based on intermolecular hydride β-H transfer were proposed. Current work not only provides a high-performance and high-stability catalytic system to selectively produce GVL from LA or its esters, but also sheds light on the catalytic mechanism of the CTH process at the molecular level.

Fluorobenzoic acids (FBAs) are used as chemical tracers in enhanced oil recovery and reduction in their limit of detection is a crucial issue. GC-MS is a versatile tool to detect and quantify FBAs at very low limits of concentration, but they require esterification prior to analysis by GC-MS. The present article presents a study of the catalytic methyl esterification of fluorinated aromatic carboxylic acids (FBAs) using methanol as methyl source and UiO-66-NH 2 as a heterogeneous catalyst. The reaction time was reduced to 10 hours which is a 58% reduction in time over the traditional BF 3 ·MeOH complex as derivatizing agent. The yield of the esterification reaction was evaluated with respect to the BF 3 -MeOH complex and determined by GC-EI-MS. The catalytic procedure was optimized by the Taguchi model with a 99.99% fit. Good catalytic performance was observed for 23 different isomers of fluorinated aromatic acids showing a relative conversion yield of up to 169.86%, which reduced the detection limit of FBAs up to 2.60 ng mL -1 ., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The photo-Fenton reaction provides an effective strategy for the removal of organic pollution in water environments. However, it remains a great challenge to develop photo-Fenton catalysts with high photocatalytic activity, low catalyst losses and excellent recyclability. In this work, a β-FeOOH/TiO 2 /cellulose nanocomposite aerogel was fabricated as an efficient and convenient heterogeneous catalyst in the photo-Fenton system via in situ synthesis of TiO 2 and β-FeOOH NPs on a cellulose-based aerogel. The cellulose aerogel not only acted as a microreactor to prevent aggregation of particles, but also acted as a supporting material to improve the stability and reusable performance of the catalyst. Meanwhile, the synergy between TiO 2 and β-FeOOH endowed the cellulose-based nanocomposite aerogel with highly efficient photo-Fenton degradation of dyes. As a result, the composite β-FeOOH/TiO 2 /cellulose aerogel displayed high photocatalytic performance. Its removal efficiency of MB reached 97.2% under weak UV light for 65 min. There is no obvious decrease in the catalytic efficiency after 5 cycles, suggesting the stability and recyclability of the composite aerogel. This study provides a novel strategy for the preparation of efficient green heterogeneous catalysts by using renewable resources, and shows composite catalyst processes have great potential in wastewater treatment., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The green fluorescent protein (GFP) is a purely natural specialty protein that has been widely used to design synthetic fluorescent probes. In the present work we designed and synthesized a series of fluorescent compounds akin to GFP precursors by a one-step method, and investigated the luminescence properties of the fluorescent compounds by varying the substituents. We presented the first systematic summary of the photophysical data including extinction coefficients and fluorescence quantum yields for this class of fluorescent dyes. We also carried out density functional theory (DFT) calculations for these dyes to investigate the effect of electronic effects due to different substituents. These studied optical properties may provide a reference for later probe design. More interestingly, we have developed a polarity-sensitive lipid droplet probe T-LD with AIE properties on this basis. The probe exhibited not only favorable pH stability and kinetic stability in terms of optical properties, but also solvent discolouration and polarity-sensitive properties, and was able to label intracellular lipid droplets. We successfully applied the probe for intracellular lipid droplet level monitoring and zebrafish imaging.

Multifunctional integration is the focus of hydrogel-based flexible sensors, and formation of a dual network (DN) could shed light on the fabrication of hydrogels with multifunctionality and enhanced properties. In this study, a DN hydrogel was fabricated by the self-assembly of herbal molecule glycyrrhizic acid (GA) as the first hydrogel network and subsequent photocrosslinking of methacrylated sodium alginate (SA-MA) to form the second network. Profiting from the good compatibility between the two hydrogel networks, the obtained DN hydrogels with a homogeneous porous microstructure were endowed with remarkably enlarged stretching (114.5%) and compression (74.4%) strains. In addition, they were demonstrated to display excellent bacteriostatic activity (>99.9%) against Escherichia coli and Staphylococcus aureus owing to the synergetic antibacterial effect of GA and SA-MA. The DN hydrogels as strain sensors possessed high sensitivity (GF = 1.39), linear sensing ( R 2 > 0.99), rapid response (180 ms), and good stability (1300 times) for human motion detection. Besides, the DN hydrogels could also be used to conduct pressure sensing such as application of heavy weights and even human pulses. All results suggest that the developed DN hydrogels have great potential in serving as epidermal and implantable flexible sensors for human health monitoring., Competing Interests: The authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)

This study explores adsorptive removal measures to shed light on current water treatment innovations for kinetic/isotherm models and their applications to antibiotic pollutants using a broad range of biomass-based adsorbents. The structure, classifications, sources, distribution, and different techniques for the remediation of antibiotics are discussed. Unlike previous studies, a wide range of adsorbents are covered and adsorption of comprehensive classes of antibiotics onto biomass/biochar-based adsorbents are categorized as β-lactam, fluoroquinolone, sulfonamide, tetracycline, macrolides, chloramphenicol, antiseptic additives, glycosamides, reductase inhibitors, and multiple antibiotic systems. This allows for an assessment of their performance and an understanding of current research breakthroughs in applying various adsorbent materials for antibiotic removal. Distinct from other studies in the field, the theoretical basis of different isotherm and kinetics models and the corresponding experimental insights into their applications to antibiotics are discussed extensively, thereby identifying the associated strengths, limitations, and efficacy of kinetics and isotherms for describing the performances of the adsorbents. In addition, we explore the regeneration of adsorbents and the potential applications of the adsorbents in engineering. Lastly, scholars will be able to grasp the present resources employed and the future necessities for antibiotic wastewater remediation., Competing Interests: The authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)

Lapindo mud (LM) is a volcanic mud from a natural disaster that occurred 16 years ago in Sidoarjo District, East Java, Indonesia. The high amount of silica in the local materials of LM has been extracted for silica gel synthesis via hydrometallurgy methods, followed by sol-gel methods. The presence of ethanol in the synthesis process generated a unique textural property at different ratios between ethanol and sodium silicate (e/ss). Sol-gel mediated silica gel synthesis exhibited mesoporous properties with an amorphous structure, which is a characteristic of the silica gel. The silica gel exhibits silica nanoparticles over the average diameter of 2.08 nm with a spherical morphology and is connected to form an agglomeration structure. Increasing the e/ss ratio enhanced the amount of the hydroxyl group and the specific surface area ranged from 57 to 103 m 2 g -1 . The moisture adsorption performance of each silica gel showed that the silica gel with an e/ss ratio of 5 : 5 exhibited the highest adsorption capacity measured by conventional gravimetric methods and thermogravimetric analysis of 10.56% and 11.20% g water g silica -1 , respectively. These results indicated that the silica gel with an e/ss ratio has a high number of hydroxyl groups and more surface-active sites, which is beneficial for the adsorption process. The adsorption capacity of the synthesized silica gel is also higher than that of the commercial silica gel, indicating an excellent performance for desiccant applications., Competing Interests: The authors have no competing interests., (This journal is © The Royal Society of Chemistry.)

Amitrole is a non-selective triazole herbicide that is widespread used to control a variety of weeds in agriculture, but it may pollute the environment and do harm to organisms. Thus, it is of critical significance to enlist a low-cost, sensitive, stable and renewable method to detect amitrole. In this paper, electrochemical experiments were carried out using carbon fibers/reduced graphene oxide/cellulose paper electrodes, which demonstrated good electrocatalytic performance for amitrole detection. The electrochemical process of amitrole on the surface of the reduced paper electrode was a quasi-reversible reaction controlled by diffusion. Cyclic voltammetry and the amperometric i - t curve method were used for amitrole determination at a micro molar level and higher-concentration range with the following characteristics: linear range 5 × 10 -6 mol L -1 to 3 × 10 -5 mol L -1 , detection limit 2.44 × 10 -7 mol L -1 . In addition, the relative standard deviation of repeatability is 3.74% and of stability is 4.68%. The reduced paper electrode with high sensitivity, low detection limit, good stability and repeatability provides novel ideas for on-site amitrole detection in food and agriculture., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

Water-insensitive self-adhesive elastomers derived from hydrophobic deep eutectic polymers (HDEPs) are reported. With the help of hydrophobic π-π interactions and dynamic hydrogen bonding networks, the HDEPs performed excellent self-adhesive properties on various materials, even in aqueous environments.

Oral administration of combinations of specific nutrients and nutraceuticals can provide synergistic health benefits to humans. In this work, zein/carboxymethyl cellulose composite nanoparticles were successfully prepared using antisolvent precipitation methods. Zein/carboxymethyl cellulose nanoparticles with the smallest size (204.6 nm) were formed when the mass ratio of zein to CMC was 2 : 1. Hydrogen bonding and hydrophobic interactions were dominant binding forces to stabilize the composite nanoparticles. Quercetin and resveratrol were then encapsulated within these nanocarriers, which improved their resistance to both light and thermal degradation. Encapsulation of the nutraceuticals was shown to delay their release under simulated gastrointestinal conditions, which may be beneficial for some applications. Moreover, encapsulation increased the in vitro bioaccessibility of the quercetin and resveratrol. Our results indicate that zein/carboxymethyl cellulose nanoparticles can be used to co-deliver combinations of bioactive compounds, which may be useful for the development of functional foods, supplements, and pharmaceuticals.

Fast-response artificial phototropic materials are a promising tool for solar energy utilisation, yet their preparation remains challenging. Herein, we report the so-called photothermal domino strategy for constructing fast-response artificial phototropic materials. In this strategy, photothermal generation, heat conduction and thermal actuation are sequentially optimised by a coordination effect. For the first time, lignin-based organic radicals boosted by this coordination effect are used to significantly enhance photothermal conversion. Interfacial coordination bonds between lignin and an elastomer matrix promote interfacial heat conduction. Light-stimulated thermal actuation is significantly improved by coordination-assisted mechanical training. The prepared biomimetic phototropic material exhibits excellent phototropic ability, with a 2.5 s light-tracking process, showing great application potential for efficient solar energy utilisation. This strategy shows great significance for fabricating high-performance intelligent phototropic materials using widely available, green raw materials.

Lignin, one of the main components of lignocellulose, can be used as an alternative to chemical polyols in the production of polyurethane because of its abundant phenolic and alcohol hydroxyls. Traditionally, lignin is directly applied in the preparation of polyurethane; however, modified lignin has been proved to be superior, especially that obtained by the oxypropylation reaction. Therefore, lignopolyol obtained by mild and efficient oxypropylation was utilized in the production of rigid polyurethane foam in this study. Specifically, the effects of the content of lignopolyol on the chemical structure, morphological structure, mechanical properties and thermal stability of the lignin-based rigid polyurethane foam were investigated. It was found that the compressive strength of the rigid polyurethane foam was significantly improved with the addition of lignopolyol compared with that of the pure polyurethane foam, which was attributed to the fact that oxypropylation made lignin into highly branched and functionalized polyols by transforming all phenolic hydroxyls into aliphatic hydroxyls. Moreover, when the molal weight of lignopolyol accounted for 40% of the added polyols, the generated foam showed optimal uniformity and regularity, and the compressive strength reached 0.18 MPa, meeting the requirements of industrial application, below which, the amount of undesired reactions is bound to increase. As a consequence, the added amount of lignopolyol was increased as much as possible on the basis of guaranteeing the desired properties, which was more conducive to realizing the green degradation and economic synthesis of rigid polyurethane foam., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

Responsive photonic crystals have attracted extensive attention due to their features of transforming external stimuli into a variation of optical signals or structural colors. In recent years, the accumulation of heavy metal ions has become a serious threat to human health and the environment. Thus, a simple and rapid method for the accurate detection of metal ions is of great importance. Herein, an imidazole-based-silica inverse opal photonic crystal (IOPC) sensor is prepared. Three different particle sizes of SiO 2 photonic crystals were used as templates for the preparation of an IOPC. The results show that the template presents a high specific surface area and interconnected nanopores. When the nanopores adsorb copper ions, the functional monomer imidazole will chelate with copper ions to form a flat quadrilateral structure. Then the nanopores of the IOPC shrink, which will result in the red shifting of the diffraction peak to complete the visual response sensing. When immersed in different concentrations of metal ions, the structural color of the IOPC changes, making it a visual sensor. In addition, it is proved that the imidazole-modified IOPC is specifically responsive to Cu 2+ , and the structural color of the sensor will shift from green to yellow after sensing. The detection limit is as low as 1 × 10 -6 mol L -1 , and the maximum offset of the diffraction peak can reach 50 nm. Therefore, the IOPC prepared here provides an ideal platform for the fast and high selective detection of Cu 2+ , and it has potential applications in the rapid detection of other heavy metal ions.

The poor mechanical properties of chitosan physical hydrogels seriously hinder their application in the biomedical field. Inspired by the structure of cell tissues, a novel chitosan nanofiber (CSNF)/Hyaluronic acid (HA)/β-glycerophosphate disodium (β-GP) drug-loaded hydrogel was prepared by micro-dissolution and physical crosslinking. The hydrogel has a "Branch-Fruit" structure and exhibits excellent mechanical properties, good biocompatibility and cell-adhesion properties. Human cancer cells (HeLa) can adhere to the hydrogel surface, which might facilitate tumor site-specific administration of drugs. This material also exhibits high pH sensitivity, with which drug release can be triggered under acidic conditions at pH 4.00. The mechanical strength and drug release behavior of this hydrogel can be easily adjusted by varying the CSNF content., Competing Interests: The authors declare no competing financial interest., (This journal is © The Royal Society of Chemistry.)

Lithium silicates have attracted great attention in recent years due to their potential use as high-temperature (450-700 °C) sorbents for CO 2 capture. Lithium orthosilicate (Li 4 SiO 4 ) can theoretically adsorb CO 2 in amounts up to 0.36 g CO 2 per g Li 4 SiO 4 . The development of new Li 4 SiO 4 -based sorbents is hindered by a lack of knowledge of the mechanisms ruling CO 2 adsorption on Li 4 SiO 4 , especially for eutectic mixtures. In this work, the structural, electronic, thermodynamic and CO 2 capture properties of monoclinic phases of Li 4 SiO 4 and a binary (Li 3 NaSiO 4 ) eutectic mixture are investigated using density functional theory. The properties of the bulk crystal phases as well as of the relevant surfaces are analysed. Likewise, the results for CO 2 -lithium silicates indicate that CO 2 is strongly adsorbed on the oxygen sites of both sorbents through chemisorption, causing an alteration not only in the chemical structure and atomic charges of the gas, as reflected by both the angles and bond distances as well as atomic charges, but also in the cell parameters of the Li 4 SiO 4 and Li 3 NaSiO 4 systems, especially in Li 4 SiO 4 (001) and Li 3 NaSiO 4 (010) surfaces. The results confirm strong adsorption of CO 2 molecules on all the considered surfaces and materials followed by CO 2 activation as inferred from CO 2 bending, bond elongation and surface to CO 2 charge transfer, indicating CO 2 chemisorption for all cases. The Li 4 SiO 4 and Li 3 NaSiO 4 surfaces may be proposed as suitable sorbents for CO 2 capture in wide temperature ranges.

Biochar is conventionally and widely used for soil amendment or as an adsorbent for water treatment. Nevertheless, the need for transition to renewable materials has resulted in an expansion of biochar for use as a filler for polymer composites. The aim is to enhance the physical, chemical, mechanical and rheological properties of the polymer composite. The reinforcement of biochar into a polymer matrix however is still new, and limited reports are focusing on the effects of biochar towards polymer composite properties. Hence, this review highlights the unique properties of biochar and its effect on the crystallization, thermal, flammability, electrical conductivity, and mechanical properties of polymer composites. This review does not solely summarize recent studies on biochar-polymer-based composites, but also offers insights into a new direction of biochar as a renewable and superior polymer filler in the future., Competing Interests: The authors have no conflict of interest to declare., (This journal is © The Royal Society of Chemistry.)

Conductive hydrogels have emerged as promising material candidates for multifunctional strain sensors, attributed to their similarity to biological tissues, good wearability, and high accuracy of information acquisition. However, it is difficult to simultaneously manufacture conductive hydrogel-based multifunctional strain sensors with the synergistic properties of reliable healability for long-term usage and environmental degradability/recyclability for decreasing the electronic waste. This work reports a facile strategy to engineer a self-healing, recyclable and conductive strain sensor by virtue of molecular-level multi-dynamic interactions (MMDIs) including Schiff base complexes, hydrogen bonds, and coordination bonds, which were fabricated using a dialdehyde TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl)-oxidized nanofibrillated cellulose (DATNFC) pre-reinforced gelatin nanocomposite hydrogel (gelatin/DATNFC hydrogel, GDH) followed by dipping in an Fe 3+ aqueous solution. The MMDI strategy allows synchronous regulation of both bulk and interfacial interactions to obtain exciting properties that outperform those of conventional hydrogels, including extraordinary compressive stress (1310 kPa), intriguing self-healing abilities, and remarkable electrical conductivity. With these outstanding merits, the as-prepared gelatin/DATNFC/Fe 3+ hydrogel (GDIH) is developed to be a multifunctional strain sensor with appealing strain sensitivity (GF = 2.24 under 6% strain) and compressive sensitivity ( S = 1.14 kPa -1 under 15 kPa), which can be utilized to manufacture electronic skin and accurately discern subtle bodily motions, handwriting and personal signatures. Notably, this GDIH-based sensor also exhibited reliable self-healing properties for long-term usage, environmental degradability and complete recyclability for decreasing the electronic waste. In consideration of the extremely facile preparation process, biocompatibility, satisfactory functionalities, remarkable self-healing properties and recyclability, the emergence of the GDIH-based sensor is believed to propose a new strategy for the development of sustainable-multifunctional strain sensors and healthcare monitoring.

Polymer networks crosslinked with spring-like ortho -phenylene ( o P) foldamers were developed. NMR analysis indicated the o P crosslinkers were well-folded. Polymer networks with o P-based crosslinkers showed enhanced energy dissipation and elasticity compared to divinylbenzene crosslinked networks. The energy dissipation was attributed to the strain-induced reversible unfolding of the o P units. Energy dissipation increased with the number of helical turns in the foldamer.

Under transition metal catalyst-free conditions, we herein present a hydride transfer-initiated construction of novel 3-(2-aminomethyl)aryl quinolines from N -isoquinolinium salts and 2-aminobenzaldehydes, proceeding with the merits of operational simplicity, high step and atom efficiency, good substrate and functional group compatibility, and mild conditions. The products are formed by reacting with the isoquinolyl motif as a two-carbon synthon along with the cleavage of its C3-N bond. Given the interesting applications of 3-aryl quinolines, the developed chemistry is anticipated to be further applied to develop new functional products.

The conversion of biomass-derived platform molecules ( e.g. , 5-hydroxymethyl furfural (HMF)) represents a sustainable route to produce value-added chemicals. Here we report the fabrication of an N-doped carbon nanotube assembled yolk-shell polyhedron with embedded Co-CoS x nanoparticles (NPs) (Y-Co-CoS x @CN) for efficient HMF electrooxidation. DFT calculations demonstrate that the formation of the heterojunction could intensify spin polarization in Co-CoS 2 , thus achieving effective d-p coupling between the catalyst and reactant/intermediate. As expected, Y-Co-CoS x @CN exhibits excellent HMF electro-oxidation activity at a low applied potential of 1.29 V vs. RHE at 10 mA cm -2 in 0.1 M KOH with 5 mM HMF, affording an FDCA yield of 96% and FE of 93.5%. This work not only sheds light on the catalytic nature of the heterojunction and the underlying mechanisms for the enhancement of HMF electro-oxidation activity, but would also provide a descriptor for the rational design of advanced electro-catalysts., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The prevention of grain storage pests is a universal concern all over the world. It is in high demand to explore novel, safe and green insecticidal techniques to address such concerns. In this work, both raw and calcined diatomite were used as a natural insecticide to remove common grain storage pests with improved lethal effect on the saw-toothed grain beetle. Interestingly, the raw diatomite showed higher insecticidal efficiency than the calcined diatomite, and its associated insecticidal properties and preparation conditions were also optimized through orthogonal tests. The optimal conditions for processing the raw diatomite insecticide were identified as follows: the diatomite dust was 500 mesh ( A 3 ), the temperature was 25 °C ( B 1 ), the relative humidity was 65% ( C 2 ), the diatomite dosage was 20 g m -2 ( D 2 ), the influence factor order was C ≥ D > A > B . The observation of surface morphology indicated that the raw diatomite had a complete, multi hole surface morphology and good adsorption performance, whereas the structure of the calcined diatomite was uncomplete with collapsed pores, resulting in poor adsorption performance. The special pore structure and excellent adsorption capacity of diatomite make the stored grain pests lose water to lethal effect. Acute toxicity and long-term toxicity tests in mice showed that diatomite has no harmful effects on mammals. The findings from our work led to a green and effective approach in producing a highly efficient and safe storage grain insecticide., Competing Interests: The authors declare no competing financial interest., (This journal is © The Royal Society of Chemistry.)

We discovered a biological mechanism supporting microbial degradation of bio-based poly(butylene succinate- co -adipate) (PBSA) plastic in soils under ambient and future climates. Here, we show that nitrogen-fixing bacteria facilitate the microbial degradation of PBSA by enhancing fungal abundance, accelerating plastic-degrading enzyme activities, and shaping/interacting with plastic-degrading fungal communities.

Excessive exposure to ultraviolet (UV) light is harmful to human health. However, the traditional preparation of anti-UV films through the doping of UV absorbers leads to unstable products. Chemical modification of polyvinyl alcohol (PVA) to fabricate functional derivatives expand the application of these materials. Herein, a 1,4-dihydropyridine (DHP) fluorescent ring with a conjugated structure as a strong UV-absorber group was introduced onto a polyvinyl alcohol acetoacetate (PVAA) film to improve its UV-blocking performance. Firstly, PVAA was prepared via transesterification using tert -butyl acetoacetate ( t -BAA). Then, the Hantzsch reaction was carried out on the surface of the PVAA film at room temperature. The resulting film showed high transparency, bright fluorescence emission, good mechanical properties, and outstanding stability. The introduction of the hydrophobic carbon chain reduced the hydrophilicity and swelling capacity of the PVAA film. In addition, the conjugated structure endowed the fluorescent film with excellent UV-blocking performance, where almost 100% UVA and UVB spectra could be shielded. The UV-blocking properties of the prepared films were persistent when they were exposed to UV irradiation, solvents, and subjected to thermal treatment. This work presents a facile and environmentally-friendly strategy by which to fabricate a multifunctional PVA-based film, which holds great potential for application in the anti-counterfeiting and UV-blocking fields.

Aramid nanofibers (ANFs) have important applications in many fields, including electrical insulation and battery separators. However, a few limitations seriously restrict the application of ANFs currently, such as low preparation efficiency and the unclear preparation mechanism. To overcome these limitations, the present work proposes a new view-point from the perspective of reaction kinetics. The preparation efficiency was proven to essentially rely on the effective c (OH - ). With a simple pre-treatment, a kinetic advantage was created and the preparation time of ANFs was reduced from multiple hours to 10 minutes, which was a considerable step towards practical applications. Moreover, the resultant ANF membranes still exhibited excellent properties in terms of mechanical strength (tensile strength > 160 MPa), thermal stability, light transmittance, and electrical insulation (above 90 kV mm -1 ). This work not only presents an ultrafast method to produce ANFs but also provides new insights into the mechanism that will benefit the subsequent development of ANF-based materials., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)

Type V natural deep eutectic solvents based on monoterpenoids (cineole, carvone, menthol, and thymol) are studied using a combined experimental and molecular modeling approach. The reported physicochemical properties showed low viscous fluids whose properties were characterized as a function of temperature. The theoretical study combining quantum chemistry and classical molecular dynamics simulations provided a nanoscopic characterization of the fluids, particularly for the hydrogen bonding network and its relationship with the macroscopic properties. The considered fluids constitute a suitable type of solvents considering their properties, cost, origin, and sustainability in different technological applications and sow the possibility of developing type V NADES from different types of molecules, especially in the terpenoid family of compounds.

A convenient and sensitive reversible-fluorescence sensing platform for accurate monitoring of high-valence metal ions is still very challenging. As a green kind of fluorescent carbon nanomaterials, carbon dots (CDs) have captured considerable attention because of the stable fluorescence property and low cost. Herein, we fabricated a type of nitrogen-functionalized carbon dots (N-CDs) from CMC as a fluorescent reversible sensing platform for detecting various high-valence metal ions. N-CDs with a mean size of 2.3 nm were obtained and possessed 22.9% quantum yields (QY). A label-free fluorescent probe for detection of high-valence metal ions (Fe 3+ , Cr 6+ , Mn 7+ ) was established via the fluorescence quenching response. Among them, the detection limit (LOD) toward Fe 3+ ions reached 0.8 µM. We have explored the quenching mechanism of N-CDs to explain the valence state-related electron-transfer fluorescence quenching between high-valence metal ions and N-CDs. Moreover, the valence state-related fluorescence quenching phenomenon of N-CDs in aqueous solution could be effectively recovered by introducing a reducing agent (Ti 3+ ). This "turn off-on" fluorescence recovery system of N-CDs could be applied in different applications covering the selective detection of environmental high-valence metal ions and cellular imaging., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Cellulose, the most abundant natural polymer, has good biocompatibility, biodegradability, and non-toxicity, which make it and its derivatives promising candidates for the fabrication of multifunctional materials, while maintaining sustainability and environmental friendliness. The combination of electrospinning technology and cellulose (and its derivatives) provides a feasible approach to produce nanostructured porous materials with promising functionalities, flexibility, renewability and biodegradability. At the same time, it enables value-added applications of cellulose and its derivatives that are derived from nature or even biomass waste. This review summarizes and discusses the latest progress in cellulose-based electrospun nanofibers, including their construction methods and conditions, various available raw materials, and applications in multiple areas (water treatment, biomaterials, sensors, electro-conductive materials, active packaging, and so on), which are followed by the conclusion and prospects associated with future opportunities and challenges in this active research area., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Currently, it is challenging to prepare uniform hollow-structured hydrogels with tailorable comprehensive properties. Herein, making full use of the different gelation routes of polyvinyl alcohol (PVA), we propose a distinctive two-stage method for preparing hollow-structured hydrogels, which is to arrange the microstructure of the hydrogel through segmented adjustment. The mechanical properties, macrostructure, and functions of the obtained hollow hydrogel can be easily designed and edited. Specifically, the mechanical properties of the hollow hydrogel can be improved from "soft" to "hard" by changing the preparation conditions. In addition, hollow hydrogels with diverse macrostructures can also be developed through different templates, such as tubes, gloves, and rings. More importantly, the hollow hydrogels can be endowed with conductive, anti-drying, anti-freezing, and photothermal-converting functions due to the great system compatibility of the gel precursor. Benefiting from the advantages of the hollow hydrogel, the conductive gel ring-based bioelectrodes and sensors were developed. Interestingly, the adaptive gel ring-based electronics can stably record the electrophysiological and strain signals of the human body without the help of adhesive tape. This study opens more opportunities for development and applications of other hydrogel-based hollow materials., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)