Rational design of dual-ion doped cobalt-free Li-rich cathode materials for enhanced cycle stability of lithium-ion pouch cell batteries.

The synergistic effect of single-crystal structure and dual doping in Li-rich cobalt-free cathode materials was thoroughly investigated. Lithium-ion pouch cells employing Sb/Sn doped Li1.2Mn0.6Ni0.2O2 and graphite exhibited a specific capacity of 191.01 mA h g-1 at 1C rate and exceptionally stable performance upon cycling, with capacity retention of 87.24% of their initial capacity after 250 cycles at 1C rate. The strategic combination of morphology manipulation and dual ion doping has markedly diminished cation mixing and expanded the Li interstitial sites within the cathode lattice. This work offers significant insights into the mechanisms responsible for the structural decline of Li-rich cobalt-free cathodes, emphasizing the importance of stabilizing the cathode lattice structure at high potential. These findings suggest promising potential for this material to meet the demanding energy density criteria for electric vehicles. Finally, this research provides practical strategies for effectively implementing high-voltage cobalt-free cathodes, offering valuable guidance for future applications.

A new design of colorimetric films using bacterial cellulose nanocrystals derived from nata de coco for sensing volatile organic compounds.

In this work, bacterial cellulose (BC) derived from Nata de Coco is a polysaccharide material, and it is further processed into bacterial cellulose nanocrystal (BCNC) via acid hydrolysis. Then BCNC is doped with transition metals to enhance its amine/hydrogen sulfide response. Therefore, the aim of this study is to investigate the use of transition metals as indicators to detect amine and hydrogen sulfide gas for efficiently monitoring food spoilage. BCNCs were treated with various concentrations of silver nitrate (AgNO3) and copper sulfate pentahydrate (CuSO4·5H2O). Then the dropwise addition of ascorbic acid was applied to reduce Ag+ and Cu2+ to Ag0 (silver nanoparticle) and Cu0 (copper nanoparticle), which refer to red brown and red wine colors, respectively. The results indicated that BCNC/Ag nanoparticles were spherical, while BCNC/Cu nanoparticles exhibited a rod-like structure. XRD results also presented the incorporation of Ag and Cu nanoparticles, as confirmed by both crystallography structures. Furthermore, UV-Vis spectra showed the adsorption bands at 422-430 nm and 626-629 nm, belonging to Ag and Cu nanoparticles. After H2S and ammonia gas exposure, BH/Ag and BH/Cu films turned black from brown and red. In conclusion, transition metal-doped BCNCs exhibit potential for innovative food spoilage gas sensors.

Advancing lithium-sulfur battery efficiency: utilizing a 2D/2D g-C3N4@MXene heterostructure to enhance sulfur evolution reactions and regulate polysulfides under lean electrolyte conditions.

Lithium-sulfur batteries (LSBs) show promise for achieving a high energy density of 500 W h kg-1, despite challenges such as poor cycle life and low energy efficiency due to sluggish redox kinetics of lithium polysulfides (LiPSs) and sulfur's electronic insulating nature. We present a novel 2D Ti3C2 Mxene on a 2D graphitic carbon nitride (g-C3N4) heterostructure designed to enhance LiPS conversion kinetics and adsorption capacity. In a pouch cell configuration with lean electrolyte conditions (∼5 µL mg-1), the g-C3N4-Mx/S cathode exhibited excellent rate performance, delivering ∼1061 mA h g-1 at C/8 and retaining ∼773 mA h g-1 after 190 cycles with a Coulombic efficiency (CE) of 92.7%. The battery maintained a discharge capacity of 680 mA h g-1 even at 1.25 C. It operated reliably at an elevated sulfur loading of 5.9 mg cm-2, with an initial discharge capacity of ∼900 mA h g-1 and a sustained CE of over 83% throughout 190 cycles. Postmortem XPS and EIS analyses elucidated charge-discharge cycle-induced changes, highlighting the potential of this heterostructured cathode for commercial garnet LSB development.

Ratiometric electrochemical lateral flow immunoassay for the detection of Streptococcus suis serotype 2.

An electrochemical lateral flow immunoassay (eLFIA) strip with high reproducibility was developed to rapidly and accurately detect Streptococcus suis serotype 2. This proposed strip was fabricated by integrating ratiometric electrochemical detection and LFIA (R-eLFIA). The R-eLFIA exhibited excellent reproducibility, which was improved by 3.8 times compared to a single electrode. A dual-working screen-printed graphene electrode (SPGE) was designed by tuning the working electrode with electroactive species in the biosensing system. Ferrocene carboxylic acid (Fc) was used as a signal probe, and sunset yellow (SY) at one working electrode was used as an internal reference signal to provide a built-in correction for reducing the effects of inherent background current. S. suis serotype 2-specific antibodies were immobilized on a nitrocellulose membrane of LFIA, which is located on the position of Fc-SPGE. In the presence of the analyte, an immunocomplex formed on the region of Fc-SPGE, causing a decrease in Fc current while SY current remained constant. The current ratio's decrease was proportional to S. suis serotype 2's concentration. Under optimization, this biosensor showed good linearity in the range of 102-1010 CFU/mL with a limit of detection of 10 CFU/mL and achieved a rapid detection time (15 min). Moreover, the R-eLFIA biosensor exhibited excellent reproducibility and high selectivity and was applied in human serum samples. Thus, this study successfully matched the advantages of the ratiometric strategy and LFIA and has great potential to be used as an effective tool for rapidly detecting S. suis serotype 2 in clinical samples.

Fabrication of a colorimetric film based on bacterial cellulose/metal coordination framework composite for monitoring food spoilage gas.

A newly designed colorimetric sensing film has been developed to determine the spoilage gas from food deterioration. The fabrication of sensing film used for food labels based on bacterial cellulose and carboxymethyl cellulose composite film (BC/CMC) incorporated with Bis(imidazolium) tetrachlorocuprate, HIm2CuCl4 was focused. The BC/CMC composite films were prepared by vacuum filtration and then dipped into the (5-20 % w/w) HIm2CuCl4 solution. Subsequently, they were dried at 60 °C to obtain the BC/CMC-Cu film. For monitoring fish freshness, the TVB-N level was considered an indicator of determining fish spoilage. In addition, the color change was evaluated and expressed as Lab color values and total color difference (TCD). According to the sensing response, the TCD values of the sensing films had continuously changed, corresponding to the ammonia gas, which is one of the TVB-N gases. Based on the variations in Lab color values exposed to ammonia gas at room temperature, the film color shifted from the initial lime green color to the final blue color due to the substitution of metal-ligand bonding. Finally, this colorimetric sensing film can be employed as a potential food freshness indicator in intelligent packaging.

Is it possible to 3D bioprint load-bearing bone implants? A critical review.

Rehabilitative capabilities of any tissue engineered scaffold rely primarily on the triad of (i) biomechanical properties such as mechanical properties and architecture, (ii) chemical behavior such as regulation of cytokine expression, and (iii) cellular response modulation (including their recruitment and differentiation). The closer the implant can mimic the native tissue, the better it can rehabilitate the damage therein. Among the available fabrication techniques, only 3D bioprinting (3DBP) can satisfactorily replicate the inherent heterogeneity of the host tissue. However, 3DBP scaffolds typically suffer from poor mechanical properties, thereby, driving the increased research interest in development of load-bearing 3DBP orthopedic scaffolds in recent years. Typically, these scaffolds involve multi-material 3D printing, comprising of at-least one bioink and a load-bearing ink; such that mechanical and biological requirements of the biomaterials are decoupled. Ensuring high cellular survivability and good mechanical properties are of key concerns in all these studies. 3DBP of such scaffolds is in early developmental stages, and research data from only a handful of preliminary animal studies are available, owing to limitations in print-capabilities and restrictive materials library. This article presents a topically focused review of the state-of-the-art, while highlighting aspects like available 3DBP techniques; biomaterials' printability; mechanical and degradation behavior; and their overall bone-tissue rehabilitative efficacy. This collection amalgamates and critically analyses the research aimed at 3DBP of load-bearing scaffolds for fulfilling demands of personalized-medicine. We highlight the recent-advances in 3DBP techniques employing thermoplastics and phosphate-cements for load-bearing applications. Finally, we provide an outlook for possible future perspectives of 3DBP for load-bearing orthopedic applications. Overall, the article creates ample foundation for future research, as it gathers the latest and ongoing research that scientists could utilize.

Electrochemical capillary-driven microfluidic DNA sensor for HIV-1 and HCV coinfection analysis.

Electrochemical DNA sensors can be operated in either static or flow-based detection schemes. In static schemes, manual washing steps are still necessary, resulting in a tedious and time-consuming process. In contrast, in flow-based electrochemical sensors, the current response is collected when the solution flows through the electrode continuously. However, the drawback of such a flow system is the low sensitivity due to the limited time for the interaction between the capturing element and the target. Herein, we propose a novel electrochemical capillary-driven microfluidic DNA sensor to combine the advantages of static and flow-based electrochemical detection systems into a single device by incorporating burst valve technology. The microfluidic device with a two-electrode configuration was applied for the simultaneous detection of two different DNA markers, human immunodeficiency virus-1 (HIV-1) and hepatitis C virus (HCV) cDNA, via the specific interaction between pyrrolidinyl peptide nucleic acids (PNA) probes and the DNA target. The integrated system, while requiring a small sample volume (7 µL for each sample loading port) and less analysis time, achieved good performance in terms of the limits of detection (LOD) (3SDblank/slope) and quantification (LOQ) (10SDblank/slope) at 1.45 nM and 4.79 nM for HIV and 1.20 nM and 3.96 nM for HCV, respectively. The simultaneous detection of HIV-1 and HCV cDNA prepared from human blood samples showed results that are in complete agreement with the RT‒PCR assay. The results qualify this platform as a promising alternative for the analysis of either HIV-1/HCV or coinfection that can be easily adapted for other clinically important nucleic acid-based markers.

Formulation and Performance of NBR/CR-Based High-Damping Rubber Composites for Soundproof Using Orthogonal Test.

Multiple functional-material-filled nitrile butadiene rubber/chloroprene rubber (NBR/CR) acoustic composites were extensively studied and prepared. According to the orthogonal test table L25 (56), 25 groups of samples were prepared by using a low-temperature one-time rubber mixing process. With tensile strength, average transmission loss, and damping peak as indexes, the influence degree of different factors and levels on the properties of acoustic composites was quantitatively discussed and analyzed. The matrix weight analysis was employed to optimize the material formula of rubber composites, and the corresponding influence weight was given. Results showed that the acoustic composite with blending ratio of 70/30 for NBR/CR matrix had preferable mechanical and acoustic properties; adding mica powder (MP) and montmorillonite (MMT) in matrix contributed to improve all above three indexes owing to their specific lamellar structures; hollow glass beads (HGB) had a positive influence on improving acoustic property due to its hollow microcavities, however, it had a negative impact on damping property because of the smooth spherical surfaces. Accordingly, the optimal formulation was found to be NBR/CR blending ratio of 70/30, MP of 10 phr (per hundred rubber), HGB of 4 phr, and MMT of 10 phr.

Enhanced hybrid photocatalytic dry reforming using a phosphated Ni-CeO2 nanorod heterostructure.

Operating the dry reforming reaction photocatalytically presents an opportunity to produce commodity chemicals from two greenhouse gases, carbon dioxide and methane, however, the top-performing photocatalysts presented in the academic literature invariably rely on the use of precious metals. In this work, we demonstrate enhanced photocatalytic dry reforming performance through surface basicity modulation of a Ni-CeO2 photocatalyst by selectively phosphating the surface of the CeO2 nanorod support. An optimum phosphate content is observed, which leads to little photoactivity loss and carbon deposition over a 50-hour reaction period. The enhanced activity is attributed to the Lewis basic properties of the PO43- groups which improve CO2 adsorption and facilitate the formation of small nickel metal clusters on the support surface, as well as the mechanical stability of CePO4. A hybrid photochemical-photothermal reaction mechanism is demonstrated by analyzing the wavelength-dependent photocatalytic activities. The activities, turnover numbers, quantum efficiencies, and energy efficiencies are shown to be on par with other dry-reforming photocatalysts that use noble metals, representing a step forward in understanding how to stabilize ignoble nickel-based dry reforming photocatalysts. The challenges associated with comparing the performance of photocatalysts reported in the academic literature are also commented on.

Sustainable Carbon Derived from Sulfur-Free Lignins for Functional Electrical and Electrochemical Devices.

Technical lignins, kraft, soda, lignoboost, and hydrolysis lignins were used for the production of carbon particles at different carbonization temperatures, 1000 °C and 1400 °C. The results showed that the lignin source and carbonization temperature significantly influenced the carbon quality and microstructure of the carbon particles. Soda lignin carbonized up to 1400 °C showed higher degree of graphitization and exhibited the highest electrical conductivity of 335 S·m-1, which makes it suitable for applications, such as electromagnetic interference shielding and conductive composite based structural energy storage devices. The obtained carbon particles also showed high surface area and hierarchical pore structure. Kraft lignin carbonized up to 1400 °C gives the highest BET surface area of 646 m2 g-1, which makes it a good candidate for electrode materials in energy storage applications. The energy storage application has been validated in a three-electrode set up device, and a specific capacitance of 97.2 F g-1 was obtained at a current density of 0.1 A g-1 while an energy density of 1.1 Wh kg-1 was observed at a power density of 50 W kg-1. These unique characteristics demonstrated the potential of kraft lignin-based carbon particles for electrochemical energy storage applications.

Regioselective Protection and Deprotection of Nanocellulose Molecular Design Architecture: Robust Platform for Multifunctional Applications.

Regioselectively substituted nanocellulose was synthesized by protecting the primary hydroxyl group. Herein, we took advantage of the different reactivities of primary and secondary hydroxyl groups to graft large capping structures. This study mainly focuses on regioselective installation of trityl protecting groups on nanocellulose chains. The elemental analysis and nuclear magnetic resonance spectroscopy of regioselectively substituted nanofibrillated cellulose (NFC) suggested that the trityl group was successfully grafted in the primary hydroxyl group with a degree of substitution of nearly 1. Hansen solubility parameters were employed, and the binary system composed of an ionic liquid and pyridine as a base was revealed to be the optimum condition for regioselective functionalization of nanocellulose. Interestingly, the dissolution of NFC in the ionic liquid and the subsequent deprotection process of NFC substrates hardly affected the crystalline structure of NFC (3.6% decrease in crystallinity). This method may provide endless possibilities for the design of advanced engineered nanomaterials with multiple functionalities. We envisage that this protection/deprotection approach may lead to a bright future for the fabrication of multifunctional devices based on nanocellulose.

Efficacy of Biopolymer/Starch Based Antimicrobial Packaging for Chicken Breast Fillets.

Food contamination leading to the spoilage and growth of undesirable bacteria, which can occur at any stage along the food chain, is a significant problem in the food industry. In the present work, biopolymer polybutylene succinate (PBS) and polybutylene succinate/tapioca starch (PBS/TPS) films incorporating Biomaster-silver (BM) and SANAFOR® (SAN) were prepared and tested as food packaging to improve the lifespan of fresh chicken breast fillets when kept in a chiller for seven days. The incorporation of BM and SAN into both films demonstrated antimicrobial activity and could prolong the storability of chicken breast fillets until day 7. However, PBS + SAN 2%, PBS/TPS + SAN 1%, and PBS/TPS + SAN 2% films showed the lowest microbial log growth. In quality assessment, incorporation of BM and SAN into both film types enhanced the quality of the chicken breast fillets. However, PBS + SAN 1% film showed the most notable enhancement of chicken breast fillet quality, as it minimized color variation, slowed pH increment, decreased weight loss, and decelerated the hardening process of the chicken breast fillets. Therefore, we suggest that the PBS + SAN and PBS/TPS + SAN films produced in this work have potential use as antimicrobial packaging in the future.

Nanocrystalline Cellulose from Microcrystalline Cellulose of Date Palm Fibers as a Promising Candidate for Bio-Nanocomposites: Isolation and Characterization.

Date palm fiber (Phoenix dactylifera L.) is a natural biopolymer rich in lignocellulosic components. Its high cellulose content lends them to the extraction of tiny particles like microcrystalline cellulose (MCC) and nanocrystalline cellulose (NCC). These cellulose-derived small size particles can be used as an alternative biomaterial in wide fields of application due to their renewability and sustainability. In the present work, NCC (A) and NCC (B) were isolated from date palm MCC at 60 min and 90 min hydrolysis times, respectively. The isolated NCC product was subjected to characterization to study their properties differences. With the hydrolysis treatment, the yields of produced NCC could be attained at between 22% and 25%. The infrared-ray functional analysis also revealed the isolated NCC possessed a highly exposed cellulose compartment with minimized lignoresidues of lignin and hemicellulose. From morphology evaluation, the nanoparticles' size was decreased gradually from NCC (A) (7.51 nm width, 139.91 nm length) to NCC (B) (4.34 nm width, 111.51 nm length) as a result of fragmentation into cellulose fibrils. The crystallinity index was found increasing from NCC (A) to NCC (B). With 90 min hydrolysis time, NCC (B) showed the highest crystallinity index of 71% due to its great cellulose rigidity. For thermal analysis, NCC (B) also exhibited stable heat resistance, in associating with its highly crystalline cellulose structure. In conclusion, the NCC isolated from date palm MCC would be a promising biomaterial for various applications such as biomedical and food packaging applications.

Design and Ductile Behavior of Torsion Configurations in Material Extrusion to Enhance Plasticizing and Melting.

In the present work, the ductile formation mechanism of a newly proposed torsion configuration has been investigated. One of the unique attributes of this paper is the first-time disclosure of the design and fabrication of a novel prototype screw with torsional flow character validating the orthogonal test model experimentally. The torsional spiral flow patterns that occurred in the torsion channel cause a ductile deformation of polymer in the form of a spiral, which in turn enhances the radial convection, achieving an effective mass transfer of material from the top region to the bottom region and vice versa. Furthermore, the characteristic parameters of torsion configuration have a significant influence on the plasticizing and melting capability of polymer. By range analysis and weight matrix analysis, the best factor and level combination was obtained. Results indicated that the aspect ratio of the torsion channel is almost equal to 1, and the plasticizing and melting capability of polymer is optimal. This novel design innovation offers a paradigm shift in the energy-efficient plasticization of polymer compounds.

A Single Crystal Hybrid Ligand Framework of Copper(II) with Stable Intrinsic Blue-Light Luminescence in Aqueous Solution.

Single-crystal solid-liquid dual-phase hybrid organic-inorganic ligand frameworks with reversible sensing response facilitated by external stimuli have received significant attention in recent years. This report presents a significant leap in designing electronic structures that display reversible dual-phase photoluminescence properties from single-crystal hybrid ligand frameworks. Three-dimensional Cu(C3N2H4)4Cl2 complex frameworks were formed through the intermolecular hydrogen bonding and π⋯π stacking supramolecular interactions. The absorption band peaks at 627 nm were assigned to d-d transition showing 10Dq = 15,949 cm-1 and crystal field stabilization energy (CFSE) = 0.6 × 10Dq = 114.4 kJmol-1, while the ligand-to-metal charge transfer (LMCT) of complexes was displayed at 292 nm. The intense luminescence band results from LMCT present at 397 nm. Considering its structure, air stability, framework forming and stable luminescence in aqueous solution, the Cu(C3N2H4)4Cl2 complex shows potential for luminescence Cu-based sensors using emission intensity to detect heavy metal ion species.

Thermoconformational Behavior of Cellulose Nanofiber Films as a Device Substrate and Their Superior Flexibility and Durability to Glass.

The design and high-throughput manufacturing of thin renewable energy devices with high structural and atomic configurational stability are crucial for the fabrication of green electronics. Yet, this concept is still in its infancy. In this work, we report the extraordinary durability of thin molecular interlayered organic flexible energy devices based on chemically tuned cellulose nanofiber transparent films that outperform glass by decreasing the substrate weight by 50%. The nanofabricated flexible thin film has an exceptionally low thermal coefficient of expansion of 1.8 ppm/K and a stable atomic configuration under a harsh fabrication condition (over 190 °C for an extended period of 5 h). A flexible optoelectronic device using the same renewable cellulose nanofiber film substrate was found to be functionally operational over a life span of 5 years under an intermittent operating condition. The success of this device's stability opens up an entirely new frontier of applications of flexible electronics.

One-pot fabrication of flexible and luminescent nanofilm by in-situ radical polymerization of vinyl carbazole on nanofibrillated cellulose.

Photoresponsive functionalized nanofilms were prepared via radical polymerization of carbazole units on a nanofibrillated cellulose (NFC) backbone via one-pot procedure. Herein, NFC was functionalized with active carbazole units as pendant organic moieties. The nanofilms were characterized by UV-vis and fluorescence spectroscopy, Fourier transformed infrared (FTIR) and Raman spectroscopy, 13C NMR and proton NMR spectra, contact angle analysis, mechanical testing, and scanning electron microscopy (SEM). The fabricated nanofilms exhibited large tensile strength (∼110 MPa), higher hydrophobicity and luminescence activity. The results indicated that the prepared optically active nanofilms present potential applications in the fields of flexible organic light emitting devices.

Hetero-Porous, High-Surface Area Green Carbon Aerogels for the Next-Generation Energy Storage Applications.

Various carbon materials have been developed for energy storage applications to address the increasing energy demand in the world. However, the environmentally friendly, renewable, and nontoxic bio-based carbon resources have not been extensively investigated towards high-performance energy storage materials. Here, we report an anisotropic, hetero-porous, high-surface area carbon aerogel prepared from renewable resources achieving an excellent electrical double-layer capacitance. Two different green, abundant, and carbon-rich lignins which can be extracted from various biomasses, have been selected as raw materials, i.e., kraft and soda lignins, resulting in clearly distinct physical, structural as well as electrochemical characteristics of the carbon aerogels after carbonization. The obtained green carbon aerogel based on kraft lignin not only demonstrates a competitive specific capacitance as high as 163 F g-1 and energy density of 5.67 Wh kg-1 at a power density of 50 W kg-1 when assembled as a two-electrode symmetric supercapacitor, but also shows outstanding compressive mechanical properties. This reveals the great potential of the carbon aerogels developed in this study for the next-generation energy storage applications requiring green and renewable resources, lightweight, robust storage ability, and reliable mechanical integrity.

High quantum yield photoluminescent N-doped carbon dots for switch sensing and imaging.

Stable blue fluorescent nitrogen doped carbon dots (N-CDs) with a very high quantum yield up to 81% has been reported for the first time. Novel N-CDs were synthesized through an efficient and rapid one-step hydrothermal synthesis process from diethylenetriamine as nitrogen source and a novel carbon source trans-aconitic acid. The nanosized particles of N-CDs were in the range of 2-8 nm and uniformly distributed in molecular level. The N-CDs showed high selectivity toward Fe3+ with low detection limit of 10.42 nmol L-1 (with corresponding linear range of 2-50 µmol L-1) enabling them for ion detection application and also exhibited high fluorescence stability in extreme pH conditions. Novel N-CDs also presented a green emission shift under acidic condition (pH~2) which makes them a potential sensing probe for security papers, food packaging and bio-medical detection sensors. A security paper sensor device has been fabricated and its operation function has been validated by making real time detection of color. The novel and facile to manufacture carbon dots has potential applications ranging from biological nano-sensors for security document to color-switch sensing and bio-imaging.