Surface Chemistry Research Articles

High‐Resolution Thermal Sensing Using Temperature‐Sensitive Cathodoluminescence Spectroscopy in Nitrogen‐Doped Nanodiamonds

The evolution of the cathodoluminescence spectra from commercially available nanodiamonds with high density of nitrogen‐vacancy defects has been studied in a large wavelength range, from 200 to 800 nm, and temperatures from 5 to 300 K, in order to achieve a temperature probe with high spatial resolution. The full width at half maximum of the peak associated to the neutral charge state of the NV center has been found to evolve with temperature in a predictable way, although its value may vary from sample to sample. We have attributed this shift to the differences in the nanodiamonds surface chemistry.

Enhanced Olivine Reactivity in Wet Supercritical CO2 for Engineered Mineral Carbon Sequestration.

The success of CO2 mineralization as a potential solution for reducing carbon emissions hinges on understanding chemical interactions between basaltic minerals and CO2-charged fluids. This study provides a detailed analysis of olivine dissolution in CO2-water mixtures at 90 and 150 °C, 2-9 MPa, and for 8 and 24 h, in both water- and CO2-dominant conditions. By using olivine crystal sections instead of powders, surface agitation is prevented, closing the gap between laboratory studies and natural settings. Surface chemistry, texture, and cross-sectional properties were examined pre- and postreaction using a multiscale approach combining spectroscopic and imaging techniques. Results show that wet supercritical CO2 environments lead to significant olivine dissolution, forming Mg-depleted, Si-enriched etched surfaces, and under certain conditions, the formation of passivating silica precipitates. In contrast, reactions in aqueous fluids caused minimal changes in surface chemistry and texture with no silica precipitation. These observations indicate that reaction extent in the CO2-rich phase is greater relative to water-rich mixtures at equivalent temperature, pressure, and reaction duration. The presence of silica precipitates incorporating leached metals indicates limited transport of reactant away from reaction sites in a CO2-rich medium. This study semi-quantitatively evaluates reaction extents in both CO2-rich and aqueous systems across a wide range of parameters, demonstrating faster mineralization in CO2-rich environments and highlighting their potential for enhancing the CO2 storage efficiency.

Carbon nanomaterials for efficient oxygen and hydrogen evolution reactions in water splitting: A review

Water splitting has gained significant attention as a means to produce clean and sustainable hydrogen fuel through the electrochemical or photoelectrochemical decomposition of water. Efficient and cost-effective water splitting requires the development of highly active and stable catalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Carbon nanomaterials, including carbon nanotubes, graphene, and carbon nanofibers, etc., have emerged as promising candidates for catalyzing these reactions due to their unique properties, such as high surface area, excellent electrical conductivity, and chemical stability. This review article provides an overview of recent advancements in the utilization of carbon nanomaterials as catalysts or catalyst supports for the OER and HER in water splitting. It discusses various strategies employed to enhance the catalytic activity and stability of carbon nanomaterials, such as surface functionalization, hybridization with other active materials, and optimization of nanostructure and morphology. The influence of carbon nanomaterial properties, such as defect density, doping, and surface chemistry, on electrochemical performance is also explored. Furthermore, the article highlights the challenges and opportunities in the field, including scalability, long-term stability, and integration of carbon nanomaterials into practical water splitting devices. Overall, carbon nanomaterials show great potential for advancing the field of water splitting and enabling the realization of efficient and sustainable hydrogen production.

Trace‐Amount of Water as An Electrolyte Additive for Sodium Metal Electrode

AbstractThe high reactivity of water toward Na metal has raised a concern about keeping the electrolytes extra‐dried. In this work, changes in water concentration in electrolytes (with and without fluoroethylene carbonate) show changes in overpotential and the surface chemistry of Na electrodes. In a symmetric cell test, the cell with pristine electrolyte (1 M NaClO4 in ethylene carbonate:propylene carbonate) sustained only 22 cycles before reaching the safety limit (5 V) at 1 mA cm−2. Meanwhile, controlling the water content (40 ppm) extended the cell's life by 3.5 times. In fluoroethylene‐carbonate‐containing electrolytes, the optimized water concentration (40 ppm) gave the minimum overpotential (12 mV) after 170 cycles. Ex situ X‐ray photoemission spectroscopy showed that water hydrolyzed fluoroethylene carbonate, which changed the Na electrode's surface chemistry. The appropriate amount of product (NaF) stabilized the electrodes’ surfaces. Electrical impedance spectroscopy showed that the controlled traces amount of water (40 ppm) always gave the minimum values for resistances. For the pristine electrolytes, the resistances attributed to the charge‐transfer process and the solid‐electrolyte interface layer increased 51 times (from 45 Ω–2290 Ω) after cycling. Meanwhile, for the optimized sample, the resistances remarkably decreased by 93 % (from 264 Ω–19 Ω) after cycling.

Delaminated structure of Zn-doped TiO2 coatings induced by ultrasound-auxiliary micro-arc oxidation: the influence of ultrasonic power

In this study, two representative ultrasonic vibration (UV) methods were employed to fabricate Zn-doped TiO2 micro-arc oxidation (MAO) ceramic coatings with enhanced corrosion resistance on pure Ti substrate. On the one hand, the surface morphology and chemistry of the coatings are characterized as partially crystallized hydroxyapatite nanoparticles and amorphous bands rich in Ca, P, Zn, and O. On the other hand, the MAO-modified coatings exhibit much greater corrosion resistance than the bare Ti surfaces, showing a reduction in corrosion current density (icorr) by at least an order of magnitude. However, a key finding is that a lower UV power setting of 360 V (named as the TZ-optimized protocols here) surpasses the higher 900 V (named as the TZ-powerful protocols) in terms of corrosion resistance (i.e. icorr =∼1.47×10−8 A/cm2 vs ∼7.85×10−7 A/cm2, respectively) as well as adhesion strength to the substrate (the critical load of ∼6.4 N vs ∼2.9 N, respectively), which can be attributed to the delaminated structure formed at higher UV powers. This work is expected to remind the potential side effect of such delamination in ceramic coatings produced by UV-assisted MAO processes on Ti-based alloys.

CsSnBr3 and Cs3Bi2Br9: Structural, Optical Characteristics, and Application in a Schottky Barrier Diode

The search for alternatives to Pb‐based perovskites, due to concerns about stability and toxicity, has led to the exploration of Pb‐free options. Tin (Sn) and bismuth (Bi) are promising candidates, given their similar ionic radii to Pb and the isoelectronic nature of Pb2+ and Bi3+, which suggest comparable chemical properties. Among these, CsSnBr3 and Cs3Bi2Br9 are relatively underexplored but offer lower toxicity and enhanced stability while demonstrating optoelectronic properties suitable for various applications. In this study, CsSnBr3 and Cs3Bi2Br9 nanocrystals are synthesized using a colloidal method and integrated into Schottky diodes. X‐ray photoelectron spectroscopy analysis of the surface chemistry confirms improved thermal and phase stability compared to Pb‐based perovskites. Schottky diode parameters, including ideality factor, barrier height, and series resistance are assessed using conventional thermionic emission, modified Cheung's, and Norde's models. The Cs3Bi2Br9‐based Schottky diode exhibits superior electrical performance with the lowest series resistance and optimal barrier height. Electrical impedance spectroscopy results indicated that CsSnBr3 has higher resistances and lower capacitances than Cs3Bi2Br9, reflecting lower charge carrier mobility and more defects, although the R1C1 regions in both materials demonstrated faster charge dynamics, making them ideal for high‐speed applications.

LiTFSI salt concentration effect for well‐balanced ion transport and physical properties in nanocellulose‐reinforced PEO#600 solid electrolytes

AbstractPoly(ethylene oxide) (PEO) with an oxygen group serves as a reactive site for the pathway of lithium‐ion transport. Reducing the PEO crystal domain in solid electrolytes is an extremely efficient approach for enhancing the mobility of ions. The present study applied various EO/Li molar ratios to modify the physical and electrochemical properties of PEO nanocomposite reinforced by nanocellulose. An elevated lithium salt concentration causes a gradual decline in crystallinity and mechanical strength. The electrochemical performance of the 13 EO/Li molar ratio voltammogram and charge–discharge shows efficient Li‐ion transport with 5.6 × 10−4 S/cm conductivity at room temperature and 131 mA h g−1 initial discharge capacity. The shifting glass transition and melting point at lower temperatures (−40.5 to −44.5°C and 45.3–43.8°C) suggest greater ion mobility throughout the large non‐crystalline structure. Lithium ions are limited by membrane weakening and re‐crystallization caused by high lithium salt (EM_11) concentrations. EM_13 has the highest specific capacity, operating voltage, and lithium transfer number depends on balanced electrochemical performance and physical features. XPS surface chemistry analysis explains LiF, Li2CO3, and Li2O solid electrolyte interfaces (SEI) in EM samples. A lower Li2O (11.62 at.%) than LiF (38.4 at.%) after cycling enhances Li‐ion diffusion and cell reversibility.

Harnessing Novel Reduced Graphene Oxide-Based Aerogel for Efficient Organic Contaminant and Heavy Metal Removal in Aqueous Environments.

Ensuring clean water sources is pivotal for sustainable development and the well-being of communities worldwide. This study represents a pioneering effort in water purification, exploring an innovative approach utilizing modified reduced graphene oxide (rGO) aerogels. These advanced materials promise to revolutionize environmental remediation efforts, specifically removing organic contaminants from aqueous solutions. The study investigates the exceptional adsorption properties of rGO-aerogel, enhanced with cysteamine, to understand its efficacy in addressing water pollution challenges. The characterization methods utilized encompass various analytical techniques, including FE-SEM, BET, FTIR, TGA, DSC, XPS, NMR, and elemental analysis. These analyses provide valuable insights into the material's structural modifications and surface chemistry. The research comprehensively explores the intricacies of adsorption kinetics, equilibrium, and isothermal study to unravel the underlying mechanisms governing contaminant removal. MO and Ni2+ exhibited adsorption of 542.6 and 150.6 mg g-1, respectively, at 25 °C. Ni2+ has unveiled the highest removal at pH 5, and MO has shown high removal in a wide pH range (pH 4-7). Both contaminants have shown fast adsorption kinetic performance on an rGO-aerogel surface. This study aims to identify the synergistic effect of cysteamine and rGO in aerogel formation to remove heavy metals and organic contaminants. These findings mark a significant stride in advancing sustainable water-treatment methods and pioneering in synthesizing innovative materials with versatile applications in environmental contexts, offering a potential solution to the global water pollution crisis.

Probing Twist‐Induced Endocytotic Membrane Fission using Anisotropic Gold Homodimers

AbstractMembrane fission involves a crucial step of lipid remodeling, in which the dynamin collar constricts and severs the tubulated lipid membrane at the neck of budding vesicles. Nevertheless, the difficulty in accurately determining the rotational dynamics of live endocytotic vesicles poses a limit on the elucidation of dynamin‐induced membrane remodeling for endocytotic vesicle scission. Herein, we designed a DNA‐modified gold homodimer (AuHD)‐based anisotropic plasmonic probe with uniform surface chemistry, minimizing orientational fluctuation within vesicle encapsulation. Using AuHDs as cargos to image the dynamics of cargo‐containing vesicles during endocytosis, we showed that, prior to detachment from plasma membrane, the cargo‐containing vesicles underwent multiple intermittent twists of ~4° angular orientation relative to plasma membrane with a ~0.2 s dwell time. These findings suggest that the membrane torques resulting from dynamin actions in vivo constitute the pathway to membrane fission, potentially shedding light on how dynamin‐mediated lipid remodeling orchestrates membrane fission.

Coupling Manipulation of Interfacial Chemistry and Coordination Structure in Vanadium Oxides Enables Rapid Magnesium Ion Diffusion Kinetics

AbstractRechargeable magnesium batteries (RMBs) are a highly promising energy storage system due to their high volumetric capacity and intrinsic safety. However, the practical development of RMBs is hindered by the sluggish Mg2+ diffusion kinetics, including at the cathode‐electrolyte interface (CEI) and within the cathode bulk. Herein, we propose an efficient strategy to manipulate the interfacial chemistry and coordination structure in oligolayered V2O5 (L−V2O5) for achieving rapid Mg2+ diffusion kinetics. In terms of the interfacial chemistry, the specific exposed crystal planes in L−V2O5 possess strong electron donating ability, which helps to promote the degradation dynamics of C−F/C−S bonds in the electrolyte, thereby establishing the inorganic‐organic interlocking CEI layer for rapid Mg2+ diffusion. In terms of the coordination structure, the straightened V−O structure in L−V2O5 provides efficient ions diffusion path for accelerating Mg2+ diffusion in the cathode. As a result, the L−V2O5 delivers a high reversible capacity (355.3 mA h g−1 at 0.1 A g−1) and an excellent rate capability (161 mAh g−1 at 1 A g−1). Impressively, the interdigital micro‐RMBs is firstly assembled, exhibiting excellent flexibility and practicability. This work gives deeper insights into the interface and interior ions diffusion for developing high‐kinetics RMBs.

Design rules for catalysis in single-particle plasmonic nanogap reactors with precisely aligned molecular monolayers

Plasmonic nanostructures can both drive and interrogate light-driven catalytic reactions. Sensitive detection of reaction pathways is achieved by confining optical fields near the active surface. However, effective control of the reaction kinetics remains a challenge to utilize nanostructure constructs as efficient chemical reactors. Here we present a nanoreactor construct exhibiting high catalytic and optical efficiencies, based on a nanoparticle-on-mirror (NPoM) platform. We observe and track pathways of the Pd-catalysed C-C coupling reaction of molecules within a set of nanogaps presenting different chemical surfaces. Atomic monolayer coatings of Pd on the different Au facets enable tuning of the reaction kinetics of surface-bound molecules. Systematic analysis shows the catalytic efficiency of NPoM-based nanoreactors greatly improves on platforms based on aggregated nanoparticles. More importantly, we show Pd monolayers on the nanoparticle or on the mirror play significantly different roles in the surface reaction kinetics. Our data provides clear evidence for catalytic dependencies on molecular configuration in well-defined nanostructures. Such nanoreactor constructs therefore yield clearer design rules for plasmonic catalysis.

Probing Twist-Induced Endocytotic Membrane Fission using Anisotropic Gold Homodimers.

Membrane fission involves a crucial step of lipid remodeling, in which the dynamin collar constricts and severs the tubulated lipid membrane at the neck of budding vesicles. Nevertheless, the difficulty in accurately determining the rotational dynamics of live endocytotic vesicles poses a limit on the elucidation of dynamin-induced membrane remodeling for endocytotic vesicle scission. Herein, we designed a DNA-modified gold homodimer (AuHD)-based anisotropic plasmonic probe with uniform surface chemistry, minimizing orientational fluctuation within vesicle encapsulation. Using AuHDs as cargos to image the dynamics of cargo-containing vesicles during endocytosis, we showed that, prior to detachment from plasma membrane, the cargo-containing vesicles underwent multiple intermittent twists of ~4° angular orientation relative to plasma membrane with a ~0.2 s dwell time. These findings suggest that the membrane torques resulting from dynamin actions in vivo constitute the pathway to membrane fission, potentially shedding light on how dynamin-mediated lipid remodeling orchestrates membrane fission.

Robust PFAS‐Free Superhydrophobicity Exhibited in Hierarchically Nanostructured Coatings on Textiles

Long chain per‐ and polyfluorinated chemical compounds, commonly referred to as PFAS, historically offered superior breathable and flexible water‐repellent textile finishes on clothing. Now notoriously deemed “forever chemicals” for their environmental persistence and ability to bioaccumulate, they can cause a range of human health impacts including cancer and reproductive harm, which has highlighted the need for less harmful but equally superhydrophobic coatings. Inspired by the microscopically bumpy water‐repellent surfaces of lotus leaves, this work introduces a PFAS‐free hierarchical nanocoating on and within textile substrates using a multistep synthetic approach, involving fabric pretreatment to facilitate a robust particle‐to‐substrate attachment of subsequently infiltrated silica nanoparticles (NPs), followed by surface functionalization of textile‐infiltrated NPs with long‐alkyl‐chain silanes to impart PFAS‐free water repellency. The system is subjected to rigorous wash testing and found consistent superhydrophobic performance after 65 wash cycles. Furthermore, the system can be adapted as a flexible platform technology for a variety of design opportunities by changing the substrate, NP composition, and surface chemistry to suit a variety of applications. Herein, a robust, flexible, and breathable interface between fabric and water that offers a next‐generation PFAS‐free water‐repellent textile coating solution is developed.

Surface Activation of Cotton Fabric with Low-Temperature Air Plasma Treatment for Metallic Printing

In this investigation, air plasma treatment was utilised to activate the surfaces of 100% grey and bleached cotton fabrics in preparation for metallic pigment printing. The study delved into the surface morphology, wettability, and surface chemistry properties. Scanning electron microscopy (SEM) revealed roughness and grooves in the treated samples. The contact angle witnessed a 29% and 41% increase for grey and bleached fabrics, respectively, compared to their untreated counterparts. Surface chemistry analysis using FTIR and XPS provided crucial insights into the functional polar groups, such as OH and C=O, along with significantly elevated O1 peaks in both plasma-treated grey and bleached cotton fabrics. These findings contributed to the enhanced surface free energy of the fabrics, preparing them for the subsequent pigment printing process. The study explores the impact of plasma treatment on the colour fastness of grey and bleached cotton fabrics printed with gold and silver metallic pigments. Untreated fabrics exhibited poor durability, with low colour change and staining-resistance ratings, particularly for gold pigments. Plasma treatment significantly improved colour retention, adhesion, and resistance to staining for both metallic pigments, with silver outperforming gold. Rubbing fastness tests revealed that plasma treatment moderately enhanced durability, though gold remained susceptible to friction damage. Light fastness was excellent for both pigments, and plasma treatment further improved performance. Perspiration tests showed that plasma treatment bolstered resistance, particularly for gold. These findings suggest that plasma treatment enhances the stability of metallic pigments, offering potential applications in the textile industry for improved product quality and durability.

A small amount of sodium difluoro(oxalate)borate additive induces anion-derived interphases for sodium-ion batteries

In sodium-ion batteries, the properties of the electrode-electrolyte interphases (EEIs) layer formed on the electrode surface, dominate the Na+ de-solvation process and Na+ (de)intercalation behavior, thereby influencing the battery performance. Currently, both high-concentration electrolytes and localized high-concentration electrolytes facilitate the formation of anion-derived and inorganic-rich interfacial chemistry, leading to excellent electrochemical performance. However, the expensive lithium salt and/or fluorinated diluent imposes a major concern. Herein, a small amount additive of 0.5 wt% sodium difluoro(oxalate)borate (NaDFOB) with the electron-rich property is introduced into 1 mol L–1 NaClO4/propylene carbonate electrolyte to construct a robust inorganic-rich EEIs via an anion preferential adsorption-decomposition mechanism. Theoretical calculations and experimental results reveal that the DFOB– anion has a lower adsorption energy than the other components, which will be preferentially adsorbed in the inner Helmholtz plane (IHP) with the closer proximity to two electrode surfaces and thus being firstly decomposed to form inorganic-rich interphases, thereby effectively suppressing side reactions. Consequently, both Na-ion half-cells and full-cells using this electrolyte deliver excellent cycling performance. This strategy that regulates the interphase chemistry on the electrode surface through an anion preferential adsorption-decomposition strategy, provides a promising avenue for developing long-term cycling sodium-ion batteries.

Ultrathin Copper Monosulfide Films for an Optically Semitransparent, Highly Selective Ammonia Chemosensor.

Transition-metal sulfides are emerging as promising materials for chemiresistive gas sensors─a field still dominated by semiconducting metal oxides. Despite the availability of materials with tunable electronic, optical, physical, and chemical properties, few studies have moved beyond synthesis to provide strategies for enhancing gas sensing performance through material modification. Here, we present a simple, scalable synthetic strategy for developing an optically semitransparent, flexible NH3 gas sensor with a highly uniform, ultrathin CuS (covellite) active sensing layer. The optical and chemical properties of the CuS were precisely controlled near the percolation threshold of thin-film formation by varying key experimental parameters such as the Cu film thickness (<10 nm) and the sulfurization time (∼90 s) under ambient conditions. Experimental and computational studies of CuS and its NH3 sensing characteristics identify key physicochemical properties. The controlled surface chemistry and morphology of the ultrathin CuS layer demonstrate its effectiveness in functional NH3 sensing devices, which achieve a calculated detection limit of 1.38 ppm for NH3 gas at 150 °C, along with exceptional mechanical robustness and optical semitransparency in the visible-light spectrum.

Tailoring Hematite Photoanodes for Improved PEC Performance: The Role of Alcohol Species Revealed by SHAP Analysis.

We explore the synergistic effects of TiO2 underlayers and varied alcohol species in the precursor solutions on the photoelectrochemical (PEC) performance of hematite photoanodes. Utilizing a robust machine learning (ML) framework combined with comprehensive analytical data sets, we systematically investigate how these modifications influence key physical and chemical properties, directly impacting the efficiency of water splitting processes. Our approach employs an ML model that integrates SHapley Additive exPlanations (SHAP) to quantitatively assess the impact of each dominant descriptor selected in the analytical data on the PEC performance, and they were combined with the SHAP values' dependence on the experimental operations. Specifically, we focus on the type of alcohol (methanol, ethanol, butanol, and 2-ethyl-1-butanol) used in the precursor solutions as the experimental operation, examining their effects on the dominant descriptors selected in the analytical data. The results from the SHAP analysis reveal that different alcohol species significantly alter the physicochemical properties at the hematite/TiO2 interface and in bulk hematite. These changes are primarily manifested in the modulation of the density of states and resistance to promote the charge carrier transport. For example, ethanol and butanol were found to enhance the electron density of states at the interface, which correlates with higher photocurrent outputs and improved PEC activity. In contrast, methanol showed a less pronounced effect, suggesting a nuanced interaction between the alcohol molecular structure and hematite surface chemistry. These findings not only underscore the importance of tailored precursor solution chemistry for enhancing PEC performance but also highlight the power of ML tools in uncovering the underlying physical and chemical mechanisms that govern the behavior of complex material systems. This study sets a foundational approach where ML can bridge the gap between empirical observations and theoretical understanding, leading to the rational design of energy materials.

The use of interphacial energies to estimate the spreading coefficients of organic liquids by the solid polymer surface of polytetrafluoroethylene

In the article, using equations previously obtained by the author, calculations were made of the interfacial energies of a solid polymer – polytetrafluoroethylene in contact with organic liquids and their vapors. Based on the calculation results, the spreading coefficients in the studied systems were calculated. Since Young’s derivation of the equation for the cosine of the contact angle, many researchers have attempted to determine the surface energy of solids, which would, in turn, make it possible to determine the interfacial energy at the solid-melt (liquid) interface. However, on the way to solving this problem there were obstacles associated with various processes that accompany phenomena occurring on the surface of a solid body in the presence of a liquid (melt) of another body on its surface. This is not the place to list all types of processes. They are well known to specialists in the field of surface phenomena. Here are just a few of them that affect the surface properties of bodies: chemical reactions, mutual dissolution of components of solid and liquid phases, deformation of solid phases, etc. In the case of contact of the polymer with organic liquids, such obstacles do not exist. Also, since it is impossible to dwell on all publications devoted to the determination of the surface energy of solids, the article discusses specific works on determining the interfacial energy at contact angles close to or equal to zero. Since the question of the behavior of interfacial energy at a contact angle equal to zero is of fundamental importance, and there are conflicting opinions in the literature on this matter, giving the correct answer to this question is an urgent task. Using examples of calculations of interfacial energies of homologous series of organic liquids on a solid surface of polytetrafluoroethylene, we have shown that only at zero contact angle the interfacial energy is zero. In this article, using interfacial energy values, we are the first to calculate the spreading coefficients of organic liquids over the surface of a solid polymer, which, in our opinion, is also an urgent task.

3D printing of biodegradable biocomposites based on forest industrial residues by fused deposition modeling

This study investigated the impact of industrial forest residues (IFR) type and proportion on 3D-printed biocomposites (BC). Fused deposition modeling (FDM) produced BC containing up to 20 % Jack pine sawdust, wood ashes, cellulose fibers, and polylactic acid (PLA). The BC thermal stability, surface chemistry, microstructure, and physical and mechanical were investigated. Thermal stability investigations revealed that adding IRF resulted in a decline in the PLA degradation temperature, an increase in the residual mass, a decrease in the glass transition temperature, and an improvement in crystallinity. Add IRF to PLA showed an important reduction in ductility, a consistent reduction of the tensile and flexural strengths with increasing proportion but only a slight or a non-significant reduction the modulus of elasticity. Adding forest waste filler to pure PLA increased the water absorption (WA) and dimensional accuracy (TA) of the biocomposites, which was expected due to the hydrophilic character of fillers. The microstructural analysis demonstrated that a higher filler level resulted in a greater porosity, roughness, and visible filler pull-out on the filament and printed parts surfaces. Surface chemistry analysis suggested poor interactions between the PLA and the fillers and consequently poor interfacial adhesion. Furthermore, the rheological investigations confirmed that the complex viscosity and storage modulus of PLA-Jack pine's sawdust and PLA-cellulose fibers increased with filler. In contrast, the PLA-wood ashes showed opposite results. Using 3D-printed biodegradable biocomposites provided a sustainable option for reducing dependence on non-renewable plastic, valorizing the value chain of forest products, and promoting the circular economy.

Mycelium-Doped Straw Biochars for Antibiotic Control.

Straw, a predominant agricultural residue, represents a significant waste product. Harnessing its potential is of paramount importance both in terms of research and economic value. In this study, chemically pretreated corn straw was infused with distinct microbial fungal mycelium variants and subsequently transformed into a series of biochars through a process involving carbonization and activation. The findings revealed enhancements in the specific surface area and total pore volume of mycelium-doped straw biochars compared to the original corn straw biochar (BCS). Additionally, discernible disparities were observed in their physical and chemical attributes, encompassing functional groups, surface chemistry, and micro-morphology. Notably, in water-based antibiotic removal experiments focusing on tetracycline hydrochloride (TH) and chloramphenicol (CP), the mycelium-doped straw biochars outperformed BCS. Their maximum adsorption capacities for TH and CP surpassed those of alternative adsorbents, including other biochars. Impressively, even after five cycles, the biochar exhibited a removal rate exceeding 80%, attesting to its robust stability. This study successfully emphasized the efficacy of incorporating fungal mycelium to enhance the adsorption properties of straw-based biochar, introducing a new theoretical basis for the development of lignocellulosic materials.