Synergetic Effect Research Articles

Simultaneous enhancement in mechanical properties and flame retardancy of reed charcoal/polypropylene composites by graphene oxide interfacial modification

Biochar/polypropylene composites (BPCs) have great potential in automobiles and building materials due to their ease of processing and light weight. However, the inferior interfacial bonding strength between biochar and polypropylene (PP) and flammability of PP often result in the weak mechanical properties and poor flame retardancy of BPCs, which limit the practical applications of BPCs. Herein, graphene oxide (GO) is used as an active interfacial modifier to prepare graphene-reed charcoal/polypropylene (G-RC/PP) composites. Benefiting from the mechanical interlocking effect formed by GO, the G-RC/PP composites exhibit higher tensile and flexural strengths. When 1 % of GO was added (relative to mass of RC), the tensile and flexural strengths were 22.84 MPa and 50.8 MPa, respectively, which are 16 % and 22.7 % higher than pure PP. Additionally, the barrier-adsorption-dilution synergetic effects of GO enhance both the thermal stability and flame retardance of the composites. The total heat release rate of G-RC/PP composites is reduced by 71.6 % compared to RC/PP when GO was added at 1 %, resulting in a substantial reduction in fire hazards. This study offers a fresh perspective on the development of biochar/plastic composites with exceptional mechanical properties and high fire safety towards extensive applications as automotive parts and building structures.

Combine calculation and experiment to study the undesired polymerization of styrene for screening of effective inhibitors

Regarding undeniable formation of the undesired polymer (UP) in the styrene purification process, it is of vital importance to inhibit its production. To address the mentioned issue, effects of injecting antipolymers (e.g., stable nitroxide radicals (i.e., SNRs) and antioxidants (e.g., alkylhydroxylamines (AHA)) on the controlling the UP formation have been studied through density functional theory (DFT) calculations as well as experimental method in this study. In fact, electrophilicity and growth percentage were evaluated by DFT calculations and experimental approach, correspondingly. Accordingly, it was revealed that the best antipolymers in terms of inhibiting performance were 4‑hydroxy-2,2,6,6-tetramethyl piperidine 1-Oxyl (4‑hydroxy-TEMPO) and 4-oxo-2,2,6,6-tetramethylpiperidine 1-Oxyl (4-oxo-TEMPO), and from the antioxidants, N-Ethyl-N-phenyl hydroxylamine (EPHA) and N-Benzyl-N-phenyl hydroxylamine (BPHA) exhibited the best performance. In addition, the growth percentage of 18.70, 20.55, 24.85 and 46.8, were obtained for the EPHA, BPHA, 4‑hydroxy-TEMPO, and 4-oxo-TEMPO after 4 hrs of operation, correspondingly. Besides, the synergetic effects of the used inhibitors were determined experimentally. Among the evaluated inhibitors, EPHA/4‑hydroxy-TEMPO demonstrated the best synergetic effects over the control of UP formation. Finally, the blend of 4‑hydroxy-TEMPO (40 wt.%) and EPHA (60 wt.%) was obtained to be the optimum (best) inhibitor with 7.2 % polymer growth after 4 hrs of operation.

Synergetic effect of magnesium oxide expansion additive and biochar on the deformation and mechanical properties of concrete

Synergetic effect of magnesium oxide expansion additive and biochar on the deformation and mechanical properties of concrete

Current Evidence of the Application of Music in Tai Chi Exercise: Scoping Review.

Music has frequently been used in movement exercises to enhance health benefits. However, scientific evidence regarding the application of music to Tai Chi practice is limited. This scoping review aims to understand how music has been used in Tai Chi practice and whether music could be applied to Tai Chi practice to help optimize its benefits. PubMed, CINAHL, CNKI, and Weipu databases were searched. We included studies that compare Tai Chi practice experience or health outcomes between individuals practicing Tai Chi with music and those practicing Tai Chi without music. Studies published through September 2022 were identified. Two researchers (YD and YH) independently performed study selection and data extraction. Thematic analysis was used to summarize and categorize the findings of the included studies. Seven studies were included in this review. All 7 included studies are experimental studies. Practicing Tai Chi with music might lead to positive perceptions of Tai Chi practice (eg, motivation, concentration, enjoyment, compliance, and performance) and higher evaluations of Tai Chi instructional quality, especially for Tai Chi beginners. The effects of incorporating music into Tai Chi practice on health outcomes are inconclusive due to the heterogeneities of the sample size, and the intervention components, lengths, and frequencies of the included studies. Applying music to Tai Chi practice may result in positive Tai Chi practice experience and adherence, particularly for beginners, which could help improve the dissemination and implementation of Tai Chi interventions for public health. However, whether applying music to Tai Chi practice leads to synergetic effects on health outcomes needs further investigation.

Synthesis of Mesoporous Catechin Nanoparticles as Biocompatible Drug-Free Antibacterial Mesoformulation.

While polyphenolic substances stand as excellent antibacterial agents, their antimicrobial properties rely on the auxiliary support of micro-/nanostructures. Despite offering a novel avenue for enhancing polymer performance, controllable fabrication of mesoporous polymeric nanomaterials encounters significant challenges due to intricate intermolecular forces. In this article, mesoporous catechin nanoparticles have been successfully fabricated using a balanced multivariate interaction approach. The harmonization of the water-ethanol ratio and ionic strength effectively balances the forces of hydrogen bonding and π-π stacking, facilitating the controlled assembly of mesostructures. The mesoporous catechin nanoparticles exhibit a uniform spherical structure (∼100 nm), open mesopores with a diameter of ∼15 nm, and a high surface area of ∼106 m2 g-1. While exhibiting a good biocompatibility and negative surface charge, the mesoporous catechins possess outstanding antibacterial ability and function as an antibiotic mesoformulation without the necessity of loading any drugs. This mesoformulation inhibits 50% in vitro Staphylococcus aureus growth with a low concentration of ∼10 μg mL-1 and achieves complete inhibition at ∼25 μg mL-1. In a mouse wound model, accelerated wound healing and complete closure within 6-8 days are achieved. Proteomics of bacteria reveals that the excellent antibacterial property is attributed to the synergetic effect of mesoformulation's mesostructure and the catechin molecule intervening in bacterial metabolism. Overall, this work may pave a novel way for the future exploration of polymer nanomaterials and antibiotic formulations.

Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous

SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity.

Three-liquid-phase behavior in the quaternary systems of water + phosphoric acid + diisopropyl ether + tributyl phosphate/methyl isobutyl ketone at 298.2 K

The three-liquid-phase formation in the ternary system of water + phosphoric acid + diisopropyl ether (DIPE) makes the phosphoric acid extraction only effective for acid mass fractions above 0.69. To avoid the undesirable formation of the third phase and enhance acid extraction, particularly at low concentrations, two phase modifiers, methyl isobutyl ketone (MIBK) and tributyl phosphate (TBP), were systematically studied. In order to quantify the synergetic effect of the mixed solvents of DIPE+TBP and DIPE+MIBK, the liquid–liquid equilibria for the quaternary systems of H2O+H3PO4 + DIPE+TBP and H2O+H3PO4 + DIPE+MIBK were fully established for different DIPE/phase modifier (TBP or MIBK) mass ratios (90/10, 70/30, 50/50, and 20/80) at 298.2 K under atmospheric pressure using the cloud point and Othmer graphical method. Othmer-Tobias and Hand correlations were used to fit the tie-line data and assess its consistency. In addition, the behavior of the three-phase zone was also studied as a function of the phase modifiers content. Separation factor (S) and acid distribution (D2) were used to identify the most effective solvent with the potential to enhance phosphoric acid extraction from aqueous solutions.

Pd catalysts in the mild reductive depolymerization of Soda lignin: Support and Cu addition effects

This study pioneers the exploration of the structure-performance relationship of 5 wt% Pd and PdCu catalysts on 3 supports (γ-Al2O3, SiO2, and activated carbon (AC)) in the mild reductive depolymerization (MRD) of Soda lignin. While all catalysts achieve similar final weight average molecular weight (Mw) reduction (≈ 85 %), Pd/AC and PdCu/AC show significant differentiation from solvolysis already after 2 h and 3 h, compared to 6 h and 20 h for Pd and PdCu on oxide supports. This study also highlights the importance of hydrogenation of C=C bonds in monomer side-chains for maximizing monomer yields. Particularly PdCu/SiO2 is characterized by the lowest monomer yields (7 wt%) due to its low hydrogenation activity, while catalysts like Pd(Cu)/Al2O3, Pd/SiO2, and Pd/AC, with more expressed hydrogenation, achieve a total monomer yield of up to 14 wt%. Additional findings confirm that on γ-Al2O3, the co-impregnation of Cu and Pd leads to the formation of a chemical bond between Pd2+ and Cu1+, resulting in a new mixed metal oxide Pd-Cu–O phase. On SiO2, Pd2+ and Cu1+ do not form a chemical bond, however, the presence of Cu1+ in close proximity to Pd2+ significantly alters the selectivity of the PdCu/SiO2 catalyst due to synergetic effects. PdCu/AC maintains similar selectivity to Pd/AC, except for reduced hydrogenation over time, due to the lack of interaction between Pd and Cu on the AC surface. This research also delves into the MRD mechanism of Soda lignin over Pd and PdCu catalysts, focusing on the β-O-4 linkage cleavage and the subtle differences in reaction pathways depending on the catalyst. These findings bridge gaps in understanding the MRD of actual lignin feedstocks, offering valuable insights for catalyst development and process optimization.

Fano-resonant mechanism of terajet formation using graphene-covered high-index mesoscale spheres.

Photonic jet in terahertz (THz) frequency range (terajet) plays an important role in modern THz scanning systems to achieve a superresolution beyond the diffraction limit. Based on analytical simulations, we introduce a synergetic effect of a mesoscale dielectric sphere and graphene to improve the focusing properties of a particle. We show that a graphene-covered dielectric sphere is able to enhance the field behind it if the refractive index is high. This conflicts with a generally accepted statement that a jet is generated only for low-index dielectrics with n < 2. We demonstrate the tunability of the terajet characteristics with respect to the graphene Fermi energy and discover a Fano resonance causing the field increase. This design leverages the tuning properties of the graphene allowing dynamic control over the power and size of the generated terajet in real time. With high-index materials, we get the opportunity for integration of terajet-assisted imaging with semiconductor technology.

Uniaxial compressive stress-strain behavior of steel fiber reinforced geopolymer concrete confined by stirrups: Experimental study and analytical model

The compressive stress-strain relationship of confined steel fiber reinforced geopolymer concrete (SFRGC) is a basis for its structural nonlinear analysis and engineering design. This paper presents an experimental study on the stress-strain behavior of stirrup confined-SFRGC under uniaxial compression, with emphasis on the effects of stirrup spacing, stirrup strength and steel fiber (SF) volume fraction. The failure modes, stress-strain curves, energy absorption capacity and post-peak ductility were analyzed. The results demonstrated that due to the stirrup constraint and SF fiber crack-bridging effects, the integrity of specimens was significantly improved, showing notable ductile failure mode. The stress-strain behavior of core SFRGC was notably affected by the constraint level of stirrups, however, the effect of SF was mainly reflected in post-peak stress-strain branches. Reducing the stirrup spacing, improving the stirrup strength, and increasing the SF content can effectively enhance the strength and deformation characteristics of confined-SFRGC, as well as ductility. Moreover, synergetic effect of SF and stirrups on improving the deformation capacity of SFRGC was observed, whereas the peak stress and corresponding strain changed insignificantly with the SF content. In addition, the stirrups can reach yield around the peak stress point. Based on the analysis of test results, formulae for characterizing the peak stress, peak strain, elastic modulus as well as stress-strain responses of confined-SFRGC were proposed, with the effective confinement index of stirrups and fiber reinforcing factor introduced. The model predicted curves were in great agreement with the test curves.

Copper‐Cobalt Bimetallic Nanoparticles for the Acceptorless Dehydrogenation of Alcohols: A Combined Experimental and Theoretical Study

AbstractBimetallic Cu and Co nanoparticles were prepared using the polyol process. The nature of the polyol was found to be decisive to control the distribution of the two metals within the particles, resulting in either core‐shell or quasi‐alloyed structures, as shown by chemical analysis at the single particle level. The particles can be prepared over the entire composition range with a very good control of the Cu/Co molar ratio. The introduction of Cu in the synthetic system allows decreasing significantly the mean size of the resulting particles. The two sets of particles were used as unsupported catalysts for the solvent‐free acceptorless dehydrogenation of octan‐2‐ol. Very good ketone yields were measured when using the quasi‐alloyed particles while lower activities were obtained with core‐shell structures. The Cu25Co75 quasi‐alloyed catalyst could be recycled at least ten times without a significant loss in catalytic activity and particle‐scale chemical analyses confirmed that the recovered particles are still alloyed with no observed demixing. The catalytic results are discussed in the light of different exposed metal surface areas and possible synergetic effects using theoretical predictions.

LaMnO3-Mn3O4 nanocomposite: Synergetic effect towards high electrochemical performance

Metal oxides have been a focus of research for energy storage devices. Herein, xLaMnO3 – (100-x) Mn3O4 (LMO-MO) composites (xwt%: 100, 90, 70, and 50) were prepared via one-pot synthesis to elucidate the synergistic effect of the composite constituents on composite’s electrochemical performance. The X-ray diffraction analysis confirmed the presence of individual compounds in the desired ratio and phase. The X-ray photoelectron spectroscopy confirmed the presence of Mn2+ and Mn3+ oxidation states, indicating the presence of both LaMnO3 (LMO) and Mn3O4 (MO) in the composite. The electrochemical performance of composite electrodes prepared using nickel foam was assessed in 1 and 6 M KOH solutions. High specific capacitance measured via cyclic voltammetry of ∼ 770 Fg−1 at a scan rate of 1 mVs−1 was recorded for the composite of LMO-MO (70 %: 30 %) in 6 M KOH. At the same time, charge-discharge curves revealed a maximum specific capacitance of around 405 Fg−1 for an x =70 % sample at a current density of 0.5 Ag−1. The EIS studies show a reduction in the internal resistance of the composite due to the interconnected structure and reversible faradic process at the interface with a high degree of Coulombic efficiency. A higher overall electrochemical performance of the electrode was recorded in a 6 M KOH electrolyte. The enhanced electrochemical performance of the composite is attributed to efficient charge transfer kinetics through the electrode-electrolyte interface via easy electron hopping pathways between LMO and MO in the composite. These findings suggest that the studied LMO-MO composites could be a potential material for pseudocapacitor energy devices.

Multifunctional Acetaminophen Interlayer for High Efficiency and Durability Lead-Lean Perovskite Solar Cells.

Due to the easy oxidation of Sn2+, which leads to form tin vacancy defects and poor perovskite film quality, caused by the rapid crystallization rate in tin-based perovskite solar cells (PSCs), their efficiency lags far behind that of lead-based PSCs. To improve the photovoltaic (PV) performance and stability of FA0.9PEA0.1SnI3-based PSCs (T-PSCs), a small amount of Pb(SCN)2 is introduced into a perovskite precursor as an antioxidant, and acetaminophen (ACE) with various functional groups is used to modify a poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/perovskite interface. The results show that the Pb(SCN)2 additive and ACE interfacial modification can not only optimize energy level alignment in T-PSCs but also inhibit Sn2+ oxidation to reduce the trap-state density, resulting in promoted carrier transport. The synergetic effect of the Pb(SCN)2 antioxidant and ACE interfacial modification significantly reduces nonradiative recombination and improves the PV performance and stability of T-PSCs. Consequently, the unsealed T-PSCs with the Pb(SCN)2 additive and ACE modification achieve a champion efficiency of 12.04% and maintain 99% of their initial PCE after being stored in N2 for more than 2100 h, while reference T-PSCs demonstrate a champion PCE of 6.20% and retain only 72% of its initial PCE. Moreover, the modified T-PSCs without encapsulation demonstrate much better stability in humid air.

The synergetic effect of economic complexity and governance on quality of life: policy thresholds

This study aims to bridge the empirical research gap in governance-modulating effects on the link between a country’s productive structure and individuals’ well-being. In doing so, this study utilizes the economic complexity index to quantify a country’s productive structure and the social progress index to measure quality of life. The empirical strategy relies on the system-GMM approach, covering 75 developing countries from 2011 to 2021. The following conclusions were drawn from the empirical analysis. (1) Economic complexity and governance consistently and unconditionally improve quality of life. (2) Governance substantially modulates economic complexity to enhance quality of life, generating an overall positive net effect. (3) The results remain robust and consistent across several GMM specifications, regardless of whether the six governance indicators compiled by the World Bank were clustered using principal component analysis into four categories (i.e., general, political, economic, and institutional) or used individually. (4) Of the six governance indicators, government effectiveness, the rule of law, and control of corruption were found to be particularly significant, as were economic and institutional governance. (5) An additional threshold analysis was implemented to identify the critical governance levels that further improve quality of life. The thresholds for complementary policies are then established as follows: 0.8435, 1.846, and 1.717 for government effectiveness, rule of law, and corruption control, respectively, and 5.59, 3.14, and 3.32 for general, institutional, and economic governance, respectively. Consequently, economic complexity and governance are necessary and sufficient to improve well-being below these thresholds. Complementary policies are, however, necessary to sustain the overall positive impact beyond these thresholds. The findings of this study provide insights into complementary policies for leveraging economic development to improve the well-being of developing countries.

Bismuth doped g-C3N4 composites for enhanced photocatalytic degradation of ciprofloxacin

There is an increase in presence of various contaminants particularly related to antibiotics in the water sources affecting the environment. This study focusses on designing and development of innovative bismuth doped g-C3N4 for photocatalytic degradation of ciprofloxacin. Diverse Bi doped g-C3N4 catalysts, with metal loadings ranging from (0.5 – 2 wt%), were synthesized and characterized using advanced techniques. The introduction of Bi doped g-C3N4 drastically lowered the bandgap, with the introduction of Bi loadings. A highest ∼79% degradation was observed in 60 min using 1 wt% Bi doped g-C3N4, drastically outperforming bare g-C3N4 (∼63%). Kinetic studies were carried in the temperature range of (10 – 25°C), revealing an activation energy of 23.1 kJ/mol. Scavenging tests were carried with different additives (EDTA, IPA, AgNO3), among these lowest degradation (∼45%) was observed with EDTA which confirms that the h+ species controlling the degradation mechanism. Overall, this study reveals an improved photocatalytic activity attributed to better charge transfer and synergetic effects among Bi and g-C3N4, demonstrating the potential for pollutant removal present in wastewater.

Investigation of kinetics, reaction mechanisms, thermodynamics, and synergetic effects in co-pyrolysis of wood sawdust and linear low-density polyethylene using the thermogravimetric approach.

This study focused on investigating thermal degradation behaviors, kinetics, reaction mechanisms, synergistic effects, and thermodynamic parameters of wood sawdust (WSD), linear low-density polyethylene (LLDPE), and their blends (LW1:3, LW1:1, and LW3:1) during co-pyrolysis in a thermogravimetric analyzer (TGA). Thermal behavior exhibited a LW1:3 blend (25 wt.% LLDPE) showing significant mass loss at lower temperatures (150 to 300°C) compared to the individual feedstocks, such as 150 to 400°C and 300 to 520°C for WSD and LLDPE, respectively. The iso-conversional methods (KAS, FWO, and FM) were used to determine the kinetic parameters (Ea and A), and the activation energy drop was highest for the LW1:3 blend. According to the master plots, the third-order reaction (O3), nucleation (P2/3), and diffusional model (D4) were the predominant reaction mechanisms for the co-pyrolysis of the LW1:3, LW1:1, and LW3:1 blend, respectively. The thermodynamic parameters demonstrate that a small amount of plastic addition into WSD can improve the reactivity of the blend, shorten the reaction time, and cause less energy-intensive reactions. The values of ΔH, ΔG, and ΔS also confirmed the co-pyrolysis process's spontaneity and endothermic nature. The Fourier transforms infrared spectrometer (FTIR) spectra of raw feedstock, blends, and their biochar revealed some of the peaks were shifted, the intensity was reduced, and disappearance can happen when the temperature was increased. Using the experimental and theoretical/predicted activation energies, the parity chart illustrates the synergistic effects of co-pyrolysis of different blends, and the LW1:3 blend has a favorable synergistic impact. These results could be helpful in process optimization and designing an effective reactor system for co-pyrolysis.

Fabrication of MoS2-Fe3O4 heterostructure as an ultrafast and high-sensitivity NO2 gas sensor at room temperature

In this study, a novel MoS2-Fe3O4 heterostructure was fabricated for efficient detection of NO2 gas. The structural and morphological properties of MoS2-Fe3O4 composites were investigated by relevant characterization methods. The NO2 sensing performance of the sensor based on MoS2-Fe3O4 was tested. The result demonstrated that the MoS2-Fe3O4 sensor showed excellent performance with a high response of 25 and a fast response time of 6 s as exposed to 5 ppm NO2 at room temperature. In addition, this sensor also exhibited high sensitivity, satisfactory selectivity, excellent moisture resistance, favorable reproducibility and long-term stability. The enhanced gas sensing performance can be attributed to the synergetic effect of the abundant oxygen vacancy and p-n heterojunction.

3D Printing-Induced Hierarchically Aligned Nanocomposites With Exceptional Multidirectional Strain Sensing Performance.

High-performance sensors capable of detecting multidirectional strains are indispensable to understand the complex motions involved in flexible electronics. Conventional isotropic strain sensors can only measure uniaxial deformations or single stimuli, hindering their practical application fields. The answer to such challenge resides in the construction of engineered anisotropic sensing structures. Herein, a hierarchically aligned carbon nanofiber (CNF)/polydimethylsiloxane nanocomposite strain sensor is developed by one-step 3D printing. The precisely controlled printing path and shear flow bring about highly aligned nanocomposite filaments at macroscale and orientated CNF network within each filament at microscale. The periodically orientated nanocomposite filaments along with the inner aligned CNF network successfully control the strain distribution and the appearance of microcracks, giving rise to anisotropic structural response to external deformations. The synergetic effect of the multiscale structural design leads to distinguishable gauge factors of 164 and 0.5 for applied loadings along and transverse to the alignment direction, leading to an exceptional selectivity of 3.77. The real-world applications of the hierarchically aligned sensors in multiaxial movement detector and posture-correction device are further demonstrated. The above findings propose new ideas for manufacturing nanocomposites with engineered anisotropic structure and properties, verifying promising applications in emerging wearable electronics and soft robotics.

Scalable Layer-Controlled Oxidation of Bi2O2Se for Self-Rectifying Memristor Arrays With sub-pA Sneak Currents.

Smart memristors with innovative properties are crucial for the advancement of next-generation information storage and bioinspired neuromorphic computing. However, the presence of significant sneak currents in large-scale memristor arrays results in operational errors and heat accumulation, hindering their practical utility. This study successfully synthesizes a quasi-free-standing Bi2O2Se single-crystalline film and achieves layer-controlled oxidation by developing large-scale UV-assisted intercalative oxidation, resulting β-Bi2SeO5/Bi2O2Se heterostructures. The resulting β-Bi2SeO5/Bi2O2Se memristor demonstrates remarkable self-rectifying resistive switching performance (over 105 for ON/OFF and rectification ratios, as well as nonlinearity) in both nanoscale (through conductive atomic force microscopy) and microscale (through memristor array) regimes. Furthermore, the potential for scalable production of self-rectifying β-Bi2SeO5/Bi2O2Se memristor, achieving sub-pA sneak currents to minimize cross-talk effects in high-density memristor arrays is demonstrated. The memristors also exhibit ultrafast resistive switching (sub-100ns) and low power consumption (1.2 pJ) as characterized by pulse-mode testing. The findings suggest a synergetic effect of interfacial Schottky barriers and oxygen vacancy migration as the self-rectifying switching mechanism, elucidated through controllable β-Bi2SeO5 thickness modulation and theoretical ab initio calculations.

Synergetic effects of chlorinated paraffins and microplastics on microbial communities and nitrogen cycling in deep-sea cold seep sediments

Chlorinated paraffins (CPs) and microplastics (MPs) are commonly found in deep-sea cold seep sediments, where nitrogen cycling processes frequently occur. However, little is known about their combined effects on sedimentary microbial communities and nitrogen cycling in these environments. This study aimed to investigate the synergistic impacts of CPs and MPs on microbial communities and nitrogen cycling in deep-sea cold seep sediments through microcosm experiments. Our results demonstrated that the presence of CPs and MPs induced significant alterations in microbial community composition, promoting the growth of Halomonas. Furthermore, CPs and MPs were found to enhance nitrification, denitrification and anammox processes, which was evidenced by the higher abundance of genes associated with nitrification and denitrification, as well as increased activity of denitrification and anammox in the CPs and MPs-treatment groups compared to the control group. Additionally, the enhanced influence of CPs and MPs on denitrification was expected to promote nitrate-dependent and sulfate-dependent anaerobic oxidation of methane, thereby resulting in less methane released into the environment. These findings shed light on the potential consequences of simultaneous exposure to CPs and MPs on biogeochemical nitrogen cycling in deep-sea cold seep sediments.