Low Resistance Research Articles

Impact of Light on Coexistence of Memresistance, Meminductance, and Memcapacitance (MEMRIC) in Nanostructured Copper Oxide (CuO) based Random Access Memory Devices.

We demonstrated the coexistence of memresistance, memcapacitance, and meminductance non-volatile bipolar analog resistive switching in Cu (top electrode)/CuO (active layer)/ SS (bottom electrode) memory devices with and without the presence of the light. The onset of memcapacitance and meminductance is noticed from the pinched-shaped characteristics in the first and third quadrants. The variation in the scan rate also impacts the coexistence characteristics by shifting the intercept point for low resistance (LRS) and high resistance (HRS) states in positive and negative biasing voltages. The durability and retention are measured over a period of 150 cycles and 1500 s with and without light illumination. The Weibull slope for set/reset state with and without light are 106.80/114.23 and 70.21/102.25, respectively, suggesting that stability of the device increases with light illumination. Interestingly, the memcapacitance disappears after 600 cycle and after 60 . The double logarithmic I-V characteristics suggest the trap assisted conduction (higher slope > 2) in the higher external electric field, and Ohmic behaviour in the lower applied field region. Thus, the present study provides a way for low power electronics and photoresistors together with memresistance, memcapacitance, and meminductance, simultaneously, i.e., MEMRIC in a single device.

A General Strategy toward Enhanced Electrochemical and Mechanical Performance of Solid‐State Lithium Batteries through Constructing Covalently Bonded Electrode Materials/Electrolyte Interfaces

AbstractSolid‐state lithium batteries (SSLBs) offer inherent safety and high energy density for next‐generation energy storage, but the large interfacial resistance and poor physical connection between electrode materials and the solid electrolyte (SE) severely impede their practical applications. This work reports a general strategy to introduce covalent bonds between electrode materials and SE, not only reducing interfacial resistance but also enhancing electrochemical stability and mechanical robustness of SSLBs. The covalent bonding is accomplished by functionalizing electrode surfaces with C═C groups, enabling in situ copolymerization with telechelic polymers in the SE. This approach is applicable to various cathode/anode materials and SEs. Particularly, the SSLBs comprising LiFePO4 cathode, Li6.75La3Zr1.75Ta0.25O12/(polyethylene oxide (PEO)/lithium bis(trifluoromethylsulfonyl)imide (LiTFSI)/silk composite SE and metallic lithium anode exhibit a specific capacity of 158.4 mAh g−1 and can be cycled at 2 C for 2200 times with >80% retention. Additionally, the SSLBs containing the high nickel‐content LiNi0.96Co0.03Mn0.01O2 cathode can afford a high specific capacity of 201.8 mAh g−1. Comprehensive experimental examination and theoretical simulations confirm that the lowered interfacial resistance and intimately contacted electrode materials/electrolyte interfaces facilitate Li+ transport at different stages of charge. Furthermore, the covalently bonded electrode/electrolyte interfaces also endow SSLBs with outstanding mechanical stability, enabling flexible SSLB pouch cells to operate under various bending states without performance decay.

Impact of c- and m- sapphire plane orientations on the structural and electrical properties of β-Ga2O3 thin films grown by metal-organic chemical vapor deposition

Abstract This work presents a comprehensive investigation into the structural and electrical properties of Ga2O3 thin films grown via metal-organic chemical vapor deposition on both c- and m-plane sapphire substrates. Structural characterization revealed the β-Ga2O3 phase formation in both substrate orientations, with strong epitaxial (-201) preferential growth on c-plane substrates and polycrystalline films on m-plane substrates. Results show that Ga2O3/m-sapphire exhibits the lower electrical resistivity than its counterpart grown on c-sapphire. Activation energies of acceptor levels were estimated at ∼1.4 eV and ∼ 0.7 eV, for Ga2O3 films grown on c- and m-plane, respectively. This result shows that growing Ga2O3 on m-plane sapphire is beneficial to reach a weakly compensated sample. Cathodoluminescence analysis suggests that the additional low activation energy of ∼0.18 eV observed in Ga2O3 grown with the highest oxygen flow on m-plane sapphire can be associated to thermally-induced migration of self-trapped hole states.

Hydrodeoxygenation of Isoeugenol-derived Model Compound over Carbon-supported Pt and Pt-SnS Catalysts for the Production of Sustainable Jet Fuel.

This study focuses on the sustainable production of bio-jet fuel through the catalytic hydrodeoxygenation (HDO) of isoeugenol (IE). Properties of two spraying synthesis methods (in situ and ex situ metal doping) with different platinum (Pt) loading percentages. The catalyst was characterised using various techniques such as XAS, X-ray photoelectron spectroscopy, X-ray diffraction, high-resolution transmission electron microscopy (HRTEM), field-emission scanning electron microscopy (FESEM) and thermogravimetric analysis. The HRTEM and FESEM results show the successful preparation of a spherical nanoparticle doped over activated carbon, and Pt was dispersed on the outer shell of the particles. The catalytic HDO of IE showed a high yield and conversion as follows: IE conversion of 100%, liquid-phase mass balance of 95.92%, dihydroeugenol conversion of 99.32%, propylcyclohexane yield of 88.94% and HYD yield of 76.19%. Moreover, the catalyst exhibited high reusability with low metal leaching and high coke resistance for 10 cycles. The catalyst was evaluated in a continuous flow reactor for 100 h at different reaction temperatures, and interestingly, the catalyst showed low deactivation with a high half-time.

Numerical investigation of the impact of inlet and outlet ports of water jet impingement cooling modules

AbstractThe ever‐growing applications of high‐power chips have driven research efforts to enhance the performance of their active cooling modules. This study proposes a simple tweak of the cooling module's ports for lower thermal resistance. A dual‐inlet single‐outlet (CP2) jet impingement cold plate (JICP), a dual‐inlet dual‐outlet (CP3) JICP, and a single‐inlet dual‐outlet (CP4) JICP were assessed computationally and benchmarked against a single‐inlet single‐outlet JICP (CP1) at the same area ratio (AR) and average diameter (Davg) of inlet and outlet ports. The results show that the pressure losses inflate by up to 4.67 folds when using CP3 with AR = 5/3 and Davg = 3.0 mm. Yet, this design also shows the largest Nusselt number and the lowest outlet water temperature, module body temperature, average temperature of the target surface, and thermal resistance (0.07415 K/W). The thermal resistance is reduced by 34.13% using CP3 at AR = 3/5 and Davg = 6.0 mm. The temperature uniformity index was boosted to 97.5%. These enhancements are attributed to the shorter and symmetric flow path, the shorter residence time of water within the JICP, and the direct heat diffusion by the walls of the lower chamber.

Microstructure and corrosion properties of Al1-xWxN coatings for potential use in gas turbine blades

Herein, a numerical approach of Al1-xWxN thin film coatings on Inconel 738LC superalloys for thermal barrier applications has been studied and the experimental analysis includes deposition of Al1-xWxN films on Si (100), glass and transparent quartz substrates at 40 % N2 flow rate using a dual target DC reactive magnetron sputtering technique to investigate the morphology, microstructure, chemical bonding and corrosion behaviour. AFM analysis revealed the rms roughness, Sq and average roughness, Sa increased with the increasing W content from 22 to 70 at.%. It was found that Al1-xWxN films tend to form tiny valleys on the film surface because the values of surface skewness, Ssk lie below zero. The TEM image showed a branched snowflake structure for the specimen of Al0.58W0.42N films with discrete spots in the SAED pattern, confirming the microcrystalline nature. The blue-shifting of Ecorr towards positive potential confirmed the lower corrosion resistance of WN films than those of AlN. XRD spectra of Al0.58W0.42N films showed an amorphous nature devoid of peaks, which is also confirmed by the SAED pattern. The quasi-passive oxide layer formation was spontaneous for WN films compared to the AlN films. The bending vibrations of AlN and WN showed the coordination environment of the metal centre in the Al1-xWxN films. The computational results indicated that the thermal barrier properties of Al1-xWxN films decreased with the increasing W content, i.e., AIN > Al0.58 W0.42N > WN.

Promotion of aromatic amino acids of extracellular polymeric substance targeted transformation via sulfite mediated iron redox cycling in sludge solid-liquid separation

Highly hydrophilic extracellular polymeric substance (EPS) with gel-like structure seriously plagues the development of sludge deep dewatering. Oxysulfur radicals-based oxidation driven by iron-bearing mineral proposes a promising strategy for effective EPS decomposition. However, the transformation and involved interaction mechanisms of aromatic proteins are still controversial due to the complex EPS structure. Herein, sulfite mediated siderite (denoted as Fe(II)/S(IV)) was developed for targeted transformation aromatic amino acids in EPS oxidation to strengthen sludge solid-liquid separation. The enhanced sludge dewaterability were benefited from the Fe(II)/S(IV) bonded interaction assisted by Fe3+/Fe2+ as redox interface that facilitating the release of intracellular bound water via diminish the hydrophily and bind strength with solid protons. The amide region nitrogen of aromatic amino acids (especially tyrosine and tryptophan) originating from EPS presented looser structure and lower spatial site resistance, which were attributed to the exposure of hydrophobic sites in amino groups after Fe(II)/S(IV) treatment. Furthermore, the effective decline of aromatic amino acids in inner layer-EPS (loosely bound EPS and tightly bound EPS) was directed from Fe-N targeted interaction by triggering a series of sulfate-based radical chain reactions. The good correlation between electron transfer amount (R2 = 0.926) and Fe-N (R2 = 0.925) with bonding interaction demonstrated that the complexation of aromatic amino acids with Fe sites on siderite/sulfite via Fe-N bonds, accounting for efficient sludge solid-liquid separation. This study deepens the understanding of sludge organic matter targeted transformation and provides a tactic for iron-based conditioning of sludge.

Theoretical study of solidification phase change heat and mass transfer with thermal resistance and convection subjected to a time-dependent boundary condition

The solidification of phase-change materials (PCMs) is a key process that occurs commonly in materials science and metallurgy, such as in the casting of alloys and energy management systems. There is a lot of literature in this area that assumes the PCMs are in close contact with the heat source or sink. However, a non-freezing wall frequently encloses them in practical situations. This work presents a phase change problem that describes the solidification of a semi-infinite PCM with thermal resistance. We assume that time-dependent heat flux drives the solidification process. The PCM first convert into mush and then into solid, which leads to a three-region problem. The current study accounts for both conduction as well as convection heat transfer mechanisms. Unfortunately, the exact solution to such problems with time-dependent flux-type boundary conditions may not be possible. Thus, there is considerable interest in deriving the analytical solution. The space–time transformation yields the analytical solution to the problem. A numerical example of Al−Cu alloy with 5%Cu is presented to demonstrate the current study. Thermal resistance shows a pronounced impact on the temperature field. Lower thermal resistance offers faster solidification rate. It is found that as the heat transfer constant increases, the rate of propagation of solid-mush and mush-solid interfaces gets enhanced. In addition, the growth of thermal resistance is of linear nature, with variation in the value of Q. The solidified region has higher concentration than the mush region. The current study is applicable to both eutectic systems and solid solution alloys.

A practical method for the in-situ estimation of the effective thermal resistance of gas diffusion layers in PEMFC

The membrane electrode assembly of a PEM fuel cell is hotter than the gas feeding plates because heat is generated within it, and the diffusion layers are thermally resistive. The temperature gradient created, which increases as a function of the current density, is useful for evacuating the water produced in vapor form. This water transport mechanism is known as the “heat pipe effect”. The temperature gradient produces a saturation vapour pressure gradient, which in turn produces a diffusive vapor flow. Mastering water management, coupled with heat management, requires knowledge of the temperature of the MEA and therefore the effective thermal resistance of the diffusion layers. In this paper, we present an original method for estimating this thermal resistance in situ, without using heat flux sensors or directly measuring the temperature of the MEA. The method requires the ability to impose a temperature gradient between the anode and cathode plates, and to perform a hot-side water balance. Thermal resistance is deduced from the coupling between heat and water transfer. Two diffusion layers widely used by the community are tested. The GDL Sigracet 22 BB (from SGL Carbon) has a lower effective thermal resistance than the GDL Freudenberg H15C14. Variations in these thermal resistances are measured as a function of the temperature gradient imposed and of the compression ratio.

Compost incorporation and wildflowers introduction for stormwater infiltration and erosion-control vegetation cover establishment in post-construction landscapes

Urban and suburban development frequently disturbs and compacts soils, reducing infiltration rates and fertility, posing challenges for post-development vegetation establishment, and contributing to soil erosion. This study investigated the effectiveness of compost incorporation in enhancing stormwater infiltration and vegetation establishment in urban landscapes. Experimental treatments comprised a split-split plot design of vegetation mix (grass, wildflowers, and grass-wildflowers) as main plot, ground cover (hydro-mulch and excelsior) as subplot, and compost (30% Compost and No-Compost) as sub-subplot factors. Wildflower inclusion was motivated by their recognized ecological benefits, including aesthetics, pollinator habitat, and deep root systems. Vegetation cover was assessed using RGB (Red-Green-Blue) imagery and ArcGIS-based supervised image classification. Over a 24-month period, bulk density, infiltration rate, soil penetration resistance, vegetation cover, and root mass density were assessed. Results highlighted that Compost treatments consistently reduced bulk density by 19–24%, lowered soil penetration resistance to under 2 MPa at both field-capacity and water-stressed conditions, and increased infiltration rate by 2–3 times compared to No-Compost treatments. Vegetation cover assessment revealed rapid establishment with 30% compost and 60:40 grass-wildflower mix, persisting for an initial 12 months. Subsequently, all treatments exhibited similar vegetation coverage from 13 to 24 months, reaching 95–100% cover. Compost treatments had significantly higher root mass density within the top 15 cm than No-Compost, but compost addition did not alter the root profile beyond the 15 cm depth incorporation depth. The findings suggest that incorporating 30% compost and including a wildflower or grass-wildflower mix appears to be effective in enhancing stormwater infiltration and provides rapid erosion control vegetation cover establishment in post-construction landscapes.

Development of carbon dots supported on Zr-MOFs nano-composites for effective oxygen evolution reaction

Efficient hydrogen generation from water splitting is a key component of the hydrogen economy. It has been extensively researched for decades how electrochemically splitting water using electrocatalysts might provide a sustainable and environmentally friendly hydrogen energy source. Sluggish kinetics of the oxygen evolution reaction (OER) hinders the process of overall water splitting. Although metal-organic frameworks (MOFs) are attractive for generation of effective OER electrocatalysts, their activity is significantly hindered by their inherent lower conductivity. Here, we demonstrate a Zr-MOF-based composite with carbon dots (CDs) in order to increase their OER activity. Its exceptional morphology with higher porosity and greater surface area results in enhanced electrochemical activity. It reveals tremendously low onset potential, i.e., 1.40 V vs. RHE, and a remarkably small overpotential of 1.45 V vs. RHE to attain benchmark current density. It exhibited a minimal Tafel value of 37 mV/dec, conquering state-of-the-art catalysts for OER. The fabricated electrocatalyst demonstrated a lower charge transfer resistance (Rct) of 0.248 Ω, with exceptional durability for about 20 h in chronoamperometric studies and for up to 1500 CV cycles. All these results demonstrated that as-fabricated Zr-MOF-based composite is a probable and potential candidate for OER.

Bio-functionalized conductive poly(acrylic acid):poly(3,4-Ethylenedioxythiophene)-Prussian blue hybrid transducer for biosensors and bioelectronics interfaces

This study presents an innovative organic-inorganic hybrid transducer of poly(acrylic acid) (PAA), poly(3,4-ethylenedioxythiophene) (PEDOT) and Prussian blue (PB) nanocatalysts. The transducer demonstrated functionality conducive to enzyme conjugation and exhibited favorable electrochemical properties for biosensor signal transduction. Fabricated by a one-tube chemical redox method, the PAA:PEDOT-PB transducer showed long-term electrocatalytic and structural stability. The performance of the transducer was characterized by high transduction activity and low charge transfer resistance, particularly for H2O2 reduction. It achieves a linear detection range from 1.0 μM to 4.0 mM, with a sensitivity of 494±10 μA mM−1 cm‒1 and an LOD of 0.34 μM. The PAA:PEDOT-PB transducer featured a high density of carboxyl groups (DCOOH = 14.64±0.05 μmol cm-2) that promoted the immobilization of the H2O2-dependent oxidase enzyme lactate oxidase (LOx) with an EDC/S–NHS coupling agent. The LOx-PAA:PEDOT-PB transducer was developed for lactate biosensing. The transducer provided high LOx-enzyme affinity (KMapp = 1.47±0.05 mM), and a rapid response time (10 s) for lactate detection across a concentration range of 5.0 μM to 4.0 mM, showing a sensitivity of 223±3 μA mM‒1 cm‒1 and an LOD of 1.45 μM. The LOx-PAA:PEDOT-PB transducer was integrated with a flexible screen-printed electrode, incorporating a wireless, battery-free near field communication potentiostat module to measure lactate in artificial sweat on a skin model via smartphone. The PAA:PEDOT-PB transducer could enable connections with multiple bio-recognition molecules through polycarboxylic acid groups, providing potential avenues for the development of advanced biosensors.

Enhancing electrical insulation and thermal conductivity in polydimethylsiloxane polymer nanocomposites through silica coating on carbon fibers

Mesophase pitch-based carbon fibers (MPCFs) exhibit high thermal conductivity (∼900Wm-1K-1) and are considered to be an important candidate for future thermal management. However, MPCFs lead to an increase in the electrical conductivity of nanocomposites due to the low volume electrical resistivity (∼10-3 Ω·cm). The development of MPCFs nanocomposites with high thermal conductivity and good electrical insulation remains a challenging problem. In order to solve the problem, we utilized the surfactant cetyltrimethylammonium bromide (CTAB) as an anchor for hydrolysis, and employed a sol-gel method to deposit a silica coating on MPCFs (silica@MPCFs). Silica@MPCFs was used as the filler for polydimethylsiloxane (PDMS) matrix. The nanocomposites exhibit commendable thermal conductivity (achieving 1.52 Wm-1K-1) and excellent volume electrical insulation (exceeding 1013 Ω·cm) at a 30vol% concentration. Notably, both the thermal conductivity and volume electrical insulation exceed MPCFs/PDMS. This approach to electrical insulation treatment holds substantial potential for the future preparation of high-performance nanocomposites of electronic devices.

Enhanced Ultraviolet Photodetection with Ag Nanoparticle-Decorated ZnO Nanowires and Core-Shell Electrodes

Our study presents the synthesis and characterization of one-dimensional (1-D) zinc oxide (ZnO) nanorod (NR) arrays via low-temperature hydrothermal synthesis, followed by surface modification with silver nanoparticles (Ag NPs). Silver nanowires (AgNWs) are potential alternatives to indium-tin oxide, but their poor stability in atmospheric conditions poses a challenge. To address this, we developed ultrathin Ag/ZnO core-shell structured nanowire networks for ultraviolet-photodetectors (UV-PDs). This cost-effective solution process yielded high transmission (77%) and low sheet resistance (8.3 Ω/sq). We comprehensively investigated surface morphology, crystalline nature, elemental composition, optical properties, and electrical performance of both synthesized nanorod arrays and NW networks. The UV photodetector exhibited a rise time of approximately 1.35 seconds and a decay time of 8.01 seconds, both faster than pristine AgNW electrodes. Additionally, the dark current decreased from 9 nA to 3.5nA after incorporating Ag/ZnO, accompanied by a significant improvement in photocurrent. These results highlight a promising approach for high-performance UV photodetectors, leveraging the stability and conductivity of Ag/ZnO core-shell NW networks.

An efficient electrode for reversible oxygen reduction/evolution and ethylene electro-production on protonic ceramic electrochemical cells

Protonic ceramic electrochemical cells (PCECs) have demonstrated great promise for applications in the generation of electricity, and the synthesis of chemicals (for example, ethylene). However, enhancing the electrochemical reactions kinetics and stability of PCECs electrodes is one grand challenge. Here, we present a novel electrode material via a co-doping of cesium (Cs) and niobium (Nb) on PrBaCo2O6−δ with the composition of PrBa0.9Cs0.1Co1.9Nb0.1O6−δ (PBCCN), which naturally decomposes into dual phases of a double-perovskite PBCCN (DP-PBCCN, ∼92.3 wt%) and a single-perovskite Ba0.9Cs0.1Co0.95Nb0.05O3−δ (SP-BCCN, ∼7.7 wt%) under typical powder processing conditions. PBCCN exhibits a low area-specific resistance (ASR) value of 0.107 Ω cm2, an outstanding performance of 2.04 W cm−2 in fuel cell (FC) mode, a current density of −2.84 A cm−2 at 1.3 V in electrolysis cell (EC) mode, and promising reversible operational durability of 53 cycles in ∼212 h at +/− 0.5 A cm−2 and 650 oC. Cs doping generates more oxygen vacancies and accelerates the oxygen exchange kinetics, while Nb doping effectively enhances the stability, as illustrated by the analyses of X-ray photoelectron spectroscopy, and electrical conductivity relaxations. When applied as the positrode for electrochemical non-oxidative dehydrogenation of ethane (C2H6) to ethylene (C2H4) on PCECs, it displays an encouraging C2H6 conversion of 12.75% and a C2H4 selectivity of 98.4% at 1.2 V.

Treatability of odorous dioxanes/dioxolanes in source water: How does molecular flexibility and pre-oxidation affect odorant adsorption

Odorous dioxanes and dioxolanes, a class of cyclic acetals often produced as byproducts in polyester resin manufacturing, are problematic in drinking water treatment due to their low odor thresholds and resistance to conventional treatment technology. Our research focuses on the removal of ten dioxane/dioxolane compounds through oxidation and adsorption processes, exploring the key molecular properties that govern the treatmentability. We discovered that both chlorination and permanganate oxidation were largely ineffective at degrading cyclic acetals, achieving less than 20% removal even at high applicable doses. Conversely, powdered activated carbon (PAC) adsorption proved to be a more effective method, with a removal of > 90% at a PAC dosage of 10 mg/L for seven out of ten compounds. The presence of natural organic matter (NOM) reduced PAC adsorbability for all odorants, but the deterioration level substantially varied and mostly affected by structural flexibility as indicated by the number of rotatable bonds. The results of both the experimental investigation and molecular simulation corroborated the hypothesis that more rotatable bonds (from one to three here) are indicative of greater structural flexibility, which in consequence determines the susceptibility of cyclic acetals to NOM competitive adsorption. Increased structural flexibility could facilitate greater entry into silt-like micropores or achieve preferential adsorption sites with more compatible morphology against NOM competition. When pre-oxidation (chlorination and permanganate oxidation) and adsorption were applied sequentially, additional low molecular weight NOM components produced by pre-oxidation resulted in intensified NOM competition and decreased odorant adsorbability. If this combination is inevitably required for algae and odorant control, it would be beneficial to utilize a wise screen for oxidants and a reduced oxidant dose (less than 2 mg/L) to mitigate the deterioration of odorant adsorption. This study elucidates the roles of structural flexibility in influencing the treatability of dioxanes and dioxolanes, extending beyond the solely well-established effects of hydrophobicity. It also presents rational practice guidelines for the combination of pre-oxidation and adsorption in addressing odor incidents associated with dioxane and dioxolane compounds.

3D Hydrophobic Wood Membrane with Micro-nano Baffle Structure for Multifunctional Air Purification Filters: “Kill three eagles with one arrow”

Air pollution has presented an imminent threat to the world. Multifunctional filters with high filtration efficiency, low pressure drop, moisture resistance, antibacterial properties, and renewability are urgently needed to be developed. In this study, multifunctional wood filters are innovatively designed with a baffle structure combining macroscopic structural design and microscopic in-situ synthesis of silver nanoparticles (Ag NPs). The filter has excellent particle removal efficiency (PM0.3, 98.5%), exceptional volatile organic compounds (VOCs) adsorption efficiency (98.4% for formaldehyde and 91.7% for xylene), high sterilization efficiency (99.99%) and excellent regeneration ability (performance recovery to 98% of the initial). Furthermore, personal protective masks were assembled by the prepared filters, whose process of replacing element is as simple as replacement of electric mosquito incense tablets. This innovative filter holds promise for applications such as daily protection, sudden accidents and prevention and control of respiratory infectious diseases. We envision that the functionally modified Ag NPs wood filters with a multilayer structure offer a comprehensive solution for more effective air purification in polluted environment.

Designing and additive manufacturing of biomimetic interpenetrating phase zirconia-resin composite dental restorations with TPMS structure

Zirconia and resin are the most commonly utilized materials in dental restorations. However, zirconia presents significant wear on opposing teeth, whereas resin materials have low wear resistance and mechanical performances. A zirconia-resin interpenetrating phase composite (IPC) dental restoration was designed and fabricated using 3D printing and vacuum infiltration processes, incorporating zirconia scaffolds with triply periodic minimal surfaces (TPMS) structures. The mechanical and tribological performances of the IPCs were investigated through compressive and tribological experiments and finite element analysis, elucidating the influence of zirconia volumetric fraction. Results showed that IPCs exhibit excellent mechanical and tribological compatibilities, which can reduce the damage and wear of the antagonistic teeth. This designing and manufacturing strategy enables the IPC restorations with promising applications in dentistry.

Fucoidan from Sargassum hemiphyllum (Turner) C. Agardh inhibits human hepatoma cell (HepG2) through cell cycle arrest and apoptotic induction

Cancer has become one of the most serious diseases threatening human health, while traditional chemotherapeutic drugs have serious side effects. Drugs of marine origin have attracted many scholars due to their remarkable effectiveness, low drug resistance and low adverse reactions. In this study, the fucoidan DF1 and DF2 extracted from Sargassum hemiphyllum (Turner) C. Agardh were used to explore their effects on induced HepG2 hepatoma cell apoptosis and their relevant molecular mechanisms of apoptosis in HepG2 cells were analyzed by flow cytometry and western blotting assay. DF1 and DF2 could induce excess intracellular reactive oxygen species (ROS) production in HepG2 cells and lead to stimulation of the mitochondrial apoptotic pathway, up-regulate the protein expressions of Bax, Cytochrome C and Cleaved-Caspase-3/8, and down-regulate the protein expressions of Bcl-2 and Caspase-3/8/9. Meanwhile, DF1 and DF2 could induce HepG2 cell cycle arrest in the S-phase and up-regulate the protein expression of p21, and down-regulate the expression of Cyclin A and CDK2. This study provides a scientific basis for the development of VC/H2O2-treated fucoidans as anticancer drugs or adjuvant drugs.

Fabrication of Low-Emissivity Glass with Antibacterial Properties by Coating Cu/AZO Thin Films

This study explores the feasibility of using Cu/AZO thin films as low-emissivity materials with antibacterial properties, fabricated using the linear sputtering method. The linear sputtering technique deposits thin films onto continuous substrates, offering high throughput, uniform coatings, and precise control over film properties. In this research, Cu/AZO thin films underwent either vacuum annealing or hydrogen plasma annealing treatments. The Cu layer imparts antibacterial properties, while the AZO layer primarily provides thermal insulation. Experimental results show that annealing treatments enhance both photoelectric performance and antibacterial capability. Annealed Cu/AZO films exhibit lower resistivity and emissivity. Among the samples, those subjected to vacuum annealing at 400 °C are most suitable for low-emissivity applications, with an average visible light transmittance of 60%, an emissivity of 0.16, and an antibacterial activity value of 8.8. The Cu/AZO films proposed in this study effectively combine antibacterial and thermal insulation properties, making them relevant for the field of green materials.