Environmentally friendly and waste-free production of photocatalytic filters involving spark ablation and calcination processes for enhanced and durable photocatalytic performance.

The coating of filter media with silver is typically achieved by chemical deposition and aerosol processes. Whilst useful, such approaches struggle to provide uniform coating and are prone to blockage. To address these issues, an in situ method for coating glass fibers is presented via the dopamine-mediated electroless metallization method, yielding filters with low air resistance and excellent antibacterial performance. It is found that the filtration efficiency of the filters is between 94 and 97% and much higher than that of silver-coated filters produced using conventional dipping methods (85%). Additionally, measured pressure drops ranged between 100 and 150 Pa, which are lower than those associated with dipped filters (171.1 Pa). Survival rates of Escherichia coli and Bacillus subtilis bacteria exposed to the filters decreased to 0 and 15.7%+/- 1.49, respectively after 2 h, with no bacteria surviving after 6 h. In contrast, survival rates of E. coli and B. subtilis bacteria on the uncoated filters are 92.5% and 89.5% after 6 h. Taken together, these results confirm that the in situ deposition of silver onto fiber surfaces effectively reduces pore clogging, yielding low air resistance filters that can be applied for microbial filtration and inhibition in a range of environments. Glass fiber filter is coated via the dopamine-mediated electroless metallization method, yielding higher filtration efficiency (97%) and lower pressure drop (150 Pa) than the silver-coated filters produced by dipping method (171 Pa). Survival rates of Escherichia coli and Bacillus subtilis bacteria decreased to 0-15.7%, respectively after 2 h, with no bacteria surviving after 6 h. image

The solid electrolyte interphase (SEI) is a key component of a lithium-ion battery forming during the first few dis-/charge cycles at the interface between the anode and the electrolyte. The SEI passivates the anode-electrolyte interface by inhibiting further electrolyte decomposition extending the battery's cycle life. Insights into SEI growth and evolution in terms of structure and composition remain difficult to access. To unravel the formation of the SEI layer during the first cycles, operando electrochemical liquid cell scanning transmission electron microscopy (ec-LC-STEM) is employed to monitor in real time the nanoscale processes that occur at the anode-electrolyte interface in their native electrolyte environment [1]. The results show that the formation of the SEI layer is not a one-step process, but comprises multiple steps. The growth of the SEI is initiated at low potential during the first charge by decomposition of electrolyte leading to the nucleation of inorganic nanoparticles. Thereafter, the growth continues during subsequent cycles by forming an island-like layer. Eventually, a thick dense layer is formed with a mosaic structure composed of larger inorganic patches embedded in a matrix of organic compounds. While the mosaic model for the structure of the SEI is generally accepted, our observations document for the first time how the complex structure of the SEI is built up during dis-/charge cycling. [1] W. Dachraoui, R. Pauer, C. Battaglia, R. Erni, ACS Nano 2023, 17, 20434

Flame retardance of epoxy resins is usually imparted using suitable additives and/or properly modified curing agents. Herein, via a two-step green synthetic procedure, the chemical modification of the epoxy matrix with reactive silicon and phosphorus precursors is explored to obtain nanocomposites with intrinsic flame-retardant features. Nanoscale phase separation occurs in the first step, forming an inverse micelle system in which polar nanodomains act as nanoreactors for the hydrolysis of silanes (Si precursors), giving rise to silica lamellar nanocrystals (SLNCs). In the second step, inside the silica nanodomains, the formation of stable Si-O-P bonds occurs because the reactivity of phosphoric acid (P precursor) with the oxirane rings of the polymer chain is balanced by its tendency to diffuse into polar nanodomains. Intriguingly, the use of phosphoric acid alone in epoxy composite manufacturing leads to a wormlike morphology of the network, whereas its addition in the presence of silanes results in the formation of SLNCs with a thinner interlayer distance. The morphology of the hybrid Si/P-epoxy nanocomposites, comprising organic and inorganic co-continuous phases, can confer, through a prevalent mechanism in the condensed phase, interesting flame-retardant performances, namely, the absence of dripping during vertical burning tests, the formation of a large amount of coherent char after combustion, and a remarkable reduction (up to 27.7%) in the peak of heat release rate. The above characteristics make these nanostructured hybrid materials very promising for the manufacturing of epoxy systems with enhanced fire behavior (e.g., coatings, sealants, matrices for reinforced composites), even containing a low amount of specific flame retardants and thus keeping good viscoelastic properties.

Nanofiber membranes (NFMs) coated with noble metals are intensively researched for various applications such as wearable electronics, environmental sensors, and point of care diagnostics. To achieve the desired functionality while minimizing costs, a combination of facile coating methods and accurate microstructural designs is required, but remains elusive. Herein, novel conductive and porous membranes are designed based on a facile and scalable approach to fabricating conformally coated gold layers on electrospun PVDF fibers (Au-PVDF-NFMs) via electroless plating. The deposition of a conformal and fully interconnected gold layer with an average thickness of circa 38 nm on the surface of nanofibers is confirmed by systematic characterizations. The high-conjunction gold layers endows a high electrical conductivity to the membranes, yielding a low sheet resistance of 1.2 Ω/sq. In addition, the membranes show integrated functionalities such as hydrophobicity and gas permeability. Notably, the NFMs also show excellent mechanical durability under both stretching and bending, with negligible conductivity losses after 1000 test cycles. Thanks to these properties, the Au-PVDF-NFMs demonstrates practical suitability as gas diffusion electrodes (GDEs) for electrochemical CO2 reduction. The Au-PVDF-NFMs exhibit a substantial Faradaic efficiency towards CO, as high as ∼ 85 % at −0.7 V vs reversible hydrogen electrode (RHE), and are able to reach current densities of 100 mA cm−2 at −0.95 V versus RHE.

The solid electrolyte interphase (SEI) is a key component of a lithium-ion battery forming during the first few dischage/charge cycles at the interface between the anode and the electrolyte. The SEI passivates the anode-electrolyte interface by inhibiting further electrolyte decomposition, extending the battery's cycle life. Insights into SEI growth and evolution in terms of structure and composition remain difficult to access. To unravel the formation of the SEI layer during the first cycles, operando electrochemical liquid cell scanning transmission electron microscopy (ec-LC-STEM) is employed to monitor in real time the nanoscale processes that occur at the anode-electrolyte interface in their native electrolyte environment. The results show that the formation of the SEI layer is not a one-step process but comprises multiple steps. The growth of the SEI is initiated at low potential during the first charge by decomposition of the electrolyte leading to the nucleation of inorganic nanoparticles. Thereafter, the growth continues during subsequent cycles by forming an island-like layer. Eventually, a dense layer is formed with a mosaic structure composed of larger inorganic patches embedded in a matrix of organic compounds. While the mosaic model for the structure of the SEI is generally accepted, our observations document in detail how the complex structure of the SEI is built up during discharge/charge cycling.

The crystallization behavior of lipids is relevant in many fields such as adipose tissue formation and regeneration, forensic investigations and food production. Using a lipid model system composed of triacylglycerols, we study the formation of crystalline structures under laminar shear flows across various length scales by polarized light-, scanning electron-, and atomic force microscopy, as well as laser diffraction spectroscopy. The shear rate during crystallization γ̇cryst influences the acyl-chain length structure and promotes domain growth into the flow direction thereby transforming the crystallites from oblate into prolate particles. Concentration dependent aggregation of crystallites into clusters is the rate limiting step for floc and floc network formation. At high γ̇cryst, fast crystallite cluster formation at smaller equilibrium diameters is promoted. The high crystallite cluster concentration induces their aggregation into flocs which form weak networks. At low γ̇cryst, floc generation is limited by the low amount of crystallite clusters leading to slow growth of larger flocs and forming of strong networks. The findings in this work have potential implications ranging from the design of injectable soft tissue fillers for adipose tissue regeneration, to the crystalline network formation in microorganism derived lipids, up to a more energy-efficient production of chocolate confectionery.

Inspired by the solar-light-driven oxygen transportation in aquatic plants, a biomimetic sustainable light-driven aerogel pump with a surface layer containing black manganese oxide (MnO2) as an optical absorber is developed. The flow intensity of the pumped air is controlled by the pore structure of nanofilbrillated cellulose, urea-modified chitosan, or polymethylsilsesquioxane (PMSQ) aerogels. The MnO2-induced photothermal conversion drives both the passive gas flow and the catalytic degradation of volatile organic pollutants. All investigated aerogels demonstrate superior pumping compared to benchmarked Knudsen pump systems, but the inorganic PMSQ aerogels provide the highest flexibility in terms of the input power and photothermal degradation activity. Aerogel light-driven multifunctional gas pumps offer a broad future application potential for gas-sensing devices, air-quality mapping, and air quality control systems.

Epoxy nanocomposites containing Mg(OH)2 nanocrystals (MgNCs, 5.3 wt %) were produced via an eco-friendly “solvent-free one-pot” process. X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and thermogravimetric analysis (TGA) confirm the presence of well-dispersed MgNCs. HRTEM reveals the presence also of multisheet-silica-based nanoparticles and a tendency of MgNCs to intergrow, leading to complex nanometric structures with an intersheet size of ∼0.43 nm, which is in agreement with the lattice spacing of the Mg(OH)2 (001) planes. The synthesis of MgNCs was designed on the basis of a mechanism initially proposed for the preparation of multisheet-silica-based/epoxy nanocomposites. The successful “in situ” generation of MgNCs in the epoxy via a “solvent-free one-pot” process confirms the validity of the earlier disclosed mechanism and thus opens up possibilities of new NCs with different fillers and polymer matrix. The condition would be the availability of a nanoparticle precursor soluble in the hydrophobic resin, giving the desired phase through hydrolysis and polycondensation.

Uniformly distributed silica/epoxy nanocomposites (2 and 6 wt.% silica content) were obtained through a "solvent-free one-pot" process. The inorganic phases were obtained through "in situ" sol-gel chemistry from two precursors, tetraethyl orthosilicate (TEOS) and (3-aminopropyl)-triethoxysilane (APTES). APTES acts as a coupling agent. Surprisingly when changing TEOS/APTES molar ratio (from 2.32 to 1.25), two opposite trends of glass transformation temperature (Tg) were observed for silica loading, i.e., at lower content, a decreased Tg (for 2 wt.% silica) and at higher content an increased Tg (for 6 wt.% silica) was observed. High-Resolution Transmission Electron Microscopy (HRTEM) showed the formation of multi-sheet silica-based nanoparticles with decreasing size at a lower TEOS/APTES molar ratio. Based on a recently proposed mechanism, the experimental results can be explained by the formation of a co-continuous hybrid network due to reorganization of the epoxy matrix around two different "in situ" sol-gel derived silicatic phases, i.e., micelles formed mainly by APTES and multi-sheet silica nanoparticles. Moreover, the concentration of APTES affected the size distribution of the multi-sheet silica-based nanoparticles, leading to the formation of structures that became smaller at a higher content. Flammability and forced-combustion tests proved that the nanocomposites exhibited excellent fire retardancy.

The rheology of triacylglycerol (TAG) crystal-melt suspensions (CMSs) consisting of anhydrous milk fat (AMF), cocoa butter (CB), and palm kernel oil (PKO) as function of crystallization shear rate cryst and crystal volume fraction ΦSFC is investigated by in-line ultrasound velocity profiling - pressure difference (UVP-PD) rheometry. Measurements up to ΦSFC = 8.8% are presented. Below the percolation threshold Φc, no yield stress τ0 is observed and the viscosity η scales linearly with ΦSFC. Above Φc, a non-linear dependency of both τ0 and η as function of ΦSFC is apparent. For AMF and CB, the increase in cryst leads to a decrease in η and τ0 as function of ΦSFC, whereas for PKO based CMSs the opposite is the case. Scanning electron microscopy (SEM) and polarized light microscopy (PLM) relate these rheological findings to the microstructure of the investigated CMSs by taking the effective aspect ratio aeff and the concept of the effective crystal volume fraction ΦeffSFC into account. Foam formation by dynamically enhanced membrane foaming (DEMF) is performed directly after crystallization and reveals that depending on the CMS rheology and crystallite-, crystallite cluster- and crystal floc microstructure, a wide range of gas volume fractions between 0.05-0.6 are achievable.

The rear interface of kesterite absorbers with Mo back contact represents one of the possible sources of nonradiative voltage losses (ΔVoc,nrad) because of the reported decomposition reactions, an uncontrolled growth of MoSe2, or a nonoptimal electrical contact with high recombination. Several intermediate layers (IL), such as MoO3, TiN, and ZnO, have been tested to mitigate these issues, and efficiency improvements have been reported. However, the introduction of IL also triggers other effects such as changes in alkali diffusion, altered morphology, and modifications in the absorber composition, all factors that can also influence ΔVoc,nrad. In this study, the different effects are decoupled by designing a special sample that directly compares four rear structures (SLG, SLG/Mo, SLG/Al2O3, and SLG/Mo/Al2O3) with a Na-doped kesterite absorber optimized for a device efficiency >10%. The IL of choice is Al2O3 because of its reported beneficial effect to reduce the surface recombination velocity at the rear interface of solar cell absorbers. Identical annealing conditions and alkali distribution in the kesterite absorber are preserved, as measured by time-of-flight secondary ion mass spectrometry and energy-dispersive X-ray spectroscopy. The lowest ΔVoc,nrad of 290 mV is measured for kesterite grown on Mo, whereas the kesterite absorber on Al2O3 exhibits higher nonradiative losses up to 350 mV. The anticipated field-effect passivation from Al2O3 at the rear interface could not be observed for the kesterite absorbers prepared by the two-step process, further confirmed by an additional experiment with air annealing. Our results suggest that Mo with an in situ formed MoSe2 remains a suitable back contact for high-efficiency kesterite devices.

Organic/inorganic hybrid composite materials with the dispersed phases in sizes down to a few tens of nanometers raised very great interest. In this paper, it is shown that silica/epoxy nanocomposites with a silica content of 6 wt % may be obtained with an "in situ" sol-gel procedure starting from two precursors: tetraethyl orthosilicate (TEOS) and 3-aminopropyl-triethoxysilane (APTES). APTES also played the role of a coupling agent. The use of advanced techniques (bright-field high-resolution transmission electron microscopy, HRTEM, and combined small- and wide-angle X-ray scattering (SAXS/WAXS) performed by means of a multirange device Ganesha 300 XL+) allowed us to evidence a multisheet structure of the nanoparticles instead of the gel one typically obtained through a sol-gel route. A mechanism combining in a new manner well-assessed knowledge regarding sol-gel chemistry, emulsion formation, and Ostwald ripening allowed us to give an explanation for the formation of the observed lamellar nanoparticles.

A simple one-pot synthesis process for functionalized mesostructured silica nanoparticles (MSNP) is reported. The novel process demonstrated the possibility to achieve MSNP with a surface area up to 501 m2.g−1 using a phosphonate based nonsilane precursor such as N, N´-bis[4,6- bis(diethylphosphono)-1,3,5-triazin-yl]-1,2-diaminoethane (ED). MSNP obtained by using 20 mol% of ED achieved a surface area of 80 m2.g−1 and increasing the ED content to 30 mol% resulted in a surface area of 501 m2.g−1. Zeta potential of novel MSNPs (-65.5 and -70.0 mV) were much higher than the nanoparticle (NP) prepared from only TEOS (-49 mV), indicating the presence of a large number of –SiOH and phosphonic acid surface functional groups, as confirmed by Fouriertransform infrared spectroscopy (FT-IR) and Nuclear magnetic resonance (NMR) analysis. The functionalized MSNPs were used as an adsorbent for the removal of cationic pollutants like methylene blue (MB). The MSNP with the highest porosity displayed favorable MB adsorption behavior with ~380 mg.g−1 of MB adsorption capacity. Facile regeneration in an acidic medium (~pH 4.5) with easy recyclability (10 cycles) confirmed the practical applicability of this novel functionalized MSNPs.

Solution-processed lead sulfide quantum dots (PbS QDs) are very attractive as NIR-active semiconductors for the fabrication of cost-efficient optoelectronic devices. To control the thin film carrier transport, as well as stability, surface passivation is of crucial importance. Here, we present the successful surface passivation of PbS QDs by the formamidinium lead iodide (FAPbI3) ligand. An effective procedure for the fabrication of FAPbI3-passivated PbS QDs through a binary-phase ligand exchange protocol in hexane and n-methylformamide is demonstrated. It is shown that this solution-processed ligand exchange drastically changes the photoluminescence intensity, exciton recombination dynamics, and carrier lifetime of the nanocrystals. The solution casting of the ligand-exchanged nanocrystals into thin films results in the periodic ordering of QDs in a square superlattice with close contacts. Planar graphene/QD photodetectors fabricated with PbS QDs passivated with FAPbI3 show substantially increased thermal stability as compared to similar devices using PbS QDs passivated with commonly used methylammonium lead iodide.

Despite major technological advances within the field of cardiovascular engineering, the risk of thromboembolic events on artificial surfaces in contact with blood remains a major challenge and limits the functionality of ventricular assist devices (VADs) during mid- or long-term therapy. Here, a biomimetic blood-material interface is created via a nanofiber-based approach that promotes the endothelialization capability of elastic silicone surfaces for next-generation VADs under elevated hemodynamic loads. A blend fiber membrane made of elastic polyurethane and low-thrombogenic poly(vinylidene fluoride- co-hexafluoropropylene) was partially embedded into the surface of silicone films. These blend membranes resist fundamental irreversible deformation of the internal structure and are stably attached to the surface, while also exhibiting enhanced antithrombotic properties when compared to bare silicone. The composite material supports the formation of a stable monolayer of endothelial cells within a pulsatile flow bioreactor, resembling the physiological in vivo situation in a VAD. The nanofiber surface modification concept thus presents a promising approach for the future design of advanced elastic composite materials that are particularly interesting for applications in contact with blood.

A fast and simple, one-step synthesis for the preparation of silica aerogel powders is reported. A waterglass based sol was prepared without prior ion-exchange and stirred with an immiscible organic phase (heptane) that contains the hydrophobization agent (hexamethyldisilazane). The addition of nitric acid triggers gelation and subsequently the hydrophobization of this hydrogel, which causes the gel particles to transfer from the aqueous into the organic phase, whilst the sodium and nitrate ions are retained in the aqueous phase. The resulting organogel slurry is then converted into a silica aerogel powder by means of ambient pressure drying. The addition of phase transfer agents, ethanol and isopropanol in particular, strongly influences the final silica aerogel properties, including tap density, hydrophobicity, particle size distribution, surface chemistry (solid-state NMR), and microstructure (TEM, SEM, nitrogen sorption). The addition of intermediate amounts of phase transfer agent strongly improves the aerogel properties, but these positive effects disappear when larger quantities are added. Under optimal conditions, silica aerogel powders with high mesoporosity, surface areas above 800 m(2)/g, tap densities as low as 0.083 g/cm(3), and thermal conductivities below 20 mW m(-1) K-1 can be produced in a one-step process within just over two hours. The direct use of waterglass as an inexpensive silica precursor provides a great opportunity to reduce the production cost of silica aerogel powders for thermal insulation applications.

Today, post-mortem computed tomography (CT) is routinely used for forensic identification. Mobile energy-dispersive X-ray fluorescence (EDXRF) spectroscopy of a dentition is a method of identification that has the potential to be easier and cheaper than CT, although it cannot be used with every dentition. In challenging cases, combining both techniques could facilitate the process of identification and prove to be advantageous over chemical analyses. Nine dental restorative material brands were analyzed using EDXRF spectroscopy. Their differentiability was assessed by comparing each material's x-ray fluorescence spectrum and then comparing the spectra to previous research investigating differentiability in CT. To verify EDXRF's precision and accuracy, select dental specimens underwent comparative electron beam excited x-ray spectroscopy (EDS) scans, while the impact of the restorative surface area was studied by scanning a row of dental specimens with varying restorative surface areas (n = 10). EDXRF was able to differentiate all 36 possible pairs of dental filling materials; however, dual-energy CT was only able to differentiate 33 out of 36. The EDS scans showed correlating x-ray fluorescence peaks on the x-ray spectra compared to our EDXRF. In addition, the surface area showed no influence on the differentiability of the dental filling materials. EDXRF has the potential to facilitate corpse identification by differentiating and comparing restorative materials, providing more information compared to post-mortem CT alone. Despite not being able to explicitly identify a brand without a control sample or database, its fast and mobile use could accelerate daily routines or mass victim identification processes. To achieve this goal, further development of EDXRF scanners for this application and further studies evaluating the method within a specific routine need to be performed.