Additional Electron Research Articles

Encapsulated Fe3C boosted electrocatalytic performance for oxygen reduction reaction of N-doped carbon nanotube

The shortcomings of precious metal based catalysts have limited the development of novel energies. So, developing low-cost and high performance transition metal based catalysts is one of the most feasible way to substitute the precious metal based catalysts. In all of the developed catalysts for oxygen reduction reactions (ORR), the iron-based nitrogen doped carbon nanotube (N-CNT) show great promise. In this paper, N-CNT with Fe3C encapsulated based catalysts (Fe3C@N-CNT) were synthesized. The encapsulation structure of Fe3C@N-CNT was confirmed by HAADF-STEM, XANES, XPS, XRD, SEM and other methods. XANES tests show that the doped nitrogen of Fe3C changed the length of Fe-C bond and furtherly influenced the electron transfer between encapsulated Fe3C and outer layer N-CNT. Electrochemical tests showed that the half-wave potential and onset potential ORR of 750 °C calcinated Fe3C@N-CNT were 90 mV higher than that of 20 wt.% Pt/C. The additional electric field between Fe3C and N-CNT modulated the C-N bond of surface N-CNT and enhanced the catalytic performance for ORR. This paper reveal that constructing encapsulated additional electron providing center is an effective way to design high performance catalysts.

Unveiling the mechanism underlying in−situ enhancement on anammox system by sulfide: Integration of biological and isotope analysis

The in−situ utilization of sulfide to remove the nitrate produced during the anaerobic ammonium oxidation (anammox) process can avoid prolonged sludge acclimatization, facilitating the rapid initiation of coupled nitrogen removal processes. However, the understanding of in−situ enhancement on anammox system by sulfide remains unclear. Herein, sulfide (Na2S) was introduced as an additional electron donor to remove the nitrate derived from the anammox under varying sulfide/nitrogen (S/N, S2−-S/NO3–-N, molar ratio) ratios (0.004–4.375). The underlying mechanisms were elucidated by molecular biology techniques including flow cytometry, quantitative polymerase chain reaction, and 16S rRNA amplicon sequencing, alongside isotope tracer analysis. Results revealed that anammox reactors, when operated with in−situ sulfide addition, exhibited a significant enhancement in total nitrogen removal efficiency (NRE) ranging from 11.5%−41.7% (achieved 96%), with the optimal S/N ratios of 0.01−0.8. Isotope tracer analysis indicated the successful coupling of the anammox, sulfur autotrophic denitrification (SADN), and dissimilatory nitrate reduction to ammonium (DNRA) processes within the system, with their contributions to nitrogen removal being 46%−50%, 24%−30%, and 20%−22%, respectively. Moreover, a notable increase in the abundance of sulfur–oxidizing bacteria (SOB) (20%−40% increase) and DNRA bacteria (10%−20% increase) were observed. Effective collaboration was further supported by the sustained viability of microbial communities. It is speculated that the heightened presence of SOB and DNRA bacteria created a low toxicity environment by converting sulfide to biogenic sulfur, thereby promoting the well−being of anammox bacteria. However, the excessive dosage of sulfide (S/N=1.8) intensified the DNRA process (contribution>35%) and weakened the anammox process, leading to an increase in effluent NH4+-N concentration and a decline in NRE. This study confirms that the in−situ adding an appropriate amount of sulfide favors achieving complete nitrogen removal in anammox system, which provides a novel avenue to resolve the issue of the residual nitrate in anammox process.

Role of cavity strong coupling on single electron transfer reaction rate at electrode-electrolyte interface.

The physicochemical properties of molecules can be modulated through polariton formation under strong electromagnetic confinement. Here, we discuss the possibility of exploiting this phenomenon to increase the electron transfer rate at an electrode-electrolyte interface. Electron transfer theory under strong electromagnetic confinement can be extended to the electrode-electrolyte interface, and single-electron transfer reactions can be simulated using Gerischer's theory. Although single electron transfer in free space is well described using Marcus theory, the vacuum electric field can facilitate an additional electron transfer pathway via virtual photon excitation under cavity strong coupling conditions. Therefore, this binary reaction pathway for single electron transfer can yield a quasi-two-particle electron transfer process. This quantum behavior can dominate when the mode volume is small and when there are a large number of molecules in the vacuum electric field. Exploitation of polaritons in single electron transfer reactions can lead to enhanced electrochemical energy conversion systems.

Influence of an ultrathin Mn ‘spy layer’ on the static and dynamic magnetic coupling within FePt/NiFe bilayers

Abstract We explore whether insertion of an ultrathin Mn ‘spy layer’ within a magnetic hard/soft bilayer can enable depth-sensitive element-specific measurements of the static and dynamic magnetization, while avoiding significant disruption of the original magnetic state. MgO(110)/FePt(100 Å)/NiFe(200 Å)/Mn(t Mn Å)/NiFe(200 Å) samples with Mn thicknesses of t Mn = 0, 5, and 10 Å were fabricated by magnetron sputtering and studied by element-selective x-ray magnetic circular dichroism (XMCD), vector network analyzer ferromagnetic resonance (VNA-FMR), and x-ray detected ferromagnetic resonance (XFMR). For t Mn = 5 Å, the magnetic reversal properties remain broadly similar to t Mn = 0 Å. For t Mn = 10 Å, the two NiFe layers decouple with XMCD hysteresis loops at the Mn edge showing two switching events that suggest the presence of two distinct Mn-containing regions. While the Mn moments within each region have ferromagnetic order, their relative alignment is antiparallel at high field. Analysis of the magnetic data and additional scanning transmission electron microscopy measurements point to the presence of a Mn layer at the lower NiFe/Mn interface, and the formation of a NiFeMn alloy at the upper Mn/NiFe interface. The Mn moments of the former region lie antiparallel to those of the underlying NiFe layer. The VNA-FMR data suggests that for t Mn = 5 and 10 Å, the interfacial exchange coupling at the FePt/NiFe is suppressed and the in-plane uniaxial magnetic anisotropy of the NiFe is increased, perhaps due to migration of Mn towards the buried interface. The above findings show that Mn is a problematic magnetic spy, and that a Mn thickness of less than 5 Å would be required.

Open Sn Framework Structure Hosting Bi Guest atoms-Synthesis, Crystal and Electronic Structure of Na13Sn26Bi.

The large variety of structures of Zintl phases are generally well understood since their anionic substructures follow bonding rules according to the valence concept. But there are also exceptions, which make the semiconductors especially interesting in terms of structure-property relationships. Although several Na-Sn-Pnictides with a variety of structural motives are known, up to this point no ternary compound in the Na-Sn-Bi system has been described. In this paper we present the Zintl-phase Na13Sn25.73Bi1.27 comprising a complex, open-framework structure of Sn atoms, with one mixed Sn/Bi site, hosting Na atoms. An additional Bi atom is loosely connected with only weak contacts to the framework filling a larger cavity within the network. According to band structure calculations of the two ordered variants with either full occupation of the mixed site with Sn or Bi, resulting in Na13Sn26Bi and Na13Sn24Bi3, respectively, both compounds are semiconductors with band gaps of 0.5 eV. A comparison of the band structures with the structurally related binary compounds Na5Sn13 and Na7Sn12 shows that only the perfectly charge balanced Na7Sn12 is a semiconductor whereas Na5Sn13 is metallic. The rather specific electronic situation in the ternary compound is traced back to the loosely bound Bi atom, which acts as a guest atom according to Bix@Na13Sn26-yBiy, with x=1 and y=0.27, capable to change its oxidation state and thus to uptake additional electrons allowing the system to be a semiconductor. Therefore, Na13Sn25.73Bi1.27 can be understood as a rare example of an open framework structure of Sn atoms comprising Bi atoms in the cavities.

Iron Selenide Intercalated by Uncharged Molecules: Superconductivity in FeSe(C2H7NO)0.3

AbstractThe charge‐neutral intercalated iron selenide compound FeSe(C2H7NO)0.3 is formed from FeSe(C2H8N2)0.3 through amine exchange under solvothermal conditions. Although the exchanged molecules are of similar size, the distance of the FeSe‐layers increases from 10.68 Å to 13.58 Å. The combination of X‐ray diffraction and DFT calculations suggests a chemically reasonable, albeit somewhat simplified, model for the orientation of the molecules between the FeSe‐layers, which interact via weak hydrogen bonds. The neutral guest species is unable to transfer charge to the FeSe layers, which remain electronically undoped. While the starting compound is non‐superconducting, the resulting product exhibits a transition to superconductivity at Tc=14 K. The topology of the calculated Fermi surface undergoes only minimal alteration with increased layer spacing, a change that is considerably less pronounced than that observed with electron doping. Our findings indicate that undoped FeSe layers become superconducting when the interlayer distance is sufficiently large, while the highest critical temperatures necessitate additional electron doping.

Highly Sensitive Phased Array Probes based on Capacitive Micromachined Ultrasonic Transducers

Capacitive Micromachined Ultrasonic Transducers (CMUTs) offer a wide freedom of design for ultrasonic phased arrays. They are characterized, in comparison to piezoelectric transducers, by a higher sensitivity in receiving and a wider bandwidth based on their physical properties. Especially in combination with integrated preamplifiers the high receiving sensitivity compensates or rather overcompensates the lower transmission power of the CMUT in single probe applications with pulse-echo technique. This asymmetric behavior opens new opportunities in the application. In medical diagnostics it allows to meet the maximum permissible ultrasonic radiation force with the best sensitivity. In nondestructive testing the transmission power can be increased by the combination of a piezoelectric probe for transmitting and a CMUT probe for receiving. Especially in double probe techniques, such as pitch-catch or time-of-flight diffraction (TOFD), this is an efficient extension of the conventional approach with two piezoelectric transducers. The CMUT array probes developed by Fraunhofer IPMS with integrated preamplifier and bias voltage converter powered by a standard USB-A connector can be applied as one to one substitute for piezoelectric phased arrays with commercially available ultrasonic devices without adaption or additional electronics. The CMUT arrays are best suited for immersion technique and medical sonography because of their natural matching to water-like materials. They are applicable as well for solid surfaces with a special coating. We present the first results of ultrasonic imaging with our CMUT array probes in comparison with a commercially available piezoelectric phased array probe.

Earth-abundant FeSO4-based conversion-type cathode for rechargeable sodium-ion batteries

Sodium-ion batteries (SIBs) have gained prominence as the ideal choice for next-generation large-scale energy storage systems owing to advantages such as sodium abundance and cost-effectiveness. However, their synthesis requires harsh conditions such as high pressure and temperature, and the cathode materials exhibit poor electrical conductivity and sluggish kinetics, hindering SIBs from meeting the requirements for practical applications. In this study, a conversion-type Gr/FeSO4 nanocomposite based on earth-abundant and environmentally friendly elements was developed using a high-energy mechanical ball-milling method. The conversion reaction in FeSO4 was triggered via a simple direct-contact pre-sodiation method, wherein the FeSO4 particles were reversibly converted to Fe0 and Na2SO4 and recovered in the next charging process. Meanwhile, graphene in Gr/FeSO4 acted as a conductive matrix that provided additional electron transfer paths, resulting in increased ionic and electronic conductivities and enhanced diffusion kinetics. Owing to these matrices, the as-prepared Gr/FeSO4 nanocomposite exhibited remarkable long-term cyclability. This study highlights the advantages of combining pre-sodiation and conversion reactions for cathodes and demonstrates the feasibility of employing naturally abundant FeSO4 for high-performance SIBs.

Intracellular Gold Nanocluster/Organic Semiconductor Heterostructure for Enhancing Photosynthesis.

Photosynthetic microorganisms, which rely on light-driven electron transfer, store solar energy in self-energy carriers and convert it into bioenergy. Although these microorganisms can operate light-induced charge separation with nearly 100 % quantum efficiency, their practical applications are inherently limited by the photosynthetic energy conversion efficiency. Artificial semiconductors can induce an electronic response to photoexcitation, providing additional excited electrons for natural photosynthesis to improve solar conversion efficiency. However, challenges remain in importing exogenous electrons across cell membranes. In this work, we have developed an engineered gold nanocluster/organic semiconductor heterostructure (AuNCs@OFTF) to couple the intracellular electron transport chain of living cyanobacteria. AuNCs@OFTF exhibits a prolonged excited state lifetime and effective charge separation. The internalized AuNCs@OFTF permits its photogenerated electrons to participate in the downstream of photosystem II and construct an oriented electronic highway, which enables a five-fold increase in photocurrent in living cyanobacteria. Moreover, the binding events of AuNCs@OFTF established an abiotic-biotic electronic interface at the thylakoid membrane to enhance electron flux and finally furnished nicotinamide adenine dinucleotide phosphate. Thus, AuNCs@OFTF can be exploited to spatiotemporally manipulate and enhance the solar conversion of living cyanobacteria in cells, providing an extended nanotechnology for re-engineering photosynthetic pathways.

Intracellular Gold Nanocluster/Organic Semiconductor Heterostructure for Enhancing Photosynthesis

AbstractPhotosynthetic microorganisms, which rely on light‐driven electron transfer, store solar energy in self‐energy carriers and convert it into bioenergy. Although these microorganisms can operate light‐induced charge separation with nearly 100 % quantum efficiency, their practical applications are inherently limited by the photosynthetic energy conversion efficiency. Artificial semiconductors can induce an electronic response to photoexcitation, providing additional excited electrons for natural photosynthesis to improve solar conversion efficiency. However, challenges remain in importing exogenous electrons across cell membranes. In this work, we have developed an engineered gold nanocluster/organic semiconductor heterostructure (AuNCs@OFTF) to couple the intracellular electron transport chain of living cyanobacteria. AuNCs@OFTF exhibits a prolonged excited state lifetime and effective charge separation. The internalized AuNCs@OFTF permits its photogenerated electrons to participate in the downstream of photosystem II and construct an oriented electronic highway, which enables a five‐fold increase in photocurrent in living cyanobacteria. Moreover, the binding events of AuNCs@OFTF established an abiotic‐biotic electronic interface at the thylakoid membrane to enhance electron flux and finally furnished nicotinamide adenine dinucleotide phosphate. Thus, AuNCs@OFTF can be exploited to spatiotemporally manipulate and enhance the solar conversion of living cyanobacteria in cells, providing an extended nanotechnology for re‐engineering photosynthetic pathways.

Absence of Additional Stretching-Induced Electron Scattering in Highly Conductive Cross-linked Nanocomposites with Negligible Tunneling Barrier Height and Width.

The intrinsic resistance of stretchable materials is dependent on strain, following Ohm's law. Here the invariable resistance of highly conductive cross-linked nanocomposites over 53% strain is reported, where additional electron scattering is absent with stretching. The in situ generated uniformly dispersed small silver nanosatellite particles (diameter=3.6nm) realize a short tunneling barrier width of 4.1nm in cross-linked silicone rubber matrix. Furthermore, the barrier height can be precisely controlled by the gap state energy level modulation in silicone rubber using cross-linkers. The negligible barrier height (0.01eV) and short barrier width, achieved by the silver nanosatellite particles in cross-linked silicone rubber, dramatically increase the electrical conductivity (51710Scm-1) by more than 4 orders of magnitude. The high conductance is also maintained over 53% strain. The quantum tunneling behavior is observed when the barrier height is increased, following the Simmons approximation theory. The transport becomes diffusive, following Ohm's law, when the barrier width is increased beyond 10.3nm. This study provides a novel strain-invariant resistance mechanism in highly conductive cross-linked nanocomposites.

Photocatalytic Tricyclization of Enediynes for the Synthesis of Chromenoquinolines in Continuous Flow.

A photocatalyzed radical-initiated tricyclization of enediynes was developed to synthesize a range of hitherto unknown sulfonated chromenoquinolines with moderate to excellent yields under continuous operational conditions. The reaction mechanism involves a complex series of steps including alkyl radical capture by sulfur dioxide (SO2), radical addition, 6-exo-dig/6-exo-dig/6-endo-trig tricyclization, and single electron transfer (SET). This cascade of reactions results in the direct formation of a pentacyclic framework structure, along with the creation of up to three new rings and five chemical bonds in a single step. This photocatalytic protocol exhibits a diverse substrate scope, remarkable tolerance to functional groups, and scalable adaptability.

Efficient sorbent/catalyst composites for CO2-mediated oxidative dehydrogenation of ethane via isothermal integrated CO2 capture and utilization

The isothermal integrated CO2 capture and utilization to produce ethylene (ICCU-ODHE) performances of dual functional materials (DFM) were improved by doping five transition metal elements (Fe, Co, Ni, Cu, Zn). The results show that the DFM doped with Zn exhibits excellent ICCU-ODHE performance with an ethylene yield of 35.1 %. The results based on in-situ XPS and DFT calculation show that the doping transition metal elements can reduce the energy barriers for activating ethane and CO2. It is mainly because doping transition metal elements with strong electronegativity can increase the coordinative unsaturated Cr3+ ions to adsorb more ethane molecules, meanwhile, the doping also reduces the charge density of Cr3+ and generates additional unfilled electron orbitals facilitating charge transfer to improve the CO2 and ethane activation. However, the decrease in charge density can increase the difficulty of ethylene desorption and reduce the ethylene selectivity. In addition, the cyclic regeneration experiment shows that the ICCU-ODHE performance of DFM can decrease with the increase of cycles, however, significant performance restoration is achievable after regeneration in the air at 650 °C, attributed to the limited graphitization of coke deposition on the DFM.

Enhanced dopamine detection using Ti3C2Tx/rGO/Pt ternary composite synthesized via microwave-assisted hydrothermal method

A novel electrochemical sensing platform for dopamine (DA) detection was developed by fabricating the ternary composite of Ti3C2Tx MXene (M) and reduced graphene oxide (rGO) with platinum nanoparticles (Pt NPs) through microwave-assisted hydrothermal heating. The exceptional electrical conductivity and rich surface chemistry of MXene provide abundant active catalytic sites for electrochemical reactions, while the large surface area of rGO facilitates ion and electron pathways. The integration of rGO in the MXene sheet, forming MXene-rGO (M_rGO) heterostructure composite, imparts long-term stability to the 2D heterostructure while providing additional electron pathways and significantly enhancing conductivity. Pt NPs synergistically increased the electrocatalytic activity of the electrochemical sensor's performance. Ternary nanocomposites were fabricated with different weight percentages (wt.%) of Pt NPs, ranging from 5 to 20. Characterizations of the samples (rGO, M, M_rGO, and 5–20 wt% Pt@M_rGO) were conducted through X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy (RAMAN), and X-ray spectroscopy (XPS). Electrochemical evaluations of the samples were investigated in 0.1 M phosphate buffer solution (PBS) using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) analyses. The analysis revealed that the ternary composite with 5 wt% of Pt NPs (5% Pt@M_rGO) exhibited a uniform well-distribution of Pt NPs and the highest oxidation peak for DA oxidation in CV studies. The presence of metal nanoparticles, aided by the synergistic effects between the MXene and rGO, resulted in an excellent DA sensor with a 0.147 μM detection limit from 1 to 14 μM linearity range. The sensor demonstrated outstanding selectivity, reproducibility (RSD values of 8.10%), repeatability (RSD value of 2.46%) and, excellent stability over 14 days. In human urine samples, the sensor exhibited excellent DA recovery (88.62–110.65%). This study significantly advances the development of electrochemical sensors for DA detection by introducing a rapid, facile and, efficient method for fabricating ternary composites. The fabricated sensor exhibited high sensitivity, excellent selectivity, and robust electrochemical performance, offering valuable insights into human and behavioral health advancements.

Long-term evaluation of soil-based bioelectrochemical green roof systems for greywater treatment

Water scarcity has generated the need to identify new sources. Due to its low organic contaminant load, greywater reuse has emerged as a potential alternative. Moreover, the search for decentralized treatment systems in urban areas has prompted research on using green roofs for greywater treatment. However, the performance of organic matter removal is limited by the type of substrate and height of the growing media. Bioelectrochemical systems (BESs) improve treatment performance by providing an additional electron acceptor (the electrode). In this study, nine reactors under three different conditions, i.e., open circuit (OC), microbial fuel cell (MFC), and microbial electrolysis cell (MEC), were built to evaluate the treatment of synthetic greywater in a substrate-growing medium composed of perlite and coconut fiber and operated in batch-cycle mode for 397 days. The results suggested that using BESs enables greywater treatment and the removal of pollutants to levels that allow their reuse for irrigation. Furthermore, electrical conductivity was reduced from 732.4 ± 41.2 μS/cm2 in OC to 637.32 ± 22.73 μS/cm2 and 543.15 ± 19.69 μS/cm2 in MEC and MFC, respectively. The soluble chemical oxygen demand in the latter treatments reached 76% removal, compared to levels above the OC, which only reached approximately 67%. Microbial community analysis revealed differences, mainly in the cathodes, showing a higher development of Flavobacterium, Azospirillum, and Zoogloea in MFCs, which could explain the higher levels of organic matter removal in the other conditions, suggesting that the BES could produce an enrichment of beneficial bacterial groups for treatment. Therefore, implementing BESs in green roofs enables sustainable long-term greywater treatment.

Biogenic amorphous FeOOH activated additional intracellular electron flow pathways for accelerating reductive dechlorination of tetrachloroethylene

Dissimilatory iron-reducing bacteria (DIRB) with extracellular electron transfer (EET) capabilities have shown significant potential for bioremediating halogenated hydrocarbon contaminated sites rich in iron and humic substances. However, the role and microbial molecular mechanisms of iron-humic acid (Fe-HA) complexes in the reductive dehalogenation process of DIRB remains inadequately elucidated. In this study, we developed a sustainable carbon cycling approach using Fe-HA complexes to modulate the electron flux from sawdust (SD), enabling almost complete reductive dechlorination by most DIRB (e.g., Shewanella oneidensis MR-1) that lack complex iron-sulfur molybdo enzymes. The SD-Fe-HA/MR-1 system achieved a 96.52% removal efficiency of tetrachloroethylene (PCE) at concentrations up to 250 μmol/L within 60 days. Material characterization revealed that DIRB facilitated the hydrolysis of macromolecular carbon sources by inducing the formation of amorphous ferrihydrite (FeOOH) in Fe-HA complexes. More importantly, the bioavailable FeOOH activated additional intracellular electron flow pathways, increasing the activity of potential dehalogenases. Transcriptome further highlight the innovative role of biogenic amorphous FeOOH in integrating intracellular redox metabolism with extracellular charge exchange to facilitate reductive dechlorination in DIRB. These findings provide novel insights into accelerating reductive dechlorination in-situ contaminated sites lacking obligate dehalogenating bacteria.

Principle of vanadium doping-induced MoS2 homojunction effect and mechanism analysis of antibacterial process under near-infrared light

MoS2 exhibits unique physical and chemical properties in its 1 T and 2H phases. Each phase has its inherent advantages and limitations. Although several biochemical properties of MoS2 have been extensively reported, the specific impacts of these phases on photothermal and antibacterial performance, the feasibility of integrating the unique advantages of both phases and the underlying dominant bactericidal mechanisms are still largely unexplored. In this work, the electronic-structural relationships of 1 T- and 2H-MoS2 were first simulated using density functional theory (DFT), which provided unique insights into how these phases affect performance. Based on these insights, a solid-state coupling interface and built-in electric field were designed between the two phases, and a 1 T/2H MoS2 homojunction was synthesized using the hydrothermal method, achieving a higher carrier separation efficiency and exhibiting excellent photothermal and antibacterial properties. Subsequently, further attempts were made to adjust the electronic structure by doping vanadium atoms. This doping not only introduces additional electrons to facilitate electron transfer but also further enhances the antibacterial capability by creating surface defects that increase the number of active sites. Finally, the synergistic antibacterial mechanism of this system was thoroughly investigated through detailed experiments and DFT theoretical analysis. The design of the homojunction, the introduction of defects, and the incorporation of heteroatoms were discussed in this paper, which pave the way for the rational design strategy of advanced two-dimensional materials and can be extended to other polycrystalline materials.

Enhanced X-band microwave shielding via Fe3O4 nanoparticle-decorated few layered nitrogen-doped reduced graphene oxides: Synthesis, characterization, and performance assessment

Currently, developing lightweight with good microwave (MW) shielding efficacy materials are exceedingly challenging. The challenging task for a few layers of nitrogen-doped reduced graphene oxide (FLN-rGO) derived from thermal N-deposition with an exfoliation under the pyrolysis process. Concurrently, nitrogen-doped heteroatoms FLN-rGO structure possessing an additional electron can enhance the electrical conductivity and function as an electroactive site that enhances MW shielding effectiveness (SE). Besides, the synthesized Fe3O4-FLN-rGO NCs are self-sustaining, lightweight, and have strong chemical stability and outstanding MA performance due to the presence of chemical interaction between each other and the development of hierarchical structure formation. The structural and chemical interaction properties of pristine and Fe3O4-FLN-rGO composites are investigated using high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). These analyses confirmed that Fe3O4 NPs are homogeneously decorated on the FLN-rGO surface and revealed the chemical interactions between Fe3O4 and N-rGO, as evidenced by the Fe–O–C bonding signal observed in the Fe3O4-N-rGO (1:2) composites. The Fe3O4 NPs demonstrated remarkable saturation magnetization (Ms) and low coercivity (Hc), indicating that quantum confinement effects moderate their soft ferromagnetic characteristics. With a lightweight shielding materials thickness of 0.5 mm, these composites demonstrated an outstanding average MW SE of 44.73 dB at 8 GHz and a superb MW attenuation value (α = 845.05), indicating their excellent efficacy as materials for advanced MW shielding applications.

Metagenomic survey reveals hydrocarbon biodegradation potential of Canadian high Arctic beaches

BackgroundDecreasing sea ice coverage across the Arctic Ocean due to climate change is expected to increase shipping activity through previously inaccessible shipping routes, including the Northwest Passage (NWP). Changing weather conditions typically encountered in the Arctic will still pose a risk for ships which could lead to an accident and the uncontrolled release of hydrocarbons onto NWP shorelines. We performed a metagenomic survey to characterize the microbial communities of various NWP shorelines and to determine whether there is a metabolic potential for hydrocarbon degradation in these microbiomes.ResultsWe observed taxonomic and functional gene evidence supporting the potential of NWP beach microbes to degrade various types of hydrocarbons. The metagenomic and metagenome-assembled genome (MAG) taxonomy showed that known hydrocarbon-degrading taxa are present in these beaches. Additionally, we detected the presence of biomarker genes of aerobic and anaerobic degradation pathways of alkane and aromatic hydrocarbons along with complete degradation pathways for aerobic alkane degradation. Alkane degradation genes were present in all samples and were also more abundant (33.8 ± 34.5 hits per million genes, HPM) than their aromatic hydrocarbon counterparts (11.7 ± 12.3 HPM). Due to the ubiquity of MAGs from the genus Rhodococcus (23.8% of the MAGs), we compared our MAGs with Rhodococcus genomes from NWP isolates obtained using hydrocarbons as the carbon source to corroborate our results and to develop a pangenome of Arctic Rhodococcus. Our analysis revealed that the biodegradation of alkanes is part of the core pangenome of this genus. We also detected nitrogen and sulfur pathways as additional energy sources and electron donors as well as carbon pathways providing alternative carbon sources. These pathways occur in the absence of hydrocarbons allowing microbes to survive in these nutrient-poor beaches.ConclusionsOur metagenomic analyses detected the genetic potential for hydrocarbon biodegradation in these NWP shoreline microbiomes. Alkane metabolism was the most prevalent type of hydrocarbon degradation observed in these tidal beach ecosystems. Our results indicate that bioremediation could be used as a cleanup strategy, but the addition of adequate amounts of N and P fertilizers, should be considered to help bacteria overcome the oligotrophic nature of NWP shorelines.

Optimizing activated carbon electrodes and improving their electrochemical performance through nitrogen doping and HNO3 modification

In order to optimize the process conditions, electrodes were prepared by mixing coal-based activated carbon (AC), polyvinylidene fluoride (PVDF), and conductive carbon black on a graphite plate. To enhance the adsorption capacity of the electrode, nitrogen-doped modification and nitric acid modification were sequentially performed on AC. Characterization methods included scanning electron microscopy (SEM), specific surface area (BET), x-ray photoelectron spectroscopy (XPS), and other analytical techniques. Contact angle and cyclic voltammetry tests were also conducted on the electrode. The experimental results showed that the modified material's specific surface area increased from 482.843 m2/g to 856.073 m2/g, the electrode's specific capacitance reached 404.56 F/g. For better utilization of AC for electrosorption, new nitrogen- and oxygen-containing functional groups were introduced to provide additional electrons, reduces the internal resistance of the material improves the electron mobility, and improves AC electrochemical performance. The removal of Cu2+ by modified AC reached 76.25 % at a Cu2+ concentration of 80 mg/L with an applied voltage of 1.5 V.