High Generation Rate Research Articles

Time-reversed biphoton source of the double-Λ spontaneous four-wave mixing process

Abstract Utilizing the double-Λ spontaneous four-wave mixing (SFWM) process, the biphoton source generates narrow-linewidth pairs of signal and probe photons. In a medium, the signal photon propagates at nearly the speed of light in a vacuum, while the probe photon propagates as slow light. Typically, signal photons arrive at the detector first and are used as the heralding photons in conventional biphoton sources. In this work, we propose using probe photons as the heralding photons to enhance the heralding probability an approach that has been overlooked previously. We also investigate a time-reversed double-Λ SFWM biphoton source using heated atomic vapor. Compared with the conventional biphoton source under the same experimental conditions, the time-reversed one exhibits a time-reversed temporal profile with a similar full-width-at-half-maximum linewidth of 3.4MHz, increased the heralding efficiency by a factor of 5.3, and enhanced the detection rate by 1.3 times. With the time-reversed source, we achieved a heralding probability of 82±6% and a generation rate of (1.8±0.2)×106 pairs/s, referring to biphotons collected within polarization-maintained single-mode optical fibers. Furthermore, the time-reversed temporal profile is more suitable for quantum memory. Simulation results show that, at an optical depth of 150 (or 50), the storage efficiency of a quantum memory using the time-reversed source can reach 91% (or 81%), compared with 81% (or 67%) using the conventional source. This study demonstrates the significance of using the slow-light photon in biphoton pairs as the heralding photon for quantum operations. We have achieved a biphoton source with high heralding probability, high generation rate, and narrow linewidth in a room-temperature or hot medium.

Characterization of the Liquid Fuel Produced from Catalytic Depolymerization of Polymeric Waste Using Batch Reactor

The high rate of generation of plastic waste in the country and the fact that all other means of Municipal Plastic Waste (MPW) management techniques had failed leading to the requirement of efficient and alternative disposal technique-depolymerization. The technique involves heating the polymeric waste at an elevated temperature in an inert environment to produce condensable, non-condensable, hydrocarbon and biochar. The plastic waste was collected at the Ilokun dumpsite in Ado-Ekiti, southwest Nigeria. Each component of the waste samples was depolymerized in a batch reactor without the use of a catalyst and with the addition of 10 g of activated carbon (AC) and calcium oxide (CaO) as catalysts. The liquid fuels which were produced between the temperature range of 219 and 232 were blended with standard fuel. Fuel samples with conventional diesel and depolymerized plastic diesel were characterized based on ASTM standards. The results of the proximate and ultimate analysis indicated that percentage moisture content ranges from 0.00-0.18%, volatile matter ranges between 96.66-99.75% and percentage ash content ranges from 0.13-3.03%. Fixed carbon ranges from 0.004-0.31% while the Gross Heating Value (GHV) ranges from 42.66-45.87 MJ/kg. The CHONS analyzer indicated the percentage of carbon, hydrogen, oxygen, nitrogen, and sulfur content range 81.64-85.51%, 12-31-18.04%, 0.00-1.51%, 0.00-0.73%, and 0.10- 0.97% respectively. The results of the physiochemical properties of the samples show that the density, API gravity, Kinematic viscosity and Flash point vary from 0.76-0.83 (g/cm3), 38.98-54.68, 17-2.80 (cm2/s) and 50.0-70.0 (°C) respectively while Cloud point, Pour point, Fire point and Cetane index range from -20-15.0 (°C), -23-7 (°C), 61.0-79.0 (°C) and 38.50-47.0. The pH values of the liquid fuel samples vary from 6.60-3.30. The overall results of the characterization indicated the fuel samples have proximity to the properties of the conventional diesel following the ASTM D975, ASTM D4737, ASTM D1298, ASTM D445, ASTM D2709, and ASTM D482 standards. The depolymerized polymeric waste is sustainable, with a low cost of production. Hence a good substitute as an alternative fuel and means of wealth creation from waste.

Geminal Synergy in Pt-Co Dual-Atom Catalysts: From Synthesis to Photocatalytic Hydrogen Production.

Dual-atom catalysts (DACs) have garnered significant interest due to their high atom utilization and synergistic catalysis. However, developing a precise synthetic method for DACs and comprehending the underlying catalytic mechanisms remain challenging. In this study, we employ a photoinduced anchoring strategy to precisely synthesize PtCo DAC on graphitic carbon nitride (CN). A Co atom was anchored on CN through the lone-pair electrons of nitrogen. Upon light irradiation, photoelectrons gathering at the Co site can anchor Pt metal ions nearby, accurately facilitating the formation of heteronuclear DACs. The PtCo DAC demonstrates a remarkably high H2 generation rate from ammonia borane (AB) hydrolysis, with a TOF of 3130 molH2 molPt-1 min-1 at 298 K. This TOF value is approximately 3.2 times higher than that of the Pt single-atom photocatalyst. Importantly, the PtCo DAC shows good stability, achieving a turnover number as high as 307,982 molH2 molPt-1 at room temperature. The experimental and theoretical calculation results demonstrate that the synergy between Pt and Co optimizes the adsorption energy of AB and H2 molecules while reducing the energy barrier of the rate-determining step, thus accelerating H2 evolution from AB hydrolysis. Additionally, the introduced Co species stabilize the Pt active sites by enhancing the stability of the Pt-N bond, preventing leaching, aggregation, and deactivation. The excellent catalytic performance, good stability, and low cost of the catalysts in this work open new prospects for their practical application in hydrogen production.

Copper Nanoclusters Imparted Metalloporphyrin Based Metal-Organic Frameworks for Enhanced CO2 Electroreduction.

Strategies that can introduce catalytic auxiliary into electrocatalysts to boost the performance of electrocatalytic CO2 reduction reaction (CO2RR) are meaningful in exploring hybrid electrocatalytic systems. Here, a series of hybrid electrocatalysts (Cu NCs@MOF-545-M, M=Fe, Co and Ni) have been prepared by assembly Cu NCs with MOF-545-M (M=Fe, Co and Ni) and successfully applied in electrocatalytic CO2RR. In the obtained MOF-545-M (M=Fe, Co and Ni), the integration of Cu NCs with MOF-545-M (M=Fe, Co and Ni) can create a hybrid electrocatalytic system that enhances the charge transfer efficiency and electrocatalytic CO2RR activity. Specifically, the optimal Cu NCs@MOF-545-Co presents remarkable FECO over a wide potential range (-0.7 V to -1.0 V), high CO generation rate (8.2 mol m-2 h-1) and excellent maximum energy efficiency (69 %, -0.7 V), which is superior to Cu NCs and MOF-545-Co, and represented to be one of the best performances to date. This work demonstrates a facile approach to significantly improve the FECO by loading metal nanoclusters into MOFs, providing a valuable reference for future studies on hybridization strategies to enhance the performance of electrocatalysts.

Creating Cation Vacancies in BiOCl Nanosheets Toward Exceptional Visible-Light-Driven Photocatalytic CO2 Reduction.

BiOCl-based materials have emerged as promising photocatalysts for converting CO2 into valuable products and fuels. However, challenges such as low light absorption and inefficient charge carrier separation require effective solutions, with vacancy engineering offering a promising approach. Current research primarily focuses on anion vacancies, leaving cation vacancies less explored. In contrast, this study presents a novel method to enhance visible-light-driven photocatalysts by Bi cation vacancies in ultrathin BiOCl nanosheets through a straightforward hydrochloric acid etching process (HAE-BiOCl). These introduced Bi vacancies not only expand the light absorption range and enhance carrier separation, but also serve as active sites for CO2 adsorption. Additionally, Bi vacancies can effectively lower the activation energy of COOH- species and thereby enhance overall reaction activity. As a result, the HAE-BiOCl catalyst exhibits exceptional photocatalytic CO2 reduction performance without the need for co-catalysts or sacrificial agents. It achieves high CO generation rates of 68.39 and 17.43µmol g-1 h-1 under 300W Xe lamp and visible light irradiation, respectively. These rates are significantly higher compared to counterparts without vacancy creation and surpass those of most reported Bi-based photocatalysts. This study underscores the potential of inducing cation vacancies via acid etching as a valuable strategy for advancing photocatalysis.

Assessment of the oil and gas potential of the eastern edge of the Northern Ustyurt using new geophysical data

Purpose. Detailed substantiation of the geological structure of the eastern edge of the Northern Ustyurt, clarification of modern geological and geophysical data, as well as highlighting the mainstages of evaluating the results of exploration work to confirm the oil and gas potential and subsequent exploitation of the fields. Methodology. The authors used the following scientific methods: generalization – to systematize scientific provisions; analogy and comparison – to characterize deflection in different periods; analysis and synthesis – to substantiate geological and geophysical data; algorithmmization – to determine conceptual provisions regarding the assessment of the oil and gas bearing capacity of the trough. Findings. In order to achieve the goals, the indicators of oil and gas capacity in the areas of the eastern side of the Northern Ustyurt of different geological ages were substantiated. The geological and geophysical features of the basin dating back to 2010 compared to modern refinement of geological data were characterized. The productive and unproductive structures of the eastern side of the Northern Ustyurt are characterized, taking into account the showing of oil and gas based on deposits of different geological ages. The importance of conducting geological exploration and creating corresponding cartographic materials is justified, followed by the design of predictive graphical models, geological sections, and a detailed plan of the territory. Originality. The influence of high hydro carbon generation rates on the further identification of “oil windows” has been substantiated for the first time. The hierarchical levels of predicting the oil and gas content of the trough are identified. The necessity of improving the mechanisms for assessing oil and gas content is substantiated. Practical value. The substantiation of the features of the assessment of the oil and gas content of the of the eastern edge of the Northern Ustyurt, which should be based on forecasting promising areas of prospecting, is the key to distinguishing between productive and unproductive objects, determining their real scale and directing investment flow precisely to promising areas with minimal environmental and economic losses.

Light-emitting diodes based on intercalated transition metal dichalcogenides with suppressed efficiency roll-off at high generation rates

Light-emitting diodes based on intercalated transition metal dichalcogenides with suppressed efficiency roll-off at high generation rates

Fabrication of Gold and Silver Nanoparticles Supported on Zinc Imidazolate Metal-Organic Frameworks as Active Catalysts for Hydrogen Release from Ammonia Borane.

Well-dispersed Au and Ag nanoparticles (NPs) have been immobilized on a zinc imidazolate metal-organic framework, Zn(mim), using the "one-pot" method and tested as catalysts in ammonia borane hydrolysis. The AuNPs@Zn(mim) and AgNPs@Zn(mim) materials were characterized by FTIR, XRD, ICP-OES, TGA, BET, SEM, and TEM. The AgNPs@Zn(mim) catalyst showed a high yield (98.5%) and high hydrogen generation rate (3352.71 mL min-1 gAg -1) in NH3BH3 dehydrogenation. The determined activation energies (19.6 kJ mol-1 for AuNPs@Zn(mim) and 38.13 kJ mol-1 for AgNPs@Zn(mim)) are lower than those for most reported catalysts containing Au/Ag-MOF used in the hydrolysis of NH3BH3. Moreover, the catalysts tested here revealed good stability and reusability, preserving 71.42% (AuNPs@Zn(mim)) and 88.23% (AgNPs@Zn(mim)) of their initial catalytic activities after five consecutive cycles. In the case of AgNPs@Zn(mim), the combination of the simple and green synthesis method, low active metal content, relatively low cost, and moderate dehydrogenation conditions makes the material an excellent candidate to produce hydrogen from ammonia borane.

Unveiling O2 adsorption on non-metallic active site for selective photocatalytic H2O2 production

Photocatalytic oxygen reduction reaction (ORR) offers a promising pathway for sustainable hydrogen peroxide (H2O2) production but faces challenges in developing catalysts with good ORR selectivity. Herein, we report that tailoring O2 adsorption on non-metallic active sites can optimize ORR selectivity. This concept is demonstrated on three carbon nitrides with different atomic configurations: polymeric carbon nitride (PCN), lithium-poly triazine imide (Li-PTI), and sodium-poly heptazine imide (Na-PHI). Na-PHI emerges as a strong candidate for H2O2 production due to the end-on adsorption mode and suitable adsorption strength with O2. Synthesized Na-PHI, PCN, and Li-PTI are characterized, with Na-PHI showing superior light absorption, charge carrier separation, and remarkable selectivity (92 %) for two-electron ORR. Consequently, Na-PHI achieves a high H2O2 generation rate of 3.48 mmol g−1 h−1, surpassing Li-PTI and PCN by 9.2 and 33 times, respectively. This study underscores the importance of O2 adsorption on non-metallic active sites for selective photocatalytic H2O2 generation.

Directional Electron Flow in a Selenoviologen-Based Tetracationic Cyclophane for Enhanced Visible-Light-Driven Hydrogen Evolution.

Directional electron flow in the photocatalyst enables efficient charge separation, which is essential for efficient photocatalysis of H2 production. Here, we report a novel class of tetracationic cyclophanes (7) incorporating bipyridine Pt(II) and selenoviologen. X-ray single-crystal structures reveal that 7 not only fixes the distances and spatial positions between its individual units but also exhibits a box-like rigid electron-deficient cavity. Moreover, host-guest recognition phenomena are observed between 7 and ferrocene, forming host-guest complexes with a 1 : 1 stoichiometry. 7 exhibits good redox properties, narrow energy gaps, and strong absorption in the visible range (370-500 nm) due to containing two selenoviologen (SeV2+) units. Meanwhile, the femtosecond transient absorption (fs-TA) reveals that 7 has stabilized dicationic biradical, efficient charge separation, and facilitates directional electron flow to achieve efficient electron transfer due to the formation of rigid cyclophane and electronic architecture. Then, 7 is applied to visible-light-driven hydrogen evolution with high hydrogen production (132 μmol), generation rate (11 μmol/h), turnover number (221), and apparent quantum yield (1.7 %), which provides a simplified and efficient photocatalytic strategy for solar energy conversion.

Enhanced stability in Co0.8Ni0.2/NDMCS catalysts: Carbon nitride encapsulation for robust hydrogen generation

Catalytic hydrolysis of NaBH4 is a promising method for "on-demand" hydrogen generation, with cobalt catalysts playing a key role due to their high hydrogen generation rates. However, rapid cobalt dissolution and poor recycling hinder stable hydrogen production. This study presents a dual-mode stabilization technique using carbon nitride encapsulation to address these challenges. Co0.8Ni0.2 alloy nanoparticles (NPs) are confined within N-doped mesoporous carbon spheres (NDMCS) and encapsulated with a carbon nitride shell (∼ 5 nm thick). XPS results reveal strong non-classical metal-support interaction, increasing activation energy from 38.82 to 44.6 kJ mol−1, which controls cobalt's reactivity, leading to excellent recycling efficiency (90 % retention of initial rate, no change in particle size) in high-concentration reactants (2 %NaBH4 + 2 %NaOH). The retention rate drops to 26.8 % without this stabilization due to rapid metal dissolution. This stability of Co0.8Ni0.2 alloy in alkaline conditions has significant practical implications for hydrogen generation and other electrochemical applications.

Directional Electron Flow in a Selenoviologen‐Based Tetracationic Cyclophane for Enhanced Visible‐Light‐Driven Hydrogen Evolution

AbstractDirectional electron flow in the photocatalyst enables efficient charge separation, which is essential for efficient photocatalysis of H2 production. Here, we report a novel class of tetracationic cyclophanes (7) incorporating bipyridine Pt(II) and selenoviologen. X‐ray single‐crystal structures reveal that 7 not only fixes the distances and spatial positions between its individual units but also exhibits a box‐like rigid electron‐deficient cavity. Moreover, host–guest recognition phenomena are observed between 7 and ferrocene, forming host–guest complexes with a 1 : 1 stoichiometry. 7 exhibits good redox properties, narrow energy gaps, and strong absorption in the visible range (370–500 nm) due to containing two selenoviologen (SeV2+) units. Meanwhile, the femtosecond transient absorption (fs‐TA) reveals that 7 has stabilized dicationic biradical, efficient charge separation, and facilitates directional electron flow to achieve efficient electron transfer due to the formation of rigid cyclophane and electronic architecture. Then, 7 is applied to visible‐light‐driven hydrogen evolution with high hydrogen production (132 μmol), generation rate (11 μmol/h), turnover number (221), and apparent quantum yield (1.7 %), which provides a simplified and efficient photocatalytic strategy for solar energy conversion.

Room-temperature efficient and tunable interlayer exciton emissions in WS2/WSe2 heterobilayers at high generation rates.

Transition metal dichalcogenide (TMDC) heterobilayers (HBs) have been intensively investigated lately because they offer novel platforms for the exploration of interlayer excitons (IXs). However, the potentials of IXs in TMDC HBs have not been fully studied as efficient and tunable emitters for both photoluminescence (PL) and electroluminescence (EL) at room temperature (RT). Also, the efficiencies of the PL and EL of IXs have not been carefully quantified. In this work, we demonstrate that IX in WS2/WSe2 HBs could serve as promising emitters at high generation rates due to its immunity to efficiency roll-off. Furthermore, by applying gate voltages to balance the electron and hole concentrations and to reinforce the built-in electric fields, high PL quantum yield (QY) and EL external quantum efficiency (EQE) of ∼0.48% and ∼0.11% were achieved at RT, respectively, with generation rates exceeding 1021 cm-2·s-1, which confirms the capabilities of IXs as efficient NIR light emitters by surpassing most of the intralayer emissions from TMDCs.

One-Dimensional Single-Crystal Mesoporous TiO2 Supported CuW6O24 Clusters as Photocatalytic Cascade Nanoreactor for Boosting Reduction of CO2 to CH4.

Constructing nanoreactors with multiple active sites in well-defined crystalline mesoporous frameworks is an effective strategy for tailoring photocatalysts to address the challenging of CO2 reduction. Herein, one-dimensional (1-D) mesoporous single-crystal TiO2 nanorod (MS-TiO2-NRs, ≈110nm in length, high surface area of 117 m2 g-1, and uniform mesopores of ≈7.0nm) based nanoreactors are prepared via a droplet interface directed-assembly strategy under mild condition. By regulating the interfacial energy, the 1-D mesoporous single-crystal TiO2 can be further tuned to polycrystalline fan- and flower-like morphologies with different oxygen vacancies (Ov). The integration of single-crystal nature and mesopores with exposed oxygen vacancies make the rod-like TiO2 nanoreactors exhibit a high-photocatalytic CO2 reduction selectivity to CO (95.1%). Furthermore, photocatalytic cascade nanoreactors by in situ incorporation of CuW6O24 (W-Cu) clusters onto MS-TiO2-NRs via Ov are designed and synthesized, which improved the CO2 adsorption capacity and achieved two-step CO2-CO-CH4 photoreduction. The second step CO-to-CH4 reaction induced by W-Cu sites ensures a high generation rate of CH4 (420.4µmol g-1 h-1), along with an enhanced CH4 selectivity (≈94.3% electron selectivity). This research provides a platform for the design of mesoporous single-crystal materials, which potentially extends to a range of functional ceramics and semiconductors for various applications.

Porous polyselenoviologen with long-lived charge separated states and highly cyclic stability for heterogeneous photocatalytic reaction and hydrogen production

A highly stable heterogeneous photocatalyst, porous polyselenoviologen (POP-SeV2+), was successfully synthesized via SN2 reaction. Compared to the monomer, POP-SeV2+ exhibited strong visible-light absorption, enhanced electron acceptor property, and prolonged lifetime of radical cations. Simultaneously, the femtosecond transient absorption (fs-TA) illustrated that the formation of tetrahedral multi-cationic structure is conducive to the rapid generation of molecular excited states and extending the duration of charge-separated states. Due to its remarkable characteristics, the POP-SeV2+ was employed as a photocatalyst for visible-light-induced cross-dehydrogenative coupling (CDC) reactions with a highly efficient yield (82 %). Additionally, its utilization was further extended to the hydrogen generation, demonstrating remarkable outcomes such as a high rate of H2 generation (300 μmol·h−1·g−1), and an apparent quantum yield (0.13 %). Notably, POP-SeV2+ displayed great stability and reusability in the photocatalytic process, which can distinguish it from those soluble SeV2+-based photocatalysts. The catalytic efficiency of POP-SeV2+ remained virtually unaffected even after undergoing several recycling cycles, which not only achieved the complete heterogeneous photocatalysis of SeV2+-based systems for the first time but also provided a new strategy to improve the application effect of viologen derivatives in solar energy conversion and utilization.

Polarization-entangled photon-pair source with van der Waals 3R-WS2 crystal

Ultracompact entangled photon sources are pivotal to miniaturized quantum photonic devices. Van der Waals (vdW) nonlinear crystals promise efficient photon-pair generation and on-chip monolithic integration with nanophotonic circuitry. However, it remains challenging to generate maximally entangled Bell states of photon pairs with high purity, generation rate, and fidelity required for practical applications. Here, we realize a polarization-entangled photon-pair source based on spontaneous parametric down conversion in an ultrathin rhombohedral tungsten disulfide (3R-WS2) crystal. This vdW entangled photonic source exhibits a high photon-pair purity with a coincidence-to-accidental ratio of above 800, a generation rate of 31 Hz, and two maximally polarization-entangled Bell states with fidelities exceeding 0.93 and entanglement degree over 0.97. These results stem from scalable optical nonlinearity, enhanced second-order susceptibility by electronic transitions, and a well-defined symmetry-enabled selection rule inherent in 3R-WS2. Our polarization entangled photon source can be integrated with photonic structures for generating more complex entangled states, thus paving an avenue for advanced quantum photonic systems toward computation and metrology.

الوضع الراهن لتداول المخلفات الصلبة في المنطقة الغربية من ليبيا

Proper planning for solid waste management, as well as working to provide appropriate data and statistics related to the causes of the problem, are among the most important effective means that contribute to achieving sustainable development. Since the problem of waste accumulation has become a source of concern, this study aimed to evaluate the current situation of municipal solid waste in the western region of Libya and estimate the effects of some social and economic factors on the waste generation. Working teams have been formed to communicate with the competent official authorities to collect the necessary data regarding waste management, amount of generation, composition, means of transporting waste and transfer stations. The data were analyzed and the obtained results showed that the estimated quantity of solid waste generated from Surman, Sabratha and Al-Jameel was 31,450 tons/year at a rate of 0.95 kg/capita/day, 61,700 tons/year at a rate 1.3 kg/capita/day and 33,600 tons/year at a rate of 1 kg/capita/day, respectively. Comparing these rates with generation rates for different Libyan cities shows that the highest generation rate was in the municipality of Sabratha. The average percentages of the various components of the composition of solid household waste generated by the population of the study area compared to the Tripoli and Benghazi area were close to each other. In general, food waste constitutes the largest percentage and in a larger quantity in Benghazi. As for solid waste management in general in terms of transportation and disposal, it is uneven as a result of poor planning and the lack of devices and equipment necessary to collect and transport waste from cities to the landfill site. Solid waste is considered a national wealth that can generate significant returns due to the possibility of recycling and using most of its components. Random disposal wastes materials that may be of high economic value, in addition to the accompanying negative effects on the environment and health.

Calcium Citrate Amount and Gelatine Source Impact on Hydroxyapatite Formation in Bone Regeneration Material in Simulated Body Fluid.

Bone grafting is crucial for bone regeneration. Recent studies have proposed the use of calcium citrate (CC) as a potential graft material. Notably, citrate does not inhibit hydroxyapatite (HAp) formation at specific calcium-to-citrate molar ratios. Octacalcium phosphate (OCP)/gelatine (Gel) composites, which are commonly produced from porcine Gel, are valued for their biodegradability and bone replacement capability. This study introduces fish Gel as an alternative to porcine Gel because of its wide acceptance and eco-friendliness. This is the first study to examine the interaction effects between two osteogenic materials, OCP/CC, and the influence of different gelatine matrix components on HAp formation in an SBF. Samples with varying CC contents were immersed in an SBF for 7 d and analysed using various techniques, confirming that high CC doses prevent HAp formation, whereas lower doses facilitate it. Notably, small-sized OCP/CC/porcine Gel composites exhibit a high HAp generation rate. Porcine Gel composites form denser HAp clusters, whereas fish Gel composites form larger spherical HAps. This suggests that lower CC doses not only avoid inhibiting HAp formation but also enhance it with the OCP/Gel composite. Compared with porcine Gel, fish Gel composites show less nucleation but an increased crystal growth for HAp.

Exoelectrogenic behaviors of Shewanella oneidensis MR-1 and cytochrome knock-out mutants on smooth electrodes of different materials

The development of anodes supporting a high rate of current generation stands as a crucial and challenging aspect in microbial electrochemical systems. A well-defined electrode surface morphology is essential for comprehending the impact of material intrinsic properties on microbial current generation, offering molecular insights into the respiration of exoelectrogens with electrodes made of diverse materials. We fabricated smooth electrodes (root mean square roughness below 10 nm) using four materials, each representing a distinct class of materials commonly utilized to construct bioanodes. These electrodes were employed to investigate current generation, electrochemical characteristics, and biofilm formation by Shewanella oneidensis MR-1 and mutants lacking cytochromes MtrC (ΔmtrC), MtrA (ΔmtrA), or CymA (ΔcymA). In reactors inoculated with MR-1, the poly(3,4-ethylenedioxythiophene) polystyrene sulfonate electrodes demonstrated a current density of 12.5 ± 1.1 μA cm-2, surpassing the 3.57 ± 0.50 μA cm-2 observed with indium tin oxide electrodes, while current generation levels by gold and glassy carbon electrodes fell in between. This disparity was not attributed to distinct biofilm formations by MR-1, as it formed stable monolayer biofilms on all types of working electrodes. At least five electron transfer pathways were identified in the MR-1 Vammograms, with the activities of these pathways depending on the electrode materials. The effectiveness of both endogenous and exogenous electron mediators varied with the electrode materials involved. Additionally, a phenazine compound exhibited diverse formal potentials when interacting with the biofilm and different types of electrodes. The mutants displayed varying degrees of impaired current generation and biofilm formation capabilities, with ΔmtrA and ΔcymA being the most affected regardless of the electrode used. However, for a specific mutant, the overall current generation, relative contribution by individual pathways, and biofilm formations underwent significant changes based on the electrode materials employed.

Observation of highly correlated ultrabright biphotons through increased atomic ensemble density in spontaneous four-wave mixing

The pairing ratio, a crucial metric assessing a biphoton source's ability to generate correlated photon pairs, remains underexplored despite theoretical predictions. This study presents experimental findings on the pairing ratio, utilizing a double-Λ spontaneous four-wave mixing biphoton source in cold atoms. At an optical depth (OD) of 20, we achieved an ultrahigh biphoton generation rate of up to 1.3×107 per second, with a successful pairing ratio of 61%. Increasing the OD to 120 significantly improved the pairing ratio to 89%, while maintaining a consistent biphoton generation rate. This achievement, marked by high generation rates and robust biphoton pairing, holds great promise for advancing efficiency in quantum communication and information processing. Additionally, in a scenario with a lower biphoton generation rate of 5.0×104 per second, we attained an impressive signal-to-background ratio of 241 for the biphoton wavepacket, surpassing the Cauchy-Schwarz criterion by approximately 1.5×104 times. Published by the American Physical Society 2024