No matter whether a system is operated manually or automatically controlled by computer, the system’s vulnerability always exists. Earthquake Disaster Reduction System (EDRS) belongs to the category of information sy...No matter whether a system is operated manually or automatically controlled by computer, the system’s vulnerability always exists. Earthquake Disaster Reduction System (EDRS) belongs to the category of information system. According to the features of security for EDRS, the steps and the methods on how to build the EDRS security were analyzed. The EDRS security features, security strategies and security measures were also given through a distributed EDRS skeleton that has been applied. Because there was still no appointed and authoritative agency or organization to certify and test EDRS security in China, a national information technology security certification center was introduced and suggested for the certification of the EDRS security. Finally, several discussions and tendencies for the EDRS development were presented.展开更多
Through investigation on the international development trend of earthquake disaster reduction system(EDRS)researches,a well finished Daqing Oilfield EDRS is introduced.Based on the PC System,redevelopment of the EDRS ...Through investigation on the international development trend of earthquake disaster reduction system(EDRS)researches,a well finished Daqing Oilfield EDRS is introduced.Based on the PC System,redevelopment of the EDRS skeleton is well discussed,including the technical skeleton,function composition,structures of software and hardware,redevelopment languages,database,and remote linking and calling of analysis modules.Meanwhile,it is pointed out that extending and utilizing the function of remote sensing information on the basis of the current distributed EDRS skeleton will become another study direction of EDRS.展开更多
Stannous chloride dihydrate is used as an efficient catalyst in reductive cyclization of 2-nitro-5- substituted aniline Schiff base leading to stable 2,5-disubstitued benzimidazole derivatives in excellent yields with...Stannous chloride dihydrate is used as an efficient catalyst in reductive cyclization of 2-nitro-5- substituted aniline Schiff base leading to stable 2,5-disubstitued benzimidazole derivatives in excellent yields with good purity. It provides a novel method of synthesis of 2,5-disubstitued benzimidazole under reductive system at room temperature.展开更多
s: Vinous aromatic nitro compounds could be selectively and rapidly reduced to the corresponding amines in excellent yields by potassium borohydride - bismuth chloride/ethanol-water, a new and facile reductive system.
Water scarcity is an escalating global crisis,posing a severe threat to populations worldwide.Consequently,exploring various materials to remove emerging contaminants from freshwater sources has garnered significant a...Water scarcity is an escalating global crisis,posing a severe threat to populations worldwide.Consequently,exploring various materials to remove emerging contaminants from freshwater sources has garnered significant attention.In this regard,single-atom catalysis(SACs) has emerged as a catalyst of scientific progress in water purification and treatment methodologies during recent decades.SACs exhibit exceptional catalytic activity,selectivity and stability,due to their near-perfect atom utilization,highly unsaturated coordination environment and uniform reaction centers.However,a comprehensive and critical review encompassing the successful integration of SACs into water purification processes needs to be completed.This review aims to accentuate recent trends by presenting the synthesis,structure,and environment and energy application-relevant properties of SACs.The results show that a comprehensive and multi-perspective summary of the advantages of SACs in environmental remediation can have significant benefits,such as fast kinetics,costeffectiveness,selectivity.The oxidation and reduction processes of SACs and functional SACs materials in water purification were emphasized.Furthermore,the last section is devoted to the current research gaps and further perspectives on the application of SACs in water treatment,which are summarized and analyzed.展开更多
Solid waste and air pollution are never ending environmental problems that can be partially solved by turning waste into useful bio-products. In this study, enzymatic solutions were developed by formulating enzymatic ...Solid waste and air pollution are never ending environmental problems that can be partially solved by turning waste into useful bio-products. In this study, enzymatic solutions were developed by formulating enzymatic solutions from fish intestines and fruit peels. This aimed to help in biodegradation of organic solid wastes. Organic waste samples were treated with formulated enzymatic solutions for 7 days in aerated set-up for aerobic degradation. Biodegradability and odor of the waste samples were compared with commercial enzymatic solution. Determination of evolved carbon dioxide (CO2) using gravimetric analysis (GA) was used to determine the percent biodegradability, Dt, of organic solid waste and odor-ranking method was used to determine the odor intensity of the organic waste samples. The result showed that the weight loss and percentage biodegradability of organic waste sample treated with formulated enzymatic solution is comparable with that of the commercial enzymatic solution. In terms of odor intensity, waste treated with the product, formulated enzymatic solution (FES) is also comparable to the waste treated with commercial enzymatic solution. Thus, implying that the developed FES is as efficient as that of the commercial enzymatic solution. These significant results will be helpful to future researchers in providing ways on improving the degradation of organic solid waste and mitigating the increasing glitches on our environment. Enzyme kinetics, physical and chemical properties studies of the solution were recommended for future researchers to accurately determine the effectiveness of the formulated enzymatic solution in the degradation of organic solid waste.展开更多
In this study,we present a self-driven photoelectrocatalytic(SD-PEC)system that effectively treats complex uranium-bearing wastewaters for both uranium recovery and organic matter decomposition while generating power....In this study,we present a self-driven photoelectrocatalytic(SD-PEC)system that effectively treats complex uranium-bearing wastewaters for both uranium recovery and organic matter decomposition while generating power.The system utilizes a titanium dioxide nanorod array(TNR)photoelectrode coupled with a silicon solar cell to optimize electron transport,while the cathode is composed of a carbon fiber coated with carboxylated carbon nanotubes(CCNT/CF),which efficiently reduce UO_(2)^(2+).The results demonstrate significant removal efficiency of uranium(complete removal in 25 min at a rate constant of~0.248 min^(-1)),as well as substantial degradation of organic impurities.Furthermore,the system generates sufficient power output to light an LED lamp and exhibits superior performance under various complex wastewater conditions,including simulated seawater and real uranium tailings wastewater.These findings underscore the potential of the SD-PEC system as a versatile approach for sustainable treatment and energy recovery of radioactive wastewater.The significance of this research extends to global environmental challenges,offering an innovative solution for managing radioactive wastewater while simultaneously contributing to renewable energy generation.展开更多
An analytical method is proposed with the “stiffness gradient of the response” as a sensitivity metric, and the relationships between the vibration responses and stiffness changes are established. First, a 2-degree-...An analytical method is proposed with the “stiffness gradient of the response” as a sensitivity metric, and the relationships between the vibration responses and stiffness changes are established. First, a 2-degree-of-freedom (DOF) system is used as an example to propose a stiffness gradient-based evaluation method, taking the effective control bandwidth ratio as a metric of effectiveness. The results show that there is an optimal mass ratio in both variable mass and variable stiffness cases. Then, a typical 16-DOF system is used to investigate the frequency domain characteristics of the stiffness gradient values in the complex system. The distributions of stiffness gradient values show multiple peak intervals corresponding to the sensitive regions for vibration control. By assigning random mass parameters, a significant exponential decay relationship between the subsystem’s mass and effective control is identified, emphasizing the importance of the optimal mass ratio. The finite-element simulation results of solid plate models with springs and oscillators further validate the theoretical results. In short, the gradient value of stiffness effectively quantifies the effects of subsystems on vibration control, providing an analytical tool for active control in complex systems. The identified exponential decay relationship offers meaningful guidance for implementation strategies.展开更多
This study demonstrates the electrochemical reduction of carbon monoxide(COR)at high current densities in a zero-gap electrolyzer cell and cell stack.By systematically optimizing both the commercially available membra...This study demonstrates the electrochemical reduction of carbon monoxide(COR)at high current densities in a zero-gap electrolyzer cell and cell stack.By systematically optimizing both the commercially available membrane electrode assembly components(including binder content and gas diffusion layer)and the operating conditions,we could perform COR at current densities up to 1.4 A cm^(-2)with a maximum C2+selectivity of 90%.We demonstrated the scale-up to a 3×100 cm^(2)electrolyzer stack that can sustain stable operation at 1 A cm^(-2)for several hours without significant performance decay and with a total C2+selectivity of~80%and an ethylene selectivity of~40%.We provide critical insights into the holistic optimization of key system parameters,without using special catalysts or surface additives,which can pave the way for scalable and industrially viable COR processes.展开更多
Gas turbine rotors are complex dynamic systems with high-dimensional,discrete,and multi-source nonlinear coupling characteristics.Significant amounts of resources and time are spent during the process of solving dynam...Gas turbine rotors are complex dynamic systems with high-dimensional,discrete,and multi-source nonlinear coupling characteristics.Significant amounts of resources and time are spent during the process of solving dynamic characteristics.Therefore,it is necessary to design a lowdimensional model that can well reflect the dynamic characteristics of high-dimensional system.To build such a low-dimensional model,this study developed a dimensionality reduction method considering global order energy distribution by modifying the proper orthogonal decomposition theory.First,sensitivity analysis of key dimensionality reduction parameters to the energy distribution was conducted.Then a high-dimensional rotor-bearing system considering the nonlinear stiffness and oil film force was reduced,and the accuracy and the reusability of the low-dimensional model under different operating conditions were examined.Finally,the response results of a multi-disk rotor-bearing test bench were reduced using the proposed method,and spectrum results were then compared experimentally.Numerical and experimental results demonstrate that,during the dimensionality reduction process,the solution period of dynamic response results has the most significant influence on the accuracy of energy preservation.The transient signal in the transformation matrix mainly affects the high-order energy distribution of the rotor system.The larger the proportion of steady-state signals is,the closer the energy tends to accumulate towards lower orders.The low-dimensional rotor model accurately reflects the frequency response characteristics of the original high-dimensional system with an accuracy of up to 98%.The proposed dimensionality reduction method exhibits significant application potential in the dynamic analysis of highdimensional systems coupled with strong nonlinearities under variable operating conditions.展开更多
Layered transition metal hydroxides show distinct advantages in separately co-catalyzing CO_(2)reduction and H_(2)O oxidation at the electron-accumulating and hole-accumulating sites of wrapped heterojunction photocat...Layered transition metal hydroxides show distinct advantages in separately co-catalyzing CO_(2)reduction and H_(2)O oxidation at the electron-accumulating and hole-accumulating sites of wrapped heterojunction photocatalysts,while concurrently preventing side reactions and photocorrosion on the semiconductor surface.Herein,Ni-Co bimetallic hydroxides with varying Ni/Co molar ratios(Ni_(x)Co_(1-x)(OH)_(2),x=1,0.75,0.5,0.25,and 0)were grown in situ on a model 2D/2D S-scheme heterojunction composed of Cu_(2)O nanosheets and Fe_(2)O_(3)nanoplates to form a series of Cu_(2)O/Fe_(2)O_(3)@Ni_(x)Co_(1-x)(OH)_(2)(CF@NiCo)photocatalysts.The combined experimental and theoretical investigation demonstrates that incorporating an appropriate amount of Co into Ni(OH)_(2)not only modulates the energy band structure of Ni_(x)Co_(1-x)(OH)_(2),balances the electron-and hole-trapping abilities of the bifunctional cocatalyst and maximizes the charge separation efficiency of the heterojunction,but also regulates the d-band center of Ni_(x)Co_(1-x)(OH)_(2),reinforcing the adsorption and activation of CO_(2)and H_(2)O on the cocatalyst surface and lowering the rate-limiting barriers in the CO_(2)-to-CO and H_(2)O-to-O_(2)conversion.Benefiting from the Ni-Co synergy,the redox reactions proceed stoichiometrically.The optimized CF@Ni_(0.75)Co_(0.25)achieves CO and O_(2)yields of 552.7 and 313.0μmol gcat^(-1)h^(-1),respectively,11.3/9.9,1.6/1.7,and 4.5/5.9-fold higher than those of CF,CF@Ni,and CF@Co.This study offers valuable insights into the design of bifunctional noble-metal-free cocatalysts for high-performance artificial photosynthesis.展开更多
Experts and officials shared their insights on poverty reduction cooperation and sustainable development during the 2025 International Seminar on Global Poverty Reduction Partnerships.
Controllable synthesis of ultrathin metallene nanosheets and rational design of their spatial arrangement in favor of electrochemical catalysis are critical for their renewable energy applications.Here,a biomimetic de...Controllable synthesis of ultrathin metallene nanosheets and rational design of their spatial arrangement in favor of electrochemical catalysis are critical for their renewable energy applications.Here,a biomimetic design of“Trunk-Branch-Leaf”strategy is proposed to prepare the ultrathin edge-riched Zn-ene“leaves”with a thickness of~2.5 nm,adjacent Zn-ene cross-linked with each other,which are supported by copper nanoneedle“branches”on copper mesh“trunks,”named as Zn-ene/Cu-CM.The resulting superstructure enables the formation of an interconnected network and multiple channels,which can be used as an electrocatalytic CO_(2) reduction reaction(CO_(2)RR)electrode to allow a fast charge and mass transfer as well as a large electrolyte reservoir.By virtue of the distinctive structure,the obtained Zn-ene/Cu-CM electrode exhibits excellent selectivity and activity toward CO production with a maximum Faradaic efficiency of 91.3%and incredible partial current density up to 40 mA cm^(−2),outperforming most of the state-of-the-art Zn-based electrodes for CO_(2) reduction.The phenolphthalein color probe combined with in situ attenuated total reflection-infrared spectroscopy uncovered the formation of the localized pseudo-alkaline microenvironment at the interface of the Zn-ene/Cu-CM electrode.Theoretical calculations confirmed that the localized pH as the origin is responsible for the adsorption of CO_(2) at the interface and the generation of *COOH and *CO intermediates.This study offers valuable insights into developing efficient electrodes through synergistic regulation of reaction microenvironments and active sites,thereby facilitating the electrolysis of practical CO_(2) conversion.展开更多
The development of Pt-free catalysts for the oxygen reduction reaction(ORR)is a great issue for meeting the cost challenges of proton exchange membrane fuel cells(PEMFCs)in commercial applications.In this work,a serie...The development of Pt-free catalysts for the oxygen reduction reaction(ORR)is a great issue for meeting the cost challenges of proton exchange membrane fuel cells(PEMFCs)in commercial applications.In this work,a series of RuCo/C catalysts were synthesized by NaBH4 reduction method under the premise that the total metal mass percentage was 20%.X-ray diffraction(XRD)patterns and scanning electron microscopy(SEM)confirmed the formation of single-phase nanoparticles with an average size of 33 nm.Cyclic voltammograms(CV)and linear sweep voltammograms(LSV)tests indicated that RuCo(2:1)/C catalyst had the optimal ORR properties.Additionally,the RuCo(2:1)/C catalyst remarkably sustained 98.1% of its activity even after 3000 cycles,surpassing the performance of Pt/C(84.8%).Analysis of the elemental state of the catalyst surface after cycling using X-ray photoelectron spectroscopy(XPS)revealed that the Ru^(0) percentage of RuCo(2:1)/C decreased by 2.2%(from 66.3% to 64.1%),while the Pt^(0) percentage of Pt/C decreased by 7.1%(from 53.3% to 46.2%).It is suggested that the synergy between Ru and Co holds the potential to pave the way for future low-cost and highly stable ORR catalysts,offering significant promise in the context of PEMFCs.展开更多
Heteroatom-doped carbon is considered a promising alternative to commercial Pt/C as an efficient catalyst for the oxygen reduction reaction(ORR).This study presents the synthesis of iron-loaded,sulfur and nitrogen co-...Heteroatom-doped carbon is considered a promising alternative to commercial Pt/C as an efficient catalyst for the oxygen reduction reaction(ORR).This study presents the synthesis of iron-loaded,sulfur and nitrogen co-doped carbon(Fe/SNC)via in situ incorporation of 2-aminothiazole molecules into zeolitic imidazolate framework-8(ZIF-8)through coordination between metal ions and organic ligands.Sulfur and nitrogen doping in carbon supports effectively modulates the electronic structure of the catalyst,increases the Brunauer-Emmett-Teller surface area,and exposes more Fe-N_(x)active centers.Fe-loaded,S and N co-doped carbon with Fe/S molar ratio of 1:10(Fe/SNC-10)exhibits a half-wave potential of 0.902 V vs.RHE.After 5000 cycles of cyclic voltammetry,its half-wave potential decreases by only 20 mV vs.RHE,indicating excellent stability.Due to sulfur s lower electronegativity,the electronic structure of the Fe-N_(x)active center is modulated.Additionally,the larger atomic radius of sulfur introduces defects into the carbon support.As a result,Fe/SNC-10 demonstrates superior ORR activity and stability in alkaline solution compared with Fe-loaded N-doped carbon(Fe/NC).Furthermore,the zinc-air battery assembled with the Fe/SNC-10 catalyst shows enhanced performance relative to those assembled with Fe/NC and Pt/C catalysts.This work offers a novel design strategy for advanced energy storage and conversion applications.展开更多
Using photoelectrocatalytic CO_(2) reduction reaction(CO_(2)RR)to produce valuable fuels is a fascinating way to alleviate environmental issues and energy crises.Bismuth-based(Bi-based)catalysts have attracted widespr...Using photoelectrocatalytic CO_(2) reduction reaction(CO_(2)RR)to produce valuable fuels is a fascinating way to alleviate environmental issues and energy crises.Bismuth-based(Bi-based)catalysts have attracted widespread attention for CO_(2)RR due to their high catalytic activity,selectivity,excellent stability,and low cost.However,they still need to be further improved to meet the needs of industrial applications.This review article comprehensively summarizes the recent advances in regulation strategies of Bi-based catalysts and can be divided into six categories:(1)defect engineering,(2)atomic doping engineering,(3)organic framework engineering,(4)inorganic heterojunction engineering,(5)crystal face engineering,and(6)alloying and polarization engineering.Meanwhile,the corresponding catalytic mechanisms of each regulation strategy will also be discussed in detail,aiming to enable researchers to understand the structure-property relationship of the improved Bibased catalysts fundamentally.Finally,the challenges and future opportunities of the Bi-based catalysts in the photoelectrocatalytic CO_(2)RR application field will also be featured from the perspectives of the(1)combination or synergy of multiple regulatory strategies,(2)revealing formation mechanism and realizing controllable synthesis,and(3)in situ multiscale investigation of activation pathways and uncovering the catalytic mechanisms.On the one hand,through the comparative analysis and mechanism explanation of the six major regulatory strategies,a multidimensional knowledge framework of the structure-activity relationship of Bi-based catalysts can be constructed for researchers,which not only deepens the atomic-level understanding of catalytic active sites,charge transport paths,and the adsorption behavior of intermediate products,but also provides theoretical guiding principles for the controllable design of new catalysts;on the other hand,the promising collaborative regulation strategies,controllable synthetic paths,and the in situ multiscale characterization techniques presented in this work provides a paradigm reference for shortening the research and development cycle of high-performance catalysts,conducive to facilitating the transition of photoelectrocatalytic CO_(2)RR technology from the laboratory routes to industrial application.展开更多
Seawater zinc-air batteries are promising energy storage devices due to their high energy density and utilization of seawater electrolytes.However,their efficiency is hindered by the sluggish oxygen reduction reaction...Seawater zinc-air batteries are promising energy storage devices due to their high energy density and utilization of seawater electrolytes.However,their efficiency is hindered by the sluggish oxygen reduction reaction(ORR)and chlorideinduced degradation over conventional catalysts.In this study,we proposed a universal synthetic strategy to construct heteroatom axially coordinated Fe–N_(4) single-atom seawater catalyst materials(Cl–Fe–N_(4) and S–Fe–N_(4)).X-ray absorption spectroscopy confirmed their five-coordinated square pyramidal structure.Systematic evaluation of catalytic activities revealed that compared with S–Fe–N_(4),Cl–Fe–N_(4) exhibits smaller electrochemical active surface area and specific surface area,yet demonstrates higher limiting current density(5.8 mA cm^(−2)).The assembled zinc-air batteries using Cl–Fe–N_(4) showed superior power density(187.7 mW cm^(−2) at 245.1 mA cm^(−2)),indicating that Cl axial coordination more effectively enhances the intrinsic ORR activity.Moreover,Cl–Fe–N_(4) demonstrates stronger Cl−poisoning resistance in seawater environments.Chronoamperometry tests and zinc-air battery cycling performance evaluations confirmed its enhanced stability.Density functional theory calculations revealed that the introduction of heteroatoms in the axial direction regulates the electron center of Fe single atom,leading to more active reaction intermediates and increased electron density of Fe single sites,thereby enhancing the reduction in adsorbed intermediates and hence the overall ORR catalytic activity.展开更多
Owing to their global search capabilities and gradient-free operation,metaheuristic algorithms are widely applied to a wide range of optimization problems.However,their computational demands become prohibitive when ta...Owing to their global search capabilities and gradient-free operation,metaheuristic algorithms are widely applied to a wide range of optimization problems.However,their computational demands become prohibitive when tackling high-dimensional optimization challenges.To effectively address these challenges,this study introduces cooperative metaheuristics integrating dynamic dimension reduction(DR).Building upon particle swarm optimization(PSO)and differential evolution(DE),the proposed cooperative methods C-PSO and C-DE are developed.In the proposed methods,the modified principal components analysis(PCA)is utilized to reduce the dimension of design variables,thereby decreasing computational costs.The dynamic DR strategy implements periodic execution of modified PCA after a fixed number of iterations,resulting in the important dimensions being dynamically identified.Compared with the static one,the dynamic DR strategy can achieve precise identification of important dimensions,thereby enabling accelerated convergence toward optimal solutions.Furthermore,the influence of cumulative contribution rate thresholds on optimization problems with different dimensions is investigated.Metaheuristic algorithms(PSO,DE)and cooperative metaheuristics(C-PSO,C-DE)are examined by 15 benchmark functions and two engineering design problems(speed reducer and composite pressure vessel).Comparative results demonstrate that the cooperative methods achieve significantly superior performance compared to standard methods in both solution accuracy and computational efficiency.Compared to standard metaheuristic algorithms,cooperative metaheuristics achieve a reduction in computational cost of at least 40%.The cooperative metaheuristics can be effectively used to tackle both high-dimensional unconstrained and constrained optimization problems.展开更多
Accelerated industrialization combined with over-applied nitrogen fertilizers results in serious nitrate pollution insurface and ground water,disrupting the balance of the global nitrogen cycle.Electrochemical nitrate...Accelerated industrialization combined with over-applied nitrogen fertilizers results in serious nitrate pollution insurface and ground water,disrupting the balance of the global nitrogen cycle.Electrochemical nitrate reduction(eNO_(3)RR)emerges as an attractive strategy to simultaneously enable nitrate removal and decentralized ammo-nia fabrication,restoring the globally perturbed nitrogen cycle.However,complex deoxygenation-hydrogenationprocesses and sluggish proton-electron transfer kinetics significantly hinder practical application of eNO_(3)RR.In this study,we developed carbon-coated Cu-Ni bimetallic catalysts derived from metal-organic frameworks(MOFs)to facilitate eNO_(3)RR.The unique structural features of catalyst promote enhanced synergy between Cuand Ni,effectively addressing critical challenges in nitrate reduction.Comprehensive structural and electrochem-ical analysis demonstrate that electrochemical nitrate-to-nitrite conversion mainly takes place on active Cu sites,the introduction of Ni could efficiently accelerate the generation of aquatic active hydrogen,promoting the hy-drogenation of oxynitrides during eNO_(3)RR.In addition,Ni introduction could push up the d-band center of thecatalyst,thus enhancing the adsorption and activation of nitrate and the corresponding intermediates.Detailedreaction pathways for nitrate-to-ammonia conversion are illuminated by rotating disk electrode(RDE),in-situFourier-transform infrared spectroscopy,in-situ Raman spectrum and electrochemical impedance spectroscopy(EIS).Benefiting from the synergistic effect of Cu and Ni,optimum catalyst exhibited excellent nitrate reductionperformance.This work provides a new idea for elucidating the underlying eNO_(3)RR reaction mechanisms andcontributes a promising strategy for designing efficient bimetallic electrocatalysts.展开更多
Fe reducing bacteria(FRB),through extracellular electron transfer(EET)pathway,can reduce Fe(III)nanoparticles,thereby affecting the migration,transformation,and degradation of pollutants.However,the interaction of Fe(...Fe reducing bacteria(FRB),through extracellular electron transfer(EET)pathway,can reduce Fe(III)nanoparticles,thereby affecting the migration,transformation,and degradation of pollutants.However,the interaction of Fe(III)nanoparticles with the most commonly identified FRB,Geobacter sulfurreducens PCA,remains poorly understood.Herein,we demonstrated that the synergistic role of outer membrane proteins and periplasmic proteins in the EET process for-Fe_(2)O_(3),Fe3O4,and𝛽α-FeOOH nanoparticles by construction of multiple gene knockout strain.oxpG(involved in the type II secretion system)and omcST(outer membrane c-type cytochrome)medi-ated pathways accounted for approximately 67%of the total reduction of𝛼α-Fe_(2)O_(3) nanoparticles.The residual reduction of𝛼α-Fe_(2)O_(3) nanoparticles in∆oxpG-omcST strain was likely caused by redox-active substances in cell supernatant.Conversely,the reduction of dissolved Fe(III)was almost unaffected in∆oxpG-omcST strain at the same concentration.However,at high dissolved Fe(III)concentration,the reduction significantly decreased due to the formation of Fe(III)nanoparticles,suggesting that this EET process is specific to Fe(III)nanoparticles.Overall,our study provided a more comprehensive understanding for the EET pathways between G.sulfurreducens PCA and different Fe(III)species,enriching our knowledge on the role of microorganisms in iron biogeochemical cycles and remediation strategies of pollutants.展开更多
文摘No matter whether a system is operated manually or automatically controlled by computer, the system’s vulnerability always exists. Earthquake Disaster Reduction System (EDRS) belongs to the category of information system. According to the features of security for EDRS, the steps and the methods on how to build the EDRS security were analyzed. The EDRS security features, security strategies and security measures were also given through a distributed EDRS skeleton that has been applied. Because there was still no appointed and authoritative agency or organization to certify and test EDRS security in China, a national information technology security certification center was introduced and suggested for the certification of the EDRS security. Finally, several discussions and tendencies for the EDRS development were presented.
基金Sponsored by the National Project of Scientific and Technical Supporting Programs (Grant No. 2006BAC13B02)the Returned Study Overseas Foundation of Heilongjiang Province (Grant No. LC06C37)Institute of Engineering Mechanics, China Earthquake Administration Science Foundation (Grant No. 2006B04)
文摘Through investigation on the international development trend of earthquake disaster reduction system(EDRS)researches,a well finished Daqing Oilfield EDRS is introduced.Based on the PC System,redevelopment of the EDRS skeleton is well discussed,including the technical skeleton,function composition,structures of software and hardware,redevelopment languages,database,and remote linking and calling of analysis modules.Meanwhile,it is pointed out that extending and utilizing the function of remote sensing information on the basis of the current distributed EDRS skeleton will become another study direction of EDRS.
基金supported by Shanghai Municipal Natural Science Foundation(No.12ZR1434900)International Collabora-tion on Drugs and Diagnostics Innovation of Tropical Diseases in China(International S&T Cooperation 2010DFB73280)
文摘Stannous chloride dihydrate is used as an efficient catalyst in reductive cyclization of 2-nitro-5- substituted aniline Schiff base leading to stable 2,5-disubstitued benzimidazole derivatives in excellent yields with good purity. It provides a novel method of synthesis of 2,5-disubstitued benzimidazole under reductive system at room temperature.
文摘s: Vinous aromatic nitro compounds could be selectively and rapidly reduced to the corresponding amines in excellent yields by potassium borohydride - bismuth chloride/ethanol-water, a new and facile reductive system.
基金financially supported by the National Natural Science Foundation of China (No.52200055)the Natural Science Foundation of Jiangsu Province (No.BK20210483)+1 种基金China Postdoctoral Science Foundation (No.2022T150271)the Natural Science Research of Jiangsu Higher Education Institutions of China (No.23KJB610001)。
文摘Water scarcity is an escalating global crisis,posing a severe threat to populations worldwide.Consequently,exploring various materials to remove emerging contaminants from freshwater sources has garnered significant attention.In this regard,single-atom catalysis(SACs) has emerged as a catalyst of scientific progress in water purification and treatment methodologies during recent decades.SACs exhibit exceptional catalytic activity,selectivity and stability,due to their near-perfect atom utilization,highly unsaturated coordination environment and uniform reaction centers.However,a comprehensive and critical review encompassing the successful integration of SACs into water purification processes needs to be completed.This review aims to accentuate recent trends by presenting the synthesis,structure,and environment and energy application-relevant properties of SACs.The results show that a comprehensive and multi-perspective summary of the advantages of SACs in environmental remediation can have significant benefits,such as fast kinetics,costeffectiveness,selectivity.The oxidation and reduction processes of SACs and functional SACs materials in water purification were emphasized.Furthermore,the last section is devoted to the current research gaps and further perspectives on the application of SACs in water treatment,which are summarized and analyzed.
文摘Solid waste and air pollution are never ending environmental problems that can be partially solved by turning waste into useful bio-products. In this study, enzymatic solutions were developed by formulating enzymatic solutions from fish intestines and fruit peels. This aimed to help in biodegradation of organic solid wastes. Organic waste samples were treated with formulated enzymatic solutions for 7 days in aerated set-up for aerobic degradation. Biodegradability and odor of the waste samples were compared with commercial enzymatic solution. Determination of evolved carbon dioxide (CO2) using gravimetric analysis (GA) was used to determine the percent biodegradability, Dt, of organic solid waste and odor-ranking method was used to determine the odor intensity of the organic waste samples. The result showed that the weight loss and percentage biodegradability of organic waste sample treated with formulated enzymatic solution is comparable with that of the commercial enzymatic solution. In terms of odor intensity, waste treated with the product, formulated enzymatic solution (FES) is also comparable to the waste treated with commercial enzymatic solution. Thus, implying that the developed FES is as efficient as that of the commercial enzymatic solution. These significant results will be helpful to future researchers in providing ways on improving the degradation of organic solid waste and mitigating the increasing glitches on our environment. Enzyme kinetics, physical and chemical properties studies of the solution were recommended for future researchers to accurately determine the effectiveness of the formulated enzymatic solution in the degradation of organic solid waste.
基金supported by the National Natural Science Foundation of China(Nos.52170083,51808143)the Science and Technology Innovation Program of Hunan Province(No.2022RC1125)the Hunan Provincial Natural Science Foundation of China(No.2021JJ20007)。
文摘In this study,we present a self-driven photoelectrocatalytic(SD-PEC)system that effectively treats complex uranium-bearing wastewaters for both uranium recovery and organic matter decomposition while generating power.The system utilizes a titanium dioxide nanorod array(TNR)photoelectrode coupled with a silicon solar cell to optimize electron transport,while the cathode is composed of a carbon fiber coated with carboxylated carbon nanotubes(CCNT/CF),which efficiently reduce UO_(2)^(2+).The results demonstrate significant removal efficiency of uranium(complete removal in 25 min at a rate constant of~0.248 min^(-1)),as well as substantial degradation of organic impurities.Furthermore,the system generates sufficient power output to light an LED lamp and exhibits superior performance under various complex wastewater conditions,including simulated seawater and real uranium tailings wastewater.These findings underscore the potential of the SD-PEC system as a versatile approach for sustainable treatment and energy recovery of radioactive wastewater.The significance of this research extends to global environmental challenges,offering an innovative solution for managing radioactive wastewater while simultaneously contributing to renewable energy generation.
基金Project supported by the National Natural Science Foundation of China(Nos.52241103 and 52322505)the Natural Science Foundation of Hunan Province of China(No.2023JJ10055)。
文摘An analytical method is proposed with the “stiffness gradient of the response” as a sensitivity metric, and the relationships between the vibration responses and stiffness changes are established. First, a 2-degree-of-freedom (DOF) system is used as an example to propose a stiffness gradient-based evaluation method, taking the effective control bandwidth ratio as a metric of effectiveness. The results show that there is an optimal mass ratio in both variable mass and variable stiffness cases. Then, a typical 16-DOF system is used to investigate the frequency domain characteristics of the stiffness gradient values in the complex system. The distributions of stiffness gradient values show multiple peak intervals corresponding to the sensitive regions for vibration control. By assigning random mass parameters, a significant exponential decay relationship between the subsystem’s mass and effective control is identified, emphasizing the importance of the optimal mass ratio. The finite-element simulation results of solid plate models with springs and oscillators further validate the theoretical results. In short, the gradient value of stiffness effectively quantifies the effects of subsystems on vibration control, providing an analytical tool for active control in complex systems. The identified exponential decay relationship offers meaningful guidance for implementation strategies.
基金Nemzeti Kutatási Fejlesztésiés Innovációs Hivatal,Grant/Award Number:RRF-2.3.1-21-2022-00009Horizon 2020 Framework Programme,Grant/Award Number:862453。
文摘This study demonstrates the electrochemical reduction of carbon monoxide(COR)at high current densities in a zero-gap electrolyzer cell and cell stack.By systematically optimizing both the commercially available membrane electrode assembly components(including binder content and gas diffusion layer)and the operating conditions,we could perform COR at current densities up to 1.4 A cm^(-2)with a maximum C2+selectivity of 90%.We demonstrated the scale-up to a 3×100 cm^(2)electrolyzer stack that can sustain stable operation at 1 A cm^(-2)for several hours without significant performance decay and with a total C2+selectivity of~80%and an ethylene selectivity of~40%.We provide critical insights into the holistic optimization of key system parameters,without using special catalysts or surface additives,which can pave the way for scalable and industrially viable COR processes.
基金supported by the China Postdoctoral Science Foundation(No.2024M764171)the Postdoctoral Research Start-up Funds,China(No.AUGA5710027424)+1 种基金the National Natural Science Foundation of China(No.U2341237)the Development and construction funds for the School of Mechatronics Engineering of HIT,China(No.CBQQ8880103624)。
文摘Gas turbine rotors are complex dynamic systems with high-dimensional,discrete,and multi-source nonlinear coupling characteristics.Significant amounts of resources and time are spent during the process of solving dynamic characteristics.Therefore,it is necessary to design a lowdimensional model that can well reflect the dynamic characteristics of high-dimensional system.To build such a low-dimensional model,this study developed a dimensionality reduction method considering global order energy distribution by modifying the proper orthogonal decomposition theory.First,sensitivity analysis of key dimensionality reduction parameters to the energy distribution was conducted.Then a high-dimensional rotor-bearing system considering the nonlinear stiffness and oil film force was reduced,and the accuracy and the reusability of the low-dimensional model under different operating conditions were examined.Finally,the response results of a multi-disk rotor-bearing test bench were reduced using the proposed method,and spectrum results were then compared experimentally.Numerical and experimental results demonstrate that,during the dimensionality reduction process,the solution period of dynamic response results has the most significant influence on the accuracy of energy preservation.The transient signal in the transformation matrix mainly affects the high-order energy distribution of the rotor system.The larger the proportion of steady-state signals is,the closer the energy tends to accumulate towards lower orders.The low-dimensional rotor model accurately reflects the frequency response characteristics of the original high-dimensional system with an accuracy of up to 98%.The proposed dimensionality reduction method exhibits significant application potential in the dynamic analysis of highdimensional systems coupled with strong nonlinearities under variable operating conditions.
文摘Layered transition metal hydroxides show distinct advantages in separately co-catalyzing CO_(2)reduction and H_(2)O oxidation at the electron-accumulating and hole-accumulating sites of wrapped heterojunction photocatalysts,while concurrently preventing side reactions and photocorrosion on the semiconductor surface.Herein,Ni-Co bimetallic hydroxides with varying Ni/Co molar ratios(Ni_(x)Co_(1-x)(OH)_(2),x=1,0.75,0.5,0.25,and 0)were grown in situ on a model 2D/2D S-scheme heterojunction composed of Cu_(2)O nanosheets and Fe_(2)O_(3)nanoplates to form a series of Cu_(2)O/Fe_(2)O_(3)@Ni_(x)Co_(1-x)(OH)_(2)(CF@NiCo)photocatalysts.The combined experimental and theoretical investigation demonstrates that incorporating an appropriate amount of Co into Ni(OH)_(2)not only modulates the energy band structure of Ni_(x)Co_(1-x)(OH)_(2),balances the electron-and hole-trapping abilities of the bifunctional cocatalyst and maximizes the charge separation efficiency of the heterojunction,but also regulates the d-band center of Ni_(x)Co_(1-x)(OH)_(2),reinforcing the adsorption and activation of CO_(2)and H_(2)O on the cocatalyst surface and lowering the rate-limiting barriers in the CO_(2)-to-CO and H_(2)O-to-O_(2)conversion.Benefiting from the Ni-Co synergy,the redox reactions proceed stoichiometrically.The optimized CF@Ni_(0.75)Co_(0.25)achieves CO and O_(2)yields of 552.7 and 313.0μmol gcat^(-1)h^(-1),respectively,11.3/9.9,1.6/1.7,and 4.5/5.9-fold higher than those of CF,CF@Ni,and CF@Co.This study offers valuable insights into the design of bifunctional noble-metal-free cocatalysts for high-performance artificial photosynthesis.
文摘Experts and officials shared their insights on poverty reduction cooperation and sustainable development during the 2025 International Seminar on Global Poverty Reduction Partnerships.
基金supports of the National Natural Science Foundation of China(NSFC)(52021004,52394202)key project of the Joint Fund for Innovation and Development of Chongqing Natural Science Foundation(CSTB2022NSCQ-LZX0013)+1 种基金the National Natural Science Foundation of China(NSFC)(52301232,and 52476056)the Natural Science Foundation of Chongqing Province(2024NSCQ-MSX1109).
文摘Controllable synthesis of ultrathin metallene nanosheets and rational design of their spatial arrangement in favor of electrochemical catalysis are critical for their renewable energy applications.Here,a biomimetic design of“Trunk-Branch-Leaf”strategy is proposed to prepare the ultrathin edge-riched Zn-ene“leaves”with a thickness of~2.5 nm,adjacent Zn-ene cross-linked with each other,which are supported by copper nanoneedle“branches”on copper mesh“trunks,”named as Zn-ene/Cu-CM.The resulting superstructure enables the formation of an interconnected network and multiple channels,which can be used as an electrocatalytic CO_(2) reduction reaction(CO_(2)RR)electrode to allow a fast charge and mass transfer as well as a large electrolyte reservoir.By virtue of the distinctive structure,the obtained Zn-ene/Cu-CM electrode exhibits excellent selectivity and activity toward CO production with a maximum Faradaic efficiency of 91.3%and incredible partial current density up to 40 mA cm^(−2),outperforming most of the state-of-the-art Zn-based electrodes for CO_(2) reduction.The phenolphthalein color probe combined with in situ attenuated total reflection-infrared spectroscopy uncovered the formation of the localized pseudo-alkaline microenvironment at the interface of the Zn-ene/Cu-CM electrode.Theoretical calculations confirmed that the localized pH as the origin is responsible for the adsorption of CO_(2) at the interface and the generation of *COOH and *CO intermediates.This study offers valuable insights into developing efficient electrodes through synergistic regulation of reaction microenvironments and active sites,thereby facilitating the electrolysis of practical CO_(2) conversion.
基金Funded by the 111 Project(No.B17034)Open Project of Hubei Key Laboratory of Power System Design and Test for Electrical Vehicle(No.ZDSYS202212)+1 种基金Innovative Research Team Development Program of Ministry of Education of China(No.IRT_17R83)the Science and Technology Project of China Southern Power Grid Co.,Ltd.(No.GDKJXM20222546)。
文摘The development of Pt-free catalysts for the oxygen reduction reaction(ORR)is a great issue for meeting the cost challenges of proton exchange membrane fuel cells(PEMFCs)in commercial applications.In this work,a series of RuCo/C catalysts were synthesized by NaBH4 reduction method under the premise that the total metal mass percentage was 20%.X-ray diffraction(XRD)patterns and scanning electron microscopy(SEM)confirmed the formation of single-phase nanoparticles with an average size of 33 nm.Cyclic voltammograms(CV)and linear sweep voltammograms(LSV)tests indicated that RuCo(2:1)/C catalyst had the optimal ORR properties.Additionally,the RuCo(2:1)/C catalyst remarkably sustained 98.1% of its activity even after 3000 cycles,surpassing the performance of Pt/C(84.8%).Analysis of the elemental state of the catalyst surface after cycling using X-ray photoelectron spectroscopy(XPS)revealed that the Ru^(0) percentage of RuCo(2:1)/C decreased by 2.2%(from 66.3% to 64.1%),while the Pt^(0) percentage of Pt/C decreased by 7.1%(from 53.3% to 46.2%).It is suggested that the synergy between Ru and Co holds the potential to pave the way for future low-cost and highly stable ORR catalysts,offering significant promise in the context of PEMFCs.
基金financial support of the National Natural Science Foundation of China(No.52472271)the National Key Research and Development Program of China(No.2023YFE0115800)。
文摘Heteroatom-doped carbon is considered a promising alternative to commercial Pt/C as an efficient catalyst for the oxygen reduction reaction(ORR).This study presents the synthesis of iron-loaded,sulfur and nitrogen co-doped carbon(Fe/SNC)via in situ incorporation of 2-aminothiazole molecules into zeolitic imidazolate framework-8(ZIF-8)through coordination between metal ions and organic ligands.Sulfur and nitrogen doping in carbon supports effectively modulates the electronic structure of the catalyst,increases the Brunauer-Emmett-Teller surface area,and exposes more Fe-N_(x)active centers.Fe-loaded,S and N co-doped carbon with Fe/S molar ratio of 1:10(Fe/SNC-10)exhibits a half-wave potential of 0.902 V vs.RHE.After 5000 cycles of cyclic voltammetry,its half-wave potential decreases by only 20 mV vs.RHE,indicating excellent stability.Due to sulfur s lower electronegativity,the electronic structure of the Fe-N_(x)active center is modulated.Additionally,the larger atomic radius of sulfur introduces defects into the carbon support.As a result,Fe/SNC-10 demonstrates superior ORR activity and stability in alkaline solution compared with Fe-loaded N-doped carbon(Fe/NC).Furthermore,the zinc-air battery assembled with the Fe/SNC-10 catalyst shows enhanced performance relative to those assembled with Fe/NC and Pt/C catalysts.This work offers a novel design strategy for advanced energy storage and conversion applications.
基金supports from the National Natural Science Foundation of China(Grant Nos.12305372 and 22376217)the National Key Research&Development Program of China(Grant Nos.2022YFA1603802 and 2022YFB3504100)+1 种基金the projects of the key laboratory of advanced energy materials chemistry,ministry of education(Nankai University)key laboratory of Jiangxi Province for persistent pollutants prevention control and resource reuse(2023SSY02061)are gratefully acknowledged.
文摘Using photoelectrocatalytic CO_(2) reduction reaction(CO_(2)RR)to produce valuable fuels is a fascinating way to alleviate environmental issues and energy crises.Bismuth-based(Bi-based)catalysts have attracted widespread attention for CO_(2)RR due to their high catalytic activity,selectivity,excellent stability,and low cost.However,they still need to be further improved to meet the needs of industrial applications.This review article comprehensively summarizes the recent advances in regulation strategies of Bi-based catalysts and can be divided into six categories:(1)defect engineering,(2)atomic doping engineering,(3)organic framework engineering,(4)inorganic heterojunction engineering,(5)crystal face engineering,and(6)alloying and polarization engineering.Meanwhile,the corresponding catalytic mechanisms of each regulation strategy will also be discussed in detail,aiming to enable researchers to understand the structure-property relationship of the improved Bibased catalysts fundamentally.Finally,the challenges and future opportunities of the Bi-based catalysts in the photoelectrocatalytic CO_(2)RR application field will also be featured from the perspectives of the(1)combination or synergy of multiple regulatory strategies,(2)revealing formation mechanism and realizing controllable synthesis,and(3)in situ multiscale investigation of activation pathways and uncovering the catalytic mechanisms.On the one hand,through the comparative analysis and mechanism explanation of the six major regulatory strategies,a multidimensional knowledge framework of the structure-activity relationship of Bi-based catalysts can be constructed for researchers,which not only deepens the atomic-level understanding of catalytic active sites,charge transport paths,and the adsorption behavior of intermediate products,but also provides theoretical guiding principles for the controllable design of new catalysts;on the other hand,the promising collaborative regulation strategies,controllable synthetic paths,and the in situ multiscale characterization techniques presented in this work provides a paradigm reference for shortening the research and development cycle of high-performance catalysts,conducive to facilitating the transition of photoelectrocatalytic CO_(2)RR technology from the laboratory routes to industrial application.
基金funded by the Innovative Research Group Project of the National Natural Science Foundation of China(52121004)the Research Development Fund(No.RDF-21-02-060)by Xi’an Jiaotong-Liverpool University+1 种基金support received from the Suzhou Industrial Park High Quality Innovation Platform of Functional Molecular Materials and Devices(YZCXPT2023105)the XJTLU Advanced Materials Research Center(AMRC).
文摘Seawater zinc-air batteries are promising energy storage devices due to their high energy density and utilization of seawater electrolytes.However,their efficiency is hindered by the sluggish oxygen reduction reaction(ORR)and chlorideinduced degradation over conventional catalysts.In this study,we proposed a universal synthetic strategy to construct heteroatom axially coordinated Fe–N_(4) single-atom seawater catalyst materials(Cl–Fe–N_(4) and S–Fe–N_(4)).X-ray absorption spectroscopy confirmed their five-coordinated square pyramidal structure.Systematic evaluation of catalytic activities revealed that compared with S–Fe–N_(4),Cl–Fe–N_(4) exhibits smaller electrochemical active surface area and specific surface area,yet demonstrates higher limiting current density(5.8 mA cm^(−2)).The assembled zinc-air batteries using Cl–Fe–N_(4) showed superior power density(187.7 mW cm^(−2) at 245.1 mA cm^(−2)),indicating that Cl axial coordination more effectively enhances the intrinsic ORR activity.Moreover,Cl–Fe–N_(4) demonstrates stronger Cl−poisoning resistance in seawater environments.Chronoamperometry tests and zinc-air battery cycling performance evaluations confirmed its enhanced stability.Density functional theory calculations revealed that the introduction of heteroatoms in the axial direction regulates the electron center of Fe single atom,leading to more active reaction intermediates and increased electron density of Fe single sites,thereby enhancing the reduction in adsorbed intermediates and hence the overall ORR catalytic activity.
基金funded by National Natural Science Foundation of China(Nos.12402142,11832013 and 11572134)Natural Science Foundation of Hubei Province(No.2024AFB235)+1 种基金Hubei Provincial Department of Education Science and Technology Research Project(No.Q20221714)the Opening Foundation of Hubei Key Laboratory of Digital Textile Equipment(Nos.DTL2023019 and DTL2022012).
文摘Owing to their global search capabilities and gradient-free operation,metaheuristic algorithms are widely applied to a wide range of optimization problems.However,their computational demands become prohibitive when tackling high-dimensional optimization challenges.To effectively address these challenges,this study introduces cooperative metaheuristics integrating dynamic dimension reduction(DR).Building upon particle swarm optimization(PSO)and differential evolution(DE),the proposed cooperative methods C-PSO and C-DE are developed.In the proposed methods,the modified principal components analysis(PCA)is utilized to reduce the dimension of design variables,thereby decreasing computational costs.The dynamic DR strategy implements periodic execution of modified PCA after a fixed number of iterations,resulting in the important dimensions being dynamically identified.Compared with the static one,the dynamic DR strategy can achieve precise identification of important dimensions,thereby enabling accelerated convergence toward optimal solutions.Furthermore,the influence of cumulative contribution rate thresholds on optimization problems with different dimensions is investigated.Metaheuristic algorithms(PSO,DE)and cooperative metaheuristics(C-PSO,C-DE)are examined by 15 benchmark functions and two engineering design problems(speed reducer and composite pressure vessel).Comparative results demonstrate that the cooperative methods achieve significantly superior performance compared to standard methods in both solution accuracy and computational efficiency.Compared to standard metaheuristic algorithms,cooperative metaheuristics achieve a reduction in computational cost of at least 40%.The cooperative metaheuristics can be effectively used to tackle both high-dimensional unconstrained and constrained optimization problems.
基金supported by the Natural Science Foundation of China(No.52101279)the Key Scientific Research Foundation of Education department of Hunan Province(No.24A0003)the Scientific Research Project of Education Department of Hunan Province(No.21B000)and the Fundamental Research Funds for the Central Universities of Central South University.
文摘Accelerated industrialization combined with over-applied nitrogen fertilizers results in serious nitrate pollution insurface and ground water,disrupting the balance of the global nitrogen cycle.Electrochemical nitrate reduction(eNO_(3)RR)emerges as an attractive strategy to simultaneously enable nitrate removal and decentralized ammo-nia fabrication,restoring the globally perturbed nitrogen cycle.However,complex deoxygenation-hydrogenationprocesses and sluggish proton-electron transfer kinetics significantly hinder practical application of eNO_(3)RR.In this study,we developed carbon-coated Cu-Ni bimetallic catalysts derived from metal-organic frameworks(MOFs)to facilitate eNO_(3)RR.The unique structural features of catalyst promote enhanced synergy between Cuand Ni,effectively addressing critical challenges in nitrate reduction.Comprehensive structural and electrochem-ical analysis demonstrate that electrochemical nitrate-to-nitrite conversion mainly takes place on active Cu sites,the introduction of Ni could efficiently accelerate the generation of aquatic active hydrogen,promoting the hy-drogenation of oxynitrides during eNO_(3)RR.In addition,Ni introduction could push up the d-band center of thecatalyst,thus enhancing the adsorption and activation of nitrate and the corresponding intermediates.Detailedreaction pathways for nitrate-to-ammonia conversion are illuminated by rotating disk electrode(RDE),in-situFourier-transform infrared spectroscopy,in-situ Raman spectrum and electrochemical impedance spectroscopy(EIS).Benefiting from the synergistic effect of Cu and Ni,optimum catalyst exhibited excellent nitrate reductionperformance.This work provides a new idea for elucidating the underlying eNO_(3)RR reaction mechanisms andcontributes a promising strategy for designing efficient bimetallic electrocatalysts.
基金supported by the National Key Research and Development Project(No.2020YFA0907500)the National Natural Science Foundation of China(No.22476206)+1 种基金the supports from the National Young Top-Notch Talents(No.W03070030)Youth Innovation Promotion Association of the Chinese Academy of Sciences(No.Y202011).
文摘Fe reducing bacteria(FRB),through extracellular electron transfer(EET)pathway,can reduce Fe(III)nanoparticles,thereby affecting the migration,transformation,and degradation of pollutants.However,the interaction of Fe(III)nanoparticles with the most commonly identified FRB,Geobacter sulfurreducens PCA,remains poorly understood.Herein,we demonstrated that the synergistic role of outer membrane proteins and periplasmic proteins in the EET process for-Fe_(2)O_(3),Fe3O4,and𝛽α-FeOOH nanoparticles by construction of multiple gene knockout strain.oxpG(involved in the type II secretion system)and omcST(outer membrane c-type cytochrome)medi-ated pathways accounted for approximately 67%of the total reduction of𝛼α-Fe_(2)O_(3) nanoparticles.The residual reduction of𝛼α-Fe_(2)O_(3) nanoparticles in∆oxpG-omcST strain was likely caused by redox-active substances in cell supernatant.Conversely,the reduction of dissolved Fe(III)was almost unaffected in∆oxpG-omcST strain at the same concentration.However,at high dissolved Fe(III)concentration,the reduction significantly decreased due to the formation of Fe(III)nanoparticles,suggesting that this EET process is specific to Fe(III)nanoparticles.Overall,our study provided a more comprehensive understanding for the EET pathways between G.sulfurreducens PCA and different Fe(III)species,enriching our knowledge on the role of microorganisms in iron biogeochemical cycles and remediation strategies of pollutants.
