This work restored the erosion thickness of the top surface of each Cretaceous formations penetrated by the typical well in the Hari sag,and simulated the subsidence burial history of this well with software BasinMod....This work restored the erosion thickness of the top surface of each Cretaceous formations penetrated by the typical well in the Hari sag,and simulated the subsidence burial history of this well with software BasinMod.It is firstly pointed out that the tectonic subsidence evolution of the Hari sag since the Cretaceous can be divided into four phases:initial subsidence phase,rapid subsidence phase,uplift and erosion phase,and stable slow subsidence phase.A detailed reconstruction of the tectonothermal evolution and hydrocarbon generation histories of typical well was undertaken using the EASY R%model,which is constrained by vitrinite reflectance(R)and homogenization temperatures of fluid inclusions.In the rapid subsidence phase,the peak period of hydrocarbon generation was reached at c.a.105.59 Ma with the increasing thermal evolution degree.A concomitant rapid increase in paleotemperatures occurred and reached a maximum geothermal gradient of about 43-45℃/km.The main hydrocarbon generation period ensued around 105.59-80.00 Ma and the greatest buried depth of the Hari sag was reached at c.a.80.00 Ma,when the maximum paleo-temperature was over 180℃.Subsequently,the sag entered an uplift and erosion phase followed by a stable slow subsidence phase during which the temperature gradient,thermal evolution,and hydrocarbon generation decreased gradually.The hydrocarbon accumulation period was discussed based on homogenization temperatures of inclusions and it is believed that two periods of rapid hydrocarbon accumulation events occurred during the Cretaceous rapid subsidence phase.The first accumulation period observed in the Bayingebi Formation(Kb)occurred primarily around 105.59-103.50 Ma with temperatures of 125-150℃.The second accumulation period observed in the Suhongtu Formation(Ks)occurred primarily around84.00-80.00 Ma with temperatures of 120-130℃.The second is the major accumulation period,and the accumulation mainly occurred in the Late Cretaceous.The hydrocarbon accumulation process was comprehensively controlled by tectono-thermal evolution and hydrocarbon generation history.During the rapid subsidence phase,the paleo temperature and geothermal gradient increased rapidly and resulted in increasing thermal evolution extending into the peak period of hydrocarbon generation,which is the key reason for hydrocarbon filling and accumulation.展开更多
The Liwan Sag,with an area of 4000 km-2,is one of the deepwater sags in the Zhujiang River(Pearl River)Mouth Basin,northern South China Sea.Inspired by the exploration success in oil and gas resources in the deepwater...The Liwan Sag,with an area of 4000 km-2,is one of the deepwater sags in the Zhujiang River(Pearl River)Mouth Basin,northern South China Sea.Inspired by the exploration success in oil and gas resources in the deepwater sags worldwide,we conducted the thermal modeling to investigate the tectono-thermal history of the Liwan Sag,which has been widely thought to be important to understand tectonic activities as well as hydrocarbon potential of a basin.Using the multi-stage finite stretching model,the tectonic subsidence history and the thermal history have been obtained for 12 artificial wells,which were constructed on basis of one seismic profile newly acquired in the study area.Two stages of rifting during the time periods of 49–33.9 Ma and 33.9–23 Ma can be recognized from the tectonic subsidence pattern,and there are two phases of heating processes corresponding to the rifting.The reconstructed average basal paleo-heat flow values at the end of the rifting events are-70.5 and-94.2 mW/m^2 respectively.Following the heating periods,the study area has undergone a persistent thermal attenuation phase since 23 Ma and the basal heat flow cooled down to-71.8–82.5 mW/m^2 at present.展开更多
The Qaidam basin is the largest intermountain basin inside Tibet, and is one of the three major petroliferous basins in western China. This study discussed the geothermal field and tectono-thermal evolution of the bas...The Qaidam basin is the largest intermountain basin inside Tibet, and is one of the three major petroliferous basins in western China. This study discussed the geothermal field and tectono-thermal evolution of the basin, in an effort to provide evidence for intracontinental or intraplate continental dynamics and basin dynamics, petroleum resources assessment, and to serve petroleum production.展开更多
A composite electrocatalyst,CoMoNiO-S/NF-110(NF is nickel foam),was synthesized through electrodeposition,followed by pyrolysis and then the vulcanization process.CoMoNiO-S/NF-110 exhibited a structure where Ni3S2 and...A composite electrocatalyst,CoMoNiO-S/NF-110(NF is nickel foam),was synthesized through electrodeposition,followed by pyrolysis and then the vulcanization process.CoMoNiO-S/NF-110 exhibited a structure where Ni3S2 and Mo2S3 nanoparticles were integrated at the edges of Co3O4 nanosheets,creating a rich,heterogeneous interface that enhances the synergistic effects of each component.In an alkaline electrolyte,the synthesized CoMoNiO-S/NF-110 exhibited superior electrocatalytic performance for oxygen evolution reaction(OER),achieving current densities of 100 and 200 mA·cm^(-2) with low overpotentials of 199.4 and 224.4 mV,respectively,outperforming RuO2 and several high-performance Mo and Ni-based catalysts.This excellent performance is attributed to the rich interface formed between the components and active sites exposed by the defect structure.展开更多
The poor electrical conductivity of metal-organic frameworks(MOFs)limits their electrocatalytic performance in the oxygen evolution reaction(OER).In this study,a Py@Co-MOF composite material based on pyrene(Py)molecul...The poor electrical conductivity of metal-organic frameworks(MOFs)limits their electrocatalytic performance in the oxygen evolution reaction(OER).In this study,a Py@Co-MOF composite material based on pyrene(Py)molecules and{[Co2(BINDI)(DMA)_(2)]·DMA}_(n)(Co-MOF,H4BINDI=N,N'-bis(5-isophthalic acid)naphthalenediimide,DMA=N,N-dimethylacetamide)was synthesized via a one-pot method,leveragingπ-πinteractions between pyrene and Co-MOF to modulate electrical conductivity.Results demonstrate that the Py@Co-MOF catalyst exhibited significantly enhanced OER performance compared to pure Co-MOF or pyrene-based electrodes,achieving an overpotential of 246 mV at a current density of 10 mA·cm^(-2) along with excellent stability.Density functional theory(DFT)calculations reveal that the formation of O*in the second step is the rate-determining step(RDS)during the OER process on Co-MOF,with an energy barrier of 0.85 eV due to the weak adsorption affinity of the OH*intermediate for Co sites.CCDC:2419276.展开更多
The efficiency and stability of catalysts for photocatalytic hydrogen evolution(PHE)are largely governed by the charge transfer behaviors across the heterojunction interfaces.In this study,CuO,a typical semiconductor ...The efficiency and stability of catalysts for photocatalytic hydrogen evolution(PHE)are largely governed by the charge transfer behaviors across the heterojunction interfaces.In this study,CuO,a typical semiconductor featuring a broad spectral absorption range,is successfully employed as the electron acceptor to combine with CdS for constructing a S-scheme heterojunction.The optimized photocatalyst(CdSCuO2∶1)delivers an exceptional hydrogen evolution rate of 18.89 mmol/(g·h),4.15-fold higher compared with bare CdS.X-ray photoelectron spectroscopy(XPS)and ultraviolet-visible diffuse reflection absorption spectroscopy(UV-vis DRS)confirmed the S-scheme band structure of the composites.Moreover,the surface photovoltage(SPV)and electron paramagnetic resonance(EPR)indicated that the photogenerated electrons and photogenerated holes of CdS-CuO2∶1 were respectively transferred to the conduction band(CB)of CdS with a higher reduction potential and the valence band(VB)of CuO with a higher oxidation potential under illumination,as expected for the S-scheme mechanism.Density-functional-theory calculations of the electron density difference(EDD)disclose an interfacial electric field oriented from CdS to CuO.This built-in field suppresses charge recombination and accelerates carrier migration,rationalizing the markedly enhanced PHE activity.This study offers a novel strategy for designing S-scheme heterojunctions with high light harvesting and charge utilization toward sustainable solar-tohydrogen conversion.展开更多
Developing efficient and durable electrocatalysts for acidic oxygen evolution reaction(OER)is pivotal for advancing proton exchange membrane water electrolysis(PEMWEs),yet balancing activity and stability remains a fo...Developing efficient and durable electrocatalysts for acidic oxygen evolution reaction(OER)is pivotal for advancing proton exchange membrane water electrolysis(PEMWEs),yet balancing activity and stability remains a formidable challenge.Herein,we propose a dual-engineering strategy to stabilize Ru-based catalysts by synergizing the oxygen vacancy site-synergized mechanism-lattice oxygen mechanism(OVSM-LOM)with Ru-N bond stabilization.The engineered RuO_(2)@NCC catalyst exhibits exceptional OER performance in 0.5 M H2SO4,achieving an ultralow overpotential of 215 mV at 10 mA cm^(-2) and prolonged stability for over 327 h.The catalyst delivers 300 h of continuous operation at 1 A cm^(-2),with a negligible degradation rate of only 0.067 mV h-1,further demonstrating its potential for practical application.Oxygen vacancies unlock the OVSM-LOM pathway,bypassing the sluggish adsorbate evolution mechanism(AEM)and accelerating reaction kinetics,while the Ru-N bonds suppress Ru dissolution by anchoring low-valent Ru centers.Quasi-in situ X-ray photoelectron spectroscopy(XPS),X-ray absorption spectroscopy(XAS),and isotopic labeling experiments confirm the lattice oxygen participation with *O formation as the rate-determining step.The Ru-N bonds reinforce the structural integrity by stabilizing low-valent Ru centers and inhibiting overoxidation.Theoretical calculations further verify that the synergistic interaction between OVs and Ru-O(N)active sites optimizes the Ru d-band center and stabilizes intermediates,while Ru-N coordination enhances structural integrity.This study establishes a novel paradigm for designing robust acidic OER catalysts through defect and coordination engineering,bridging the gap between activity and stability for sustainable energy technologies.展开更多
Hydrogen production by electrolysis of water is a key technology to achieve green hydrogen energy economy,but it relies on advanced catalyst materials with high efficiency,stability,and wide pH adaptability.In this st...Hydrogen production by electrolysis of water is a key technology to achieve green hydrogen energy economy,but it relies on advanced catalyst materials with high efficiency,stability,and wide pH adaptability.In this study,Ni,Ru,and Pt ternary metals were embedded into nitrogen-doped hollow carbon spheres(NHCSs)by hydrothermal tandem heat treatment to form ternary supported metal nanoparticles with high dispersion and ultra-small particle size(~1.3 nm),which realized efficient hydrogen evolution from multi-scenario electrocatalytic water splitting.In the whole pH range,the performance of NiRuPt/NHCSs is better than that of commercial Pt/C catalyst,and the overpotentials under alkaline,neutral,and acidic conditions are as low as 15.5,20.0,and 29.5 mV,respectively.Under industrial conditions,NiRuPt/NHCSs also have excellent hydrogen evolution reaction(HER)performance,achieving efficient electrolysis of seawater for hydrogen production,and achieving Ampere-level hydrogen production at low voltage(~1.76 V)on integrated membrane electrode assemblies.Density functional theory(DFT)calculations show that in the NiRuPt ternary metal,the Pt site is conducive to promoting the desorption of*H to form H_(2),the Ru site is conducive to promoting the capture of H_(2)O,and the Ni site is conducive to promoting the dissociation of H_(2)O.Therefore,the formed NiRuPt ternary metal synergistically promotes multi-scenario efficient electrolysis of water to produce hydrogen.This study provides a new idea for the design of multi-component metal/carbon-based composite catalysts,and promotes the development of non-noble metal/noble metal composite catalysts in hydrogen production by electrolysis of water.展开更多
Serbisütherapy(ST)is a distinctive external treatment modality within traditional Mongolian medicine(TMM),historically developed within a nomadic cultural framework.This study presents a comprehensive philologica...Serbisütherapy(ST)is a distinctive external treatment modality within traditional Mongolian medicine(TMM),historically developed within a nomadic cultural framework.This study presents a comprehensive philological and historical analysis of ST,tracing its evolution from early battlefield applications to contemporary clinical use.By critically examining classical Mongolian medical texts alongside modern case studies,we aim to systematize ST’s therapeutic methods,indications,and limitations,while exploring its mechanisms of action through both traditional theory and modern biomedical perspectives.ST has undergone significant transformation,shifting from whole-body cavity immersion in the 13th century to targeted,organ-specific applications in modern practice.Its four primary methods–Covering,Mounted,Organ Placement,and Suction–demonstrate efficacy in treating cold-natured diseases,musculoskeletal disorders,gynecological conditions,and certain emergencies.ST embodies the core principles of TMM,particularly the balance of the“Three Roots”and the correction of cold-induced pathologies through heat.Despite challenges related to standardization,cultural translation,and regulatory acceptance,ST holds translational potential for integrative medicine.Future research should prioritize mechanistic validation,clinical standardization,and the development of biocompatible thermal technologies to bridge traditional practice with modern healthcare systems.展开更多
Oxygen evolution reaction(OER)is a key step in hydrogen production by water electrolysis technology.How-ever,developing efficient,stable,and low-cost OER electrocatalysts is still challenging.This article presents the...Oxygen evolution reaction(OER)is a key step in hydrogen production by water electrolysis technology.How-ever,developing efficient,stable,and low-cost OER electrocatalysts is still challenging.This article presents the preparation of a series of novel copper iridium nanocatalysts with heterostructures and low iridium content for OER.The electrochemical tests revealed higher OER of Cu@Ir_(0.3) catalyst under acidic conditions with a generated current density of 10 mA/cm^(2) at only 284 mV overpotential.The corresponding OER mass activity was estimated to be 1.057 A/mgIr,a value 8.39-fold higher than that of the commercial IrO_(2).After 50 h of endurance testing,the Cu@Ir_(0.3) catalyst preserved excellent catalytic activity with a negligible rise in overpotential and maintained a good heterostructures.Cu@Ir_(0.3) The excellent OER activity can be attributed to its heterostructure,as con-firmed by density functional theory(DFT)calculations,indicating that Cu@Ir The coupling between isoquanta causes charge redistribution,optimizing the adsorption energy of unsaturated Ir sites for oxygen intermediates and reducing the energy barrier of OER free energy determining the rate step.In summary,this method provides a new approach for designing efficient,stable,and low iridium content OER catalysts.展开更多
Deep insights into electrocatalytic mechanisms are vital for the rational design of catalysts for oxygen evolution reaction(OER).Mechanistically,the OER driven by adsorbate evolution mechanism(AEM)is limited by the li...Deep insights into electrocatalytic mechanisms are vital for the rational design of catalysts for oxygen evolution reaction(OER).Mechanistically,the OER driven by adsorbate evolution mechanism(AEM)is limited by the linear scaling relationship,thereby exhibiting large overpotentials.In the lattice oxygen mechanism(LOM),the OER can be enhanced by enabling direct O_(2)formation.However,this enhancement is accompanied by the generation of oxygen vacancies,which presents a significant challenge to the long-term stability of LOMOER,particularly when operating at high current densities.Recently,the*O-*O coupling mechanism(OCM)has emerged as a promising alternative;it not only breaks the linear scaling relationship but also ensures catalytic stability.This review encapsulates the cutting-edge advancements in electrocatalysts that are grounded in the OCM,offering a detailed interpretation on the foundational principles guiding the design of OCM-OER catalysts.It also highlights recent theoretical investigations combining machine learning(ML)with density functional theory(DFT)calculations to reveal OER mechanisms.At the end of this review,the challenges and opportunities associated with OCM-OER electrocatalysts are discussed.展开更多
The dissimilar 2B06 and 7B04 Al alloy joints were prepared by refill friction stir spot welding(RFSSW),and the microstructural evolution and corrosion behavior of the joints were investigated.Based on microstructural ...The dissimilar 2B06 and 7B04 Al alloy joints were prepared by refill friction stir spot welding(RFSSW),and the microstructural evolution and corrosion behavior of the joints were investigated.Based on microstructural analysis,the welded joints exhibit distinct microstructural zones,including the stir zone(SZ),thermomechanically affected zone(TMAZ),and heat-affected zone(HAZ).The grain size of each zone is in the order of HAZ>TMAZ>SZ.Notably,the TMAZ and HAZ contain significantly larger secondary-phase particles compared to the SZ,with particle size in the HAZ increasing at higher rotational speeds.Electrochemical tests indicate that corrosion susceptibility follows the sequence of HAZ>TMAZ>SZ>BM,with greater sensitivity observed at increased rotational speeds.Post-corrosion mechanical performance degradation primarily arises from crevice corrosion at joint overlaps,but not from the changes in the microstructure.展开更多
Heterostructure engineering has emerged as a promising strategy to enhance the electrochemical CO_(2)reduction reaction(CO_(2)RR)by optimizing interfacial electron transfer.Herein,we report a novel octahedral SnS_(2)/...Heterostructure engineering has emerged as a promising strategy to enhance the electrochemical CO_(2)reduction reaction(CO_(2)RR)by optimizing interfacial electron transfer.Herein,we report a novel octahedral SnS_(2)/SnO_(2)heterojunction catalyst synthesized via an ion-exchange vulcanization method,which achieves exceptional activity and selectivity for CO_(2)-toformate conversion.Through in-situ Raman spectroscopy,ex-situ X-ray diffraction(XRD),and X-ray photoelectron spectroscopy(XPS),we demonstrate that the octahedral SnS_(2)/SnO_(2)heterojunction dynamically restructures into a sulfur-doped Sn/SnO_(2)(Sn(S)/SnO_(2))heterostructure under operating conditions.Density functional theory(DFT)calculations reveal that the Sn(S)/SnO_(2)interface facilitates electron transfer from SnO_(2)to metallic Sn(S),generating a built-in electric field that stabilizes Sn^(4+)in SnO_(2)and accelerates proton-coupled electron transfer to*OCHO intermediates.Consequently,the catalyst achieves a formate Faradaic efficiency exceeding 90% over a broad potential window(-0.6 to -1.0 V vs.reversible hydrogen electrode(RHE))with a high partial current density of -280 mA·cm^(-2),surpassing most reported Sn-based catalysts.This work elucidates the structural dynamics and interfacial enhancement mechanisms of heterojunction catalysts,offering a rational design principle for advanced CO_(2)RR electrocatalysts.展开更多
The tectonic settings of the different stages of the magmatic activity in the middle-south section of the Da Hinggan Mts. are analyzed through measuring the isotopic ages of the Mesozoic volcano-plutonic rocks from th...The tectonic settings of the different stages of the magmatic activity in the middle-south section of the Da Hinggan Mts. are analyzed through measuring the isotopic ages of the Mesozoic volcano-plutonic rocks from this area, and thus the tectono-magmatic evolution series are consequently determined as the initial mantle upwelling marked by the Late Triassic invasion of basic-ultrabasic rocks containing mantle-source enclaves, middle-upper crust extension marked by intrusion of the Early-Middle Jurassic diobase dike swarms, dramatic ruption of the Late Jurassic trachitic volcanic rocks, the Early Cretaceous nonorogenic alkalic-subalkalic granite invasion and the formation of the basic dike swarms and basalts. It is thus inferred that the uprise of the Da Hinggan Mts. in the Mesozoic is closely reiated to the upwelling of the deep magma in the mantle upwarping settings.展开更多
Thirteen observed heat flow values in combination with relevant geological and geophysical information are employed in the current paper to conduct a model study by means of direct inversion. The modeling demonstrates...Thirteen observed heat flow values in combination with relevant geological and geophysical information are employed in the current paper to conduct a model study by means of direct inversion. The modeling demonstrates the tectono-thermal evolution of the Tibetan Plateau during the last 40 Ma since the continent-continent collision. The authors stress the fact that the tectonic deformations of terranes are usually the inducing factors for the deep-seated thermal activities in the crust and upper mantle. On this basis a series of kinematic equations of 3-D deformations of terranes in forms of shortening-thickening-uplifting-erosion-mass sliding were deduced using the principle of plate kinematics. These equations are further used as systematically defined initial and boundary conditions for simulating the integrated processes of tectono-thermal evolution, The results of the model study suggest that there exist sharp differences in the tectono-thermal evolution between the old northern terranes and the new southern ones. However, even in the warm terranes in the south, the scale of the deep-seated thermal processes is lower than that uxnally expected.展开更多
Ⅰ. IMPLICATIONS OF THE INTEGRATED STUDY OF THE TECTONO-THERMAL EVOLUTIONRef. [1] reported 13 heat flow values along the profile from Yadong to the Qaidam Basin for the first time. After further systematic analysis an...Ⅰ. IMPLICATIONS OF THE INTEGRATED STUDY OF THE TECTONO-THERMAL EVOLUTIONRef. [1] reported 13 heat flow values along the profile from Yadong to the Qaidam Basin for the first time. After further systematic analysis and verification, these data together with the latitudes and longitudes of the heat flow sites, depth interval of linear sections, tem-展开更多
Apatite(U-Th)/He and fission track dating and tectono-thermal history modeling were used to reconstruct the Meso-Cenozoic tectonic evolution of the Huangling paleo-uplift in the Middle Yangtze Block,South China.The te...Apatite(U-Th)/He and fission track dating and tectono-thermal history modeling were used to reconstruct the Meso-Cenozoic tectonic evolution of the Huangling paleo-uplift in the Middle Yangtze Block,South China.The tectono-thermal evolution showed different tectonic exhumation/subsidence processes in the tectonic evolution of the foreland basin.The apatite(U-Th)/He ages ranged from 31.3 to 77.8 Ma,recording the thermal events of the Cenozoic Himalayan movement and indicating progressive exhumation extending from the southeast to the northwest.The thermal information of the Mesozoic Yanshan movement period was recorded by the apatite fission track age with a pooled age of 93.8 to 147 Ma.The exhumation of the Huangling paleo-uplift began in the Late Jurassic.The tectono-thermal evolution was characterized by a rapid uplift during 140-115 Ma,subsidence during 115-60 Ma,a rapid uplift during 40-30 Ma,and a slow uplift from 30 Ma to the present.The western Hunan-Hubei Depression was exhumed in the Middle Jurassic,and the tectono-thermal evolution was characterized by a rapid uplift during 160-135 Ma,a slow uplift during 135-50 Ma,a rapid uplift during 50-25 Ma,and a slow uplift from 25 Ma to the present.This Cenozoic exhumation was a response to the far field effect of the eastward growth of the Tibetan Plateau.The Cretaceous basins exposed in the surrounding areas of the Huangling paleo-uplift(Zigui basin,Yichang slope,and Huaguoping synclinorium)are foreland basins formed by the bi-directional compression of the Qinling-Dabie orogenic belt and the Xuefengshan intracontinental deformation system.展开更多
The utilization of iron coke provides a green pathway for low-carbon ironmaking.To uncover the influence mechanism of iron ore on the behavior and kinetics of iron coke gasification,the effect of iron ore on the micro...The utilization of iron coke provides a green pathway for low-carbon ironmaking.To uncover the influence mechanism of iron ore on the behavior and kinetics of iron coke gasification,the effect of iron ore on the microstructure of iron coke was investigated.Furthermore,a comparative study of the gasification reactions between iron coke and coke was conducted through non-isothermal thermogravimetric method.The findings indicate that compared to coke,iron coke exhibits an augmentation in micropores and specific surface area,and the micropores further extend and interconnect.This provides more adsorption sites for CO_(2) molecules during the gasification process,resulting in a reduction in the initial gasification temperature of iron coke.Accelerating the heating rate in non-isothermal gasification can enhance the reactivity of iron coke.The metallic iron reduced from iron ore is embedded in the carbon matrix,reducing the orderliness of the carbon structure,which is primarily responsible for the heightened reactivity of the carbon atoms.The kinetic study indicates that the random pore model can effectively represent the gasification process of iron coke due to its rich pore structure.Moreover,as the proportion of iron ore increases,the activation energy for the carbon gasification gradually decreases,from 246.2 kJ/mol for coke to 192.5 kJ/mol for iron coke 15wt%.展开更多
Gradient magnetic heterointerfaces have injected infinite vitality in optimizing impedance matching,adjusting dielectric/magnetic resonance and promoting electromagnetic(EM)wave absorption,but still exist a significan...Gradient magnetic heterointerfaces have injected infinite vitality in optimizing impedance matching,adjusting dielectric/magnetic resonance and promoting electromagnetic(EM)wave absorption,but still exist a significant challenging in regulating local phase evolution.Herein,accordion-shaped Co/Co_(3)O_(4)@N-doped carbon nanosheets(Co/Co_(3)O_(4)@NC)with gradient magnetic heterointerfaces have been fabricated via the cooperative high-temperature carbonization and lowtemperature oxidation process.The results indicate that the surface epitaxial growth of crystal Co_(3)O_(4) domains on local Co nanoparticles realizes the adjustment of magnetic-heteroatomic components,which are beneficial for optimizing impedance matching and interfacial polarization.Moreover,gradient magnetic heterointerfaces simultaneously realize magnetic coupling,and long-range magnetic diffraction.Specifically,the synthesized Co/Co_(3)O_(4)@NC absorbents display the strong electromagnetic wave attenuation capability of−53.5 dB at a thickness of 3.0 mm with an effective absorption bandwidth of 5.36 GHz,both are superior to those of single magnetic domains embedded in carbon matrix.This design concept provides us an inspiration in optimizing interfacial polarization,regulating magnetic coupling and promoting electromagnetic wave absorption.展开更多
Binary composites(ZIF-67/rGO)were synthesized by one-step precipitation method using cobalt nitrate hexahydrate as metal source,2-methylimidazole as organic ligand,and reduced graphene oxide(rGO)as carbon carrier.Then...Binary composites(ZIF-67/rGO)were synthesized by one-step precipitation method using cobalt nitrate hexahydrate as metal source,2-methylimidazole as organic ligand,and reduced graphene oxide(rGO)as carbon carrier.Then Ru3+was introduced for ion exchange,and the porous Ru-doped Co_(3)O_(4)/rGO(Ru-Co_(3)O_(4)/rGO)composite electrocatalyst was prepared by annealing.The phase structure,morphology,and valence state of the catalyst were analyzed by X-ray powder diffraction(XRD),scanning electron microscope(SEM),transmission electron microscopy(TEM),and X-ray photoelectron spectroscopy(XPS).In 1 mol·L^(-1)KOH,the oxygen evolution reaction(OER)performance of the catalyst was measured by linear sweep voltammetry,cyclic voltammetry,and chronoamperometry.The results show that the combination of Ru doping and rGO provides a fast channel for collaborative electron transfer.At the same time,rGO as a carbon carrier can improve the electrical conductivity of Ru-Co_(3)O_(4)particles,and the uniformly dispersed nanoparticles enable the reactants to diffuse freely on the catalyst.The results showed that the electrochemical performance of Ru-Co_(3)O_(4)/rGO was much better than that of Co_(3)O_(4)/rGO,and the overpotential of Ru-Co_(3)O_(4)/rGO was 363.5 mV at the current density of 50 mA·cm^(-2).展开更多
基金supported by the project of"Constraints on Lithospheric Dynamic Evolution and Hydrocarbon Accumulation from Late Mesozoic Paleo-geothermal Field in Ordos and Qinshui Basins"(grant No.41630312)the National Nature Science Foundation of China(grants No.41372208 and 40534019)+1 种基金the Open Found of the State Key Laboratory of Ore Deposit Geochemistry,CAS(grant No.201304)supported by international program for Ph.D.candidates,Sun Yat-Sen University
文摘This work restored the erosion thickness of the top surface of each Cretaceous formations penetrated by the typical well in the Hari sag,and simulated the subsidence burial history of this well with software BasinMod.It is firstly pointed out that the tectonic subsidence evolution of the Hari sag since the Cretaceous can be divided into four phases:initial subsidence phase,rapid subsidence phase,uplift and erosion phase,and stable slow subsidence phase.A detailed reconstruction of the tectonothermal evolution and hydrocarbon generation histories of typical well was undertaken using the EASY R%model,which is constrained by vitrinite reflectance(R)and homogenization temperatures of fluid inclusions.In the rapid subsidence phase,the peak period of hydrocarbon generation was reached at c.a.105.59 Ma with the increasing thermal evolution degree.A concomitant rapid increase in paleotemperatures occurred and reached a maximum geothermal gradient of about 43-45℃/km.The main hydrocarbon generation period ensued around 105.59-80.00 Ma and the greatest buried depth of the Hari sag was reached at c.a.80.00 Ma,when the maximum paleo-temperature was over 180℃.Subsequently,the sag entered an uplift and erosion phase followed by a stable slow subsidence phase during which the temperature gradient,thermal evolution,and hydrocarbon generation decreased gradually.The hydrocarbon accumulation period was discussed based on homogenization temperatures of inclusions and it is believed that two periods of rapid hydrocarbon accumulation events occurred during the Cretaceous rapid subsidence phase.The first accumulation period observed in the Bayingebi Formation(Kb)occurred primarily around 105.59-103.50 Ma with temperatures of 125-150℃.The second accumulation period observed in the Suhongtu Formation(Ks)occurred primarily around84.00-80.00 Ma with temperatures of 120-130℃.The second is the major accumulation period,and the accumulation mainly occurred in the Late Cretaceous.The hydrocarbon accumulation process was comprehensively controlled by tectono-thermal evolution and hydrocarbon generation history.During the rapid subsidence phase,the paleo temperature and geothermal gradient increased rapidly and resulted in increasing thermal evolution extending into the peak period of hydrocarbon generation,which is the key reason for hydrocarbon filling and accumulation.
基金The Program of the Key Technologies for Petroleum Exploration in Deep Oceanic Areas under contract No.2011ZX05025-006-05the Chinese Postdoc Fund,No.58 General Fund,2015 under contract No.2015M582636the National Natural Science Foundation of China under contract No.41602251
文摘The Liwan Sag,with an area of 4000 km-2,is one of the deepwater sags in the Zhujiang River(Pearl River)Mouth Basin,northern South China Sea.Inspired by the exploration success in oil and gas resources in the deepwater sags worldwide,we conducted the thermal modeling to investigate the tectono-thermal history of the Liwan Sag,which has been widely thought to be important to understand tectonic activities as well as hydrocarbon potential of a basin.Using the multi-stage finite stretching model,the tectonic subsidence history and the thermal history have been obtained for 12 artificial wells,which were constructed on basis of one seismic profile newly acquired in the study area.Two stages of rifting during the time periods of 49–33.9 Ma and 33.9–23 Ma can be recognized from the tectonic subsidence pattern,and there are two phases of heating processes corresponding to the rifting.The reconstructed average basal paleo-heat flow values at the end of the rifting events are-70.5 and-94.2 mW/m^2 respectively.Following the heating periods,the study area has undergone a persistent thermal attenuation phase since 23 Ma and the basal heat flow cooled down to-71.8–82.5 mW/m^2 at present.
基金financially supported by National Natural Science Fund of China (grant no.41302202)Basic Scientific Research Project of Institute of Geological Mechanics (no.DZLXJK201305)
文摘The Qaidam basin is the largest intermountain basin inside Tibet, and is one of the three major petroliferous basins in western China. This study discussed the geothermal field and tectono-thermal evolution of the basin, in an effort to provide evidence for intracontinental or intraplate continental dynamics and basin dynamics, petroleum resources assessment, and to serve petroleum production.
文摘A composite electrocatalyst,CoMoNiO-S/NF-110(NF is nickel foam),was synthesized through electrodeposition,followed by pyrolysis and then the vulcanization process.CoMoNiO-S/NF-110 exhibited a structure where Ni3S2 and Mo2S3 nanoparticles were integrated at the edges of Co3O4 nanosheets,creating a rich,heterogeneous interface that enhances the synergistic effects of each component.In an alkaline electrolyte,the synthesized CoMoNiO-S/NF-110 exhibited superior electrocatalytic performance for oxygen evolution reaction(OER),achieving current densities of 100 and 200 mA·cm^(-2) with low overpotentials of 199.4 and 224.4 mV,respectively,outperforming RuO2 and several high-performance Mo and Ni-based catalysts.This excellent performance is attributed to the rich interface formed between the components and active sites exposed by the defect structure.
文摘The poor electrical conductivity of metal-organic frameworks(MOFs)limits their electrocatalytic performance in the oxygen evolution reaction(OER).In this study,a Py@Co-MOF composite material based on pyrene(Py)molecules and{[Co2(BINDI)(DMA)_(2)]·DMA}_(n)(Co-MOF,H4BINDI=N,N'-bis(5-isophthalic acid)naphthalenediimide,DMA=N,N-dimethylacetamide)was synthesized via a one-pot method,leveragingπ-πinteractions between pyrene and Co-MOF to modulate electrical conductivity.Results demonstrate that the Py@Co-MOF catalyst exhibited significantly enhanced OER performance compared to pure Co-MOF or pyrene-based electrodes,achieving an overpotential of 246 mV at a current density of 10 mA·cm^(-2) along with excellent stability.Density functional theory(DFT)calculations reveal that the formation of O*in the second step is the rate-determining step(RDS)during the OER process on Co-MOF,with an energy barrier of 0.85 eV due to the weak adsorption affinity of the OH*intermediate for Co sites.CCDC:2419276.
文摘The efficiency and stability of catalysts for photocatalytic hydrogen evolution(PHE)are largely governed by the charge transfer behaviors across the heterojunction interfaces.In this study,CuO,a typical semiconductor featuring a broad spectral absorption range,is successfully employed as the electron acceptor to combine with CdS for constructing a S-scheme heterojunction.The optimized photocatalyst(CdSCuO2∶1)delivers an exceptional hydrogen evolution rate of 18.89 mmol/(g·h),4.15-fold higher compared with bare CdS.X-ray photoelectron spectroscopy(XPS)and ultraviolet-visible diffuse reflection absorption spectroscopy(UV-vis DRS)confirmed the S-scheme band structure of the composites.Moreover,the surface photovoltage(SPV)and electron paramagnetic resonance(EPR)indicated that the photogenerated electrons and photogenerated holes of CdS-CuO2∶1 were respectively transferred to the conduction band(CB)of CdS with a higher reduction potential and the valence band(VB)of CuO with a higher oxidation potential under illumination,as expected for the S-scheme mechanism.Density-functional-theory calculations of the electron density difference(EDD)disclose an interfacial electric field oriented from CdS to CuO.This built-in field suppresses charge recombination and accelerates carrier migration,rationalizing the markedly enhanced PHE activity.This study offers a novel strategy for designing S-scheme heterojunctions with high light harvesting and charge utilization toward sustainable solar-tohydrogen conversion.
基金support from the National Natural Science Foundation of China(Nos.12305373 and 52276220)the Guangzhou Basic Research Program(No.SL2024A04J00234).
文摘Developing efficient and durable electrocatalysts for acidic oxygen evolution reaction(OER)is pivotal for advancing proton exchange membrane water electrolysis(PEMWEs),yet balancing activity and stability remains a formidable challenge.Herein,we propose a dual-engineering strategy to stabilize Ru-based catalysts by synergizing the oxygen vacancy site-synergized mechanism-lattice oxygen mechanism(OVSM-LOM)with Ru-N bond stabilization.The engineered RuO_(2)@NCC catalyst exhibits exceptional OER performance in 0.5 M H2SO4,achieving an ultralow overpotential of 215 mV at 10 mA cm^(-2) and prolonged stability for over 327 h.The catalyst delivers 300 h of continuous operation at 1 A cm^(-2),with a negligible degradation rate of only 0.067 mV h-1,further demonstrating its potential for practical application.Oxygen vacancies unlock the OVSM-LOM pathway,bypassing the sluggish adsorbate evolution mechanism(AEM)and accelerating reaction kinetics,while the Ru-N bonds suppress Ru dissolution by anchoring low-valent Ru centers.Quasi-in situ X-ray photoelectron spectroscopy(XPS),X-ray absorption spectroscopy(XAS),and isotopic labeling experiments confirm the lattice oxygen participation with *O formation as the rate-determining step.The Ru-N bonds reinforce the structural integrity by stabilizing low-valent Ru centers and inhibiting overoxidation.Theoretical calculations further verify that the synergistic interaction between OVs and Ru-O(N)active sites optimizes the Ru d-band center and stabilizes intermediates,while Ru-N coordination enhances structural integrity.This study establishes a novel paradigm for designing robust acidic OER catalysts through defect and coordination engineering,bridging the gap between activity and stability for sustainable energy technologies.
基金financially supported by the Yunnan Fundamental Research Projects(Nos.202401CF070026 and 202501AT070017)the Scientific Research Fund Project of Yunnan Provincial Education Department(No.2024J0134)+1 种基金the Xingdian Talent Program of Yunnan Province,and the Scientific and Technological Project of Yunnan Precious Metals Laboratory(No.YPML-20240502065)Xinjiang Key Laboratory of Novel Functional Materials Chemistry Open Science Project(No.XJLNFMC-202406).
文摘Hydrogen production by electrolysis of water is a key technology to achieve green hydrogen energy economy,but it relies on advanced catalyst materials with high efficiency,stability,and wide pH adaptability.In this study,Ni,Ru,and Pt ternary metals were embedded into nitrogen-doped hollow carbon spheres(NHCSs)by hydrothermal tandem heat treatment to form ternary supported metal nanoparticles with high dispersion and ultra-small particle size(~1.3 nm),which realized efficient hydrogen evolution from multi-scenario electrocatalytic water splitting.In the whole pH range,the performance of NiRuPt/NHCSs is better than that of commercial Pt/C catalyst,and the overpotentials under alkaline,neutral,and acidic conditions are as low as 15.5,20.0,and 29.5 mV,respectively.Under industrial conditions,NiRuPt/NHCSs also have excellent hydrogen evolution reaction(HER)performance,achieving efficient electrolysis of seawater for hydrogen production,and achieving Ampere-level hydrogen production at low voltage(~1.76 V)on integrated membrane electrode assemblies.Density functional theory(DFT)calculations show that in the NiRuPt ternary metal,the Pt site is conducive to promoting the desorption of*H to form H_(2),the Ru site is conducive to promoting the capture of H_(2)O,and the Ni site is conducive to promoting the dissociation of H_(2)O.Therefore,the formed NiRuPt ternary metal synergistically promotes multi-scenario efficient electrolysis of water to produce hydrogen.This study provides a new idea for the design of multi-component metal/carbon-based composite catalysts,and promotes the development of non-noble metal/noble metal composite catalysts in hydrogen production by electrolysis of water.
基金supported by The China Ethnic Medicine Association Research Grant(No.2023MY055-81)Science and Technology Program of the Joint Fund of Scientific Research for the Public Hospitals of Inner Mongolia Academy of Medical Sciences(2023GLLHD177,2023GLLH0174)Inner Mongolia Autonomous Region Regional Medical Center for Specialized Care(2025).
文摘Serbisütherapy(ST)is a distinctive external treatment modality within traditional Mongolian medicine(TMM),historically developed within a nomadic cultural framework.This study presents a comprehensive philological and historical analysis of ST,tracing its evolution from early battlefield applications to contemporary clinical use.By critically examining classical Mongolian medical texts alongside modern case studies,we aim to systematize ST’s therapeutic methods,indications,and limitations,while exploring its mechanisms of action through both traditional theory and modern biomedical perspectives.ST has undergone significant transformation,shifting from whole-body cavity immersion in the 13th century to targeted,organ-specific applications in modern practice.Its four primary methods–Covering,Mounted,Organ Placement,and Suction–demonstrate efficacy in treating cold-natured diseases,musculoskeletal disorders,gynecological conditions,and certain emergencies.ST embodies the core principles of TMM,particularly the balance of the“Three Roots”and the correction of cold-induced pathologies through heat.Despite challenges related to standardization,cultural translation,and regulatory acceptance,ST holds translational potential for integrative medicine.Future research should prioritize mechanistic validation,clinical standardization,and the development of biocompatible thermal technologies to bridge traditional practice with modern healthcare systems.
基金supported by the Major Science and Technology Special Plan of Yunnan Province(Nos.202302AB080012 and 202402AB080004)the National Natural Science Foundation of China(No.22264025)+1 种基金the Basic Research Foundation of Yunnan Province(Nos.202401AS070033 and 202501AT070055)the Reserve talents for young and middleaged academic and technical leaders project of Yunnan Province(No.202405AC350071).
文摘Oxygen evolution reaction(OER)is a key step in hydrogen production by water electrolysis technology.How-ever,developing efficient,stable,and low-cost OER electrocatalysts is still challenging.This article presents the preparation of a series of novel copper iridium nanocatalysts with heterostructures and low iridium content for OER.The electrochemical tests revealed higher OER of Cu@Ir_(0.3) catalyst under acidic conditions with a generated current density of 10 mA/cm^(2) at only 284 mV overpotential.The corresponding OER mass activity was estimated to be 1.057 A/mgIr,a value 8.39-fold higher than that of the commercial IrO_(2).After 50 h of endurance testing,the Cu@Ir_(0.3) catalyst preserved excellent catalytic activity with a negligible rise in overpotential and maintained a good heterostructures.Cu@Ir_(0.3) The excellent OER activity can be attributed to its heterostructure,as con-firmed by density functional theory(DFT)calculations,indicating that Cu@Ir The coupling between isoquanta causes charge redistribution,optimizing the adsorption energy of unsaturated Ir sites for oxygen intermediates and reducing the energy barrier of OER free energy determining the rate step.In summary,this method provides a new approach for designing efficient,stable,and low iridium content OER catalysts.
基金supported by the National Natural Science Foundation of China(Nos.22373063 and 22302005)Fundamental Research Funds for the Central Universities of China(No.GK202203002)+1 种基金China Postdoctoral Science Foundation(No.2023M730044)Technology Innovation Leading Program of Shaanxi(Program No.2023KXJ-007).
文摘Deep insights into electrocatalytic mechanisms are vital for the rational design of catalysts for oxygen evolution reaction(OER).Mechanistically,the OER driven by adsorbate evolution mechanism(AEM)is limited by the linear scaling relationship,thereby exhibiting large overpotentials.In the lattice oxygen mechanism(LOM),the OER can be enhanced by enabling direct O_(2)formation.However,this enhancement is accompanied by the generation of oxygen vacancies,which presents a significant challenge to the long-term stability of LOMOER,particularly when operating at high current densities.Recently,the*O-*O coupling mechanism(OCM)has emerged as a promising alternative;it not only breaks the linear scaling relationship but also ensures catalytic stability.This review encapsulates the cutting-edge advancements in electrocatalysts that are grounded in the OCM,offering a detailed interpretation on the foundational principles guiding the design of OCM-OER catalysts.It also highlights recent theoretical investigations combining machine learning(ML)with density functional theory(DFT)calculations to reveal OER mechanisms.At the end of this review,the challenges and opportunities associated with OCM-OER electrocatalysts are discussed.
基金supported by the National Natural Science Foundation of China (Nos. 52075449, 51975480)。
文摘The dissimilar 2B06 and 7B04 Al alloy joints were prepared by refill friction stir spot welding(RFSSW),and the microstructural evolution and corrosion behavior of the joints were investigated.Based on microstructural analysis,the welded joints exhibit distinct microstructural zones,including the stir zone(SZ),thermomechanically affected zone(TMAZ),and heat-affected zone(HAZ).The grain size of each zone is in the order of HAZ>TMAZ>SZ.Notably,the TMAZ and HAZ contain significantly larger secondary-phase particles compared to the SZ,with particle size in the HAZ increasing at higher rotational speeds.Electrochemical tests indicate that corrosion susceptibility follows the sequence of HAZ>TMAZ>SZ>BM,with greater sensitivity observed at increased rotational speeds.Post-corrosion mechanical performance degradation primarily arises from crevice corrosion at joint overlaps,but not from the changes in the microstructure.
基金the Natural Science Foundation of Jiangsu Province(No.BK20253049)the Science and Technology Program of Xuzhou(No.KC25028)+3 种基金the Basic Science(Natural Science)Research Project of Higher Education Institutions in Jiangsu Province(No.25KJB430013)the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(No.24KJA150003)the National Natural Science Foundation of China(No.22271122)the Xuzhou Key Research and Development Program(Social Development)(No.KC23298).
文摘Heterostructure engineering has emerged as a promising strategy to enhance the electrochemical CO_(2)reduction reaction(CO_(2)RR)by optimizing interfacial electron transfer.Herein,we report a novel octahedral SnS_(2)/SnO_(2)heterojunction catalyst synthesized via an ion-exchange vulcanization method,which achieves exceptional activity and selectivity for CO_(2)-toformate conversion.Through in-situ Raman spectroscopy,ex-situ X-ray diffraction(XRD),and X-ray photoelectron spectroscopy(XPS),we demonstrate that the octahedral SnS_(2)/SnO_(2)heterojunction dynamically restructures into a sulfur-doped Sn/SnO_(2)(Sn(S)/SnO_(2))heterostructure under operating conditions.Density functional theory(DFT)calculations reveal that the Sn(S)/SnO_(2)interface facilitates electron transfer from SnO_(2)to metallic Sn(S),generating a built-in electric field that stabilizes Sn^(4+)in SnO_(2)and accelerates proton-coupled electron transfer to*OCHO intermediates.Consequently,the catalyst achieves a formate Faradaic efficiency exceeding 90% over a broad potential window(-0.6 to -1.0 V vs.reversible hydrogen electrode(RHE))with a high partial current density of -280 mA·cm^(-2),surpassing most reported Sn-based catalysts.This work elucidates the structural dynamics and interfacial enhancement mechanisms of heterojunction catalysts,offering a rational design principle for advanced CO_(2)RR electrocatalysts.
文摘The tectonic settings of the different stages of the magmatic activity in the middle-south section of the Da Hinggan Mts. are analyzed through measuring the isotopic ages of the Mesozoic volcano-plutonic rocks from this area, and thus the tectono-magmatic evolution series are consequently determined as the initial mantle upwelling marked by the Late Triassic invasion of basic-ultrabasic rocks containing mantle-source enclaves, middle-upper crust extension marked by intrusion of the Early-Middle Jurassic diobase dike swarms, dramatic ruption of the Late Jurassic trachitic volcanic rocks, the Early Cretaceous nonorogenic alkalic-subalkalic granite invasion and the formation of the basic dike swarms and basalts. It is thus inferred that the uprise of the Da Hinggan Mts. in the Mesozoic is closely reiated to the upwelling of the deep magma in the mantle upwarping settings.
基金Project supported by the National Natural Science Foundation of China.
文摘Thirteen observed heat flow values in combination with relevant geological and geophysical information are employed in the current paper to conduct a model study by means of direct inversion. The modeling demonstrates the tectono-thermal evolution of the Tibetan Plateau during the last 40 Ma since the continent-continent collision. The authors stress the fact that the tectonic deformations of terranes are usually the inducing factors for the deep-seated thermal activities in the crust and upper mantle. On this basis a series of kinematic equations of 3-D deformations of terranes in forms of shortening-thickening-uplifting-erosion-mass sliding were deduced using the principle of plate kinematics. These equations are further used as systematically defined initial and boundary conditions for simulating the integrated processes of tectono-thermal evolution, The results of the model study suggest that there exist sharp differences in the tectono-thermal evolution between the old northern terranes and the new southern ones. However, even in the warm terranes in the south, the scale of the deep-seated thermal processes is lower than that uxnally expected.
基金Project supported by the National Natural Science Foundation of China.
文摘Ⅰ. IMPLICATIONS OF THE INTEGRATED STUDY OF THE TECTONO-THERMAL EVOLUTIONRef. [1] reported 13 heat flow values along the profile from Yadong to the Qaidam Basin for the first time. After further systematic analysis and verification, these data together with the latitudes and longitudes of the heat flow sites, depth interval of linear sections, tem-
基金funded by the National Natural Science Foundation of China(U2244208,42302138)China Postdoctoral Science Foundation(No.2020M733869)Science Foundation of China University of Petroleum,Beijing(No.2462023XKBH003).
文摘Apatite(U-Th)/He and fission track dating and tectono-thermal history modeling were used to reconstruct the Meso-Cenozoic tectonic evolution of the Huangling paleo-uplift in the Middle Yangtze Block,South China.The tectono-thermal evolution showed different tectonic exhumation/subsidence processes in the tectonic evolution of the foreland basin.The apatite(U-Th)/He ages ranged from 31.3 to 77.8 Ma,recording the thermal events of the Cenozoic Himalayan movement and indicating progressive exhumation extending from the southeast to the northwest.The thermal information of the Mesozoic Yanshan movement period was recorded by the apatite fission track age with a pooled age of 93.8 to 147 Ma.The exhumation of the Huangling paleo-uplift began in the Late Jurassic.The tectono-thermal evolution was characterized by a rapid uplift during 140-115 Ma,subsidence during 115-60 Ma,a rapid uplift during 40-30 Ma,and a slow uplift from 30 Ma to the present.The western Hunan-Hubei Depression was exhumed in the Middle Jurassic,and the tectono-thermal evolution was characterized by a rapid uplift during 160-135 Ma,a slow uplift during 135-50 Ma,a rapid uplift during 50-25 Ma,and a slow uplift from 25 Ma to the present.This Cenozoic exhumation was a response to the far field effect of the eastward growth of the Tibetan Plateau.The Cretaceous basins exposed in the surrounding areas of the Huangling paleo-uplift(Zigui basin,Yichang slope,and Huaguoping synclinorium)are foreland basins formed by the bi-directional compression of the Qinling-Dabie orogenic belt and the Xuefengshan intracontinental deformation system.
基金financially supported by the National Science Foundation of China(Nos.51974212 and 52274316)the China Baowu Low Carbon Metallurgy Innovation Foundation(No.BWLCF202116)+1 种基金the Science and Technology Major Project of Wuhan(No.2023020302020572)the Foundation of Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education(No.FMRUlab23-04)。
文摘The utilization of iron coke provides a green pathway for low-carbon ironmaking.To uncover the influence mechanism of iron ore on the behavior and kinetics of iron coke gasification,the effect of iron ore on the microstructure of iron coke was investigated.Furthermore,a comparative study of the gasification reactions between iron coke and coke was conducted through non-isothermal thermogravimetric method.The findings indicate that compared to coke,iron coke exhibits an augmentation in micropores and specific surface area,and the micropores further extend and interconnect.This provides more adsorption sites for CO_(2) molecules during the gasification process,resulting in a reduction in the initial gasification temperature of iron coke.Accelerating the heating rate in non-isothermal gasification can enhance the reactivity of iron coke.The metallic iron reduced from iron ore is embedded in the carbon matrix,reducing the orderliness of the carbon structure,which is primarily responsible for the heightened reactivity of the carbon atoms.The kinetic study indicates that the random pore model can effectively represent the gasification process of iron coke due to its rich pore structure.Moreover,as the proportion of iron ore increases,the activation energy for the carbon gasification gradually decreases,from 246.2 kJ/mol for coke to 192.5 kJ/mol for iron coke 15wt%.
基金financially supported by the National Natural Science Foundation of China(52373271)Science,Technology and Innovation Commission of Shenzhen Municipality under Grant(KCXFZ20201221173004012)+1 种基金National Key Research and Development Program of Shaanxi Province(No.2023-YBNY-271)Open Testing Foundation of the Analytical&Testing Center of Northwestern Polytechnical University(2023T019).
文摘Gradient magnetic heterointerfaces have injected infinite vitality in optimizing impedance matching,adjusting dielectric/magnetic resonance and promoting electromagnetic(EM)wave absorption,but still exist a significant challenging in regulating local phase evolution.Herein,accordion-shaped Co/Co_(3)O_(4)@N-doped carbon nanosheets(Co/Co_(3)O_(4)@NC)with gradient magnetic heterointerfaces have been fabricated via the cooperative high-temperature carbonization and lowtemperature oxidation process.The results indicate that the surface epitaxial growth of crystal Co_(3)O_(4) domains on local Co nanoparticles realizes the adjustment of magnetic-heteroatomic components,which are beneficial for optimizing impedance matching and interfacial polarization.Moreover,gradient magnetic heterointerfaces simultaneously realize magnetic coupling,and long-range magnetic diffraction.Specifically,the synthesized Co/Co_(3)O_(4)@NC absorbents display the strong electromagnetic wave attenuation capability of−53.5 dB at a thickness of 3.0 mm with an effective absorption bandwidth of 5.36 GHz,both are superior to those of single magnetic domains embedded in carbon matrix.This design concept provides us an inspiration in optimizing interfacial polarization,regulating magnetic coupling and promoting electromagnetic wave absorption.
文摘Binary composites(ZIF-67/rGO)were synthesized by one-step precipitation method using cobalt nitrate hexahydrate as metal source,2-methylimidazole as organic ligand,and reduced graphene oxide(rGO)as carbon carrier.Then Ru3+was introduced for ion exchange,and the porous Ru-doped Co_(3)O_(4)/rGO(Ru-Co_(3)O_(4)/rGO)composite electrocatalyst was prepared by annealing.The phase structure,morphology,and valence state of the catalyst were analyzed by X-ray powder diffraction(XRD),scanning electron microscope(SEM),transmission electron microscopy(TEM),and X-ray photoelectron spectroscopy(XPS).In 1 mol·L^(-1)KOH,the oxygen evolution reaction(OER)performance of the catalyst was measured by linear sweep voltammetry,cyclic voltammetry,and chronoamperometry.The results show that the combination of Ru doping and rGO provides a fast channel for collaborative electron transfer.At the same time,rGO as a carbon carrier can improve the electrical conductivity of Ru-Co_(3)O_(4)particles,and the uniformly dispersed nanoparticles enable the reactants to diffuse freely on the catalyst.The results showed that the electrochemical performance of Ru-Co_(3)O_(4)/rGO was much better than that of Co_(3)O_(4)/rGO,and the overpotential of Ru-Co_(3)O_(4)/rGO was 363.5 mV at the current density of 50 mA·cm^(-2).
