Insight into structure evolution of carbon nitrides and its energy conversion as luminescence

A series of carbon nitride(CN)materials represented by graphitic carbon nitride(g-C_(3)N_(4))have been widely used in bioimaging,biosensing,and other fields in recent years due to their nontoxicity,low cost,and high luminescent quantum efficiency.What is more attractive is that the luminescent properties such as wavelength and intensity can be regulated by controlling the structure at the molecular level.Hence,it is time to summarize the related research on CN structural evolution and make a prospect on future developments.In this review,we first summarize the research history and multiple structural evolution of CN.Then,the progress of improving the luminescence performance of CN through structural evolution was discussed.Significantly,the relationship between CN structure evolution and energy conversion in the forms of photoluminescence,chemiluminescence,and electrochemiluminescence was reviewed.Finally,key challenges and opportunities such as nanoscale dispersion strategy,luminous efficiency improving methods,standardization evaluation,and macroscopic preparation of CN are highlighted.

Mineralogical characteristics,metallurgical properties and phase structure evolution of Ca-rich hematite sintering

In order to study the sintering characteristics of Ca-rich iron ore,chemical analysis,laser diffraction,scanning electron microscopy,XRD-Rietveld method,and micro-sintering were used to analyze the mineralogical properties and sintering pot tests were used to study the sintering behavior.In addition,a grey correlation mathematical model was used to calculate and compare the comprehensive sintering performance under different calcium-rich iron ore contents.The results demonstrate that the Ca-rich iron ore has coarse grain size and strong self-fusing characteristics with Ca element in the form of calcite(CaCO_(3)) and the liquid phase produced by the self-fusing of the calcium-rich iron ore is well crystallized.Its application with a 20wt%content in sintering improves sinter productivity,reduces fuel consumption,enhances reduction index,and improves gas permeability in blast furnace by 0.45 t/(m^(2)·h),6.11 kg/t,6.17%,and 65.39 kPa·℃,respectively.The Ca-rich iron ore sintering can improve the calorific value of sintering flue gas compared with magnetite sintering,which is conducive to recovering heat for secondary use.As the content of the Ca-rich iron ore increases,sinter agglomeration shifts from localized liquid-phase bonding to a combination of localized liquid-phase bonding and iron oxide crystal connection.Based on an examination of the greater weight value of productivity with grey correlation analysis,the Ca-rich iron ore is beneficial for the comprehensive index of sintering in the range of 0-20wt%content.Therefore,it may be used in sintering with magnetite concentrates as the major ore species.

Effects of compressing and remelting in SIMA processing on semi-solid structure evolution of an Al-Zn wrought alloy

Structure evolution of an Al-Zn wrought alloy in remelting processing in thestrain induced melt activated (SIMA) serai-solid procedure was observed, and effects of factors, theremelting temperature, the holding time, and the compression strain, on structures and grain sizesof the alloy were investigated. The results show that (1) the proper temperature of remelting is inthe range of 610 to 615℃; (2) the grain size in specimen with greater compression strain is smallerthan that with smaller compression strain in condition of the same remelting temperature andholding time, and the grain size in local area with great local equivalent strain is smaller thanthat with small one; (3) liquid occurs in form of cluster in matrix during remelting and itsquantity increases with remelting time increasing; liquid in specimen with great compression strainoccurs earlier than that with small one, and quantity of liquid in the center of specimen withgreater local equivalent strain is greater than that in the two ends of it; (4) distortion energyafter deforming in matrix of the alloy is the significant factor to activate melting of matrix atlocal area with great local equivalent strain.

Surface structure evolution of cathode materials for Li-ion batteries

Lithium ion batteries are important electrochemical energy storage devices for consumer electronics and the most promising candidates for electrical/hybrid vehicles. The surface chemistry influences the performance of the batteries significantly. In this short review, the ewlution of the surface struture of the cathode materials at different states of the pristine, storage and electrochemical reaclions are summarized. The main methods for the surface modification are also introduced.

Densification and Structure Evolution of ZrB_(2)-ZrO_(2) Composites Prepared by Plasma Activated Sintering using ZrB2@ZrO2 Powder

The densification and the structure evolution of the plasma activated sintered(PAS sintered)ZrB_(2)-ZrO_(2) composite via the ZrO_(2)-coated ZrB_(2) powder(ZrB_(2)@ZrO_(2))prepared by in situ passivation method were investigated.The composition and microstructure were characterized by XRD,Raman,SEM,and EDS techniques.The coated powder has excellent sintering performance.The relative density of the composite reaches above 90%at 1200℃,and the main sintering process occurs between ZrO_(2) particles.While at above 1500℃,the relative density reaches above 95%and the main sintering process occurs between ZrB_(2) and ZrO_(2) particles.With the increase of ZrO_(2) coating content,the structure of the sintered body changes from ZrB_(2) continuous network structure to island structure.When the content is 20%,an island structure is formed.Increasing the ZrO_(2) content further causes the overheating of ZrO_(2).Thus,the best sintering performance reaches when the coating content is 20wt%.

Structure Evolution of Bulk Metallic Glass Zr_(52.5)Ni_(14.6)Al_10Cu_(17.9)Ti_5 during Annealing

Bulk metallic glass Zr_52.5Ni_14.6Al_10Cu_17.9Ti_5 was prepared by melt injection casting method. Its glass transition and crystallization temperatures were determined by differential scanning calorimetry (DSC) to be 631 K and 710 K respectively. By analysis of X-ray diffractometry (XRD) and transmission electron microscopy (TEM ), the predominant crystallized phase of Zr_2Ni0.67O0.33 distributed on glass state matrix was detected after annealing at 673 K for 600 s. The transformation to Zr_2Ni_0.67O_0.33 and a small amount of ZrAl and Zr_2Cu took place after annealing for 600 s at temperature from 703 K to 723 K. With increasing annealing temperature from 753 K to 823 K, the amounts of ZrAl and Zr_2Cu increased, but the size of the crystals did not significantly change. The transformation to Zr_2Ni_0.67O_0.33 is interface-controlled, but is diffusion-controlled to Zr_2Cu and ZrAl. With increasing annealing temperature up to 200 K above T_x, the nanometer grains became very fine because of the increase of nucleation rate for Zr_2Cu and ZrAl.

Pore structure evolution of lacustrine organic-rich shale from the second member of the Kongdian formation in the Cangdong Sag,Bohai Bay Basin,China

Pyrolysis experiments were conducted on lacustrine organic-rich shale from Cangdong Sag in Bohai Bay Basin,China,to investigate the impact of hydrocarbon generation on shale pore structure evolution.Thermal evolution is found to control the transformation of organic matter,hydrocarbon products characteristics,and pore structure changes.Furthermore,pore volume and specific surface area increase with increasing maturity.In low-mature stage,the retained oil content begins to increase,pore volumes show slight changes,and primary pores are occluded by the generated crude oil of high molecular weight and density.In the oil-window stage,the retained oil content rapidly increases and reaches maximum,and pore volumes gradually increase with increasing thermal maturity.At high mature stage,the retained oil content begins to decrease,and the pore volume increases considerably owing to the expulsion of liquid hydrocarbon.In over mature stage,natural gas content significantly increases and kerogen transforms to asphalt.Numerous organic pores are formed and the pore size gradually increases,resulting from the connection of organic pores caused the increasing thermal stress.This study lays a foundation for understanding variation of hydrocarbon products during the thermal evolution of lacustrine shales and its relationship with the evolution of shale reservoirs.

Studies of Structure Evolution of Nanostructured Hf_(11)Ni_(89) Alloy

A nanostructured Hf11Ni89 ribbon sample was prepared by melt-spinning. It was found that the as-quenched sample is composed of a major HfNi5 compound nanophase and an interfacial magnetic Ni(Hf) solid solution phase. The structure evolution of the sample was studied by using X-ray difFraction (XRD), transmission electron microscopy (TEM), difFerential scanning calorimetry (DSC), resistivity and magnetothermal analysis. Upon heating, a second precipitation process of the Ni(Hf) phase prior to grain growth wa5 detected by means of both structural analysis and physical property measurements. The measurement results are discussed based on the relationship between microstructure and physical properties.

Structure Evolution of China Aviation Network Based on Hierarchical Model

The annual passenger volume of airport reflected its passenger transport scale and the role in aviation network.The airports in whole country were divided into three layers:first layer airports,second layer airports and third layer airports.The airlines from the first layer airports consisted the first layer aviation network.The airlines from the second layer airports consisted the second layer aviation network.The airlines from the third layer airports consisted the third layer aviation network.The structure and function of different layer aviation network had significant differences.These differences were shown in the number of airlines,average number of airlines of each airport,annual passenger volume of airport and average passenger volume of each airline.National aviation network hierarchical model was constructed to describe the whole country aviation network.The matrix was built to describe the airline number,annual passenger volume,average number of airlines,average passenger volume of each airport and airline rate of aviation network.The index of national aviation network structure was constructed to show the ratio of index between different aviation network layer to describe the aviation network structure.The structure index was built to illustrate the macrostructural features of national aviation network.The statistics data in year 1988,1994,2001,2008 and 2015 of China aviation network were analyzed and basic data matrixes,basic index matrixes and structure index matrixes were calculated.The trend of ratio of corresponding index between the first layer and the second layer showed the change of basic structure of China aviation network.At meantime,the tendency of ratio of corresponding index between the third layer and the second layer also showed the change of basic structure.The trend of network general structure index illustrated that the large scaled new airports and airlines construction had significant influence on the national aviation network structure.

Structure evolution of oxygen removal from porous carbon for optimizing supercapacitor performance

The presence of oxygen functional groups is detrimental to the capacitive performance of porous carbon electrode in organic electrolyte. In this regards, hydrogen thermal reduction has been demonstrated effective approach in removing the unstable surface oxygen while maintaining the high porosity of carbon matrix. However, the exact evolution mechanism of various oxygen species during this process, as well as the correlation with electrochemical properties, is still under development. Herein, biomass-based porous carbon is adopted as the model material to trace its structure evolution of oxygen removal under hydrogen thermal reduction process with the temperature range of 400–800 °C. The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700°C. XPS, TPRMS and Boehm titration results indicate that the oxygen elimination undergoes three distinctive stages(intermolecular dehydration, hydrogenation and decomposition reactions). The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700 °C. Benefiting from the stable electrochemical interface and the optimized porous structure, the as-obtained HAC-700 exhibit significantly suppressed self-discharge and leak current, with improved cycling stability, which is attributable to the stabilization of electrochemical interface between carbon surface and electrolyte. The result provides insights for rational design of surface chemistry for high-performance carbon electrode towards advanced energy storage.

Carbon Emission Effects Driven by Evolution of Chinese Dietary Structure from 1987 to 2020

Exploring carbon emission effects based on the evolution of residents’ dietary structure to achieve the carbon neutrality goal and mitigate climate change is an important task.This study took China as the research object(data excluding Hong Kong,Macao and Taiwan) and used the carbon emission coefficient method to quantitatively measure the food carbon emissions from 1987–2020,then analyzed the carbon emission effects under the evolution of dietary structure.The results showed that during the study period,the Chinese dietary structure gradually changed to a high-carbon consumption pattern.The dietary structure of urban residents developed to a balanced one,while that of rural residents developed to a high-quality one.During the study period,the per capita food carbon emissions and total food consumption of Chinese showed an increasing trend.The per capita food carbon emissions of residents in urban and rural showed an overall upward trend.The total food carbon emissions in urban increased significantly,while that in rural increased first and then decreased.The influence of beef and mutton on carbon emissions is the highest in dietary structure.Compared with the balanced dietary pattern,the food carbon emissions of Chinese residents had not yet reached the peak,but were evolving to a high-carbon consumption pattern.

Evolution of molecular structure of TATB under shock loading from transient Raman spectroscopic technique

By combination of the transient Raman spectroscopic measurement and the density functional theoretical calculations,the structural evolution and stability of TATB under shock compression was investigated.Due to the improvement in synchronization control between two-stage light gas gun and the transient Raman spectra acquisition,as well as the sample preparation,the Raman peak of the N-O mode of TATB was firstly observed under shock pressure up to 13.6 GPa,noticeably higher than the upper limit of 8.5 GPa reported in available literatures.By taking into account of the continuous shift of the main peak and other observed Raman peaks,we did not distinguish any structural transition or any new species.Moreover,both the present Raman spectra and the time-resolved radiation of TATB during shock loading showed that TATB exhibits higher chemical stability than previous declaration.To reveal the detailed structural response and evolution of TATB under compression,the density functional theoretical calculations were conducted,and it was found that the pressure make N-O bond lengths shorter,nitro bond angles larger,and intermolecular and intra-molecular hydrogen bond interactions enhanced.The observed red shift of Raman peak was ascribed to the abnormal enhancement of H-bound effect on the scissor vibration mode of the nitro group.

Fe-lnduced Electronic Transfer and Structural Evolution of Lotus Pod-Like CoNiFeP_(x)@P,N-C Heterostructure for Sustainable Oxygen Evolution

Transition metal phosphides with metallic properties are a promising candidate for electrocatalytic water oxidation,and developing highly active and stable metal phosphide-based oxygen evolution reaction catalysts is still challenging.Herein,we present a facile ion exchange and phosphating processes to transform intestine-like CoNiP_(x)@P,N-C into lotus pod-like CoNiFeP_(x)@P,N-C heterostructure in which numerous P,N-codoped carboncoated CoNiFeP_(x)nanoparticles tightly anchors on the 2D carbon matrix.Meanwhile,the as-prepared CoNiFeP_(x)@P,N-C enables a core-shell structure,high specific surface area,and hierarchical pore structure,which present abundant heterointerfaces and fully exposed active sites.Notably,the incorporation of Fe can also induce electron transfer in CoNiP_(x)@P,IM-C,thereby promoting the oxygen evolution reaction.Consequently,CoNiFeP_(x)@P,IM-C delivers a low overpotential of 278 mV(vs RHE)at a current density of10 mA cm^(-1)and inherits excellent long-term stability with no observable current density decay after 30 h of chronoamperometry test.This work not only highlights heteroatom induction to tune the electronic structure but also provides a facile approach for developing advanced and stable oxygen evolution reaction electrocatalysts with abundant heterointerfaces.

In-situ study for the elastic structure evolutions of threedimensional Ir-O framework during the oxygen evolution reaction in acid

Understanding the dynamic structural and chemical evolutions at the catalyst-electrolyte interfaces is crucial for the development of active and stable electrocatalysts.In this work,β-Li_(2)IrO_(3)is employed as a model catalyst for the oxygen evolution reaction(OER).Its elastic three-dimensional Ir-O framework enables us to investigate the Li^(+)cation dissolution-induced structure evolutions and the formation mechanism of amorphous IrO_(x)species.Electrochemical measurements by rotating ring disk electrode(RRDE)reveal that up to 60%of the measured OER current can be ascribed to catalyst degradation.A series of in-situ X-ray diffraction spectroscopy(XRD),X-ray absorption spectroscopy(XAS),and Raman spectroscopy are conducted.Structure vibration is observed with oxidation states of Ir being reduced abnormally during OER at high potentials.It’s hypothesized that the reversible proton intercalations are responsible for the Ir turn-over mechanism.Results of this work demonstrate a stable and elastic iridate structure and reveal the initial catalyst degradation behaviors during OER in acid media.

Insight into the ammonia torrefaction and pyrolysis system of cellulose:Unraveling the evolution of chemical structure and nitrogen migration mechanism

This study aimed to investigate the mechanism of nitrogen doping,migration,and conversion during ammonia torrefaction and also explore the evolution law of the chemical structure of cellulose.The results showed that the ammonia torrefaction pretreatment could significantly optimize the distribution of nitrogen and oxygen elements in cellulose.The carbon skeleton first captured the active nitrogenous radicals to form-NHn-N,and pyridine-N and pyrrole-N originated from the conversion of-NHn-N.The existence of C=O played a major role in the immobilization of nitrogen.The nitrogen in bio-oil exists mainly in the form of five-and six-membered heterocycles.The correlation analysis showed that the main precursors for the formation of nitrogenous heterocyclic compounds were five-membered Oheterocyclic compounds.Finally,the product distribution characteristics in the torrefaction-pyrolysis systems were summarized,and the nitrogen doping and conversion mechanisms were proposed.This study expanded the boundaries of cellulose pretreatment and the production of high-value chemicals.

Local atomic structure evolution of liquid gadolinium and yttrium during solidification:An ab initio study

Local atomic structure evolution of pure gadolinium(Gd)and yttrium(Y)during solidification was investigated by using ab initio molecular dynamics(AIMD)simulation.The calculated results indicate that the local short-range order(SRO)in liquid Gd and Y is similar to some transitional metals with an asymmetric shape of the second peak in static structure factors.Moreover,the formation of icosahedral local motifs as a function of temperature decreases the diffusivity,which explains the connection between structure evolution and dynamic properties.In examining the topological structures of both systems,we demonstrate that small atomic displacement leads to two different types of topological sixfold rings in liquid and solid states.All analyses yield a systematic study about rare earth metals Gd and Y at the atomic level.

In-situ observation and analysis of solidified structure evolution of S50C steel in soaking furnace

The evolution of solidified structure of S50C steel during heat treatment in compact strip production process was studied through an ultra-high-temperature confocal scanning laser microscope.It was found that the solidified structure consisted of dendritic crystals with secondary dendrite arm spacing ranging in 32-120μm,where carbon segregation was evident,and the dendrite arms wereα-Fe.The insignificant change was observed at a soaking temperature of 1180℃,whereas at 1300℃,the finer structure firstly disappeared,and then,the coarsening decreased,indicating that carbon tended to be homogenized.Therefore,the microsegregation was improved at 1300℃for 15 min.The phase transformation ofα-Fe→γ-Fe enhanced the carbon diffusion,and the evolution of the equivalent radius req was controlled by carbon diffusion.The diffusion coefficient of carbon(D=15μm2/s)was determined by using the inverse problem method.

In-situ study on structure evolution and gasification reactivity of biomass char with K and Ca catalysts at carbon dioxide atmosphere

The structural evolution and gasification reactivity of biochar prepared from the pyrolysis of wheat straw were investigated by in-situ Raman spectroscopy and thermogravimetric analysis.The Raman spectra consisted of a combination of four Lorentzian bands(D1,D2,D4,G)and one Gaussian band(D3)in the first-order region.The experimental results showed that the addition of catalysts or the presence of ash could improve the CO_(2) gasification reactivity of biochar and result in a larger ID1/IG ratio and a lower IG/IALL ratio,meaning that the carbon structure was less ordered,and there were also more active sites such as amorphous carbon and cross-linked structures;Ca-based catalysts and K-based catalysts changed the evolution of biochar structure in a different way in CO_(2) atmosphere,the ID3/ID1 of Ca-based biochar was close to the value of non-catalyst biochar and decreased slowly,indicating that the Ca-based catalysts can stabilize the aromatic rings,while the IG/IALL of K-based biochar decreases significantly and the ID3/ID1 increased significantly,indicating the increase of carbon structure defects and the cracking of large aromatic rings in bio-char into small ones;a scheme of K and Ca reaction with biochar in CO_(2) gasification process was proposed.

Structural attributes,evolution and petroleum geological significances of the Tongnan negative structure in the central Sichuan Basin,SW China

The Tongnan secondary negative structure in central Sichuan Basin has controls and influences on the structural framework and petroleum geological conditions in the Gaoshiti-Moxi area.To clarify the controls and influences,the deformation characteristics,structural attributes and evolution process of the Tongnan negative structure were investigated through a series of qualitative and quantitative methods such as balanced profile restoration,area-depth-strain(ADS)analysis,and structural geometric forward numerical simulation,after comprehensive structural interpretation of high-precision 3D seismic data.The results are obtained in three aspects.First,above and below the P/AnP(Permian/pre-Permian)unconformity,the Tongnan negative structure demonstrates vertical differential structural deformation.It experiences two stages of structural stacking and reworking:extensional depression(from the Sinian Dengying Formation to the Permian),and compressional syncline deformation(after the Jurassic).The multi-phase trishear deformation of the preexisting deep normal faults dominated the extensional depression.The primary depression episodes occurred in the periods from the end of Late Proterozoic to the deposition of the 1st–2nd members of the Dengying Formation,and from the deposition of Lower Cambrian Longwangmiao Formation–Middle–Upper Cambrian until the Ordovician.Second,the multi-stage evolution process of the Tongnan negative structure controlled the oil and gas migration and adjustment and present-day differential gas and water distribution between the Tongnan negative structure and the Gaoshiti and Moxi-Longnüsi structural highs.Third,the Ordovician,which is limitedly distributed in the Tongnan negative structure and is truncated by the P/AnP unconformity on the top,has basic geological conditions for the formation of weathering karst carbonate reservoirs.It is a new petroleum target deserving attention.

The Microstructure Evolution of Intrinsic Microcrystalline Silicon Films and Its Influence on the Photovoltaic Performance of Thin-Film Silicon Solar Cells

Hydrogenated microcrystalline silicon （μc-Si：H） intrinsic films and solar cells are prepared by plasma enhanced chemical vapor deposition （PECVD） with various hydrogen dilution ratios. The influence of hydrogen dilution ratios on electrical characteristics is investigated to study the phase transition from amorphous to microcrystalline silicon. During the deposition process,the optical emission spectroscopy （OES） from plasma is recorded and compared with the Raman spectra of the films,by which the microstructure evolution of different 1-12 dilution ratios and its influence on the performance of μc-Si： H n-i-p solar cells is investigated.