The amount of impervious surface area increases with rapid urbanization.Remote sensing indices are used to detect impervious surface areas quickly,cheaply and accurately.This study used Landsat-OLI and Sentiel-2A MSI ...The amount of impervious surface area increases with rapid urbanization.Remote sensing indices are used to detect impervious surface areas quickly,cheaply and accurately.This study used Landsat-OLI and Sentiel-2A MSI images in the province of Ankara to compare six impervious surface extraction indices:Normalized Difference Builtup Index(NDBI),Combinational Biophysical Composition Index(CBCI),Normalized Impervious Surface Index(NISI),Urban Index(UI),Index-based Built-up Index(IBI),Enhanced Normalized Difference Impervious Surfaces Index(ENDISI).Spectral discrimination index(SDI)and error matrix were used to evaluate the performance of the indexes.In addition,a visual evaluation of the performance of the indices was made on different surface areas in the study area.展开更多
Iron oxide nanoparticles(IONPs)with intrinsic peroxidase(POD)-mimic activity have gained significant attention as nanozymes.Reducing sizes of IONPs is the mostly applied strategy to boost their enzymatic activity due ...Iron oxide nanoparticles(IONPs)with intrinsic peroxidase(POD)-mimic activity have gained significant attention as nanozymes.Reducing sizes of IONPs is the mostly applied strategy to boost their enzymatic activity due to their high specific surface areas.Herein,we synthesized a series of uniformly sized IONPs ranging from3.17 to 21.2 nm,and found that POD activity of IONPs is not monotone increased by reducing their sizes,with the optimal size of 7.82 nm rather than smaller sized 3.17 nm.The reason for this unnormal phenomenon is that electronic structure also had great influence on POD activity,especially at the ultrasmall size region.Since Fe^(2+)are with higher enzymatic activity than Fe^(3+),3.17 nm IONPs although have the largest specific surface area,are prone to be oxidized,which reduced their iron content and ratio of Fe^(2+)to Fe^(3+),and consequently decreased their POD activity.By intentionally oxidized 7.82 nm IONPs in air,POD activity was obviously reduced,illustrating electronic structure cannot be overlooked.At the larger sized region ranging from 7.82 to 21.2 nm,oxidation degree of IONPs is similar,and surface electronic structure had a negligible effect on POD activity,and therefore,POD activity is predominantly influenced by specific surface area.By using the optimized 7.82 nm IONPs,tumor growth was obviously inhibited,demonstrating their potential in cancer therapeutics.Our results reveal that the designing of nanozymes should comprehensively balance their influence of surface electronic structure and specific surface area.展开更多
Mo_(2)CT_(x)MXene is a novel two-dimensional material,which is generally made by the etching of inorganic acid solutions,such as hydrofluoric acid(HF)or hydrochloric acid(HCl).Those solutions are always corrosive and ...Mo_(2)CT_(x)MXene is a novel two-dimensional material,which is generally made by the etching of inorganic acid solutions,such as hydrofluoric acid(HF)or hydrochloric acid(HCl).Those solutions are always corrosive and hazardous.In this paper,a mild organic acid,acetic acid(CH_(3)COOH),was selected to synthesize Mo_(2)CT_(x)MXene.30 mL acetic acid(HAc)with the concentration of 13 mol/L was mixed with 2 g acetate(CH_(3)COONa or CH_(3)COOK)and 10 mL water to make etching solution(NaAc+HAc or KAc+HAc).In the solution,the concentration of CH_(3)COO^(-)was 10 mol/L,the concentration of Na^(+)/K^(+)is 0.6/0.5 mol/L.The pH value is 2.8.Mo_(2)CT_(x)was obtained by hydrothermal etching at 240℃for 1 d.Compared with the general method of HF etching,the etchant is milder and the etching process is safer.On the surface of Mo_(2)CT_(x)nanosheet made by this method,acetate group(CH_(3)COO^(-))was adsorbed as termination,which is larger than the F/O/OH termination of that made by general HF etching.The lattice parameter c(LP c)of Mo_(2)CT_(x)etched with NaAc+HAc/KAc+HAc is 21.09Å/20.89Å.Moreover,the specific surface areas of the samples etched by NaAc+HAc and KAc+HAc were 18.1 m^(2)/g and 14.1 m^(2)/g,respectively,which were much larger than those etched by conventional methods.As the anode of lithium-ion battery,the specific capacity under current density of 100 mA/g at 100 th cycle was 108 mA·h/g,which is higher than the capacity of samples made by general HF etching.This work reports a novel method to make Mo_(2)CT_(x)MXene by the solution of mild acetic acid.The samples made by this method had very high specific surface area and relatively high lithium-storage performance.展开更多
We build a computer program to reconstruct convex bodies using even L_(p)surface area measures for p≥1.Firstly,we transform the minimization problem Pi,which is equivalent to solving the even L_(p)Minkowski problem,i...We build a computer program to reconstruct convex bodies using even L_(p)surface area measures for p≥1.Firstly,we transform the minimization problem Pi,which is equivalent to solving the even L_(p)Minkowski problem,into a convex optimization problem P4 with a finite number of constraints.This transformation makes it suitable for computational resolution.Then,we prove that the approximate solutions obtained by solving the problem P4 converge to the theoretical solution when N and k are sufficiently large.Finally,based on the convex optimization problem P_(4),we provide an algorithm for reconstructing convex bodies from even L_(p)surface area measures,and present several examples implemented using MATLAB.展开更多
A procedure of low temperature solid-phase sintering（LTSS） was carried out to fabricate sintered metal fibrous media（SMFM） with high specific surface area.Stainless steel fibers which were produced by cutting proc...A procedure of low temperature solid-phase sintering（LTSS） was carried out to fabricate sintered metal fibrous media（SMFM） with high specific surface area.Stainless steel fibers which were produced by cutting process were first plated with a coarse copper coating layer by electroless plating process.A low-temperature sintering process was then completed at about 800 °C for 1 h under the protection of hydrogen atmosphere.The results show that a novel SMFM with complex surface morphology and high specific surface area（0.2 m2/g） can be obtained in this way.The effect of sintering temperature on the surface morphology and specific surface area of SMFM was studied by means of scanning electron microscopy and Brunauer-Emmett-Teller.The damage of micro-structure during the sintering process mainly contributed to the loss of specific surface area of SMFM and the optimal sintering temperature was 800 °C.展开更多
According to the notion of Orlicz mixed volume, in this paper, we extend L_p-dual affine surface area to the Orlicz version. Further, we obtain the affine isoperimetric inequality and the Blachke-Santaló inequali...According to the notion of Orlicz mixed volume, in this paper, we extend L_p-dual affine surface area to the Orlicz version. Further, we obtain the affine isoperimetric inequality and the Blachke-Santaló inequality for the dual Orlicz affine surface area. Besides, we also get the monotonicity inequality for Orlicz dual affine surface area.展开更多
Four methods, including voltammetric measurement of double layer capacitance, surface oxides reduction, under potential deposition of Cu and carbon monoxide （CO） stripping have been applied to evaluate the real surf...Four methods, including voltammetric measurement of double layer capacitance, surface oxides reduction, under potential deposition of Cu and carbon monoxide （CO） stripping have been applied to evaluate the real surface area of a polycrystalline Pd （pc-Pd） electrode. The results reveal that the second and third methods lead to consistent results with deviations below 5%. And from the determined double layer capacitance and CO stripping charge, it is deduced that the double layer capacity unit area is 23.1±0.4μF/cm2 and the saturated CO adlayer should be ca. 0.66 ML in order to ensure that the real surface area as determined is consistent with the other two techniques. The applicability as well as the attentions when applying these techniques for the determination of the real surface area of pc-Pd electrodes have been discussed.展开更多
The high-surface area nano-CeO2 was prepared by Ce（NO3）3 by precipitation method, with surfactant cetyhrimethyl ammonium bromide （CTAB） as templating agent. The effects of the precipitating agents, reaction temper...The high-surface area nano-CeO2 was prepared by Ce（NO3）3 by precipitation method, with surfactant cetyhrimethyl ammonium bromide （CTAB） as templating agent. The effects of the precipitating agents, reaction temperature, ageing time, and calcination temperature on the surface area, as well as the pore structure and the mean crystallite size of nano-CeO2 were studied. It was found that the reaction of Ce（NO3）3 with NaOH in the presence of CTAB at 90℃ for 12 h yieldsed a cerium oxide/surfaetant mixture, which after calcination at 400℃ resulted in high-surface area nano-CeO2. The mean crystallite size of CeO2 was approximately 6 nm, surface area was in excess of 200 m^2· g ^- 1, pore size was approximately 9 nm, and the pore distribution was concentrative. Moreover, the surface area can still reach 147 m^2·g^- 1 after calcination at 700 ℃, which showed the good thermal stability of the CeO2. The number of oxygen vacancies in the structure of CeO2 corresponded with the surface area of CeO2, and the high surface area was propitious to the formalion of oxygen vacancies.展开更多
Developing efficient oxygen evolution reaction(OER) electrocatalysts such as transition metal sulfides(TMSs) is of great importance to advance renewable hydrogen fuel toward further practical applications.Herein,NiCoS...Developing efficient oxygen evolution reaction(OER) electrocatalysts such as transition metal sulfides(TMSs) is of great importance to advance renewable hydrogen fuel toward further practical applications.Herein,NiCoS_(2) nanoparticles well decorated on double-sided N-doped reduced graphene oxide sheets(NiCoS_(2)/rGO) are prepared from an Al-containing ternary NiCoAl-layered double hydroxide precursor(NiCoAl-LDH) grown on GO support as an OER electrocatalyst.The Al-confinementassisted sulfurization,followed by selective acid treatment,endows the resulting NiCoS_(2)/rGO composite with the advantages:well-dispersed NiCoS_(2) nanoparticles,dualsided rGO support,as well as a large specific surface area of 119.4 m^(2)·g^(-1) and meso-/macroporous size distribution.The NiCoS_(2)/rGO electrocatalyst exhibits an overpotential of 273 mV at 10 mA·cm^(-2) and a good stability of 24 h,which outperform those of the counterparts of NiS_(2)/rGO and CoS_(2)/rGO.The results of electrochemical active surface area and electrochemical impedance spectra experimentally provide convincing rationales of the information of active sites and good conductivity,both underpin the enhanced electrocatalytic performances.展开更多
Pure and Zr, La or Pr-doped cerium oxides were characterised by transmission electron microscopy (TEM), N2 adsorption-desorption at –196 oC and X-ray diffraction (XRD). For crystal sizes calculation, the Scherrer and...Pure and Zr, La or Pr-doped cerium oxides were characterised by transmission electron microscopy (TEM), N2 adsorption-desorption at –196 oC and X-ray diffraction (XRD). For crystal sizes calculation, the Scherrer and Williamson-Hall equations were compared, and the relationship between surface area and crystal size was critically discussed. It was demonstrated that the Williamson-Hall equation must be used instead of the Scherrer equation to calculate crystal sizes, since the latter equation underestimated ...展开更多
Mesoporous CeO2 particles with high surface area were synthesized using a modified evaporation-induced self assembly(EISA) method which combined citric acid as complexing agent.As-prepared powder and further thermal t...Mesoporous CeO2 particles with high surface area were synthesized using a modified evaporation-induced self assembly(EISA) method which combined citric acid as complexing agent.As-prepared powder and further thermal treatment samples were characterized by X-ray diffraction(XRD),transmission electron microscopy(TEM),selected area electron diffraction(SAED),Fourier transform infrared spectrometer(FTIR),thermogravimetry and differential thermal analysis(TG-DTA),Brunauer-Emmett-Teller(BET) and Barrett-Joyner-Ha...展开更多
Soil organic carbon(SOC)can act as a sink or source of atmospheric carbon dioxide;therefore,it is important to understand the amount and composition of SOC in terrestrial ecosystems,the spatial variation in SOC,and th...Soil organic carbon(SOC)can act as a sink or source of atmospheric carbon dioxide;therefore,it is important to understand the amount and composition of SOC in terrestrial ecosystems,the spatial variation in SOC,and the underlying mechanisms that stabilize SOC.In this study,density fractionation and acid hydrolysis were used to assess the spatial variation in SOC,the heavy fraction of organic carbon(HFOC),and the resistant organic carbon(ROC)in soils of the southern Hulun Buir region,northeastern China,and to identify the major factors that contribute to this variation.The results showed that as the contents of clay and silt particles(0–50μm)increased,both methylene blue(MB)adsorption by soil minerals and microaggregate contents increased in the 0–20 and 20–40 cm soil layers(P<0.05).Although varying with vegetation types,SOC,HFOC,and ROC contents increased significantly with the content of clay and silt particles, MB adsorption by soil minerals,and microaggregate content(P<0.05),suggesting that soil texture,the MB adsorption by soil minerals,and microaggregate abundance might be important factors influencing the spatial heterogeneity of carbon contents in soils of the southern Hulun Buir region.展开更多
As a substitute for synthetic ammonia under mild condition, electrocatalytic nitrogen reduction reaction(NRR) provides a hopeful approach for the development of ammonia. Nevertheless, the current development of NRR el...As a substitute for synthetic ammonia under mild condition, electrocatalytic nitrogen reduction reaction(NRR) provides a hopeful approach for the development of ammonia. Nevertheless, the current development of NRR electrocatalysts is far from enough and a systematic research is needed to gain a better improvement. This article presents that 2 D C_(3)N_(4)-NV with a large specific surface area and abundant nitrogen vacancies is prepared by a simple and feasible method, and used as a metal-free catalyst for electrocatalytic NRR. Experiment result and density functional theory(DFT) calculation reveal that nitrogen vacancies in 2 D C_(3)N_(4)-NV can act as an efficient active site for catalytic NRR, which is conducive to capturing and activating N_(2), lowering Gibbs free energy(DG) in reaction and inhibiting hydrogen evolution reaction(HER) at the same time. In addition, the larger specific surface area also makes more active site exposed, which is good for the contact between the electrolyte and the active site, thus enhancing its NRR activity. The electrocatalyst shows an excellent catalytic activity for NRR in 0.1 M HCl, including Faradaic efficiency of 10.96%, NH_(3) yields of 17.85 lg h^(-1) mg_(cat)^(-1)., and good stability(over 20 h).展开更多
In this paper, three kinds of MgO with different specific surface area were prepared, and their effects on the catalytic performance of nickel catalysts for the carbon dioxide reforming of methane were investigated. T...In this paper, three kinds of MgO with different specific surface area were prepared, and their effects on the catalytic performance of nickel catalysts for the carbon dioxide reforming of methane were investigated. The results showed that MgO support with the higher specific surface area led to the higher dispersion of the active metal, which resulted in the higher initial activity. On the other hand, the specific surface area of MgO materials might not be the dominant factor for the basicity of support to chemisorb and activate CO2, which was another important factor for the performance of catalysts. Herein, Ni/MgO(CA) catalyst with proper specific surface area and strong ability to activate CO2exhibited stable catalytic property and the carbon species deposited on the Ni/MgO(CA) catalyst after 10 h of reaction at 650 ?C were mainly activated carbon species.展开更多
In this work,a facile"carbonization-activation"strategy is developed to synthesize N,P-codoped hierarchical porous carbon.Phosphoric acid is innovatively introduced during the hydrothermal process to achieve...In this work,a facile"carbonization-activation"strategy is developed to synthesize N,P-codoped hierarchical porous carbon.Phosphoric acid is innovatively introduced during the hydrothermal process to achieve in-situ P doping as well as create abundant pores,and the employment of sodamide is of vital importance to simultaneously serve as activating agent and N-source to succeed a high-level N doping.Thus,the obtained samples exhibit a unique three-dimensional hierarchical structure with an ultra-high specific surface area(3646 m^(2)g^(-1))and ultra-high N-doping level(9.81 at.%).Computational analyses confirm that N,P co-doping and higher N content can enhance active sites and widen potential differences of carbon materials to improve their capacitance.The as-prepared carbon materials demonstrate superior electrochemical performances,such as an ultra-high capacitance of 586 Fg^(-1)at 1 Ag^(-1),a superior rate capability of 409 Fg^(-1)at 20 Ag^(-1),and excellent long-term stability of 97%capacitance retention after10,000 cycles in 6 M KOH.Moreover,an assembled symmetric supercapacitor delivers a high energy density of 28.1 Wh kg^(-1)at the power density of 450 W kg^(-1)in 1 M Na_(2)SO_(4),demonstrating a great potential for applications in supercapacitors.展开更多
Adding fumed silica(Si0_(2))has been considered as an effective method for tailoring the phase morphology and performance of elastomer-toughened plastic binary blends.It has been demonstrated that the selective distri...Adding fumed silica(Si0_(2))has been considered as an effective method for tailoring the phase morphology and performance of elastomer-toughened plastic binary blends.It has been demonstrated that the selective distribution of SiO_(2) plays a decisive role in the mechanical properties of plastic/elastomer/SiO_(2)nanocomposites,especially for the impact toughness.In this work,we aim to illuminate the role of specific surface area in controlling their selective distribution of fumed SiO_(2) and consequent mechanical properties of plastic/elastomer binary blends.Three types of SiO_(2) with different specific surface areas were incorporated into polylactide/ethylene-co-vinyl-acetate(PLA/EVA)model blends by melt blending directly.It was found that the selective distribution of SiO_(2) is largely determined by their specific surface areas,i.e.SiO_(2) nanoparticles with low specific surface area has a stronger tendency to be located at the interface between PLA matrix and EVA dispersed phase as compared to those with high specific surface area.The specific surface area-dependent interfacial selective distribution of SiO_(2) is mainly attributed to the extent of increased viscosity of EVA dispersed phase in which SiO_(2)nanoparticles are initially dispersed and resultant migration rate of SiO_(2) nanoparticles.The interfacial localized SiO_(2) nanoparticles induce an obvious enhancement in the impact toughness with strength and modulus well maintained.More importantly,in the case of the same interfacial distribution,toughening efficiency is increased with the specific surface area of SiO_(2).Therefore,this is an optimum specific surface area of SiO_(2) for the toughening.This work not only provides a novel way to manipulate the selective distribution of SiO_(2) in elastomer-toughened plastic blends toward high-performance,but also gives a deep insight into the role of interfacial localized nanoparticles in the toughening mechanism.展开更多
Preparation of rice husk ash with high specific surface area and chemical reactivity of the product are reported in this paper. The amorphous rice husk ash with high specific surface area of 311 m2·g-1 was produc...Preparation of rice husk ash with high specific surface area and chemical reactivity of the product are reported in this paper. The amorphous rice husk ash with high specific surface area of 311 m2·g-1 was produced by heating acid treated rice husk at 700℃ for 4 h. The isotherms of rice husk ash are similar in shape to type Ⅱof Brunaner's classification with mesopores being predominant. The rice husk ash has a high chemical reactivity,especially that pretreated with acid. This chemical reactivity depends on ashing temperature and pretreatment conditions. There is an exponential relation between the specific surface area of rice husk ash and the change in the conductivity of saturated Ca(OH)2 solution with rice husk ash, from which the specific surface area can be known according to the conductivity change.展开更多
The porous cubic yttrium oxides with high specific surface area were prepared yttrium nitrate and its complex formed with methyl salicylate. The specific surface area by the explosive decomposition of and properties o...The porous cubic yttrium oxides with high specific surface area were prepared yttrium nitrate and its complex formed with methyl salicylate. The specific surface area by the explosive decomposition of and properties of powders synthesized at various temperatures were characterized using BET, X-ray diffraction （XRD）, infrared spectra （IR）, and scanning electron microscopy （SEM）. The results indicate that the highest specific surface area is found to be 65.37 m^2·g^-1 at the calcination temperature of 600 ℃, and then decreases to 20.33 m2· g^- 1 with the calcination temperature rising from 600 to 900 ℃. The powders show strong surface activity for adsorping water and carbon dioxide in air, which also decreases with the rising calcination temperature. The drop both on the surface area and surface activity of samples at higher temperatures may be due to pore-narrowing（sintering） effects.展开更多
Potassium-ion hybrid capacitors(PIHCs)are widely regarded as highly promising energy storage devices,due to their exceptional energy density,impressive power density,and abundant potassium resources.Unfortunately,rest...Potassium-ion hybrid capacitors(PIHCs)are widely regarded as highly promising energy storage devices,due to their exceptional energy density,impressive power density,and abundant potassium resources.Unfortunately,restricted by the inherent capacitive storage mechanism,the carbon cathodes possess a much lower specific capacity than battery-type anodes.Therefore,designing high-performance carbon cathodes is extremely urgent for the development of PIHCs.Herein,N,O codoped porous carbon(NOPC)was fabricated through the NaCl hard template method and combined KOH/melamine chemical activation technique,displaying the characteristics of abundant N/O content(4.7 at%/16.9 at%),ultrahigh specific surface area(3092 m^(2)g^(-1))and hierarchical pore network.The designed NOPC cathode delivers a high specific capacity(164.4 mAh.g^(-1)at 0.05 A.g^(-1))and superior cyclability(95.1%retention ratio at 2 A·g^(-1)over 2500 cycles).Notably,the adjustable ratio of micropores to mesopores facilitates the achievement of the optimal bal-ance between capacity and rate capability.Moreover,the pseudocapacitance can be further augmented through the incorporation of N/O functional groups.As expected,the graphite//NOPC based PIHC possesses a high energy density of 113 Wh·kg-at 747 W·kg^(-1)and excellent capacity retention of 84.4% fter 400 cycles at 1.0 A·g^(-1).This work introduces a novel strategy for designing carbon cathodes that enhances the electrochemical performance of PIHCs.展开更多
The reactive surface area, an important parameter controlling mineral reactions, affects the amount of mineralization trapping of CO2 which affects the long-term CO2 storage. The effect of the reactive surface area on...The reactive surface area, an important parameter controlling mineral reactions, affects the amount of mineralization trapping of CO2 which affects the long-term CO2 storage. The effect of the reactive surface area on the mineralization trapping of CO2 was numerically simulated for CO2 storage in saline aquifers. Three kinds of minerals, including anorthite, calcite and kaolinite, are involved in the mineral reactions. This paper models the relationship between the specific surface area and the grain diameter of anorthite based on experimental data from literature （Brantley and Mellott, 2000）. When the reactive surface areas of anorthite and calcite decrease from 838 to 83.8 m^2/m^3, the percentage of mineralization trapping of CO： after 500 years decreases from 11.8% to 0.65%. The amount of dissolved anorthite and the amounts of precipitated kaolinite and calcite decrease significantly when the reactive surface areas ofanorthite and calcite decrease from 838 to 83.8 m2/m3. Calcite is initially dissolved in the brine and then precipitates during the geochemical reactions between CO2-H20 and the minerals. Different reactive surface areas of anorthite and calcite lead to different times from dissolution to precipitation. The pH of the brine decreases with decreasing reactive surface areas of anorthite and calcite which influences the acidity of the saline aquifer. The gas saturation between the upper and lower parts of the saline aquifer increases with decreasing reactive surface areas of anorthite and calcite. The mass density distribution of brine solution shows that the CO2^＋brine solution region increases with decreasing reactive surface areas ofanorthite and calcite.展开更多
文摘The amount of impervious surface area increases with rapid urbanization.Remote sensing indices are used to detect impervious surface areas quickly,cheaply and accurately.This study used Landsat-OLI and Sentiel-2A MSI images in the province of Ankara to compare six impervious surface extraction indices:Normalized Difference Builtup Index(NDBI),Combinational Biophysical Composition Index(CBCI),Normalized Impervious Surface Index(NISI),Urban Index(UI),Index-based Built-up Index(IBI),Enhanced Normalized Difference Impervious Surfaces Index(ENDISI).Spectral discrimination index(SDI)and error matrix were used to evaluate the performance of the indexes.In addition,a visual evaluation of the performance of the indices was made on different surface areas in the study area.
基金financially supported by the Natural Science Foundation of Zhejiang Province(No.LR22E010001)the National Natural Science Foundation of China(No.52073258)+1 种基金the Fundamental Research Funds for the Provincial Universities of Zhejiang(No.RF-B2022006)the R&D Program of Zhejiang University of Technology(No.KYY-HX-20190730)
文摘Iron oxide nanoparticles(IONPs)with intrinsic peroxidase(POD)-mimic activity have gained significant attention as nanozymes.Reducing sizes of IONPs is the mostly applied strategy to boost their enzymatic activity due to their high specific surface areas.Herein,we synthesized a series of uniformly sized IONPs ranging from3.17 to 21.2 nm,and found that POD activity of IONPs is not monotone increased by reducing their sizes,with the optimal size of 7.82 nm rather than smaller sized 3.17 nm.The reason for this unnormal phenomenon is that electronic structure also had great influence on POD activity,especially at the ultrasmall size region.Since Fe^(2+)are with higher enzymatic activity than Fe^(3+),3.17 nm IONPs although have the largest specific surface area,are prone to be oxidized,which reduced their iron content and ratio of Fe^(2+)to Fe^(3+),and consequently decreased their POD activity.By intentionally oxidized 7.82 nm IONPs in air,POD activity was obviously reduced,illustrating electronic structure cannot be overlooked.At the larger sized region ranging from 7.82 to 21.2 nm,oxidation degree of IONPs is similar,and surface electronic structure had a negligible effect on POD activity,and therefore,POD activity is predominantly influenced by specific surface area.By using the optimized 7.82 nm IONPs,tumor growth was obviously inhibited,demonstrating their potential in cancer therapeutics.Our results reveal that the designing of nanozymes should comprehensively balance their influence of surface electronic structure and specific surface area.
基金Projects(52372284,52275187,62004143)supported by the National Natural Science Foundation of ChinaProject(2022BAA084)supported by the Key R&D Program of Hubei Province,ChinaProject(232300421135)supported by the Natural Science Foundation of Henan Province,China。
文摘Mo_(2)CT_(x)MXene is a novel two-dimensional material,which is generally made by the etching of inorganic acid solutions,such as hydrofluoric acid(HF)or hydrochloric acid(HCl).Those solutions are always corrosive and hazardous.In this paper,a mild organic acid,acetic acid(CH_(3)COOH),was selected to synthesize Mo_(2)CT_(x)MXene.30 mL acetic acid(HAc)with the concentration of 13 mol/L was mixed with 2 g acetate(CH_(3)COONa or CH_(3)COOK)and 10 mL water to make etching solution(NaAc+HAc or KAc+HAc).In the solution,the concentration of CH_(3)COO^(-)was 10 mol/L,the concentration of Na^(+)/K^(+)is 0.6/0.5 mol/L.The pH value is 2.8.Mo_(2)CT_(x)was obtained by hydrothermal etching at 240℃for 1 d.Compared with the general method of HF etching,the etchant is milder and the etching process is safer.On the surface of Mo_(2)CT_(x)nanosheet made by this method,acetate group(CH_(3)COO^(-))was adsorbed as termination,which is larger than the F/O/OH termination of that made by general HF etching.The lattice parameter c(LP c)of Mo_(2)CT_(x)etched with NaAc+HAc/KAc+HAc is 21.09Å/20.89Å.Moreover,the specific surface areas of the samples etched by NaAc+HAc and KAc+HAc were 18.1 m^(2)/g and 14.1 m^(2)/g,respectively,which were much larger than those etched by conventional methods.As the anode of lithium-ion battery,the specific capacity under current density of 100 mA/g at 100 th cycle was 108 mA·h/g,which is higher than the capacity of samples made by general HF etching.This work reports a novel method to make Mo_(2)CT_(x)MXene by the solution of mild acetic acid.The samples made by this method had very high specific surface area and relatively high lithium-storage performance.
文摘We build a computer program to reconstruct convex bodies using even L_(p)surface area measures for p≥1.Firstly,we transform the minimization problem Pi,which is equivalent to solving the even L_(p)Minkowski problem,into a convex optimization problem P4 with a finite number of constraints.This transformation makes it suitable for computational resolution.Then,we prove that the approximate solutions obtained by solving the problem P4 converge to the theoretical solution when N and k are sufficiently large.Finally,based on the convex optimization problem P_(4),we provide an algorithm for reconstructing convex bodies from even L_(p)surface area measures,and present several examples implemented using MATLAB.
基金Project (50930005) supported by the National Natural Science Foundation of ChinaProject (U0834002) supported by the Key Programof NSFC-Guangdong Joint Funds of China+1 种基金Project (LYM09024) supported by Training Program for Excellent Young Teachers withInnovation of Guangdong University, ChinaProject (2009ZM0121) supported by the Fundamental Research Funds for the CentralUniversities of South China University of Technology,China
文摘A procedure of low temperature solid-phase sintering（LTSS） was carried out to fabricate sintered metal fibrous media（SMFM） with high specific surface area.Stainless steel fibers which were produced by cutting process were first plated with a coarse copper coating layer by electroless plating process.A low-temperature sintering process was then completed at about 800 °C for 1 h under the protection of hydrogen atmosphere.The results show that a novel SMFM with complex surface morphology and high specific surface area（0.2 m2/g） can be obtained in this way.The effect of sintering temperature on the surface morphology and specific surface area of SMFM was studied by means of scanning electron microscopy and Brunauer-Emmett-Teller.The damage of micro-structure during the sintering process mainly contributed to the loss of specific surface area of SMFM and the optimal sintering temperature was 800 °C.
基金Supported by the National Natural Science Foundation of China(11161019,11561020)the Science and Technology Plan of Gansu Province(145RJZG227)
文摘According to the notion of Orlicz mixed volume, in this paper, we extend L_p-dual affine surface area to the Orlicz version. Further, we obtain the affine isoperimetric inequality and the Blachke-Santaló inequality for the dual Orlicz affine surface area. Besides, we also get the monotonicity inequality for Orlicz dual affine surface area.
文摘Four methods, including voltammetric measurement of double layer capacitance, surface oxides reduction, under potential deposition of Cu and carbon monoxide （CO） stripping have been applied to evaluate the real surface area of a polycrystalline Pd （pc-Pd） electrode. The results reveal that the second and third methods lead to consistent results with deviations below 5%. And from the determined double layer capacitance and CO stripping charge, it is deduced that the double layer capacity unit area is 23.1±0.4μF/cm2 and the saturated CO adlayer should be ca. 0.66 ML in order to ensure that the real surface area as determined is consistent with the other two techniques. The applicability as well as the attentions when applying these techniques for the determination of the real surface area of pc-Pd electrodes have been discussed.
基金Project supported by the National Natural Science Foundation of China (20473075)
文摘The high-surface area nano-CeO2 was prepared by Ce（NO3）3 by precipitation method, with surfactant cetyhrimethyl ammonium bromide （CTAB） as templating agent. The effects of the precipitating agents, reaction temperature, ageing time, and calcination temperature on the surface area, as well as the pore structure and the mean crystallite size of nano-CeO2 were studied. It was found that the reaction of Ce（NO3）3 with NaOH in the presence of CTAB at 90℃ for 12 h yieldsed a cerium oxide/surfaetant mixture, which after calcination at 400℃ resulted in high-surface area nano-CeO2. The mean crystallite size of CeO2 was approximately 6 nm, surface area was in excess of 200 m^2· g ^- 1, pore size was approximately 9 nm, and the pore distribution was concentrative. Moreover, the surface area can still reach 147 m^2·g^- 1 after calcination at 700 ℃, which showed the good thermal stability of the CeO2. The number of oxygen vacancies in the structure of CeO2 corresponded with the surface area of CeO2, and the high surface area was propitious to the formalion of oxygen vacancies.
基金financially supported by the National Natural Science Foundation of China(No.U1607128)。
文摘Developing efficient oxygen evolution reaction(OER) electrocatalysts such as transition metal sulfides(TMSs) is of great importance to advance renewable hydrogen fuel toward further practical applications.Herein,NiCoS_(2) nanoparticles well decorated on double-sided N-doped reduced graphene oxide sheets(NiCoS_(2)/rGO) are prepared from an Al-containing ternary NiCoAl-layered double hydroxide precursor(NiCoAl-LDH) grown on GO support as an OER electrocatalyst.The Al-confinementassisted sulfurization,followed by selective acid treatment,endows the resulting NiCoS_(2)/rGO composite with the advantages:well-dispersed NiCoS_(2) nanoparticles,dualsided rGO support,as well as a large specific surface area of 119.4 m^(2)·g^(-1) and meso-/macroporous size distribution.The NiCoS_(2)/rGO electrocatalyst exhibits an overpotential of 273 mV at 10 mA·cm^(-2) and a good stability of 24 h,which outperform those of the counterparts of NiS_(2)/rGO and CoS_(2)/rGO.The results of electrochemical active surface area and electrochemical impedance spectra experimentally provide convincing rationales of the information of active sites and good conductivity,both underpin the enhanced electrocatalytic performances.
基金Project supported by the Spanish Ministry of Science and Innovation (CIT-420000-2009-48 project, partially funded with FEDER resources)
文摘Pure and Zr, La or Pr-doped cerium oxides were characterised by transmission electron microscopy (TEM), N2 adsorption-desorption at –196 oC and X-ray diffraction (XRD). For crystal sizes calculation, the Scherrer and Williamson-Hall equations were compared, and the relationship between surface area and crystal size was critically discussed. It was demonstrated that the Williamson-Hall equation must be used instead of the Scherrer equation to calculate crystal sizes, since the latter equation underestimated ...
基金supported by the National Natural Science Foundation of China (20771047)the Natural Science Foundation of Jiangsu Province (BK2008541)+1 种基金Jiangsu Graduate Student Innovation Grant (CX82Z-007Z)Jiangsu University Innovation Grant (1293000425)
文摘Mesoporous CeO2 particles with high surface area were synthesized using a modified evaporation-induced self assembly(EISA) method which combined citric acid as complexing agent.As-prepared powder and further thermal treatment samples were characterized by X-ray diffraction(XRD),transmission electron microscopy(TEM),selected area electron diffraction(SAED),Fourier transform infrared spectrometer(FTIR),thermogravimetry and differential thermal analysis(TG-DTA),Brunauer-Emmett-Teller(BET) and Barrett-Joyner-Ha...
基金Project supported by the National Natural Science Foundation of China(Nos.40321101 and 40071036)the Major State Basic Research Development Program of China(973 Program)(No.2002CB412503)
文摘Soil organic carbon(SOC)can act as a sink or source of atmospheric carbon dioxide;therefore,it is important to understand the amount and composition of SOC in terrestrial ecosystems,the spatial variation in SOC,and the underlying mechanisms that stabilize SOC.In this study,density fractionation and acid hydrolysis were used to assess the spatial variation in SOC,the heavy fraction of organic carbon(HFOC),and the resistant organic carbon(ROC)in soils of the southern Hulun Buir region,northeastern China,and to identify the major factors that contribute to this variation.The results showed that as the contents of clay and silt particles(0–50μm)increased,both methylene blue(MB)adsorption by soil minerals and microaggregate contents increased in the 0–20 and 20–40 cm soil layers(P<0.05).Although varying with vegetation types,SOC,HFOC,and ROC contents increased significantly with the content of clay and silt particles, MB adsorption by soil minerals,and microaggregate content(P<0.05),suggesting that soil texture,the MB adsorption by soil minerals,and microaggregate abundance might be important factors influencing the spatial heterogeneity of carbon contents in soils of the southern Hulun Buir region.
基金funded by the National Natural Science Foundation of China (21802058 and 21872066)the Fundamental Research Funds for the Central Universities (China, lzujbky-2020-42)the Natural Science Foundation of Gansu Province (20JR5RA225)。
文摘As a substitute for synthetic ammonia under mild condition, electrocatalytic nitrogen reduction reaction(NRR) provides a hopeful approach for the development of ammonia. Nevertheless, the current development of NRR electrocatalysts is far from enough and a systematic research is needed to gain a better improvement. This article presents that 2 D C_(3)N_(4)-NV with a large specific surface area and abundant nitrogen vacancies is prepared by a simple and feasible method, and used as a metal-free catalyst for electrocatalytic NRR. Experiment result and density functional theory(DFT) calculation reveal that nitrogen vacancies in 2 D C_(3)N_(4)-NV can act as an efficient active site for catalytic NRR, which is conducive to capturing and activating N_(2), lowering Gibbs free energy(DG) in reaction and inhibiting hydrogen evolution reaction(HER) at the same time. In addition, the larger specific surface area also makes more active site exposed, which is good for the contact between the electrolyte and the active site, thus enhancing its NRR activity. The electrocatalyst shows an excellent catalytic activity for NRR in 0.1 M HCl, including Faradaic efficiency of 10.96%, NH_(3) yields of 17.85 lg h^(-1) mg_(cat)^(-1)., and good stability(over 20 h).
基金supported by the South-Central University for Nationalities(CZZ12002)
文摘In this paper, three kinds of MgO with different specific surface area were prepared, and their effects on the catalytic performance of nickel catalysts for the carbon dioxide reforming of methane were investigated. The results showed that MgO support with the higher specific surface area led to the higher dispersion of the active metal, which resulted in the higher initial activity. On the other hand, the specific surface area of MgO materials might not be the dominant factor for the basicity of support to chemisorb and activate CO2, which was another important factor for the performance of catalysts. Herein, Ni/MgO(CA) catalyst with proper specific surface area and strong ability to activate CO2exhibited stable catalytic property and the carbon species deposited on the Ni/MgO(CA) catalyst after 10 h of reaction at 650 ?C were mainly activated carbon species.
基金financially supported by the National Natural Science Foundation of China(Nos.21776147,21606140,61604086,and 21905153)the Qingdao Municipal Science and Technology Bureau,China(19-6-1-91-nsh)+2 种基金the International Science&Technology Cooperation Program of China(No.2014DFA60150)the Department of Science and Technology of Shandong Province(Nos.ZR2018BB066 and 2016GGX104010)the Chemcloudcomputing of National Supercomputing Center in Shenzhen(Shenzhen CloudComputing Center)。
文摘In this work,a facile"carbonization-activation"strategy is developed to synthesize N,P-codoped hierarchical porous carbon.Phosphoric acid is innovatively introduced during the hydrothermal process to achieve in-situ P doping as well as create abundant pores,and the employment of sodamide is of vital importance to simultaneously serve as activating agent and N-source to succeed a high-level N doping.Thus,the obtained samples exhibit a unique three-dimensional hierarchical structure with an ultra-high specific surface area(3646 m^(2)g^(-1))and ultra-high N-doping level(9.81 at.%).Computational analyses confirm that N,P co-doping and higher N content can enhance active sites and widen potential differences of carbon materials to improve their capacitance.The as-prepared carbon materials demonstrate superior electrochemical performances,such as an ultra-high capacitance of 586 Fg^(-1)at 1 Ag^(-1),a superior rate capability of 409 Fg^(-1)at 20 Ag^(-1),and excellent long-term stability of 97%capacitance retention after10,000 cycles in 6 M KOH.Moreover,an assembled symmetric supercapacitor delivers a high energy density of 28.1 Wh kg^(-1)at the power density of 450 W kg^(-1)in 1 M Na_(2)SO_(4),demonstrating a great potential for applications in supercapacitors.
基金the National Natural Science Foundation of China(No.51803130)China Postdoctoral Science Foundation(No.2018M640915)+1 种基金Sichuan Science and Technology Program(No.2019JDRC010)Fundamental Research Funds for Central Universities.
文摘Adding fumed silica(Si0_(2))has been considered as an effective method for tailoring the phase morphology and performance of elastomer-toughened plastic binary blends.It has been demonstrated that the selective distribution of SiO_(2) plays a decisive role in the mechanical properties of plastic/elastomer/SiO_(2)nanocomposites,especially for the impact toughness.In this work,we aim to illuminate the role of specific surface area in controlling their selective distribution of fumed SiO_(2) and consequent mechanical properties of plastic/elastomer binary blends.Three types of SiO_(2) with different specific surface areas were incorporated into polylactide/ethylene-co-vinyl-acetate(PLA/EVA)model blends by melt blending directly.It was found that the selective distribution of SiO_(2) is largely determined by their specific surface areas,i.e.SiO_(2) nanoparticles with low specific surface area has a stronger tendency to be located at the interface between PLA matrix and EVA dispersed phase as compared to those with high specific surface area.The specific surface area-dependent interfacial selective distribution of SiO_(2) is mainly attributed to the extent of increased viscosity of EVA dispersed phase in which SiO_(2)nanoparticles are initially dispersed and resultant migration rate of SiO_(2) nanoparticles.The interfacial localized SiO_(2) nanoparticles induce an obvious enhancement in the impact toughness with strength and modulus well maintained.More importantly,in the case of the same interfacial distribution,toughening efficiency is increased with the specific surface area of SiO_(2).Therefore,this is an optimum specific surface area of SiO_(2) for the toughening.This work not only provides a novel way to manipulate the selective distribution of SiO_(2) in elastomer-toughened plastic blends toward high-performance,but also gives a deep insight into the role of interfacial localized nanoparticles in the toughening mechanism.
文摘Preparation of rice husk ash with high specific surface area and chemical reactivity of the product are reported in this paper. The amorphous rice husk ash with high specific surface area of 311 m2·g-1 was produced by heating acid treated rice husk at 700℃ for 4 h. The isotherms of rice husk ash are similar in shape to type Ⅱof Brunaner's classification with mesopores being predominant. The rice husk ash has a high chemical reactivity,especially that pretreated with acid. This chemical reactivity depends on ashing temperature and pretreatment conditions. There is an exponential relation between the specific surface area of rice husk ash and the change in the conductivity of saturated Ca(OH)2 solution with rice husk ash, from which the specific surface area can be known according to the conductivity change.
文摘The porous cubic yttrium oxides with high specific surface area were prepared yttrium nitrate and its complex formed with methyl salicylate. The specific surface area by the explosive decomposition of and properties of powders synthesized at various temperatures were characterized using BET, X-ray diffraction （XRD）, infrared spectra （IR）, and scanning electron microscopy （SEM）. The results indicate that the highest specific surface area is found to be 65.37 m^2·g^-1 at the calcination temperature of 600 ℃, and then decreases to 20.33 m2· g^- 1 with the calcination temperature rising from 600 to 900 ℃. The powders show strong surface activity for adsorping water and carbon dioxide in air, which also decreases with the rising calcination temperature. The drop both on the surface area and surface activity of samples at higher temperatures may be due to pore-narrowing（sintering） effects.
基金financially supported by the National Natural Science Foundation of China(Nos.22179123 and52002138)Taishan Scholar Program of Shandong Province+1 种基金China(No.tsqn202211048)the Fundamental Research Funds for the Central Universities(Nos.202262010 and 862201013190)。
文摘Potassium-ion hybrid capacitors(PIHCs)are widely regarded as highly promising energy storage devices,due to their exceptional energy density,impressive power density,and abundant potassium resources.Unfortunately,restricted by the inherent capacitive storage mechanism,the carbon cathodes possess a much lower specific capacity than battery-type anodes.Therefore,designing high-performance carbon cathodes is extremely urgent for the development of PIHCs.Herein,N,O codoped porous carbon(NOPC)was fabricated through the NaCl hard template method and combined KOH/melamine chemical activation technique,displaying the characteristics of abundant N/O content(4.7 at%/16.9 at%),ultrahigh specific surface area(3092 m^(2)g^(-1))and hierarchical pore network.The designed NOPC cathode delivers a high specific capacity(164.4 mAh.g^(-1)at 0.05 A.g^(-1))and superior cyclability(95.1%retention ratio at 2 A·g^(-1)over 2500 cycles).Notably,the adjustable ratio of micropores to mesopores facilitates the achievement of the optimal bal-ance between capacity and rate capability.Moreover,the pseudocapacitance can be further augmented through the incorporation of N/O functional groups.As expected,the graphite//NOPC based PIHC possesses a high energy density of 113 Wh·kg-at 747 W·kg^(-1)and excellent capacity retention of 84.4% fter 400 cycles at 1.0 A·g^(-1).This work introduces a novel strategy for designing carbon cathodes that enhances the electrochemical performance of PIHCs.
基金supported by the National Natural Science Foundation of China (Grant No. 50906043)the Tsinghua University Initiative Scientific Research Program(2009THZ02232)The first author did this study while at Geoscience Australia sponsored by CAGS (China-Australia Geological Storage of CO2Project)
文摘The reactive surface area, an important parameter controlling mineral reactions, affects the amount of mineralization trapping of CO2 which affects the long-term CO2 storage. The effect of the reactive surface area on the mineralization trapping of CO2 was numerically simulated for CO2 storage in saline aquifers. Three kinds of minerals, including anorthite, calcite and kaolinite, are involved in the mineral reactions. This paper models the relationship between the specific surface area and the grain diameter of anorthite based on experimental data from literature （Brantley and Mellott, 2000）. When the reactive surface areas of anorthite and calcite decrease from 838 to 83.8 m^2/m^3, the percentage of mineralization trapping of CO： after 500 years decreases from 11.8% to 0.65%. The amount of dissolved anorthite and the amounts of precipitated kaolinite and calcite decrease significantly when the reactive surface areas ofanorthite and calcite decrease from 838 to 83.8 m2/m3. Calcite is initially dissolved in the brine and then precipitates during the geochemical reactions between CO2-H20 and the minerals. Different reactive surface areas of anorthite and calcite lead to different times from dissolution to precipitation. The pH of the brine decreases with decreasing reactive surface areas of anorthite and calcite which influences the acidity of the saline aquifer. The gas saturation between the upper and lower parts of the saline aquifer increases with decreasing reactive surface areas of anorthite and calcite. The mass density distribution of brine solution shows that the CO2^＋brine solution region increases with decreasing reactive surface areas ofanorthite and calcite.
