This work describes the discharge characteristics and acetone degradation with plasma under different electric fields based on a coaxial cylindrical dielectric barrier discharge(DBD)device energized by pulsed power.It...This work describes the discharge characteristics and acetone degradation with plasma under different electric fields based on a coaxial cylindrical dielectric barrier discharge(DBD)device energized by pulsed power.It is found that the segmented electrodes with appropriate spacing in coaxial cylindrical DBD are beneficial to the plasma ionization.In this work,the plasma distribution,discharge thermal effect,ionization of reactive species,and acetone degradation performance in coaxial cylindrical DBD with different segmented electrodes are systematically investigated.The experimental results show that segmented electrodes with a certain distance can cause additional ionization in the non-electrode-covered region between adjacent electrodes,thus enlarging the plasma region compared with a single electrode with equivalent total electrode length.The additional ionization involved the inner volume discharge between the quartz tubes and the outer surface discharge along the surface of the external quartz tube.The spatial distributions of the inner volume discharge and external surface discharge were predominantly governed by the radial and axial components of the inter-electrode electric field,respectively.The external surface discharge exhibited significant suppression when the electrode spacing was<1.5 mm,and it reached its maximum length at 3 mm spacing.When the electrode distance increased to 7-9 mm,a weak ionizing region appeared in the middle of the adjacent electrodes,which could be attributed to the gradual attenuation of the radial component with the increasing electrode spacing.A higher thermal effect and better oxidation of acetone to CO_(x)(CO and CO_(2))were achieved with the segmented electrode;the dual-segment configuration(3 mm per electrode)achieved a reactor temperature of 63.4℃,representing a 10℃enhancement over comparable single-electrode systems.Similarly,the CO_(2)and CO concentration reached 328.8 mg/m3and 105.7 mg/m3,respectively,in two 3 mm long segmented electrodes,which was an increase of 12.2%and 25.6%,respectively,compared with the single electrode.Notably,considering the equivalent ionization of the inner discharge with different electrodes,the enhanced thermal effects and CO_(x)conversion efficiency directly correlate with the expanded plasma zone induced by electrode segmentation.This work provides critical insights into optimizing electrode configurations for efficient plasma-assisted volatile organic compound degradation systems.展开更多
Acetone is a common volatile organic compound that can cause harm to human health when inhaled in small amounts.Therefore,the development of fast response and low detection limit acetone sensors becomes crucial.In thi...Acetone is a common volatile organic compound that can cause harm to human health when inhaled in small amounts.Therefore,the development of fast response and low detection limit acetone sensors becomes crucial.In this study,a core-shell spherical TiO_(2) sensor with a rich pore structure was designed.This sensor exhibited excellent sensing properties,including higher responsiveness(100 ppm acetone,R_(a)/R_(g)=80),lower detection limit(10 ppb)and short response time(8 s).The problem is that the sensing mechanism between TiO_(2) and acetone is not thoroughly analyzed.To gain further insight,the interaction process of TiO_(2) core-shell spheres and acetone under varying oxygen content environments was investigated by dynamic testing,X-ray photoelectron spectroscopy,in-situ Fourier transform infrared spectroscopy and gas chromatography-mass spectrometry.The research results show that acetone not only adsorbs on the surface of the material and reacts with adsorbed oxygen,but also undergoes catalytic oxidation reaction with TiO_(2) core-shell spheres.Significantly,in high oxygen content environments,acetone undergoes oxidation to form intermediates such as acids and anhydrides that are difficult to desorpt on the surface of the material,thus prolonging the recovery time of the sensor.The discovery of this sensing process will provide some guidance for the design of acetone sensing materials in the future.Meanwhile,this also imparts valuable references and insights for the investigation of the mechanism and application of other sensitive metal oxide materials.展开更多
Low-concentration acetone detection is of great importance for acetone sensor in the fields of environmental protection and noninvasive diagnosis.In this work,mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)n-p heterojunctions were...Low-concentration acetone detection is of great importance for acetone sensor in the fields of environmental protection and noninvasive diagnosis.In this work,mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)n-p heterojunctions were constructed for efficient improvement of low-concentration acetone gas sensing.The gas-sensing results indicated that the mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)composites with a significantly large specific surface area exhibited significantlyenhanced acetone gas-sensitive performance compared to pure Fe_(2)O_(3).The Fe_(2)O_(3)/Cr_(2)O_(3)composites demonstrated a high response,good selectivity and excellent stability over200 days to 10 ppm acetone at 220℃.And the theoretical detection limit was calculated to reach 0.285 ppm acetone.A feasible acetone sensing mechanism was proposed through electronic band structure and density functional theory.The improved low-concentration acetone sensing performance was due to the formed mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)n-p heterojunctions with a large specific surface area.The Fe_(2)O_(3)/Cr_(2)O_(3)composites showed excellent acetone gas-sensitive performance,which could be a promising candidate for developing low-concentration acetone sensing devices at low working temperatures.展开更多
Nickel ferrite nano-powders were prepared by microwave radiating low-temperature solid-state reaction method, and then modified with Ag by dipping method. The crystal structure and morphology of the samples were chara...Nickel ferrite nano-powders were prepared by microwave radiating low-temperature solid-state reaction method, and then modified with Ag by dipping method. The crystal structure and morphology of the samples were characterized by means of X-ray diffraction（XRD）, scanning electron microscopy （SEM） and X-ray photoelectron spectroscopy （XPS）. The gas sensing properties of the samples were also investigated. The results reveal that the Ag, as amorphous structure, can efficiently prevent the reuniting and growing-up of nanosized NiFe2O4 grains, and 1.5% Ag modified NiFe2O4 sensor has a better sensitivity, up to 43, for acetone gas than 1.5%Ag mixed NiFe2O4 sensor prepared by low-temperature solid-state reaction, at an optimal working voltage of 4.5 V. The quick response time （1 s） and fast recovery time （～10 s） are the main characteristics of this sensor.展开更多
A synthetic method of dialkylideneacetones has been developed. Compared with known protocols, the method employed catalytic Ca(OH)_2 as the cheap, mild base catalyst and dilute aqueous EtOH(20%, v/v)as the green and s...A synthetic method of dialkylideneacetones has been developed. Compared with known protocols, the method employed catalytic Ca(OH)_2 as the cheap, mild base catalyst and dilute aqueous EtOH(20%, v/v)as the green and safe solvent. The procedure was easily operated: In most cases, the product could be isolated by a simple filtration, and purified by washing with water. This paper provided experimental details of the reactions, which could be applied in gram-scale synthesis and should be a very reliable and practical protocol to prepare these useful compounds in laboratory and at the industrial level.展开更多
The morphologic changes and growth status of PC12 cells were observed after intervened by different concentrations of methanol, ethanol, acetone, glycerol and the toxic concentrations were ascertained. Four kinds of o...The morphologic changes and growth status of PC12 cells were observed after intervened by different concentrations of methanol, ethanol, acetone, glycerol and the toxic concentrations were ascertained. Four kinds of organic solvents al showed certain cytotoxicity to PC12 cells. Compared with other three kinds of or-ganic solvents, ethanol showed the most obvious cytotoxicity to PC12 cells and the cellviability would be reduced to 60% if the concentration of ethanol was 20 ml/L and the intervention lasted for 24 h. Under the same condition, the reduced per-centages of cellviability for acetone and ethanol were 20% and 15% respectively. Glycerol also showed cytotoxicity to PC12 cells, especial y as the concentration was raised gradual y, but the toxicity was relatively mild. This study would provide refer-ence material for subsequent pharmacological studies.展开更多
Mesoporous semiconducting metal oxides(SMOs)heterojunctions are appealing sensors for gas detecting.However,due to the different hydrolysis and condensation mechanism of every metal precursor and the contradiction bet...Mesoporous semiconducting metal oxides(SMOs)heterojunctions are appealing sensors for gas detecting.However,due to the different hydrolysis and condensation mechanism of every metal precursor and the contradiction between high crystallinity and high surface area,the synthesis of mesoporous SMOs heterojunctions with highly o rdered mesostructures,highly crystallized frameworks,and high surface area remains a huge challenge.In this work,we develop a novel"acid-base pair"adjusted solvent evaporation induced self-assembly(EISA)strategy to prepare highly crystallized ordered mesoporous TiO2/WO3(OM-TiO2/WO3)heterojunctions.The WCl6 and titanium isopropoxide(TIPO)are used as the precursors,respectively,which function as the"acid-base pair",enabling the coassembly with the structure directing agent(PEO-b-PS)into highly ordered meso structures.In addition,PEO-b-PS can be converted to rigid carbon which can protect the meso structures from collapse during the crystallization process.The resultant OM-TiO2/WO3 heterojunctions possess primitive cubic mesostructures,large pore size(~21.1 nm),highly crystalline frameworks and surface area(~98 m2/g).As a sensor for acetone,the obtained OM-TiO2/WO3 show excellent re sponse/recovery perfo rmance(3 s/5 s),good linear dependence,repeatability,selectivity,and long-term stability(35 days).展开更多
Acetone,as widely used reagents in industry and laboratories,are extremely harmful to the human.So the detection of acetone gas concentrations and leaks in special environments at room temperature is essential.Herein,...Acetone,as widely used reagents in industry and laboratories,are extremely harmful to the human.So the detection of acetone gas concentrations and leaks in special environments at room temperature is essential.Herein,the nanocomposite combining SnO-SnO_(2)(p-n junction)and Ti_(3)C_(2)T_(x) MXene was successfully synthesized by a one-step hydrothermal method.Because of the existence of a small amount of oxygen during the hydrothermal conditions,part of the p-type SnO was oxidized to n-type SnO_(2),forming in-situ p-n junctions on the surface of Sn O.The hamburger-like SnO-SnO_(2)/Ti_(3)C_(2)T_(x) sensor exhibited improved acetone gas sensing response of 12.1(R_(g)/R_(a))at room temperature,which were nearly 11 and 4 times higher than those of pristine Ti_(3)C_(2)T_(x) and pristine SnO-SnO_(2),respectively.Moreover,it expressed a short recovery time(9 s)and outstanding reproducibility.Because of the different work functions,the Schottky barrier was formed between the SnO and the Ti_(3)C_(2)T_(x) nanosheets,acting as a hole accumulation layer(HALs)between Ti_(3)C_(2)T_(x) and tin oxides.Herein,the sensing mechanism based on the formation of hetero-junctions and high conductivity of the metallic phase of Ti_(3)C_(2)T_(x) MXene in SnO-SnO_(2)/Ti_(3)C_(2)T_(x) sensors was discussed in detail.展开更多
Currently,SmFeO_(3)-based sensors are an effective platform for detecting acetone gas.However,they require high operating temperatures,which increases energy consumption and safety hazards,and their response is low wh...Currently,SmFeO_(3)-based sensors are an effective platform for detecting acetone gas.However,they require high operating temperatures,which increases energy consumption and safety hazards,and their response is low when the gas concentration is at 10^(-9)(PPB),which cannot meet the requirements of using exhaled breath to pre-diagnose diabetes.Herein,Pd-SmFeO_(3)hollow nanotubes with an extremely high specific surface area and porosity were synthesized by electrospinning.After Pd doping,the specific surface area improved by more than two times,and the acetone response improved by more than three times.In addition,the response further improved by more than 1.5 times,and the optimum operating temperature reduced by 100℃under light irradiation.Moreover,the relative humidity adaptability,long-term stability,and selectivity of the material were significantly improved after Pd doping or light irradiation.Finally,the acetone concentration in a person’s exhaled breath was detected by a Pd-SmFeO_(3)-based gas sensor,and the error was less than 10%compared to that obtained by gas chromatography-mass spectrometry method.展开更多
Ternary Au/Fe2O3-ZnO gas-sensing materials were synthesized by combining co-precipitation and microwave irradiation process.The as-prepared Au/Fe2O3-ZnO was characterized with X-ray diffractometer and scanning electro...Ternary Au/Fe2O3-ZnO gas-sensing materials were synthesized by combining co-precipitation and microwave irradiation process.The as-prepared Au/Fe2O3-ZnO was characterized with X-ray diffractometer and scanning electron microscope,and its gas-sensing performance was measured using a gas-sensor analysis system.The results show that the as-prepared products consist of hexagonal wurtzite ZnO,face-centered cubic gold nanoparticles and orthorhombic Fe2O3crystallines.The Au/Fe2O3-ZnO based sensor has a very high selectivity to ethanol and acetone,and also has high sensitivity(154)at a low working temperature(270°C)and an extremely fast response(1s)against acetone.It is found that the selectivity can be adjusted by Fe2O3content added in the ternary materials.It possesses a worth looking forward prospect to practical applications in acetone detecting and administrating field.展开更多
In recent years, clinical studies have found that acetone concentration in exhaled breath can be taken as a characteristic marker of diabetes. Metal-oxide-semiconductor (MOS) materials are widely used in acetone gas s...In recent years, clinical studies have found that acetone concentration in exhaled breath can be taken as a characteristic marker of diabetes. Metal-oxide-semiconductor (MOS) materials are widely used in acetone gas sensors due to their low cost, high sensitivity, fast response/recovery time, and easy integration. This paper reviews recent progress in acetone sensors based on MOS materials for diabetes diagnosis. The methods of improving the performance of acetone sensor have been explored for comparison, especially in high humidity conditions. We summarize the current excellent methods of preparations of sensors based on MOSs and hope to provide some help for the progress of acetone sensors in the diagnosis of diabetes.展开更多
The PdC12 was mixed with nanocrystalline powders LaFeO3 and subsequently followed by an annealing of 800 ℃. PdO phase was formed and almost distributed uniformly on the surface of LaFeO3 nano-particles. With an incre...The PdC12 was mixed with nanocrystalline powders LaFeO3 and subsequently followed by an annealing of 800 ℃. PdO phase was formed and almost distributed uniformly on the surface of LaFeO3 nano-particles. With an increase of PdO amounts in composite powders, sensing sensitivity Rg/Ra to low concentration acetone or ethanol for Pd doped LaFeO3 sensors increased at first, underwent the maximum with 2 wt.% PdC12 dopant, and then doped again. Interestingly, appropriate Pd doping in LaFeO3 changed the selectivity behavior of gas sensing. LaFeO3 sensor showed good selectivity to ethanol, but 2 wt.% Pd doped LaFeO3 sensor showed good selectivity to acetone. The sensitivity for LaFeO3 at 200 ℃was 1.32 to 1 ppm ethanol, and 1.19 to 1 ppm acetone. Whereas the sensitivity for 2 wt.% Pd doped LaFeO3 at 200 ℃ was 1.53 to 1 ppm ethanol, and 1.9 to 1 ppm acetone. The 2 wt.% Pd doped LaFeO3 sensor at 200 ℃ showed very short response time （4 s） and recovery time （2 s） to 1 ppm acetone gas, respectively. Such results showed that 2 wt.% Pd doped LaFeO3 sensor is a new promising sensing candidate for detecting low concentration acetone.展开更多
Three-dimensionally ordered mesoporous Fe2O3（meso-Fe2O3） and its supported Au, Pd,and Au-Pd alloy（xA uP dy/meso-Fe2O3; x = 0.08–0.72 wt.%; Pd/Au molar ratio（y） = 1.48–1.85）photocatalysts have been prepared via...Three-dimensionally ordered mesoporous Fe2O3（meso-Fe2O3） and its supported Au, Pd,and Au-Pd alloy（xA uP dy/meso-Fe2O3; x = 0.08–0.72 wt.%; Pd/Au molar ratio（y） = 1.48–1.85）photocatalysts have been prepared via the KIT-6-templating and polyvinyl alcohol-protected reduction routes, respectively. Physical properties of the samples were characterized, and their photocatalytic activities were evaluated for the photocatalytic oxidation of acetone in the presence of a small amount of H2O2 under visible-light illumination. It was found that the meso-Fe2O3 was rhombohedral in crystal structure. The as-obtained samples displayed a high surface area of 111.0–140.8 m^2/g and a bandgap energy of 1.98–2.12 eV. The Au, Pd and/or Au–Pd alloy nanoparticles（NPs） with a size of 3–4 nm were uniformly dispersed on the surface of the meso-Fe2O3 support. The 0.72 wt.% AuP d1.48/meso-Fe2O3 sample performed the best in the presence of 0.06 mol/L H2O2 aqueous solution, showing a 100% acetone conversion within4 hr of visible-light illumination. It was concluded that the good performance of 0.72 wt.%AuPd（1.48）/meso-Fe2O3 for photocatalytic acetone oxidation was associated with its ordered mesoporous structure, high adsorbed oxygen species concentration, plasmonic resonance effect between AuPd（1.48） NPs and meso-Fe2O3, and effective separation of the photogenerated charge carriers. In addition, the introduction of H2O2 and the involvement of the photo-Fenton process also played important roles in enhancing the photocatalytic activity of 0.72 wt.%AuPd（1.48）/meso-Fe2O3.展开更多
In the present work, we synthesized Sm2O3 doped SnO2 in order to prepare a selective acetone sensor with fast response, quick recovery and good repeatability. Pure as well as 2 mol.%, 4 mol.%, 6 mol.% and 8 mol.% Sm2O...In the present work, we synthesized Sm2O3 doped SnO2 in order to prepare a selective acetone sensor with fast response, quick recovery and good repeatability. Pure as well as 2 mol.%, 4 mol.%, 6 mol.% and 8 mol.% Sm2O3 doped SnO2 nanostructured samples were synthesized by using a co-precipitation method. The characterization of the samples was done by thermogravimetric and differential thermo-gravimetric analysis（TG-DTA）, X-ray diffraction（XRD）, field emission gun-scanning electron microscopy（FEG-SEM）, energy dispersive analysis by X-rays（EDAX）, high resolution scanning electron microscopy（HR-TEM）, selected area X-ray diffraction（SAED）, Brunauer-Emmet-Teller（BET） and ultraviolet-visible-near infrared（UV-Vis-NIR） spectroscopy techniques. The gas response studies of liquid petroleum gas, ammonia, ethanol and acetone vapor were carried out. The results showed that Sm doping systematically lowered operating temperature and enhanced the gas response and selectivity for acetone. The response and recovery time for 6 mol.% Sm2O3 doped SnO2 thick film at the operating temperature of 250 °C were 15 and 24 s, respectively.展开更多
TiO2hollow microspheres(TiO2‐HMSs)have attracted much attention because of their high photoreactivity,low density,and good permeability.However,anatase TiO2‐HMSs have poor thermal stability.In this study,surface‐fl...TiO2hollow microspheres(TiO2‐HMSs)have attracted much attention because of their high photoreactivity,low density,and good permeability.However,anatase TiO2‐HMSs have poor thermal stability.In this study,surface‐fluorinated TiO2‐HMSs were assembled from hollow nanoparticles by the hydrothermal reaction of the mixed Ti(SO4)2–NH4HF–H2O2solution at180°C.The effect of the calcination temperature on the structure and photoreactivity of the TiO2‐HMSs was systematically investigated,which was evaluated by photocatalytic oxidation of acetone in air under ultraviolet irradiation.We found that after calcination at300°C,the photoreactivity of the TiO2‐HMSs decreases from1.39×10?3min?1(TiO2‐HMS precursor)to0.82×10?3min?1because of removal of surface‐adsorbed fluoride ions.With increasing calcination temperature from300to900°C,the building blocks of the TiO2‐HMSs evolve from truncated bipyramidal shaped hollow nanoparticles to round solid nanoparticles,and the photoreactivity of the TiO2‐HMSs steady increases from0.82×10?3to2.09×10?3min?1because of enhanced crystallization.Further increasing the calcination temperature to1000and1100°C results in a decrease of the photoreactivity,which is ascribed to a sharp decrease of the Brunauer–Emmett–Teller surface area and the beginning of the anatase–rutile phase transformation at1100°C.The effect of surface‐adsorbed fluoride ions on the thermal stability of the TiO2‐HMSs is also discussed.展开更多
The heterostructured NiWO_(4)/WO_(3) nanotubes(Ni/W NTs)were synthesized by using a facile self-assembly method on the sacrificial polystyrene(PS)nanofibers templates.Then,the Pt-decorated NiWO_(4)/WO_(3)(Pt@Ni/W)comp...The heterostructured NiWO_(4)/WO_(3) nanotubes(Ni/W NTs)were synthesized by using a facile self-assembly method on the sacrificial polystyrene(PS)nanofibers templates.Then,the Pt-decorated NiWO_(4)/WO_(3)(Pt@Ni/W)composite NTs were obtained through using an ultrasonic mixing method.The experimental results display that the order of gas-sensing performance is Pt@Ni/W>Ni/W>WO_(3).The 2wt.%Pt@Ni/W-5 NTs indicate the supreme acetone-sensing response(R_(air)/R_(gas)=58.4 at 100×10^(−6))at 375℃,which is 10.6 and 1.53 times that of the WO_(3) and NiWO_(4)/WO_(3) NTs,respectively.Additionally,the 2wt.%Pt@Ni/W-5 NTs also exhibit the dramatically high selectivity toward acetone against ethanol,methanal,methanol,NH_(3) and toluene.The Pt-decorated Ni/W NTs show the excellent responsivity and stability toward acetone,which is ascribed to the construction of heterostructured NiWO_(4)/WO_(3) and the spill-over effect of Pt nanoparticles.展开更多
MnO_(x)-CeO_(2) catalysts are developed by hydrolysis driving redox method using acetate precursor(3 Mn1 Ce-Ac) and nitrate precursor(3 Mn1 Ce-N) for the selective catalytic reduction(SCR) of NO_(x) by NH_(3).A counte...MnO_(x)-CeO_(2) catalysts are developed by hydrolysis driving redox method using acetate precursor(3 Mn1 Ce-Ac) and nitrate precursor(3 Mn1 Ce-N) for the selective catalytic reduction(SCR) of NO_(x) by NH_(3).A counterpart sample(Cop-3 Mn1 Ce) was prepared by the NH_(3)·H_(2) O co-precipitation method for comparison purpose.Combining the results of physicochemical properties characterization and performance test,we find that the 3 Mn1 Ce-Ac catalyst with some nanorod structures is highly active for the deNOx process.The SCR activity of the 3 Mn1 Ce-Ac catalyst is more admirable than the 3 Mn1 Ce-N and the Cop-3 Mn1 Ce catalysts due to plentiful Lewis acid sites,excellent low-temperature reducibility,and superior surface area resulted from O_(2) generation during the pre paration procedure.The 3 Mn1 Ce-Ac still exhibits the greatest performance for the deNO_(x )process when gaseous acetone is in the SCR feed gas.The NOx conversion and N2 selectivity over the 3 Mn1 Ce-Ac are both improved by gaseous acetone above150℃ due to the inhibition of SCR undesired side reactions(NSCR & C-O reactions) and "slow-SCR" process.展开更多
Solvothermal reaction of imidazolyl-based synthon with deprotonated adipic acid produced a new coordination complex {[Zn（BIDPE）(hdc)]·2 H;O}n（1）. The structure was characterized by single-crystal X-ray crysta...Solvothermal reaction of imidazolyl-based synthon with deprotonated adipic acid produced a new coordination complex {[Zn（BIDPE）(hdc)]·2 H;O}n（1）. The structure was characterized by single-crystal X-ray crystallography. It crystallizes in monoclinic, space group C2/m, at 293 K: a = 12.005（2）, b = 17.956（3）, c = 12.039（2） ?, β = 113.089（3）°, V = 2387.3（7） ?;, Z = 4, Dc = 1.524 g·cm-3, μ（Mo Ka） = 1.082 mm–1 and F（000） = 1136. 5942 reflections were measured and 2180 independent reflections（Rint = 0.0679） were used in further refinement. Complex 1 reveals 1D double-stranded chains containing [Zn;（BIDPE）;] and [Zn;（hdc）;] metallocyclic rings. The adjacent chains are linked by H-bonding and π···π interactions to form a 3D network. Thermal stability and luminescence property were studied. Interestingly, the luminescent emission of 1 can be quenched by the addition of trace amount of acetone, demonstrating its potential application for sensitive detecting acetone.展开更多
Using van der Waals corrected density functional theory(vdW-DF) method we have investigated the adsorption of acetone molecule on pristine and Pt-doped graphene.Several active sites for both the interacting systems ha...Using van der Waals corrected density functional theory(vdW-DF) method we have investigated the adsorption of acetone molecule on pristine and Pt-doped graphene.Several active sites for both the interacting systems have been considered in the adsorption process including full geometry optimization.We have analyzed the structural and electrical properties of energetically favorable configurations.The results show that adsorption of acetone molecule on the Pt-doped graphene is energetically preferable.The binding energy and bonding distance are determined to be-5.277 eV and 2.206 A,respectively,accompanying with charge transfer of 1.11 e.Furthermore,the Pt-0 bond is rather significantly elongated when acetone is adsorbed on Pt-doped graphene.Compared to pristine graphene,the Pt-doped graphene has stronger interaction with the acetone and may provide more sensitive signai for a single acetone molecule.Meanwhile,practically,the band gap of Pt-doped graphene would become reduced after acetone adsorption.Consequently,our first-principles study presents evidence for a coherent benchmark for the applicability of Pt-doped graphene for acetone adsorption and detection.展开更多
The acetone-sensing properties of the undoped and Pd doped perovskite-type oxides NdFeO3 were investigated from room temperature to 400°C. The perovskite-type NdFeO3 was synthesized by a sol-gel method, and the d...The acetone-sensing properties of the undoped and Pd doped perovskite-type oxides NdFeO3 were investigated from room temperature to 400°C. The perovskite-type NdFeO3 was synthesized by a sol-gel method, and the dopants Pd with the content from 1wt% to 5wt% were implanted into NdFeO3 nanoparticles by thermal diffusion. X-ray diffraction （XRD） and scanning electron microscopy （SEM） techniques show that NdFeO3 is an orthorhombic structure with the average particle size of about 40 nm. A giant acetone-sensing response of 675.7 is observed when the Pd content in NdFeO3 powders is about 3wt%. The response and recovery time of the sensor to the 5×10–4 acetone gas are 16 and 1 s, respectively. At the same time, it performs a good selectivity to acetone gas and may be a new promising material candidate for the acetone-sensor development.展开更多
文摘This work describes the discharge characteristics and acetone degradation with plasma under different electric fields based on a coaxial cylindrical dielectric barrier discharge(DBD)device energized by pulsed power.It is found that the segmented electrodes with appropriate spacing in coaxial cylindrical DBD are beneficial to the plasma ionization.In this work,the plasma distribution,discharge thermal effect,ionization of reactive species,and acetone degradation performance in coaxial cylindrical DBD with different segmented electrodes are systematically investigated.The experimental results show that segmented electrodes with a certain distance can cause additional ionization in the non-electrode-covered region between adjacent electrodes,thus enlarging the plasma region compared with a single electrode with equivalent total electrode length.The additional ionization involved the inner volume discharge between the quartz tubes and the outer surface discharge along the surface of the external quartz tube.The spatial distributions of the inner volume discharge and external surface discharge were predominantly governed by the radial and axial components of the inter-electrode electric field,respectively.The external surface discharge exhibited significant suppression when the electrode spacing was<1.5 mm,and it reached its maximum length at 3 mm spacing.When the electrode distance increased to 7-9 mm,a weak ionizing region appeared in the middle of the adjacent electrodes,which could be attributed to the gradual attenuation of the radial component with the increasing electrode spacing.A higher thermal effect and better oxidation of acetone to CO_(x)(CO and CO_(2))were achieved with the segmented electrode;the dual-segment configuration(3 mm per electrode)achieved a reactor temperature of 63.4℃,representing a 10℃enhancement over comparable single-electrode systems.Similarly,the CO_(2)and CO concentration reached 328.8 mg/m3and 105.7 mg/m3,respectively,in two 3 mm long segmented electrodes,which was an increase of 12.2%and 25.6%,respectively,compared with the single electrode.Notably,considering the equivalent ionization of the inner discharge with different electrodes,the enhanced thermal effects and CO_(x)conversion efficiency directly correlate with the expanded plasma zone induced by electrode segmentation.This work provides critical insights into optimizing electrode configurations for efficient plasma-assisted volatile organic compound degradation systems.
基金supported by the National Natural Science Foundation of China(Nos.21771060 and 61271126)the International Science&Technology Cooperation Program of China(No.2016YFE0115100)+2 种基金Heilongjiang Provincial Natural Science Foundation of China(No.LH_(2)023B021)Reform and Development Fund Project of Local University supported by the Central Government,Heilongjiang Touyan Innovation Team Program,New Era Excellent Master’s and Doctoral Dissertations of Heilongjiang Province(No.LJYXL2023-020)Basic Scientific Research Project for Heilongjiang Provincial Colleges and Universities(No.2023-KYYWF-1482).
文摘Acetone is a common volatile organic compound that can cause harm to human health when inhaled in small amounts.Therefore,the development of fast response and low detection limit acetone sensors becomes crucial.In this study,a core-shell spherical TiO_(2) sensor with a rich pore structure was designed.This sensor exhibited excellent sensing properties,including higher responsiveness(100 ppm acetone,R_(a)/R_(g)=80),lower detection limit(10 ppb)and short response time(8 s).The problem is that the sensing mechanism between TiO_(2) and acetone is not thoroughly analyzed.To gain further insight,the interaction process of TiO_(2) core-shell spheres and acetone under varying oxygen content environments was investigated by dynamic testing,X-ray photoelectron spectroscopy,in-situ Fourier transform infrared spectroscopy and gas chromatography-mass spectrometry.The research results show that acetone not only adsorbs on the surface of the material and reacts with adsorbed oxygen,but also undergoes catalytic oxidation reaction with TiO_(2) core-shell spheres.Significantly,in high oxygen content environments,acetone undergoes oxidation to form intermediates such as acids and anhydrides that are difficult to desorpt on the surface of the material,thus prolonging the recovery time of the sensor.The discovery of this sensing process will provide some guidance for the design of acetone sensing materials in the future.Meanwhile,this also imparts valuable references and insights for the investigation of the mechanism and application of other sensitive metal oxide materials.
基金financially supported by the National Natural Science Foundation of China(Nos.62374154 and12374128)the National Key R&D Program of China(Nos.2022YFB3903200 and 2022YFB3903203)
文摘Low-concentration acetone detection is of great importance for acetone sensor in the fields of environmental protection and noninvasive diagnosis.In this work,mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)n-p heterojunctions were constructed for efficient improvement of low-concentration acetone gas sensing.The gas-sensing results indicated that the mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)composites with a significantly large specific surface area exhibited significantlyenhanced acetone gas-sensitive performance compared to pure Fe_(2)O_(3).The Fe_(2)O_(3)/Cr_(2)O_(3)composites demonstrated a high response,good selectivity and excellent stability over200 days to 10 ppm acetone at 220℃.And the theoretical detection limit was calculated to reach 0.285 ppm acetone.A feasible acetone sensing mechanism was proposed through electronic band structure and density functional theory.The improved low-concentration acetone sensing performance was due to the formed mesoporous Fe_(2)O_(3)/Cr_(2)O_(3)n-p heterojunctions with a large specific surface area.The Fe_(2)O_(3)/Cr_(2)O_(3)composites showed excellent acetone gas-sensitive performance,which could be a promising candidate for developing low-concentration acetone sensing devices at low working temperatures.
基金Project (2006BS04035) supported by the Youth Scientific Research Foundation of Shandong Province, China
文摘Nickel ferrite nano-powders were prepared by microwave radiating low-temperature solid-state reaction method, and then modified with Ag by dipping method. The crystal structure and morphology of the samples were characterized by means of X-ray diffraction（XRD）, scanning electron microscopy （SEM） and X-ray photoelectron spectroscopy （XPS）. The gas sensing properties of the samples were also investigated. The results reveal that the Ag, as amorphous structure, can efficiently prevent the reuniting and growing-up of nanosized NiFe2O4 grains, and 1.5% Ag modified NiFe2O4 sensor has a better sensitivity, up to 43, for acetone gas than 1.5%Ag mixed NiFe2O4 sensor prepared by low-temperature solid-state reaction, at an optimal working voltage of 4.5 V. The quick response time （1 s） and fast recovery time （～10 s） are the main characteristics of this sensor.
基金the National Natural Science Foundation of China (Nos. 21202141, 21672163)Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)+3 种基金Top-notch Academic Programs Project of Jiangsu Higher Education Institutions (TAPP)the high level talent support project of Yangzhou University (top-notch talent, L. Yu)Yangzhou Natural Science Foundation (No. YZ2014040)the Natural Science Foundation of Guangling College (No. ZKZD17005) for financial support
文摘A synthetic method of dialkylideneacetones has been developed. Compared with known protocols, the method employed catalytic Ca(OH)_2 as the cheap, mild base catalyst and dilute aqueous EtOH(20%, v/v)as the green and safe solvent. The procedure was easily operated: In most cases, the product could be isolated by a simple filtration, and purified by washing with water. This paper provided experimental details of the reactions, which could be applied in gram-scale synthesis and should be a very reliable and practical protocol to prepare these useful compounds in laboratory and at the industrial level.
文摘The morphologic changes and growth status of PC12 cells were observed after intervened by different concentrations of methanol, ethanol, acetone, glycerol and the toxic concentrations were ascertained. Four kinds of organic solvents al showed certain cytotoxicity to PC12 cells. Compared with other three kinds of or-ganic solvents, ethanol showed the most obvious cytotoxicity to PC12 cells and the cellviability would be reduced to 60% if the concentration of ethanol was 20 ml/L and the intervention lasted for 24 h. Under the same condition, the reduced per-centages of cellviability for acetone and ethanol were 20% and 15% respectively. Glycerol also showed cytotoxicity to PC12 cells, especial y as the concentration was raised gradual y, but the toxicity was relatively mild. This study would provide refer-ence material for subsequent pharmacological studies.
基金supported by the National Natural Science Foundation of China(Nos.51822202 and 51772050)China Postdoctoral Science Foundation(No.2019M651342)+2 种基金Shanghai Rising-Star Program(No.18QA1400100)Youth Top-notch Talent Support Program of Shanghai,the Shanghai Committee of Science and Technology,China(No.19520713200)DHU Distinguished Young Professor Program and Fundamental Research Funds for the Central Universities。
文摘Mesoporous semiconducting metal oxides(SMOs)heterojunctions are appealing sensors for gas detecting.However,due to the different hydrolysis and condensation mechanism of every metal precursor and the contradiction between high crystallinity and high surface area,the synthesis of mesoporous SMOs heterojunctions with highly o rdered mesostructures,highly crystallized frameworks,and high surface area remains a huge challenge.In this work,we develop a novel"acid-base pair"adjusted solvent evaporation induced self-assembly(EISA)strategy to prepare highly crystallized ordered mesoporous TiO2/WO3(OM-TiO2/WO3)heterojunctions.The WCl6 and titanium isopropoxide(TIPO)are used as the precursors,respectively,which function as the"acid-base pair",enabling the coassembly with the structure directing agent(PEO-b-PS)into highly ordered meso structures.In addition,PEO-b-PS can be converted to rigid carbon which can protect the meso structures from collapse during the crystallization process.The resultant OM-TiO2/WO3 heterojunctions possess primitive cubic mesostructures,large pore size(~21.1 nm),highly crystalline frameworks and surface area(~98 m2/g).As a sensor for acetone,the obtained OM-TiO2/WO3 show excellent re sponse/recovery perfo rmance(3 s/5 s),good linear dependence,repeatability,selectivity,and long-term stability(35 days).
基金supported financially by the National Natural Science Foundation of China(Nos.,51572158 and 51972200)the Graduate Innovation Fund of Shaanxi University of Science&Technology+2 种基金funded by the Japan Society for the Promotion of Science(JSPS)Grant-in-Aid for the Scientific Research(KAKENHI Nos.20H00297 and Innovative Area“Mixed Anion”(No.16H06439))the Nippon Sheet Glass Foundation for Materials Science and Engineeringby the Dynamic Alliance for Open Innovations Bridging Human,Environment and Materials,the Cooperative Research Program of“Network Joint Research Center for Materials and Devices”。
文摘Acetone,as widely used reagents in industry and laboratories,are extremely harmful to the human.So the detection of acetone gas concentrations and leaks in special environments at room temperature is essential.Herein,the nanocomposite combining SnO-SnO_(2)(p-n junction)and Ti_(3)C_(2)T_(x) MXene was successfully synthesized by a one-step hydrothermal method.Because of the existence of a small amount of oxygen during the hydrothermal conditions,part of the p-type SnO was oxidized to n-type SnO_(2),forming in-situ p-n junctions on the surface of Sn O.The hamburger-like SnO-SnO_(2)/Ti_(3)C_(2)T_(x) sensor exhibited improved acetone gas sensing response of 12.1(R_(g)/R_(a))at room temperature,which were nearly 11 and 4 times higher than those of pristine Ti_(3)C_(2)T_(x) and pristine SnO-SnO_(2),respectively.Moreover,it expressed a short recovery time(9 s)and outstanding reproducibility.Because of the different work functions,the Schottky barrier was formed between the SnO and the Ti_(3)C_(2)T_(x) nanosheets,acting as a hole accumulation layer(HALs)between Ti_(3)C_(2)T_(x) and tin oxides.Herein,the sensing mechanism based on the formation of hetero-junctions and high conductivity of the metallic phase of Ti_(3)C_(2)T_(x) MXene in SnO-SnO_(2)/Ti_(3)C_(2)T_(x) sensors was discussed in detail.
基金financially supported by Shandong Natural Science Foundation(No.ZR2021QE265)the Fundamental Research Funds of Taishan University(No.Y01-2020015)+1 种基金the National Natural Science Foundation of China(Nos.61574098,61204051)Shandong Province Key Research and Development Program(No.2019GGX101016)。
文摘Currently,SmFeO_(3)-based sensors are an effective platform for detecting acetone gas.However,they require high operating temperatures,which increases energy consumption and safety hazards,and their response is low when the gas concentration is at 10^(-9)(PPB),which cannot meet the requirements of using exhaled breath to pre-diagnose diabetes.Herein,Pd-SmFeO_(3)hollow nanotubes with an extremely high specific surface area and porosity were synthesized by electrospinning.After Pd doping,the specific surface area improved by more than two times,and the acetone response improved by more than three times.In addition,the response further improved by more than 1.5 times,and the optimum operating temperature reduced by 100℃under light irradiation.Moreover,the relative humidity adaptability,long-term stability,and selectivity of the material were significantly improved after Pd doping or light irradiation.Finally,the acetone concentration in a person’s exhaled breath was detected by a Pd-SmFeO_(3)-based gas sensor,and the error was less than 10%compared to that obtained by gas chromatography-mass spectrometry method.
基金Project(30916014103) supported by the Fundamental Research Funds for the Central Universities,China
文摘Ternary Au/Fe2O3-ZnO gas-sensing materials were synthesized by combining co-precipitation and microwave irradiation process.The as-prepared Au/Fe2O3-ZnO was characterized with X-ray diffractometer and scanning electron microscope,and its gas-sensing performance was measured using a gas-sensor analysis system.The results show that the as-prepared products consist of hexagonal wurtzite ZnO,face-centered cubic gold nanoparticles and orthorhombic Fe2O3crystallines.The Au/Fe2O3-ZnO based sensor has a very high selectivity to ethanol and acetone,and also has high sensitivity(154)at a low working temperature(270°C)and an extremely fast response(1s)against acetone.It is found that the selectivity can be adjusted by Fe2O3content added in the ternary materials.It possesses a worth looking forward prospect to practical applications in acetone detecting and administrating field.
文摘In recent years, clinical studies have found that acetone concentration in exhaled breath can be taken as a characteristic marker of diabetes. Metal-oxide-semiconductor (MOS) materials are widely used in acetone gas sensors due to their low cost, high sensitivity, fast response/recovery time, and easy integration. This paper reviews recent progress in acetone sensors based on MOS materials for diabetes diagnosis. The methods of improving the performance of acetone sensor have been explored for comparison, especially in high humidity conditions. We summarize the current excellent methods of preparations of sensors based on MOSs and hope to provide some help for the progress of acetone sensors in the diagnosis of diabetes.
基金Project supported by Shandong Natural Science Foundation(ZR2013EMM016)National Natural Science Foundation of China(51472145,51272133,51472150,J1103212)the Fundamental Research Funds for the Central Universities(DUT16RC(4)69)
文摘The PdC12 was mixed with nanocrystalline powders LaFeO3 and subsequently followed by an annealing of 800 ℃. PdO phase was formed and almost distributed uniformly on the surface of LaFeO3 nano-particles. With an increase of PdO amounts in composite powders, sensing sensitivity Rg/Ra to low concentration acetone or ethanol for Pd doped LaFeO3 sensors increased at first, underwent the maximum with 2 wt.% PdC12 dopant, and then doped again. Interestingly, appropriate Pd doping in LaFeO3 changed the selectivity behavior of gas sensing. LaFeO3 sensor showed good selectivity to ethanol, but 2 wt.% Pd doped LaFeO3 sensor showed good selectivity to acetone. The sensitivity for LaFeO3 at 200 ℃was 1.32 to 1 ppm ethanol, and 1.19 to 1 ppm acetone. Whereas the sensitivity for 2 wt.% Pd doped LaFeO3 at 200 ℃ was 1.53 to 1 ppm ethanol, and 1.9 to 1 ppm acetone. The 2 wt.% Pd doped LaFeO3 sensor at 200 ℃ showed very short response time （4 s） and recovery time （2 s） to 1 ppm acetone gas, respectively. Such results showed that 2 wt.% Pd doped LaFeO3 sensor is a new promising sensing candidate for detecting low concentration acetone.
基金supported by the National Natural Science Foundation of China (No. 21377008)the National High Technology Research and Development Program of China ("863"Program)(No. 2015AA034603)the Foundation of the Creative Research Team Construction Promotion Project of Beijing Municipal Institutions
文摘Three-dimensionally ordered mesoporous Fe2O3（meso-Fe2O3） and its supported Au, Pd,and Au-Pd alloy（xA uP dy/meso-Fe2O3; x = 0.08–0.72 wt.%; Pd/Au molar ratio（y） = 1.48–1.85）photocatalysts have been prepared via the KIT-6-templating and polyvinyl alcohol-protected reduction routes, respectively. Physical properties of the samples were characterized, and their photocatalytic activities were evaluated for the photocatalytic oxidation of acetone in the presence of a small amount of H2O2 under visible-light illumination. It was found that the meso-Fe2O3 was rhombohedral in crystal structure. The as-obtained samples displayed a high surface area of 111.0–140.8 m^2/g and a bandgap energy of 1.98–2.12 eV. The Au, Pd and/or Au–Pd alloy nanoparticles（NPs） with a size of 3–4 nm were uniformly dispersed on the surface of the meso-Fe2O3 support. The 0.72 wt.% AuP d1.48/meso-Fe2O3 sample performed the best in the presence of 0.06 mol/L H2O2 aqueous solution, showing a 100% acetone conversion within4 hr of visible-light illumination. It was concluded that the good performance of 0.72 wt.%AuPd（1.48）/meso-Fe2O3 for photocatalytic acetone oxidation was associated with its ordered mesoporous structure, high adsorbed oxygen species concentration, plasmonic resonance effect between AuPd（1.48） NPs and meso-Fe2O3, and effective separation of the photogenerated charge carriers. In addition, the introduction of H2O2 and the involvement of the photo-Fenton process also played important roles in enhancing the photocatalytic activity of 0.72 wt.%AuPd（1.48）/meso-Fe2O3.
文摘In the present work, we synthesized Sm2O3 doped SnO2 in order to prepare a selective acetone sensor with fast response, quick recovery and good repeatability. Pure as well as 2 mol.%, 4 mol.%, 6 mol.% and 8 mol.% Sm2O3 doped SnO2 nanostructured samples were synthesized by using a co-precipitation method. The characterization of the samples was done by thermogravimetric and differential thermo-gravimetric analysis（TG-DTA）, X-ray diffraction（XRD）, field emission gun-scanning electron microscopy（FEG-SEM）, energy dispersive analysis by X-rays（EDAX）, high resolution scanning electron microscopy（HR-TEM）, selected area X-ray diffraction（SAED）, Brunauer-Emmet-Teller（BET） and ultraviolet-visible-near infrared（UV-Vis-NIR） spectroscopy techniques. The gas response studies of liquid petroleum gas, ammonia, ethanol and acetone vapor were carried out. The results showed that Sm doping systematically lowered operating temperature and enhanced the gas response and selectivity for acetone. The response and recovery time for 6 mol.% Sm2O3 doped SnO2 thick film at the operating temperature of 250 °C were 15 and 24 s, respectively.
基金supported by the National Natural Science Foundation of China(51672312,21373275)the Science and Technology Program of Wuhan,China(2016010101010018,2015070504020220)the Dean’s Research Fund–04257 from the Education University of Hong Kong~~
文摘TiO2hollow microspheres(TiO2‐HMSs)have attracted much attention because of their high photoreactivity,low density,and good permeability.However,anatase TiO2‐HMSs have poor thermal stability.In this study,surface‐fluorinated TiO2‐HMSs were assembled from hollow nanoparticles by the hydrothermal reaction of the mixed Ti(SO4)2–NH4HF–H2O2solution at180°C.The effect of the calcination temperature on the structure and photoreactivity of the TiO2‐HMSs was systematically investigated,which was evaluated by photocatalytic oxidation of acetone in air under ultraviolet irradiation.We found that after calcination at300°C,the photoreactivity of the TiO2‐HMSs decreases from1.39×10?3min?1(TiO2‐HMS precursor)to0.82×10?3min?1because of removal of surface‐adsorbed fluoride ions.With increasing calcination temperature from300to900°C,the building blocks of the TiO2‐HMSs evolve from truncated bipyramidal shaped hollow nanoparticles to round solid nanoparticles,and the photoreactivity of the TiO2‐HMSs steady increases from0.82×10?3to2.09×10?3min?1because of enhanced crystallization.Further increasing the calcination temperature to1000and1100°C results in a decrease of the photoreactivity,which is ascribed to a sharp decrease of the Brunauer–Emmett–Teller surface area and the beginning of the anatase–rutile phase transformation at1100°C.The effect of surface‐adsorbed fluoride ions on the thermal stability of the TiO2‐HMSs is also discussed.
基金supported by the National Natural Science Foundation of China (Nos. 51772130, 51972145)。
文摘The heterostructured NiWO_(4)/WO_(3) nanotubes(Ni/W NTs)were synthesized by using a facile self-assembly method on the sacrificial polystyrene(PS)nanofibers templates.Then,the Pt-decorated NiWO_(4)/WO_(3)(Pt@Ni/W)composite NTs were obtained through using an ultrasonic mixing method.The experimental results display that the order of gas-sensing performance is Pt@Ni/W>Ni/W>WO_(3).The 2wt.%Pt@Ni/W-5 NTs indicate the supreme acetone-sensing response(R_(air)/R_(gas)=58.4 at 100×10^(−6))at 375℃,which is 10.6 and 1.53 times that of the WO_(3) and NiWO_(4)/WO_(3) NTs,respectively.Additionally,the 2wt.%Pt@Ni/W-5 NTs also exhibit the dramatically high selectivity toward acetone against ethanol,methanal,methanol,NH_(3) and toluene.The Pt-decorated Ni/W NTs show the excellent responsivity and stability toward acetone,which is ascribed to the construction of heterostructured NiWO_(4)/WO_(3) and the spill-over effect of Pt nanoparticles.
基金supported by the Key Laboratory of Water and Air Pollution Control of Guangdong province,China (No.2017A030314001)the National Key Research and Development Plan (No.2019YFC0214303)+1 种基金Central Public-Interest Scientific Institution Basal Research Fund (No.PM-zx703-202002-015)the National Natural Science Foundation of China (No.22076224)。
文摘MnO_(x)-CeO_(2) catalysts are developed by hydrolysis driving redox method using acetate precursor(3 Mn1 Ce-Ac) and nitrate precursor(3 Mn1 Ce-N) for the selective catalytic reduction(SCR) of NO_(x) by NH_(3).A counterpart sample(Cop-3 Mn1 Ce) was prepared by the NH_(3)·H_(2) O co-precipitation method for comparison purpose.Combining the results of physicochemical properties characterization and performance test,we find that the 3 Mn1 Ce-Ac catalyst with some nanorod structures is highly active for the deNOx process.The SCR activity of the 3 Mn1 Ce-Ac catalyst is more admirable than the 3 Mn1 Ce-N and the Cop-3 Mn1 Ce catalysts due to plentiful Lewis acid sites,excellent low-temperature reducibility,and superior surface area resulted from O_(2) generation during the pre paration procedure.The 3 Mn1 Ce-Ac still exhibits the greatest performance for the deNO_(x )process when gaseous acetone is in the SCR feed gas.The NOx conversion and N2 selectivity over the 3 Mn1 Ce-Ac are both improved by gaseous acetone above150℃ due to the inhibition of SCR undesired side reactions(NSCR & C-O reactions) and "slow-SCR" process.
基金supported by the National Natural Science Foundation of China(No.21671004,51404006)
文摘Solvothermal reaction of imidazolyl-based synthon with deprotonated adipic acid produced a new coordination complex {[Zn（BIDPE）(hdc)]·2 H;O}n（1）. The structure was characterized by single-crystal X-ray crystallography. It crystallizes in monoclinic, space group C2/m, at 293 K: a = 12.005（2）, b = 17.956（3）, c = 12.039（2） ?, β = 113.089（3）°, V = 2387.3（7） ?;, Z = 4, Dc = 1.524 g·cm-3, μ（Mo Ka） = 1.082 mm–1 and F（000） = 1136. 5942 reflections were measured and 2180 independent reflections（Rint = 0.0679） were used in further refinement. Complex 1 reveals 1D double-stranded chains containing [Zn;（BIDPE）;] and [Zn;（hdc）;] metallocyclic rings. The adjacent chains are linked by H-bonding and π···π interactions to form a 3D network. Thermal stability and luminescence property were studied. Interestingly, the luminescent emission of 1 can be quenched by the addition of trace amount of acetone, demonstrating its potential application for sensitive detecting acetone.
基金the support of this work by the Islamic Azad University,Pharmaceutical Science Branch,Tehran,Iran(IAUPS)
文摘Using van der Waals corrected density functional theory(vdW-DF) method we have investigated the adsorption of acetone molecule on pristine and Pt-doped graphene.Several active sites for both the interacting systems have been considered in the adsorption process including full geometry optimization.We have analyzed the structural and electrical properties of energetically favorable configurations.The results show that adsorption of acetone molecule on the Pt-doped graphene is energetically preferable.The binding energy and bonding distance are determined to be-5.277 eV and 2.206 A,respectively,accompanying with charge transfer of 1.11 e.Furthermore,the Pt-0 bond is rather significantly elongated when acetone is adsorbed on Pt-doped graphene.Compared to pristine graphene,the Pt-doped graphene has stronger interaction with the acetone and may provide more sensitive signai for a single acetone molecule.Meanwhile,practically,the band gap of Pt-doped graphene would become reduced after acetone adsorption.Consequently,our first-principles study presents evidence for a coherent benchmark for the applicability of Pt-doped graphene for acetone adsorption and detection.
基金supported by the National Natural Science Foundation of China (Grant Nos. 50872069 and 50872074)
文摘The acetone-sensing properties of the undoped and Pd doped perovskite-type oxides NdFeO3 were investigated from room temperature to 400°C. The perovskite-type NdFeO3 was synthesized by a sol-gel method, and the dopants Pd with the content from 1wt% to 5wt% were implanted into NdFeO3 nanoparticles by thermal diffusion. X-ray diffraction （XRD） and scanning electron microscopy （SEM） techniques show that NdFeO3 is an orthorhombic structure with the average particle size of about 40 nm. A giant acetone-sensing response of 675.7 is observed when the Pd content in NdFeO3 powders is about 3wt%. The response and recovery time of the sensor to the 5×10–4 acetone gas are 16 and 1 s, respectively. At the same time, it performs a good selectivity to acetone gas and may be a new promising material candidate for the acetone-sensor development.
