ZnO is a highly significant II-VI semiconductor known for its excellent optoelectronic properties,making it widely applicable and promising for use in light-emitting devices,solar cells,lasers,and photodetectors.The m...ZnO is a highly significant II-VI semiconductor known for its excellent optoelectronic properties,making it widely applicable and promising for use in light-emitting devices,solar cells,lasers,and photodetectors.The methods for preparing ZnO are diverse,and among them,the hydrothermal method is favored for its simplicity,ease of operation,and low cost,making it an optimal choice for ZnO single-crystal growth.Most studies investigating the effects of different hydrothermal experimental parameters on the morphology and performance of ZnO nano-materials typically focus on only 2—3 variable parameters,with few examining the impact of all possible experimental parameter changes on ZnO nano-mate-rials.The principles of the hydrothermal method and its advantages in nano-material preparation were briefly introduced in this article.The detailed discussion on the influence of various experimental parameters on the preparation of ZnO nano-materials was provided,which including reaction materials,Zn^(2+)/OH^(-)ratio,reaction time and temperature,additives,experimental equipment,and annealing conditions.The review co-vers how different experimental parameters affect the morphology and performance of the materials,as well as how different rare earth doping elements influence the performance of ZnO nano-materials.It is hoped that this work will contribute to future research on the hydrothermal synthesis of nano-materials.展开更多
Hydrothermal method was used to synthesize nanoscale particles of MnZn ferrites. The crystallites were characterized by XRD, TEM and SEM. The effects of the reaction time, temperature and additives on the product were...Hydrothermal method was used to synthesize nanoscale particles of MnZn ferrites. The crystallites were characterized by XRD, TEM and SEM. The effects of the reaction time, temperature and additives on the product were investigated. Crystallization process would be carried out above 160 ℃ for 5 h or more, higher temperature can reduce the reaction time. Additives were used to remove impurities such as Fe 2O 3, ZnMnO 3.10～15 nm pure slightly agglomerated MnZn ferrite crystallites with a narrow grain size distribution were obtained.展开更多
Mesoporous cerium-zirconium mixed oxides were prepared by hydrothermal method using cetyl trimethyl ammonium bromide (CTAB) as template. The effects of amount of template, pH value of solution and hydrothermal tempera...Mesoporous cerium-zirconium mixed oxides were prepared by hydrothermal method using cetyl trimethyl ammonium bromide (CTAB) as template. The effects of amount of template, pH value of solution and hydrothermal temperature on mesostructure of samples were systematically investigated. The final products were characterized by XRD, TEM, FT-IR, and BET. The results indicate that all the cerium-zirconium mixed oxides present a meso-structure. At molar ratio of n(CTAB)/n((Ce)+(Zr))= 0.15, pH value of 9, and hydrothermal temperature of 120 ℃, the samples obtained possess a specific surface area of 207.9 m2/g with pore diameter of 3.70 nm and pore volume of 0.19 cm3/g.展开更多
Micaceous iron oxide （MIO） with a hexagonal flaky shape was prepared by hydrothermal method. The ferric hydroxide used as precursor was obtained by an acidic leaching solution of pyrite cinders reacting with ammonia...Micaceous iron oxide （MIO） with a hexagonal flaky shape was prepared by hydrothermal method. The ferric hydroxide used as precursor was obtained by an acidic leaching solution of pyrite cinders reacting with ammonia solution. The optimal experimental conditions for preparing micaceous iron oxide were investigated by orthogonal experiments. Micaceous iron oxide can be successfully prepared when optimal parameters of total iron concentration of 2.0 mol/L, pH value of 8, n（Fe2＋）/n（Fe3＋） of 0.1, mass of seed crystal of 1 g, reaction temperature of 260 ℃ and reaction time of 30 min are applied. X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and selected area electron diffractometry （SAEM） were adopted to characterize the hydrothermal products prepared under optimal conditions. The results indicate that highly crystallized α-Fe2O3 hexagonal flakes, about 1.0-1.5 μm in diameter and 0.1 μm in thickness, are prepared. Furthermore, the quality of micaceous iron oxide prepared can meet the required characteristics of micaceous iron oxide pigments for paints （ISO 10601--2007）.展开更多
MnZn ferrite nanoscale particles were synthesized by hydrothermal method. The effects of amount of addition La3+ on the products were discussed. The product was characterized by X-ray diffraction （XRD） and transmiss...MnZn ferrite nanoscale particles were synthesized by hydrothermal method. The effects of amount of addition La3+ on the products were discussed. The product was characterized by X-ray diffraction （XRD） and transmission electron microscope （TEM）. The results show that the sample with 0.2% La3+（mass fraction） or without La3+ has only spinel phase, but the sample with mass fraction of La3+ exceeding 0.4% posses second phase besides the spinel one; and the nano-MnZn ferrites change from cube to hexagon when the mass fractions of La3+ is up to （1.2%.） TEM image of the sample with 1.2% La3+ indicates that the homogeneous hexagonal crystal is obtained and the particles are larger than those of undoped; the addition of La3+ has great influence on the crystallization of hydrothermal process and can change the shape of particles and improve their growth. The saturation magnetization of the sample with 1.2% La3+ (2.64 A·m2·kg-1) is lower than that of undoped (17.54 (A·m2·kg-1)) and it behaves superparamagnetically.展开更多
The decomposition of K-Feldspar is significant to the development and utilization of K-feldspar as potassium resources. Potassium feldspar powder was decomposed successfully by hydrothermal method using CaO additive. ...The decomposition of K-Feldspar is significant to the development and utilization of K-feldspar as potassium resources. Potassium feldspar powder was decomposed successfully by hydrothermal method using CaO additive. Tobermorite solid and KOH solution were obtained as a result of the hydrothermal decomposition.展开更多
Calcium sulfate hemihydrate (CaSO4·0.5H2O, HH) is one of the three most commonly phases of gypsum observed in natural precipitates. Calcium sulfate hemihydrate whisker is a kind of fibriform single crystal with t...Calcium sulfate hemihydrate (CaSO4·0.5H2O, HH) is one of the three most commonly phases of gypsum observed in natural precipitates. Calcium sulfate hemihydrate whisker is a kind of fibriform single crystal with the mean diameter of 1-3 μm and the mean aspect ratio of 30–80. HH whisker was the most promising reinforcement seemed to be calcium sulfate-based due to its high intensity, high corrosion-resistance, good thermal stability, non-poisonous and low price. Thus, HH whiskers combine both reinforcement and low price, may be both effective in improving mechanical performance and extending application area.展开更多
Undoped and Na-doped ZnO films were deposited by sol-gel method.The effects of sodium incorporation on structure,surface morphology and optical constants of the films were investigated.X-ray diffraction patterns show ...Undoped and Na-doped ZnO films were deposited by sol-gel method.The effects of sodium incorporation on structure,surface morphology and optical constants of the films were investigated.X-ray diffraction patterns show the hexagonal wurtzite polycrystalline structure and that the sodium incorporation leads to the change in the structural characteristics of ZnO films.The SEM observations show that the surface morphology of the films is affected by the sodium incorporation.The transmission spectra show that the average transmittance of the films is above 85% in the visible range.The absorption edge initially blue-shifts and then red-shifts with the increase of Na doping content.The optical constants of these films were calculated using transmission spectra.Refractive indices of the films in the visible range decrease at first and then increase with increasing Na doping content.展开更多
A reduced graphene oxide/Ni(OH)2 composite with excellent supercapacitive performance was synthesized by a facile hydrothermal route without organic solvents or templates used.XRD and SEM results reveal that the nicke...A reduced graphene oxide/Ni(OH)2 composite with excellent supercapacitive performance was synthesized by a facile hydrothermal route without organic solvents or templates used.XRD and SEM results reveal that the nickel hydroxide,which crystallizes into hexagonal β-Ni(OH)2 nanoflakes with a diameter less than 200 nm and a thickness of about 10 nm,is well combined with the reduced graphene oxide sheets.Electrochemical performance of the synthesized composite as an electrode material was investigated by cyclic voltammetry,electrochemical impedance spectroscopy and galvanostatic charge/discharge measurements.Its specific capacitance is determined to be 1672 F/g at a scan rate of 2 mV/s,and 696 F/g at a high scan rate of 50 mV/s.After 2000 cycles at a current density of 10 A/g,the composite exhibits a specific capacitance of 969 F/g,retaining about 86% of its initial capacitance.The composite delivers a high energy density of 83.6 W·h/kg at a power density of 1.0 kW/kg.The excellent supercapacitive performance along with the easy synthesis method allows the synthesized composite to be promising for supercapacitor applications.展开更多
Properties of hydroxyapatite （HA, Ca10（PO4）6（OH）2）, including bioactivity, biocompatibility, solubility and adsorption could be tailored over wide ranges by the control of particle composition, particle size and...Properties of hydroxyapatite （HA, Ca10（PO4）6（OH）2）, including bioactivity, biocompatibility, solubility and adsorption could be tailored over wide ranges by the control of particle composition, particle size and morphology. In order to satisfy various applications, well-crystallized pure HA nanoparticles were synthesized at moderate temperatures by hydrotherrnal synthesis, and HA nanoparticles with different lengths were obtained by adding organic additives. X-ray diffractometry （XRD） and Fourier transform infrared （FTIR） spectrometry were used to characterize these nanoparticles, and the morphologies of the HA particles were observed by transmission electron microscopy （TEM）. The results demonstrate that shorter rod-like HA particles can be prepared by adding cetyltrimethylammonium bromide （CTAB）, as the additive of CTAB can block the HA crystal growth along with c-axis. And whisker HA particles are obtained by adding ethylenediamine tetraacetic acid （EDTA）, since EDTA may have effect on the dissolution-repreeipitation process of HA.展开更多
Silver-tin oxide powders were synthesized by the hydrothermal method with Ag(NH_3)_2^+ solution and Na_2SnO_3 solution as raw materials and Na_2SO_3 as reductant. The precipitation conditions of Na2SnO3 solution and t...Silver-tin oxide powders were synthesized by the hydrothermal method with Ag(NH_3)_2^+ solution and Na_2SnO_3 solution as raw materials and Na_2SO_3 as reductant. The precipitation conditions of Na2SnO3 solution and the reduction conditions of Ag(NH_3)_2^+ were also investigated. The powders prepared were characterized by differential thermal analysis (DTA), X-ray diffraction analysis (XRD), scanning electron microscope (SEM) and energy spectrum analysis. The results show that pH value of the solution is a key parameter in the formation of Sn(OH)_4 precipitate and the reduction reaction of Ag(NH_3)_2^+ can release H+ ions, which results in synchronous precipitation of Sn(OH)_6~2- as Sn(OH)_4. The reduction of Ag(NH_3)_2^+ and precipitation of Na_2SnO_3 occur simultaneously and the coprecipitation of silver and tin oxide is reached by the hydrothermal method. The silver-tin oxide composite powders have mainly flake shape of about 0.3 μm in thickness and there exists homogeneous distribution of tin oxide and silver in the powder synthesized.展开更多
The CaCu3Ti4O12 xerogels, powders and ceramics were prepared through the sol-gel method using two kinds of organic acid （decanoic acid and decanedioic acid）. The xerogels, powders and ceramics were characterized by ...The CaCu3Ti4O12 xerogels, powders and ceramics were prepared through the sol-gel method using two kinds of organic acid （decanoic acid and decanedioic acid）. The xerogels, powders and ceramics were characterized by the methods of TG-DTG, FT-IR, XRD, SEM and TEM. The dielectric properties of the ceramics were also measured. The results indicated that the powders calcined at 850 ℃ for 2 h are both nanometer scale particles. After sintering, the ceramics mainly consist of the CaCu3Ti4O12 phase. Compared with the powders prepared using monoacid, the particle size of the powders prepared using diacid obviously increases, and the grain size, the relative density and the whole permittivity of the ceramics increase as well. Specially, the ceramic prepared using decanedioic acid has higher relative density （97.3%）, dielectric constant （316 808） and lower dielectric loss （0.242 5） at 30 ℃ （10 kIaz）展开更多
Hollow-structured Cu_(0.3)Co_(2.7)O_(4) microspheres have been synthesized by a simple one-pot template-free hydrothermal method with copper sulfate,cobalt acetate and ammonia as raw materials.The products were charac...Hollow-structured Cu_(0.3)Co_(2.7)O_(4) microspheres have been synthesized by a simple one-pot template-free hydrothermal method with copper sulfate,cobalt acetate and ammonia as raw materials.The products were characterized by powder X-ray diffraction,energy dispersive X-ray analysis,selected area electron diffraction,high-resolution transmission electron microscopy,scanning electron microscopy and BET measurements.The research results show that the hollow Cu_(0.3)Co_(2.7)O_(4) microspheres consist of single-crystalline nanocubes with the diameter of about 20 nm.The formation mechanism of hollow Cu_(0.3)Co_(2.7)O_(4) microspheres is suggested as Ostwald ripening in a solid-solution-solid process,and Cu_(0.3)Co_(2.7)O_(4) microspheres are mesoporous containing two pore sizes of 3.3 and 5.9 nm.The as-prepared Cu_(0.3)Co_(2.7)O_(4) sensors have optimal gas responses to 50×10^(−6) mg/m^(3) C_(2)H_(5)OH at 190℃.展开更多
A simple hydrothermal process followed by heat treatment was applied to the preparation of spinel Li1.05Mn1.95O4. In this process, electrolytic manganese dioxide(EMD) and LiOH·H2O were used as starting materials....A simple hydrothermal process followed by heat treatment was applied to the preparation of spinel Li1.05Mn1.95O4. In this process, electrolytic manganese dioxide(EMD) and LiOH·H2O were used as starting materials. The physiochemical properties of the synthesized samples were investigated by thermogravimetry-differential scanning calorimetry(TG-DSC), X-ray diffractometry(XRD), and scanning electronic microscopy(SEM). The results show that the hydrothermally synthesized precursor is an essential amorphous. The precursor can be easily transferred to spinel powders with a homogeneous structure and a regularly-shaped morphology by heat treatment. Li1.05Mn1.95O4 powder obtained by heat treating the precursor at 430 °C for 12 h and then calcining at 800 °C for 12 h shows an excellent cycling performance with an initial charge capacity of 118.2 mA·h·g-1 obtained at 0.5C rate and 93.8% of its original value retained after 100 cycles.展开更多
Li2Fe0.5Mn0.5SiO4 material was synthesized by a citric acid-assisted sol-gel method. The influence of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+) on the electrochemical properties of Li2Fe0.5Mn0.5...Li2Fe0.5Mn0.5SiO4 material was synthesized by a citric acid-assisted sol-gel method. The influence of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+) on the electrochemical properties of Li2Fe0.5Mn0.5SiO4 was studied. The final sample was identified as Li2Fe0.5Mn0.5SiO4 with a Pmn21 monoclinic structure by X-ray diffraction analysis. The crystal phases components and crystal phase structure of the Li2Fe0.5Mn0.4SiO4 material were improved as the increase of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+). Field-emission scanning electron microscopy verified that the Li2Fe0.5Mn0.5SiO4 particles are agglomerates of Li2Fe0.5Mn0.5SiO4 primary particles with a geometric mean diameter of 220 nm. The Li2Fe0.5Mn0.5SiO4 sample was used as an electrode material for rechargeable lithium ion batteries, and the electrochemical measurements were carried out at room temperature. The Li2Fe0.5Mn0.5SiO4 electrode delivered a first discharge capacity of 230.1 mAh/g at the current density of 10 mA/g in first cycle and about 162 mAh/g after 20 cycles at the current density of 20 mA/g.展开更多
文摘ZnO is a highly significant II-VI semiconductor known for its excellent optoelectronic properties,making it widely applicable and promising for use in light-emitting devices,solar cells,lasers,and photodetectors.The methods for preparing ZnO are diverse,and among them,the hydrothermal method is favored for its simplicity,ease of operation,and low cost,making it an optimal choice for ZnO single-crystal growth.Most studies investigating the effects of different hydrothermal experimental parameters on the morphology and performance of ZnO nano-materials typically focus on only 2—3 variable parameters,with few examining the impact of all possible experimental parameter changes on ZnO nano-mate-rials.The principles of the hydrothermal method and its advantages in nano-material preparation were briefly introduced in this article.The detailed discussion on the influence of various experimental parameters on the preparation of ZnO nano-materials was provided,which including reaction materials,Zn^(2+)/OH^(-)ratio,reaction time and temperature,additives,experimental equipment,and annealing conditions.The review co-vers how different experimental parameters affect the morphology and performance of the materials,as well as how different rare earth doping elements influence the performance of ZnO nano-materials.It is hoped that this work will contribute to future research on the hydrothermal synthesis of nano-materials.
文摘Hydrothermal method was used to synthesize nanoscale particles of MnZn ferrites. The crystallites were characterized by XRD, TEM and SEM. The effects of the reaction time, temperature and additives on the product were investigated. Crystallization process would be carried out above 160 ℃ for 5 h or more, higher temperature can reduce the reaction time. Additives were used to remove impurities such as Fe 2O 3, ZnMnO 3.10～15 nm pure slightly agglomerated MnZn ferrite crystallites with a narrow grain size distribution were obtained.
基金Project(CHCL0501) supported by Hubei Provincial Open Fund of Key Laboratory of Catalytic Material Science and Technology
文摘Mesoporous cerium-zirconium mixed oxides were prepared by hydrothermal method using cetyl trimethyl ammonium bromide (CTAB) as template. The effects of amount of template, pH value of solution and hydrothermal temperature on mesostructure of samples were systematically investigated. The final products were characterized by XRD, TEM, FT-IR, and BET. The results indicate that all the cerium-zirconium mixed oxides present a meso-structure. At molar ratio of n(CTAB)/n((Ce)+(Zr))= 0.15, pH value of 9, and hydrothermal temperature of 120 ℃, the samples obtained possess a specific surface area of 207.9 m2/g with pore diameter of 3.70 nm and pore volume of 0.19 cm3/g.
基金Project(2008A090300016) supported by Major Science & Technology Special Program of Guangdong Province,China
文摘Micaceous iron oxide （MIO） with a hexagonal flaky shape was prepared by hydrothermal method. The ferric hydroxide used as precursor was obtained by an acidic leaching solution of pyrite cinders reacting with ammonia solution. The optimal experimental conditions for preparing micaceous iron oxide were investigated by orthogonal experiments. Micaceous iron oxide can be successfully prepared when optimal parameters of total iron concentration of 2.0 mol/L, pH value of 8, n（Fe2＋）/n（Fe3＋） of 0.1, mass of seed crystal of 1 g, reaction temperature of 260 ℃ and reaction time of 30 min are applied. X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and selected area electron diffractometry （SAEM） were adopted to characterize the hydrothermal products prepared under optimal conditions. The results indicate that highly crystallized α-Fe2O3 hexagonal flakes, about 1.0-1.5 μm in diameter and 0.1 μm in thickness, are prepared. Furthermore, the quality of micaceous iron oxide prepared can meet the required characteristics of micaceous iron oxide pigments for paints （ISO 10601--2007）.
文摘MnZn ferrite nanoscale particles were synthesized by hydrothermal method. The effects of amount of addition La3+ on the products were discussed. The product was characterized by X-ray diffraction （XRD） and transmission electron microscope （TEM）. The results show that the sample with 0.2% La3+（mass fraction） or without La3+ has only spinel phase, but the sample with mass fraction of La3+ exceeding 0.4% posses second phase besides the spinel one; and the nano-MnZn ferrites change from cube to hexagon when the mass fractions of La3+ is up to （1.2%.） TEM image of the sample with 1.2% La3+ indicates that the homogeneous hexagonal crystal is obtained and the particles are larger than those of undoped; the addition of La3+ has great influence on the crystallization of hydrothermal process and can change the shape of particles and improve their growth. The saturation magnetization of the sample with 1.2% La3+ (2.64 A·m2·kg-1) is lower than that of undoped (17.54 (A·m2·kg-1)) and it behaves superparamagnetically.
基金Project supported by National Key Technologies Research and Development Program for 11th Five-year Plan (No. 2006 BAD10B04)China Geological Survey Project (No. 12120113087700)
文摘The decomposition of K-Feldspar is significant to the development and utilization of K-feldspar as potassium resources. Potassium feldspar powder was decomposed successfully by hydrothermal method using CaO additive. Tobermorite solid and KOH solution were obtained as a result of the hydrothermal decomposition.
文摘Calcium sulfate hemihydrate (CaSO4·0.5H2O, HH) is one of the three most commonly phases of gypsum observed in natural precipitates. Calcium sulfate hemihydrate whisker is a kind of fibriform single crystal with the mean diameter of 1-3 μm and the mean aspect ratio of 30–80. HH whisker was the most promising reinforcement seemed to be calcium sulfate-based due to its high intensity, high corrosion-resistance, good thermal stability, non-poisonous and low price. Thus, HH whiskers combine both reinforcement and low price, may be both effective in improving mechanical performance and extending application area.
基金Project(50872001) supported by the National Natural Science Foundation of ChinaProject(20060357003) supported by Research Fund for the Doctoral Program of Higher Education of ChinaProject(KJ2010A284) supported by the Natural Science Foundation of Anhui Higher Education Institution of China
文摘Undoped and Na-doped ZnO films were deposited by sol-gel method.The effects of sodium incorporation on structure,surface morphology and optical constants of the films were investigated.X-ray diffraction patterns show the hexagonal wurtzite polycrystalline structure and that the sodium incorporation leads to the change in the structural characteristics of ZnO films.The SEM observations show that the surface morphology of the films is affected by the sodium incorporation.The transmission spectra show that the average transmittance of the films is above 85% in the visible range.The absorption edge initially blue-shifts and then red-shifts with the increase of Na doping content.The optical constants of these films were calculated using transmission spectra.Refractive indices of the films in the visible range decrease at first and then increase with increasing Na doping content.
基金Project(KJ2012A045) supported by the Natural Science Foundation of Education Commission of Anhui Province,China
文摘A reduced graphene oxide/Ni(OH)2 composite with excellent supercapacitive performance was synthesized by a facile hydrothermal route without organic solvents or templates used.XRD and SEM results reveal that the nickel hydroxide,which crystallizes into hexagonal β-Ni(OH)2 nanoflakes with a diameter less than 200 nm and a thickness of about 10 nm,is well combined with the reduced graphene oxide sheets.Electrochemical performance of the synthesized composite as an electrode material was investigated by cyclic voltammetry,electrochemical impedance spectroscopy and galvanostatic charge/discharge measurements.Its specific capacitance is determined to be 1672 F/g at a scan rate of 2 mV/s,and 696 F/g at a high scan rate of 50 mV/s.After 2000 cycles at a current density of 10 A/g,the composite exhibits a specific capacitance of 969 F/g,retaining about 86% of its initial capacitance.The composite delivers a high energy density of 83.6 W·h/kg at a power density of 1.0 kW/kg.The excellent supercapacitive performance along with the easy synthesis method allows the synthesized composite to be promising for supercapacitor applications.
基金Project(20070410304) supported by Postdoctoral Foundation of ChinaProject(07JJ3105) supported by Hunan Provincial Natural Science Foundation of China
文摘Properties of hydroxyapatite （HA, Ca10（PO4）6（OH）2）, including bioactivity, biocompatibility, solubility and adsorption could be tailored over wide ranges by the control of particle composition, particle size and morphology. In order to satisfy various applications, well-crystallized pure HA nanoparticles were synthesized at moderate temperatures by hydrotherrnal synthesis, and HA nanoparticles with different lengths were obtained by adding organic additives. X-ray diffractometry （XRD） and Fourier transform infrared （FTIR） spectrometry were used to characterize these nanoparticles, and the morphologies of the HA particles were observed by transmission electron microscopy （TEM）. The results demonstrate that shorter rod-like HA particles can be prepared by adding cetyltrimethylammonium bromide （CTAB）, as the additive of CTAB can block the HA crystal growth along with c-axis. And whisker HA particles are obtained by adding ethylenediamine tetraacetic acid （EDTA）, since EDTA may have effect on the dissolution-repreeipitation process of HA.
基金Project(2001BA901A09)supported by the Key Program of Science and Technology Action of West China Development
文摘Silver-tin oxide powders were synthesized by the hydrothermal method with Ag(NH_3)_2^+ solution and Na_2SnO_3 solution as raw materials and Na_2SO_3 as reductant. The precipitation conditions of Na2SnO3 solution and the reduction conditions of Ag(NH_3)_2^+ were also investigated. The powders prepared were characterized by differential thermal analysis (DTA), X-ray diffraction analysis (XRD), scanning electron microscope (SEM) and energy spectrum analysis. The results show that pH value of the solution is a key parameter in the formation of Sn(OH)_4 precipitate and the reduction reaction of Ag(NH_3)_2^+ can release H+ ions, which results in synchronous precipitation of Sn(OH)_6~2- as Sn(OH)_4. The reduction of Ag(NH_3)_2^+ and precipitation of Na_2SnO_3 occur simultaneously and the coprecipitation of silver and tin oxide is reached by the hydrothermal method. The silver-tin oxide composite powders have mainly flake shape of about 0.3 μm in thickness and there exists homogeneous distribution of tin oxide and silver in the powder synthesized.
基金Projects(CC20120031,CC20110048)supported by Changzhou Science and Technology Innovation Project,China
文摘The CaCu3Ti4O12 xerogels, powders and ceramics were prepared through the sol-gel method using two kinds of organic acid （decanoic acid and decanedioic acid）. The xerogels, powders and ceramics were characterized by the methods of TG-DTG, FT-IR, XRD, SEM and TEM. The dielectric properties of the ceramics were also measured. The results indicated that the powders calcined at 850 ℃ for 2 h are both nanometer scale particles. After sintering, the ceramics mainly consist of the CaCu3Ti4O12 phase. Compared with the powders prepared using monoacid, the particle size of the powders prepared using diacid obviously increases, and the grain size, the relative density and the whole permittivity of the ceramics increase as well. Specially, the ceramic prepared using decanedioic acid has higher relative density （97.3%）, dielectric constant （316 808） and lower dielectric loss （0.242 5） at 30 ℃ （10 kIaz）
基金Project(51202066)supported by the National Natural Science Foundation of ChinaProject(NCET-13-0784)supported by the Program for New Century Excellent Talents in University of China。
文摘Hollow-structured Cu_(0.3)Co_(2.7)O_(4) microspheres have been synthesized by a simple one-pot template-free hydrothermal method with copper sulfate,cobalt acetate and ammonia as raw materials.The products were characterized by powder X-ray diffraction,energy dispersive X-ray analysis,selected area electron diffraction,high-resolution transmission electron microscopy,scanning electron microscopy and BET measurements.The research results show that the hollow Cu_(0.3)Co_(2.7)O_(4) microspheres consist of single-crystalline nanocubes with the diameter of about 20 nm.The formation mechanism of hollow Cu_(0.3)Co_(2.7)O_(4) microspheres is suggested as Ostwald ripening in a solid-solution-solid process,and Cu_(0.3)Co_(2.7)O_(4) microspheres are mesoporous containing two pore sizes of 3.3 and 5.9 nm.The as-prepared Cu_(0.3)Co_(2.7)O_(4) sensors have optimal gas responses to 50×10^(−6) mg/m^(3) C_(2)H_(5)OH at 190℃.
基金Project(50174058)supported by the National Natural Science Foundation of ChinaProject(2011A025)supported by the Glorious Laurel Scholar Program of Guangxi Zhuang Autonomous Region,China
文摘A simple hydrothermal process followed by heat treatment was applied to the preparation of spinel Li1.05Mn1.95O4. In this process, electrolytic manganese dioxide(EMD) and LiOH·H2O were used as starting materials. The physiochemical properties of the synthesized samples were investigated by thermogravimetry-differential scanning calorimetry(TG-DSC), X-ray diffractometry(XRD), and scanning electronic microscopy(SEM). The results show that the hydrothermally synthesized precursor is an essential amorphous. The precursor can be easily transferred to spinel powders with a homogeneous structure and a regularly-shaped morphology by heat treatment. Li1.05Mn1.95O4 powder obtained by heat treating the precursor at 430 °C for 12 h and then calcining at 800 °C for 12 h shows an excellent cycling performance with an initial charge capacity of 118.2 mA·h·g-1 obtained at 0.5C rate and 93.8% of its original value retained after 100 cycles.
基金Projects(13A047,10B054)supported by the Scientific Research Fund of Hunan Provincial Education Department,ChinaProjects(2011GK2002,2011FJ3160)supported by the Planned Science and Technology Project of Hunan Province,China
文摘Li2Fe0.5Mn0.5SiO4 material was synthesized by a citric acid-assisted sol-gel method. The influence of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+) on the electrochemical properties of Li2Fe0.5Mn0.5SiO4 was studied. The final sample was identified as Li2Fe0.5Mn0.5SiO4 with a Pmn21 monoclinic structure by X-ray diffraction analysis. The crystal phases components and crystal phase structure of the Li2Fe0.5Mn0.4SiO4 material were improved as the increase of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+). Field-emission scanning electron microscopy verified that the Li2Fe0.5Mn0.5SiO4 particles are agglomerates of Li2Fe0.5Mn0.5SiO4 primary particles with a geometric mean diameter of 220 nm. The Li2Fe0.5Mn0.5SiO4 sample was used as an electrode material for rechargeable lithium ion batteries, and the electrochemical measurements were carried out at room temperature. The Li2Fe0.5Mn0.5SiO4 electrode delivered a first discharge capacity of 230.1 mAh/g at the current density of 10 mA/g in first cycle and about 162 mAh/g after 20 cycles at the current density of 20 mA/g.
基金Foundation item： National Natural Science Foundation of China （51002051） Fundamental Research Funds for the Cenlxal Universities （WA1014016） Science and Technology Commission of Shanghai Municipality （09520500900）
