A series of Cr^(3+)-substituted Na_(1+x)Ti_(2−x)Cr_(x)P_(3)O_(12)(x=0.1,0.2,0.3,0.4,0.5,molar fraction)solid electrolytes were prepared by the solid-phase reaction method.The effects of Cr^(3+)ions on the phase compos...A series of Cr^(3+)-substituted Na_(1+x)Ti_(2−x)Cr_(x)P_(3)O_(12)(x=0.1,0.2,0.3,0.4,0.5,molar fraction)solid electrolytes were prepared by the solid-phase reaction method.The effects of Cr^(3+)ions on the phase composition,microstructure,and electrochemical ion conductivity of Na-based conductors were studied using X-ray powder diffraction,field emission scanning electron microscopy,and AC impedance measurement.The results show that the main crystal phase of NaTi_(2)(PO_(4))_(3) is formed in the solid electrolytes.The substitution of Ti4+sites by 15 at.%Cr^(3+)ions contributes to the enhancement of electrical conductivity,which is attributed to the combined effect of suppressing the formation of impurity phases,broadening ion channels,and improving the bonding degree of grains.Na_(1.3)Ti_(1.7)Cr_(0.3)P_(3)O_(12) electrolyte can obtain the best ionic conductivity of 6.13×10^(−6)S/cm at room temperature,which is 8 times that of the undoped NaTi_(2)(PO_(4))_(3) electrolyte.展开更多
Calcium aluminate clinkers doped with Na2O were synthesized using analytically pure reagents CaCO3, Al2O3, SiO2 and Na2CO3. The effects of Na2O-doping on the formation mechanism of calcium aluminate compounds and the ...Calcium aluminate clinkers doped with Na2O were synthesized using analytically pure reagents CaCO3, Al2O3, SiO2 and Na2CO3. The effects of Na2O-doping on the formation mechanism of calcium aluminate compounds and the crystal property of 12CaO·7Al2O3 (C12A7) cell were studied. The results show that the minerals containing Na2O mainly include 2Na2O·3CaO·5Al2O3 and Na2O·Al2O3, when the Na2O content in clinkers is less than 4.26% (mass fraction). The rest of Na2O is mainly doped in 12CaO·7Al2O3, which results in the decrease of the crystallinity of 12CaO·7Al2O3. The crystallinity of 2Na2O·3CaO·5Al2O3 is also inversely proportional to the Na2O content in clinkers. The formation processes of 2Na2O·3CaO·5Al2O3 and 12CaO·7Al2O3 can be divided into two ways, which are the direct reactions of raw materials and the transformation of CaO·Al2O3, respectively. The simulation shows that the covalency of O-Na bond in Na2O-doped 12CaO·7Al2O3 cell is weaker than those of O-Ca and O-Al bonds. The free energy of the unit cell increases because of Na2O doping, which results in the improvement of chemical activity of 12CaO·7Al2O3. The leaching efficiency of Al2O3 in clinker is improved from 34.81% to 88.17% when the Na2O content in clinkers increases from 0 to 4.26%.展开更多
Systematic studies of the transport properties of La0.67Ca0.33Mn1- FexO3 (x=0?0.3) systems showed that with x increasing Fe-doping content x the resistance increases and the insulator-metal transition temperature move...Systematic studies of the transport properties of La0.67Ca0.33Mn1- FexO3 (x=0?0.3) systems showed that with x increasing Fe-doping content x the resistance increases and the insulator-metal transition temperature moves to lower temperature. For small doping content, the transport property satisfies metal transport behavior below the transition tem- perature, and above the transition temperature it satisfies the small polaron model. This behavior can be explained by Fe3+ doping, which easily forms Fe3+-O2 -Mn4+channel, suppressing the double exchange Mn3+-O2 -Mn4+ channel and enhancing ? ? the spin scattering of Mn ions induced by antiferromagnetic clusters of Fe ions.展开更多
The structural and dielectric properties of Ba0.92Sr0.08Ti0.95Sn0.0503 (BSTS) +x(molar ratio, %) Y^3+ceramics are investigated. Combining the lattice parameters and the distortion of crystal lattice, an alternat...The structural and dielectric properties of Ba0.92Sr0.08Ti0.95Sn0.0503 (BSTS) +x(molar ratio, %) Y^3+ceramics are investigated. Combining the lattice parameters and the distortion of crystal lattice, an alternation of substitution preference of Y^3+ ion for the host cations in perovskite lattice is found. Owing to Y^3- ion entering the A site, the maximum dielectric constant is 5 627 for 1.25% Y^3+-doped samples; when Y^3- ion is more than 1.25%, it tends to occupy the B site in perovskite lattice, causing a drop in the dielectric constant. Owing to the appearance of oxygen vacancy, the optimized dielectric loss is 0.004 for 1.25% Y^3+-doped samples. The thermal stability of BSTS ceramics is significantly improved and the Curie temperature shifts to lower value with the amount of Y2O3 increased, making it a superior candidate for capacitor applications.展开更多
A facile biomolecule-assisted hydrothermal route followed by calcination has been employed for the preparation of monoclinic yttrium oxysulfate hollow spheres doped with other rare-earth ions (Yb3+ and Eu3+ or Er3...A facile biomolecule-assisted hydrothermal route followed by calcination has been employed for the preparation of monoclinic yttrium oxysulfate hollow spheres doped with other rare-earth ions (Yb3+ and Eu3+ or Er3+). The formation of hollow spheres may involve Ostwald ripening. The resulting hybrid materials were used for upconversion applications. The host crystal structure allows the easy co-doping of two different rare-earth metal ions without significantly changing the host lattice. The luminescent properties were affected by the ratio and concentration of dopant rare-earth metal ions due to energy transfer and the symmetry of the crystal field. The type of luminescent center and the crystallinity of samples were also shown to have a significant influence on the optical properties of the as-prepared products.展开更多
A facile strategy is established for constructing composite nanostructure with ultrasmall Pt nanoparticles(NPs) of ~2 nm in diameter being homogeneously embedded in N-doped carbon nanosheets. The strong coordination b...A facile strategy is established for constructing composite nanostructure with ultrasmall Pt nanoparticles(NPs) of ~2 nm in diameter being homogeneously embedded in N-doped carbon nanosheets. The strong coordination between Pt atoms in cisplatin and N atoms in pyrrole contributes to the robust embedding of Pt NP into the N-doped carbon nanosheets after annealing. Such a unique partially-embedding structure facilitates the active site exposure while stabilizing the ultrasmall Pt NPs, leading to the comparable electrochemical activities for hydrogen evolution and oxygen reduction reactions, and substantially improves durability performance compared to that of the state-of-the-art Pt/C(20 wt%).展开更多
Rare earth doping has been widely applied in many functional nanomaterials with desirable properties and functions,which would have a significant effect on the growth process of the materials.However,the controlling s...Rare earth doping has been widely applied in many functional nanomaterials with desirable properties and functions,which would have a significant effect on the growth process of the materials.However,the controlling strategy is limited into high concentration of lanthanide doping,which produces concentration quenching of the lanthanide ion luminescence with an increase in the Ln^(3+)concentration,resulting in lowering the fluorescence quantum yield of lanthanide ion.Herein,for the first time,we demonstrate simultaneous control of the structures and luminescence properties of BaCO_3nanocrystals via a small amount of Tb^(3+)doping strategy.In fact,Tb^(3+)would partially occupy Ba^(2+)sites,resulting in the changes to the structures of the BaCO_3nanocrystals,which is primarily determined by charge modulation,including the contributions from the surfaces of crystal nuclei and building blocks.These structurally modified nanocrystals exhibit tunable luminescence properties,thus emerging as potential candidates for photonic devices such as light-emitting diodes and color displays.展开更多
基金supported by the National Natural Science Foundation of China(No.51972344)the Natural Science Foundation of Hunan Province,China(No.2018JJ3646).
文摘A series of Cr^(3+)-substituted Na_(1+x)Ti_(2−x)Cr_(x)P_(3)O_(12)(x=0.1,0.2,0.3,0.4,0.5,molar fraction)solid electrolytes were prepared by the solid-phase reaction method.The effects of Cr^(3+)ions on the phase composition,microstructure,and electrochemical ion conductivity of Na-based conductors were studied using X-ray powder diffraction,field emission scanning electron microscopy,and AC impedance measurement.The results show that the main crystal phase of NaTi_(2)(PO_(4))_(3) is formed in the solid electrolytes.The substitution of Ti4+sites by 15 at.%Cr^(3+)ions contributes to the enhancement of electrical conductivity,which is attributed to the combined effect of suppressing the formation of impurity phases,broadening ion channels,and improving the bonding degree of grains.Na_(1.3)Ti_(1.7)Cr_(0.3)P_(3)O_(12) electrolyte can obtain the best ionic conductivity of 6.13×10^(−6)S/cm at room temperature,which is 8 times that of the undoped NaTi_(2)(PO_(4))_(3) electrolyte.
基金Projects(51174054,51104041,51374065)supported by the National Natural Science Foundation of ChinaProject(N130402010)supported by the Fundamental Research Funds for the Central Universities of China
文摘Calcium aluminate clinkers doped with Na2O were synthesized using analytically pure reagents CaCO3, Al2O3, SiO2 and Na2CO3. The effects of Na2O-doping on the formation mechanism of calcium aluminate compounds and the crystal property of 12CaO·7Al2O3 (C12A7) cell were studied. The results show that the minerals containing Na2O mainly include 2Na2O·3CaO·5Al2O3 and Na2O·Al2O3, when the Na2O content in clinkers is less than 4.26% (mass fraction). The rest of Na2O is mainly doped in 12CaO·7Al2O3, which results in the decrease of the crystallinity of 12CaO·7Al2O3. The crystallinity of 2Na2O·3CaO·5Al2O3 is also inversely proportional to the Na2O content in clinkers. The formation processes of 2Na2O·3CaO·5Al2O3 and 12CaO·7Al2O3 can be divided into two ways, which are the direct reactions of raw materials and the transformation of CaO·Al2O3, respectively. The simulation shows that the covalency of O-Na bond in Na2O-doped 12CaO·7Al2O3 cell is weaker than those of O-Ca and O-Al bonds. The free energy of the unit cell increases because of Na2O doping, which results in the improvement of chemical activity of 12CaO·7Al2O3. The leaching efficiency of Al2O3 in clinker is improved from 34.81% to 88.17% when the Na2O content in clinkers increases from 0 to 4.26%.
基金Project supported by the National Natural Science Foundation ofChina (No. 10274049) Foundation of the Natural Science of Zhe-jiang Province (Nos. RC015056 and 502122) Science & Tech-nology Development Foundation of the Education Committee of Sh-anghai Municipality (No. 02AK42)and the Shanghai LeadingAcademic Discipline Program (No. 01A16)
文摘Systematic studies of the transport properties of La0.67Ca0.33Mn1- FexO3 (x=0?0.3) systems showed that with x increasing Fe-doping content x the resistance increases and the insulator-metal transition temperature moves to lower temperature. For small doping content, the transport property satisfies metal transport behavior below the transition tem- perature, and above the transition temperature it satisfies the small polaron model. This behavior can be explained by Fe3+ doping, which easily forms Fe3+-O2 -Mn4+channel, suppressing the double exchange Mn3+-O2 -Mn4+ channel and enhancing ? ? the spin scattering of Mn ions induced by antiferromagnetic clusters of Fe ions.
基金Supported by Chinese Doctor Foundation of Ministry of Education of China (No20040056055)
文摘The structural and dielectric properties of Ba0.92Sr0.08Ti0.95Sn0.0503 (BSTS) +x(molar ratio, %) Y^3+ceramics are investigated. Combining the lattice parameters and the distortion of crystal lattice, an alternation of substitution preference of Y^3+ ion for the host cations in perovskite lattice is found. Owing to Y^3- ion entering the A site, the maximum dielectric constant is 5 627 for 1.25% Y^3+-doped samples; when Y^3- ion is more than 1.25%, it tends to occupy the B site in perovskite lattice, causing a drop in the dielectric constant. Owing to the appearance of oxygen vacancy, the optimized dielectric loss is 0.004 for 1.25% Y^3+-doped samples. The thermal stability of BSTS ceramics is significantly improved and the Curie temperature shifts to lower value with the amount of Y2O3 increased, making it a superior candidate for capacitor applications.
文摘A facile biomolecule-assisted hydrothermal route followed by calcination has been employed for the preparation of monoclinic yttrium oxysulfate hollow spheres doped with other rare-earth ions (Yb3+ and Eu3+ or Er3+). The formation of hollow spheres may involve Ostwald ripening. The resulting hybrid materials were used for upconversion applications. The host crystal structure allows the easy co-doping of two different rare-earth metal ions without significantly changing the host lattice. The luminescent properties were affected by the ratio and concentration of dopant rare-earth metal ions due to energy transfer and the symmetry of the crystal field. The type of luminescent center and the crystallinity of samples were also shown to have a significant influence on the optical properties of the as-prepared products.
基金supported by the National Key Basic Research Program of China(2013CB933200)the Natural Science Foundation of Shanghai(16ZR1440600)+1 种基金the State key laboratory of heavy oil processing(SKLOP201402003)the National Natural Science Foundation of China(U1510107)
文摘A facile strategy is established for constructing composite nanostructure with ultrasmall Pt nanoparticles(NPs) of ~2 nm in diameter being homogeneously embedded in N-doped carbon nanosheets. The strong coordination between Pt atoms in cisplatin and N atoms in pyrrole contributes to the robust embedding of Pt NP into the N-doped carbon nanosheets after annealing. Such a unique partially-embedding structure facilitates the active site exposure while stabilizing the ultrasmall Pt NPs, leading to the comparable electrochemical activities for hydrogen evolution and oxygen reduction reactions, and substantially improves durability performance compared to that of the state-of-the-art Pt/C(20 wt%).
基金supported by the National Natural Science Foundation of China (21403189, 21371149) Natural Science Foundation of Hebei Province (B2017203198)+1 种基金China Postdoctoral Science Foundation (2014M551047)Yanshan University Doctoral Foundation (B790)
文摘Rare earth doping has been widely applied in many functional nanomaterials with desirable properties and functions,which would have a significant effect on the growth process of the materials.However,the controlling strategy is limited into high concentration of lanthanide doping,which produces concentration quenching of the lanthanide ion luminescence with an increase in the Ln^(3+)concentration,resulting in lowering the fluorescence quantum yield of lanthanide ion.Herein,for the first time,we demonstrate simultaneous control of the structures and luminescence properties of BaCO_3nanocrystals via a small amount of Tb^(3+)doping strategy.In fact,Tb^(3+)would partially occupy Ba^(2+)sites,resulting in the changes to the structures of the BaCO_3nanocrystals,which is primarily determined by charge modulation,including the contributions from the surfaces of crystal nuclei and building blocks.These structurally modified nanocrystals exhibit tunable luminescence properties,thus emerging as potential candidates for photonic devices such as light-emitting diodes and color displays.