A lithium ion conductive solid electrolyte, L20-AI203-TiO2-SiO2-P20s glass with NASICON- type structure have been synthesized and transformed into glass-ceramic through thermal-treatment at various temperatures from 7...A lithium ion conductive solid electrolyte, L20-AI203-TiO2-SiO2-P20s glass with NASICON- type structure have been synthesized and transformed into glass-ceramic through thermal-treatment at various temperatures from 700 to 1 000 ~C for 12 h. The differential scanning calorimetry （DSC）, X-ray diffraction （XRD）, scanning electron microscopy （SEM） and complex impedance techniques were employed to characterize the samples. The experimental results indicated that the capability of glass forming in this system is superior to that of L20-A1203-TiO2-PzO~. The glass has an amorphous structure and resultant glass-ceramic mainly consisting of LiTi2（PO4）3 phases. Impurity phases AIPO4, TiO2, TiP207 and unidentified phase were observed. With the enhanced heat-treatment temperature, grain grew gradually and lithium ion conductivity of glass-ceramics increased accordingly, the related impedance semicircles were depressed gradually and even disappeared, which could be analytically explained by the coordinate action of the ＇Constant phase element＇ （CPE） model and the ＇Concept of Mismatch and Relaxation＇ model （CMR）. When the sample is devitrified at 1 000 ~C, the maximum room temperature lithium ion conductivity comes up to 4.1 x 10-4 S/cm, which is suitable for the application as an electrolyte of all-solid-state lithium batteries.展开更多
We studied the local structure and properties of six-fold coordinated silicon(Si[6]) in BaOSiO2-P2O5 glasses. Nuclear magnetic resonance(NMR) and Raman spectroscopy revealed the existence of sixfold coordinated silico...We studied the local structure and properties of six-fold coordinated silicon(Si[6]) in BaOSiO2-P2O5 glasses. Nuclear magnetic resonance(NMR) and Raman spectroscopy revealed the existence of sixfold coordinated silicon species and network former units(NFUs) in the BaO-SiO2-P2O5 glasses. The glass transition temperature(Tg), which was measured by differential scanning calorimetry, increased rapidly along with the increase of SiO2 from 0 to 10 mol%, then declined and finally increased again, which showed a "Z" trend along with the increase of SiO2 while the density of the glasses showed the opposite trend. When the addition of SiO2 is 16 mol%, Tg decreased to an extremely low value(807.9 K). Besides, the Vickers indentation hardness(Hv) had been significantly enhanced from 4.66 to 6.63 GPa by adding 16 mol% SiO2. Furthermore, the liquid fragility index(m) of the glasses declined slowly firstly and then increased rapidly when the amount of SiO2 is greater than 13 mol%.展开更多
The selective catalytic reduction of NOV with NH3 (NH3-SCR) is a very effective technology to control the emission of NOA, and the thermal stability of NH3-SCR catalyst is very important for removal of NOV from diesel...The selective catalytic reduction of NOV with NH3 (NH3-SCR) is a very effective technology to control the emission of NOA, and the thermal stability of NH3-SCR catalyst is very important for removal of NOV from diesel engines. In this work, V2O5/WO3-TiO2 (VWT) and SiO2- doped V2O5/WO3-TiO2 (VWTSi10)) catalysts were prepared by impregnation method and characterized by Brunauer- Emmett-Teller (BET), X-ray diffraction (XRD), Raman, temperature programmed reduction by hydrogen (H2-TPR), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption by ammonia (NH3- TPD). The doping of SiO2 promotes the thermal stability of V2O5/WO3-TiO? for NH3-SCR significantly. After calcination at 650 °C for 50 h, the operation window of 10% SiO2-doped V2O5/WO3-TiO2 is 220-480 °C, while the maximum NOV conversion on V2O5/WO3-TiO2 is about 77%. The presenee of SiO2 obviously blocks the transformation of TiO2 from anatase to rutile and stabilizes the dispersion of VOv and WO3 on the surface. It is available for the existence of V44 and the amount of surface acid sites increases, which inhabits the NH3 oxidation at the high temperature range and promotes NH3-SCR activity.展开更多
基金National Basic Research Program of China (No.2009CB939704)National Natural Science Foundation of China (Nos.51032005, 60808024)the Fundamental Research Funds for the Central Universities (Wuhan University of Technology)
文摘A lithium ion conductive solid electrolyte, L20-AI203-TiO2-SiO2-P20s glass with NASICON- type structure have been synthesized and transformed into glass-ceramic through thermal-treatment at various temperatures from 700 to 1 000 ~C for 12 h. The differential scanning calorimetry （DSC）, X-ray diffraction （XRD）, scanning electron microscopy （SEM） and complex impedance techniques were employed to characterize the samples. The experimental results indicated that the capability of glass forming in this system is superior to that of L20-A1203-TiO2-PzO~. The glass has an amorphous structure and resultant glass-ceramic mainly consisting of LiTi2（PO4）3 phases. Impurity phases AIPO4, TiO2, TiP207 and unidentified phase were observed. With the enhanced heat-treatment temperature, grain grew gradually and lithium ion conductivity of glass-ceramics increased accordingly, the related impedance semicircles were depressed gradually and even disappeared, which could be analytically explained by the coordinate action of the ＇Constant phase element＇ （CPE） model and the ＇Concept of Mismatch and Relaxation＇ model （CMR）. When the sample is devitrified at 1 000 ~C, the maximum room temperature lithium ion conductivity comes up to 4.1 x 10-4 S/cm, which is suitable for the application as an electrolyte of all-solid-state lithium batteries.
基金Funded by National Natural Science Foundation of China(Nos.51772223,51372180)
文摘We studied the local structure and properties of six-fold coordinated silicon(Si[6]) in BaOSiO2-P2O5 glasses. Nuclear magnetic resonance(NMR) and Raman spectroscopy revealed the existence of sixfold coordinated silicon species and network former units(NFUs) in the BaO-SiO2-P2O5 glasses. The glass transition temperature(Tg), which was measured by differential scanning calorimetry, increased rapidly along with the increase of SiO2 from 0 to 10 mol%, then declined and finally increased again, which showed a "Z" trend along with the increase of SiO2 while the density of the glasses showed the opposite trend. When the addition of SiO2 is 16 mol%, Tg decreased to an extremely low value(807.9 K). Besides, the Vickers indentation hardness(Hv) had been significantly enhanced from 4.66 to 6.63 GPa by adding 16 mol% SiO2. Furthermore, the liquid fragility index(m) of the glasses declined slowly firstly and then increased rapidly when the amount of SiO2 is greater than 13 mol%.
基金financially supported by the National Key Research and Development Program of China (No. 2016YFC0204300)the National High Technology Research and Development Program of China (No. 2015AA034603)+2 种基金the National Natural Science Foundation of China (Nos. 21333003 and 21571061)the "Shu Guang" Project of the Shanghai Municipal Education Commission (No. 12SG29)the Commission of Science and Technology of Shanghai Municipality (No. 15DZ1205305)
文摘The selective catalytic reduction of NOV with NH3 (NH3-SCR) is a very effective technology to control the emission of NOA, and the thermal stability of NH3-SCR catalyst is very important for removal of NOV from diesel engines. In this work, V2O5/WO3-TiO2 (VWT) and SiO2- doped V2O5/WO3-TiO2 (VWTSi10)) catalysts were prepared by impregnation method and characterized by Brunauer- Emmett-Teller (BET), X-ray diffraction (XRD), Raman, temperature programmed reduction by hydrogen (H2-TPR), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption by ammonia (NH3- TPD). The doping of SiO2 promotes the thermal stability of V2O5/WO3-TiO? for NH3-SCR significantly. After calcination at 650 °C for 50 h, the operation window of 10% SiO2-doped V2O5/WO3-TiO2 is 220-480 °C, while the maximum NOV conversion on V2O5/WO3-TiO2 is about 77%. The presenee of SiO2 obviously blocks the transformation of TiO2 from anatase to rutile and stabilizes the dispersion of VOv and WO3 on the surface. It is available for the existence of V44 and the amount of surface acid sites increases, which inhabits the NH3 oxidation at the high temperature range and promotes NH3-SCR activity.
