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Effect of sintering temperature on luminescence properties of borosilicate matrix blue–green emitting color conversion glass ceramics 被引量:1
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作者 Qiao-Yu Zheng Yang Li +3 位作者 Wen-Juan Wu Ming-Ming Shi Bo-Bo Yang Jun Zou 《Chinese Physics B》 SCIE EI CAS CSCD 2019年第10期550-555,共6页
The color conversion glass ceramics which were made of borosilicate matrix co-doped(SrBaSm)Si2O2N2:(Eu^3+Ce^3+) blue-green phosphors were prepared by two-step method in co-sintering. The change in luminescence propert... The color conversion glass ceramics which were made of borosilicate matrix co-doped(SrBaSm)Si2O2N2:(Eu^3+Ce^3+) blue-green phosphors were prepared by two-step method in co-sintering. The change in luminescence properties and the drift of chromaticity coordinates(CIE) of the(SrBaSm)Si2O2N2:(Eu^3+Ce^3+) blue-green phosphors and the color conversion glass ceramics were studied in the sintering temperature range from 600℃ to 800℃. The luminous intensity and internal quantum yield(QY) of the blue-green phosphors and glass ceramics decreased with the sintering temperature increasing. When the sintering temperature increased beyond 750℃, the phosphors and the color conversion glass ceramics almost had no peak in photoluminescence(PL) and excitation(PLE) spectra. The results showed that the blue-green phosphors had poor thermal stability at higher temperature. The lattice structure of the phosphors was destroyed by the glass matrix and the Ce^3+ in the phosphors was oxidized to Ce^4+, which further caused a decrease in luminescent properties of the color conversion glass ceramics. 展开更多
关键词 (SrBaSm)si2o2n2:(Eu^3+ce^3+) PHoSPHoRS blue-green color conversion glass ceramic luminescent intensity thermal quenching effects sintering temperature
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Preparation and Properties of Si2N2O Ceramics for Microwave Sintering Furnaces
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作者 ZHENG Han LI Wei +4 位作者 DU Jiaolong LI Hongxia LIU Guoqi CHEN Zihao CHEN Yongqiang 《China's Refractories》 CAS 2020年第2期42-46,共5页
Si2N2O ceramics were prepared using amorphous Si3N4 as the raw material and Li2CO3 as the sintering additive through vacuum multi-stage sintering.The influence of the Li2CO3 addition(0%,1%,2%,3%,and 5%,by mass)on the ... Si2N2O ceramics were prepared using amorphous Si3N4 as the raw material and Li2CO3 as the sintering additive through vacuum multi-stage sintering.The influence of the Li2CO3 addition(0%,1%,2%,3%,and 5%,by mass)on the phase composition,the microstructure,the porosity,the mechanical properties,the dielectric constant and the tangent of the dielectric loss angle of the porous Si2N2O ceramics was investigated.The results reveal that a suitable addition of Li2CO3 can promote the generation of Si2N2O but excessive or inadequate Li2CO3 causes decomposition of Si2N2O ceramics.The prepared porous Si2N2O ceramics have good mechanical properties,good thermal shock resistance,and low dielectric properties,which have excellent potential for application in microwave sintering furnaces. 展开更多
关键词 si2n2o porous ceramics lithium carbonate vacuum sintering dielectric properties microwave sintering
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Experimental Investigation of the Flame Propagation and Flashback Behavior of a Green Propellant Consisting of N2O and C2H4 被引量:6
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作者 Lukas Werling Felix Lauck +3 位作者 Dominic Freudenmann Nicole Rocke Helmut Ciezki Stefan Schlechtriem 《Journal of Energy and Power Engineering》 2017年第12期735-752,共18页
Regarding the research on alternatives for monopropellant hydrazine, several so called green propellants are currently under investigation or qualification. Aside others, the DLR Institute of Space Propulsion investig... Regarding the research on alternatives for monopropellant hydrazine, several so called green propellants are currently under investigation or qualification. Aside others, the DLR Institute of Space Propulsion investigates a N20/C2I-I4 premixed green propellant. During the research activities, flashback from the rocket combustion chamber into the feeding system has been identified as a major challenge when using the propellant mixture. This paper shows the results of ignition experiments conducted in a cylindrical, optical accessible ignition chamber. During the ignition and flame propagation process, pressure, temperature and high-speed video data were collected. The high speed video data were used to analyze the flame propagation speed. The obtained propagation speed was about 20 rn/s at ignition, while during further propagation of the flame speeds of up to 120 m/s were measured. Additionally, two different porous materials as flame arresting elements were tested: Porous stainless steel and porous bronze material. For both materials Peclet numbers for flashback were derived. The critical Peclet number for the sintered bronze material was around 20, while for the sintered stainless steel the critical Peclet number seems to be larger than 40. Due to the test results, sintered porous materials seem to be suitable as flashback arresters. 展开更多
关键词 Green rocket propellants ignition flame flashback n2o c2H4 premixed gases flashback an'esters porous materials.
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Correlations between Mineral Nitrogen Contents and Vertical Distribution of N20 Emission Potentials in Tropical Peat Soils Transformed into Oil Palm Plantations in Sarawak, Malaysia
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作者 Sharon Yu Ling Lau Yasuyuki Hashidoko +2 位作者 Naoki Takahashi Ryusuke Hatano Lulie Melling 《Journal of Agricultural Science and Technology(B)》 2014年第9期691-700,共10页
Tropical peat swamp forest beds that have been reclaimed for agricultural use are generally an active source of nitrous oxide (N2O) efflux, however, the mechanism by which reclaimed tropical peat soils promote the e... Tropical peat swamp forest beds that have been reclaimed for agricultural use are generally an active source of nitrous oxide (N2O) efflux, however, the mechanism by which reclaimed tropical peat soils promote the emergence of N2O emitters in soil microbial communities remains unclear. The purpose of this study was to reveal the vertical distribution of N2O emission potential and its correlation with mineral nitrogen contents in reclaimed soils. Using a culture-based N2O emission assay, the N2O emission potentials of soil at various depths (0-450 cm) were investigated in two oil palm plantations in Sarawak, Malaysia, which had elapsed times of two years (E2Y) and 10 years (El 0Y) after deforestation, respectively. On the basis of the relationship between the vertical profiles of N2O emission potentials and the contents of mineralized nitrogen in the peat soils at various depths, the impact of land management on soil microbial communities was discussed. The peat soil at plantation site E2Y showed a trend of high N2O production in deep layers (200-400 cm), whereas the older plantation site E10Y showed considerably more active N2O emission in shallow soil (10-50 cm). N2O emission potentials among the soil microbial communities at different soil depths at the E10Y site showed positive correlations with NO3- and NH4+ contents, whereas, soils obtained from the E2Y site had N2O emission potentials that were inversely proportional to the contents of NO3-. This contrasting vertical correlation between N2O-emitting potentials and mineralized nitrogen contents in bulk soils suggests that active N2O emission in deep soil at the E2Y site has maintained the original carbon-nitrogen (C/N) ratio of the peat soil, whereas at EIOY, such a regulatory system has been lost due to advanced soil degradation, leading to dynamic changes in the nitrogen cycle in shallow soil. 展开更多
关键词 n2o emitters tropical peat soil vertical n20 emission potential c/n ratio oil palm plantation.
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Fabrication of Fine-Grained Si_3N_4-Si_2N_2O Composites by Sintering Amorphous Nano-sized Silicon Nitride Powders 被引量:4
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作者 骆俊廷 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2006年第3期97-99,共3页
Si3N4-Si2N2O composites were fabricated with amorphous nano-sized silicon nitride powders by the liquid phase sintering ( LPS ). The Si2 N2O phase was generated by an in-situ reaction 2 Si3 N4 ( s ) + 1.5 02 ( g... Si3N4-Si2N2O composites were fabricated with amorphous nano-sized silicon nitride powders by the liquid phase sintering ( LPS ). The Si2 N2O phase was generated by an in-situ reaction 2 Si3 N4 ( s ) + 1.5 02 ( g ) = 3 Si2 N2O ( s ) + N2 ( g ) . The content of Si2 N2 O phase up to 60% in the volume was obtained at a sintering temperature of 1 650℃ and reduced when the sintering temperature increased or decreased, indicating the reaction is reversible. The mass loss, relative density and average grain size increased with increasing the sintering temperature. The average grain size was less than 500 nm when the sintering temperature was below 1 700 ℃. The sintering procedure contains a complex crystallization and a phase transition : amorphous silicon nitride→equiaxial α- Si3 N4→ equiaxial β- Si3 N4→ rod- like Si2 N2O→ needle- like β- Si3N4 . Small round-shaped β→ Si3 N4 particles were entrapped in the Si2 N2O grains and a high density of staking faults was situated in the middle of Si2 N2O grains at a sintering temperature of 1 650 ℃. The toughness inereased from 3.5 MPa·m^1/2 at 1 600 ℃ to 7.2 MPa· m^1/2 at 1 800 ℃ . The hardness was as high as 21.5 GPa (Vickers) at 1 600 ℃ . 展开更多
关键词 si3n4-si2n2o composite in-situ reaction amorphous nano-sized silicon nitride
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Cr2O3催化氮化制备Si3N4/SiC耐火材料及其性能 被引量:3
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作者 韩磊 赵万国 +3 位作者 李发亮 张俊 曾渊 张海军 《机械工程材料》 CAS CSCD 北大核心 2018年第10期72-76,共5页
以SiC粉和硅粉为原料,原位合成的Cr_2O_3为催化剂,采用催化氮化法制备了Si_3N_4/SiC耐火材料,研究了催化剂用量及氮化温度对耐火材料物相组成、微观形貌、物理性能和力学性能的影响。结果表明:当氮化温度为1 673K,Cr_2O_3含量(与硅粉质... 以SiC粉和硅粉为原料,原位合成的Cr_2O_3为催化剂,采用催化氮化法制备了Si_3N_4/SiC耐火材料,研究了催化剂用量及氮化温度对耐火材料物相组成、微观形貌、物理性能和力学性能的影响。结果表明:当氮化温度为1 673K,Cr_2O_3含量(与硅粉质量之比,下同)为3%时,硅粉完全氮化,耐火材料主要由颗粒状SiC和晶须状α-Si_3N_4、β-Si_3N_4等组成;随着Cr_2O_3含量的增加,Si_3N_4晶须的数量增多,长度增大,耐火材料变得致密;随氮化温度的升高,耐火材料的抗折强度和耐压强度均增大,当氮化温度为1 673K、Cr_2O_3含量为3%时,抗折强度和耐压强度均最大,分别为34MPa和132MPa。 展开更多
关键词 si3n4/sic耐火材料 cr2o3催化氮化 si3n4晶须 力学性能
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Mechanical and thermodynamic properties of the monoclinic and orthorhombic phases of SiC_2N_4 under high pressure from first principles
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作者 苗楠茜 濮春英 +4 位作者 何朝政 张飞武 卢成 卢志文 周大伟 《Chinese Physics B》 SCIE EI CAS CSCD 2014年第12期382-389,共8页
First principles calculations are preformed to systematically investigate the electronic structures, elastic and thermodynamic properties of the monoclinic and orthorhombic phases of Si C2N4 under pressure. The calcul... First principles calculations are preformed to systematically investigate the electronic structures, elastic and thermodynamic properties of the monoclinic and orthorhombic phases of Si C2N4 under pressure. The calculated structural parameters and elastic moduli are in good agreement with the available theoretical values at zero pressure. The elastic constants of the two phases under pressure are calculated by stress–strain method. It is found that both phases satisfy the mechanical stability criteria within 60 GPa. With the increase of pressure, the degree of the anisotropy decreases rapidly in the monoclinic phase, whereas it remains almost constant in the orthorhombic phase. Furthermore, using the hybrid density-functional theory, the monoclinic and orthorhombic phases are found to be wide band-gap semiconductors with band gaps of about 2.85 e V and 3.21 e V, respectively. The elastic moduli, ductile or brittle behaviors, compressional and shear wave velocities as well as Debye temperatures as a function of pressure in both phases are also investigated in detail. 展开更多
关键词 si c2n4 density functional theory Debye temperature elastic anisotropy
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Space Group of Aquaimidazolemaleatozinc, [(H_2O)(C_3H_4N_2)(O_2CCH=CHCO_2Zn)]_n
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作者 NG Seik Weng 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第1期121-121,共1页
The space group of [(H2O)(C3H4N2)(O2CCH=CHCO2Zn)]n, which was originally described in the acentric Pc space group (Liu et al., Chin. J. Struct. Chem. 2004, 23, 160~163), is re-described in the centric P21/c space g... The space group of [(H2O)(C3H4N2)(O2CCH=CHCO2Zn)]n, which was originally described in the acentric Pc space group (Liu et al., Chin. J. Struct. Chem. 2004, 23, 160~163), is re-described in the centric P21/c space group. 展开更多
关键词 ccH o2ccH=cHco2Zn Space Group of Aquaimidazolemaleatozinc o2ccH c3H4n2 H2o
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Probing into Surface Sites of Fresh Mo_2N/Al_2O_3,Mo_2C/Al_2O_3 and MoP/Al_2O_3 Catalysts by CO Adsorption and In Situ FT-IR Spectroscopy 被引量:1
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作者 Zhang Jing Wu Weicheng +1 位作者 Yan Song Zhang Dan 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2010年第4期43-45,共3页
The surface nature of fresh Mo2N/Al2O3, Mo2C/Al2O3 and/MoP/Al2O3 catalysts, which were synthesized directly in the IR cell to avoid passivation, were characterized by in situ IR spectroscopy with CO as a probe molecul... The surface nature of fresh Mo2N/Al2O3, Mo2C/Al2O3 and/MoP/Al2O3 catalysts, which were synthesized directly in the IR cell to avoid passivation, were characterized by in situ IR spectroscopy with CO as a probe molecule. CO adsorbed on fresh catalysts showed characteristic IR bands at 2045 cm-1 for Mo2N/Al2O3 catalyst, 2054 cm-1 for MozC/Al2O3 catalyst and 2037 cm-1 for MoP/Al2O3 catalyst, respectively. A strong band at 2200 cm-1 for Mo2N/Al2O3 catalyst, which could be ascribed to NCO species formed when CO reacted upon surface active nitrogen atoms, and a weak band at 2196 cm-1 for Mo2C/Al2O3 catalyst, which could be attributed to CCO species, were also detected. CO adsorbed on fresh Mo2N/Al2O3 catalyst, Mo2C/Al2O3 catalyst and MoP/Al2O3 catalyst, showed strong molecular adsorption, just like noble metals. Our experimental results are bolstered by direct IR evidence demonstrating the similarity in surface electronic property between the fresh Mo2N/Al2O3, Mo2C/Al2O3 and MoP/Al2O3 catalysts and noble metals. 展开更多
关键词 Mo2c/Al2o3 catalyst Mo2n/Al2o3 catalyst Mo2P/Al2o3 catalyst FT-IR co
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SiC晶须和Ti(C,N)颗粒协同增韧Al_2O_3陶瓷刀具的研究 被引量:13
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作者 兰俊思 丁培道 黄楠 《材料科学与工程学报》 CAS CSCD 北大核心 2004年第1期59-64,共6页
采用热压工艺烧结制备了SiCW Ti(C ,N) Al2 O3(Y2 O3)陶瓷刀具复合材料。研究了不同烧结温度(16 0 0~ 175 0℃ )下 ,材料的致密度和力学性能 (断裂韧性KIC ,维氏硬度HV和抗弯强度σf)随晶须含量 (10 %~4 0 % )的变化关系 ;探讨了SiC... 采用热压工艺烧结制备了SiCW Ti(C ,N) Al2 O3(Y2 O3)陶瓷刀具复合材料。研究了不同烧结温度(16 0 0~ 175 0℃ )下 ,材料的致密度和力学性能 (断裂韧性KIC ,维氏硬度HV和抗弯强度σf)随晶须含量 (10 %~4 0 % )的变化关系 ;探讨了SiC晶须和Ti(C ,N)颗粒对Al2 O3基体的协同增韧机理。同时与SiCW Al2 O3陶瓷及Ti(C ,N) Al2 O3陶瓷作对比研究。结果表明 :SiCW Ti(C ,N) Al2 O3(Y2 O3)陶瓷材料在 175 0℃ ,晶须含量为 2 0 %时获得最佳的综合力学性能 :KIC =7 11MPa m1 2 ,HV =2 1 16GPa ,σf=82 0MPa ;明显高于SiCW 含量为 2 0 %的SiCW Al2 O3陶瓷和不加晶须的Ti(C ,N) Al2 O3陶瓷。第三相Ti(C ,N)颗粒的加入与晶须一起产生明显的迭加增韧效果 ,而且对SiCW 的各种增韧机制起到了促进作用。 展开更多
关键词 sic晶须 TI(c n) Al2o3 陶瓷刀具 热压工艺 力学性能 致密度 复合材料
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Nano-sized carboxylates as anode materials for rechargeable lithium-ion batteries 被引量:2
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作者 Xiaoyan Wu Jie Ma +2 位作者 Yong-Sheng Hu Hong Li Liquan Chen 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2014年第3期269-273,共5页
Nano-sized caiboxylales Na2C7H3NO4 and Na2C6H2N2O4 were prepared and investigated as anode materials for lithium-ion batteries.Both carboxylates exhibit high reversible capacities around 190 mAh/g above a cut-off volt... Nano-sized caiboxylales Na2C7H3NO4 and Na2C6H2N2O4 were prepared and investigated as anode materials for lithium-ion batteries.Both carboxylates exhibit high reversible capacities around 190 mAh/g above a cut-off voltage of 0.8 V vs.Li+/Li.potentially improving the safety of the batteries.In addition,good rate performance and long cycle life of these carboxylates make them promising candidates as anode materials for lithium-ion batteries. 展开更多
关键词 cARBoXYLATES na2c7H3no4 na2c6H2n2o4 AnoDE lithium-ion batteries
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Si_3X_n(X=C,O,N;n=1,2)团簇的密度泛函研究 被引量:4
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作者 李兵 齐凯天 盛勇 《原子与分子物理学报》 CAS CSCD 北大核心 2008年第4期901-906,共6页
使用密度泛函理论(DFT)的杂化密度泛函B3LYP方法在6-31G*基组水平上对Si3Xn(X=C,O,N;n=1,2)团簇各种可能的构型进行几何结构优化,预测了各团簇的最稳定结构.并对最稳定结构的电子结构、振动特性、成键特性和电荷特性等进行了理论研究.... 使用密度泛函理论(DFT)的杂化密度泛函B3LYP方法在6-31G*基组水平上对Si3Xn(X=C,O,N;n=1,2)团簇各种可能的构型进行几何结构优化,预测了各团簇的最稳定结构.并对最稳定结构的电子结构、振动特性、成键特性和电荷特性等进行了理论研究.结果表明团簇的几何结构都是平面结构,通常Si3X2出现是Si-X键,较少出现X-X键;而Si3X中出现Si-X键和Si-Si键共存,Si3Xn(X=C,O,N;n=1,2)团簇的电荷布局分布表明这种电荷转移的作用使得团簇中所有X原子呈负电性,Si原子显正电性.处于不同位置的Si原子呈不同大小布局数,而且由于Si3X2的对称性,2个X负电性相同. 展开更多
关键词 si3Xn(X=c o n n=1 2)团簇 密度泛函理论 结构与性质
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Charge trapping behavior and its origin in Al_2O_3/SiC MIS system
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作者 刘新宇 王弋宇 +6 位作者 彭朝阳 李诚瞻 吴佳 白云 汤益丹 刘可安 申华军 《Chinese Physics B》 SCIE EI CAS CSCD 2015年第8期523-528,共6页
Charge trapping behavior and its origin in Al2O3/SiC MOS structure are investigated by analyzing the capacitance–voltage(C–V) hysteresis and the chemical composition of the interface. The C–V hysteresis is measured... Charge trapping behavior and its origin in Al2O3/SiC MOS structure are investigated by analyzing the capacitance–voltage(C–V) hysteresis and the chemical composition of the interface. The C–V hysteresis is measured as a function of oxide thickness series for an Al2O3/SiC MIS capacitor. The distribution of the trapped charges, extracted from the C–V curves, is found to mainly follow a sheet charge model rather than a bulk charge model. Therefore, the electron injection phenomenon is evaluated by using linear fitting. It is found that most of the trapped charges are not distributed exactly at the interface but are located in the bulk of the Al2O3 layers, especially close to the border. Furthermore, there is no detectable oxide interface layer in the x-ray photoelectron spectroscope(XPS) and transmission electron microscope(TEM)measurements. In addition, Rutherford back scattering(RBS) analysis shows that the width of the Al2O3/SiC interface is less than 1 nm. It could be concluded that the charge trapping sites in Al2O3/SiC structure might mainly originate from the border traps in Al2O3 film rather than the interface traps in the interfacial transition layer. 展开更多
关键词 AL2o3 si c charge trapping sites InTERFAcE
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Two New C-glucoside Flavonoids from Leaves of Crataegus pinnatifida Bge.var.major N.E.Br. 被引量:4
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作者 PeiChengZHANG SuiXuXu 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第4期337-340,共4页
Two new C-glucoside flavonoids, namely 8-C-b-D-(2-O-acetyl) glucofuranosyl apigenin and 3-O-acetylvitexin, were isolated from leaves of Crataegus pinnatifida Bge. var. major N. E. Br.. Their structures were elucidated... Two new C-glucoside flavonoids, namely 8-C-b-D-(2-O-acetyl) glucofuranosyl apigenin and 3-O-acetylvitexin, were isolated from leaves of Crataegus pinnatifida Bge. var. major N. E. Br.. Their structures were elucidated by the spectroscopic means and chemical evidence. 展开更多
关键词 crataegus pinnatifida Bge. var. major n. E. Br. RoSAcEAE 8-c-b-D-(2-o-acetyl) gluco furanosyl apigenin 3-o-acetylvitexin.
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一种二帽pseudo-Keggin结构簇合物[HN(C_2H_5)_3]_3[N(C_2H_5)_3]_2[Mo_8~ⅣMo_4~ⅤV_2~ⅣO_(38)(PO_4)]的水热合成、结构和性质研究 被引量:2
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作者 崔小兵 林之恩 杨国昱 《无机化学学报》 SCIE CAS CSCD 北大核心 2003年第1期86-90,共5页
The novel polyoxometalate, 32[Mo8ⅣMo4ⅤV2ⅣO38(PO4)], was synthesized and characterized by elementary analysis, EPR, IR spectra and X ray diffraction. The compoundcrystallizes in triclinic system, space group with a=... The novel polyoxometalate, 32[Mo8ⅣMo4ⅤV2ⅣO38(PO4)], was synthesized and characterized by elementary analysis, EPR, IR spectra and X ray diffraction. The compoundcrystallizes in triclinic system, space group with a= 1.41999(2)nm, b=1.43467(2)nm, c=1.694610(10)nm, α=95.7250(10)°, β=92.2110(10)°, γ=92.6060(10)°, V=3.42829(7)nm3, Z=2, Dc=2.388g·cm-3, Mr=2465.10g·mol-1, μ=2.489mm-1, F(000)=2388, R1=0.0584, wR2=0.1461, S=1.164. The heteropolyanion is a bi capped pseudo Keggin complex. CCDC: 186645. 展开更多
关键词 二帽pseudo-Keggin结构 簇合物 [Hn(c2H5)3]3[n(c2H5)3]2[Mo^Ⅳ8Mo^Ⅴ4V^Ⅳ2o38(Po4)] 性质 金属氧簇 水热合成 晶体结构
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超薄Si_3N_4/SiO_2(N/O)stack栅介质及器件
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作者 林钢 徐秋霞 《Journal of Semiconductors》 EI CAS CSCD 北大核心 2005年第1期115-119,共5页
成功制备了EOT(equivalentoxidethickness)为 2 1nm的Si3 N4/SiO2 (N/O)stack栅介质 ,并对其性质进行了研究 .结果表明 ,同样EOT的Si3 N4/SiO2 stack栅介质和纯SiO2 栅介质比较 ,前者在栅隧穿漏电流、抗SILC性能、栅介质寿命等方面都... 成功制备了EOT(equivalentoxidethickness)为 2 1nm的Si3 N4/SiO2 (N/O)stack栅介质 ,并对其性质进行了研究 .结果表明 ,同样EOT的Si3 N4/SiO2 stack栅介质和纯SiO2 栅介质比较 ,前者在栅隧穿漏电流、抗SILC性能、栅介质寿命等方面都远优于后者 .在此基础上 ,采用Si3 N4/SiO2 stack栅介质制备出性能优良的栅长为 0 12 μm的CMOS器件 ,器件很好地抑制了短沟道效应 .在Vds=Vgs=± 1 5V下 ,nMOSFET和pMOSFET对应的饱和电流Ion分别为5 84 3μA/ μm和 - 2 81 3μA/ μm ,对应Ioff分别是 8 3nA/ μm和 - 1 3nA/ μm . 展开更多
关键词 超薄si3n4/sio2(n/o)stack栅介质 栅隧穿漏电流 siLc特性 栅介质寿命 cMoS器件
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(C_4H_(10)N_2H)_3HSiMo_(12)O_(40)纳米颗粒的摩擦学研究
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作者 段天宝 曲黎 叶文玉 《应用化工》 CAS CSCD 2006年第11期867-870,共4页
在醇-水体系中,以H4SiMo12O40和哌嗪为原料制备了组成为(C4H10N2H)3HSiMo12O40如的纳米颗粒,以透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线粉末衍射仪(XRD)、傅立叶变换红外光谱仪(FT-IR)、紫外可见分光光度计(UV)... 在醇-水体系中,以H4SiMo12O40和哌嗪为原料制备了组成为(C4H10N2H)3HSiMo12O40如的纳米颗粒,以透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线粉末衍射仪(XRD)、傅立叶变换红外光谱仪(FT-IR)、紫外可见分光光度计(UV)、热分析仪(TG—DTA)等测试手段,对纳米颗粒的形貌、组成和结构进行了表缸,并在机械式四球长时抗磨损试验机上考察了其摩擦学性能。分散型实验结果表明,化合物在有机溶剂中良好分散(除乙醚外),红外/紫外光谱和x射线粉末衍射表明,所合成的纳米颗粒具有杂多酸Keggin骨架结构无机核,透射电镜分析表明,颗粒平均粒径约为10nm,热分析显示分解温度范围为200-425℃,作为新型有机/无机复合纳米润滑油添加剂,最佳添加浓度为0.35%时,在测试条件为负荷294N,时间30min,转速1450r/min条件下,使磨斑直径减小22.7%,摩擦系数减小14%。 展开更多
关键词 (c4H10n2H)3HsiMo12o40 KEGGIn结构 纳米颗粒 摩擦性能
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Ce^(3+)/Eu^(2+)共掺Ca_3Si_2O_4N_2荧光粉的光学特性 被引量:2
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作者 陈鸿 李晨霞 +1 位作者 华有杰 徐时清 《发光学报》 EI CAS CSCD 北大核心 2013年第10期1324-1327,共4页
采用高温固相法制备了一种新型的白光LED用Ca3Si2O4N2∶Eu2+,Ce3+,K+荧光粉。利用X射线衍射仪对样品的物相结构进行了分析,结果表明:Ce3+和K+离子的掺杂没有改变Ca3Si2O4N2∶Eu2+荧光粉的主晶相。利用荧光光谱仪对样品的发光性能进行了... 采用高温固相法制备了一种新型的白光LED用Ca3Si2O4N2∶Eu2+,Ce3+,K+荧光粉。利用X射线衍射仪对样品的物相结构进行了分析,结果表明:Ce3+和K+离子的掺杂没有改变Ca3Si2O4N2∶Eu2+荧光粉的主晶相。利用荧光光谱仪对样品的发光性能进行了测试,发现样品在355 nm激发下得到的发射光谱为峰值位于505 nm的单峰,是Eu2+离子5d-4f电子跃迁引起的。Ca3Si2O4N2∶Eu2+荧光粉通过Ce3+和K+离子的掺杂,发光明显增强。当Ce3+的摩尔分数为1%时,荧光粉的发光强度达到最大值,是单掺Eu2+离子荧光粉发光强度的168%。通过光谱重叠的方法计算Ce3+→Eu2+能量传递临界的距离为2.535 nm。 展开更多
关键词 ca3si2o4n2∶Eu2+ ce3+ 荧光粉 能量转移
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二维网状结构双核配合物[Ca_2(C_(10)H_8N_2O_4)_2(DMSO)_2(H_2O)_4]·2DMSO的合成、热分解及晶体结构 被引量:11
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作者 曹文凯 何水样 +4 位作者 赵建社 杨锐 史启祯 王大奇 窦建民 《化学学报》 SCIE CAS CSCD 北大核心 2003年第10期1612-1617,共6页
以 2 羰基丙酸水杨酰腙 (C10 H10 N2 O4)作为配体与碳酸钙在水中反应 ,在DMF (N ,N 二甲基甲酰胺 )和DMSO (二甲基亚砜 )的混合溶剂中培养了单晶 ,其组成为 [Ca2 (C10 H8N2 O4) 2 (DMSO) 2 (H2 O) 4 ]·2DMSO [C10 H8N2 O2 -4为 2 ... 以 2 羰基丙酸水杨酰腙 (C10 H10 N2 O4)作为配体与碳酸钙在水中反应 ,在DMF (N ,N 二甲基甲酰胺 )和DMSO (二甲基亚砜 )的混合溶剂中培养了单晶 ,其组成为 [Ca2 (C10 H8N2 O4) 2 (DMSO) 2 (H2 O) 4 ]·2DMSO [C10 H8N2 O2 -4为 2 羰基丙酸水杨酰腙负离子 ] .测定了单晶的结构 ,该单晶为黄色 ,属单斜晶系 ,空间群为P2 (1) /c,晶胞参数a =1 0 63 4 (3 )nm ,b =1 70 3 5(5)nm ,c =1 2 183 (3 )nm ,β=10 6 180 (5)° ,V =2 1192 (10 )nm3,Dc=1 412Mg·m- 3 ,Z =2 ,F(0 0 0 ) =944,μ =0 53 4mm- 1,GOF =0 867.所测单晶是以 2 羰基丙酸水杨酰腙羧基上的一个氧原子作为桥联的双核钙 (II)配合物 ,两个Ca2 + 均处于五角双锥的七配位环境中 ,锥底为配体 2 羰基丙酸水杨酰腙中的三个配位原子 ,以及另一 2 羰基丙酸水杨酰腙羧基上的桥联氧原子和一个水分子的配位氧原子 ,锥顶为一配位水和一配位的DMSO分子 ,即溶剂DMSO也参与了配位 ,从晶胞结构看 ,晶体中除配位的DMSO分子外 ,还有自由的DMSO溶剂分子 ,它们与配位水以氢键连接存在于晶格之中 ,在空间形成了二维网状结构 .通过TG 展开更多
关键词 二维网状结构 双核配合物 [ca2(c10H8n2o4)2(DMSo)2(H2o)4] 2DMSo 合成 热分解 晶体结构 二维网状结构双核配合物[ca2(c10H8n2o4)2(DMSo)2(H2o)4]·2DMSo的合成、热分解及晶体结构
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鼓形有机锡氧杂环羧酸簇合物[PhCH_2Sn(O)(O_2CC_4H_3S)]_6·2CH_2Cl_2 和 [PhCH_2Sn(O)(O_2CC_3H_2NO)]_6·2CH_2Cl_2的合成和晶体结构 被引量:17
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作者 尹汉东 王传华 +1 位作者 马春林 房海霞 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2003年第6期958-963,共6页
利用三苄基氧化锡与 2 -噻吩甲酸和 2 -唑甲酸反应 ,合成了六聚体苄基锡氧 2 -噻吩甲酸酯 (1 )和六聚体苄基锡氧 2 -唑甲酸酯 (2 )鼓形簇合物 .通过元素分析、红外光谱和 X射线单晶衍射对其结构进行了表征 .测试结果表明 :化合物 1... 利用三苄基氧化锡与 2 -噻吩甲酸和 2 -唑甲酸反应 ,合成了六聚体苄基锡氧 2 -噻吩甲酸酯 (1 )和六聚体苄基锡氧 2 -唑甲酸酯 (2 )鼓形簇合物 .通过元素分析、红外光谱和 X射线单晶衍射对其结构进行了表征 .测试结果表明 :化合物 1属三斜晶系 ,空间群 P1 ,a=1 . 2 76 0 (3) nm,b=1 .30 5 6 (3) nm,c=1 .334 3(3) nm,α=1 0 5 .6 5 (3)°,β=96 .2 7(3)°,γ=97.2 0 (3)°,Z=1 ,V=2 .0 997(7) nm3 ,Dc=1 .80 9g/ cm3 ,μ=2 .0 97mm- 1 ,F(0 0 0 ) =1 1 1 6 ,R=0 .0 6 5 1 ,w R=0 .1 2 92 .化合物 2属三斜晶系 ,空间群 P1 ,a=1 .2 2 4 0 (4 ) nm,b=1 .36 73(4 ) nm,c=1 .374 4(4 ) nm,α=1 0 7.76 0 (4 )°,β=98.0 6 9(5 )°,γ=91 .4 80(5 )°,Z=2 ,V=2 .1 6 31 (1 2 ) nm3 ,Dc=3.373g/ cm3 ,μ=3.799mm- 1 ,F (0 0 0 ) =2 1 36 ,R=0 .0 382 ,w R=0 .0 79.它们均为鼓形簇状结构 ,锡原子呈畸变的八面体构型 .化合物 1通过分子间 S… S近距离作用 ,形成一维链状结构 . 展开更多
关键词 鼓形有机锡氧杂环羧酸簇合物 [PhcH2Sn(o)(o2cc4H3S)]6·2cH2c12 [PhcH2Sn(o)(o2cc3H2n0)]6·2cH2cl2 合成 晶体结构 2-噻吩甲酸 2-噁唑甲酸 三苄基氧化锡
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